首页>美国卫生研究院文献>Intractable Rare Diseases Research

Intractable Rare Diseases Research

【机译】：顽固罕见疾病研究

ISSN：-
出版周期：Quarterly
语言：English

起始发布年份：2012
出版者：Tokyo : International Advancement Center for Medicine & Health Research Co.
出版地：Japan

NLM刊名缩写：Intractable Rare Dis Res

数据库引入：PubMed: v1n1, 2012-, PMC

MeSH词表主题词：Chronic Disease*; Neglected Diseases; Orphan Drug Production; Rare Diseases

备注：Also issued online. Description based on: Volume 1, number 2 (May 2012); title展开▼

期刊论文

热门论文

年度选择

更多>>

全选（0）

1.Serotonin dysregulation in Fragile X Syndrome: implications for treatment

机译：易碎X综合征中的血清素失调：对治疗的意义
- 作者：Alicia C Hanson;Randi J Hagerman
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Fragile X Syndrome fragile X mental retardation protein selective serotonin reuptake inhibitors sertraline;
2.Modeling fragile X syndrome in the Fmr1 knockout mouse

机译：在Fmr1基因敲除小鼠中建模脆性X综合征
- 作者：Tatiana M. Kazdoba;Prescott T. Leach;Jill L. Silverman;Jacqueline N. Crawley
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Fragile X Syndrome Fmr1 knockout mouse behavior phenotyping anxiety social behaviors cognition attention;
3.Fragile X spectrum disorders

机译：易碎的X光谱障碍
- 作者：Reymundo Lozano;Carolina Alba Rosero;Randi J Hagerman
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Fragile X syndrome autism spectrum disorder intellectual disability developmental delay premutation;
4.Participation of underrepresented minority children in clinical trials for Fragile X syndrome and other neurodevelopmental disorders

机译：代表性不足的少数民族儿童参与脆性X综合征和其他神经发育障碍的临床试验
- 作者：Tasleem Chechi;Salpi Siyahian;Lucy Thairu;Randi Hagerman;Reymundo Lozano
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Fragile X syndrome autism ASD clinical trials health disparities URM under represent minorities;
5.Distribution of AGG interruption patterns within nine world populations

机译：AGG中断模式在9个世界人群中的分布
- 作者：Carolyn M. Yrigollen;Stefan Sweha;Blythe Durbin-Johnson;Lili Zhou;Elizabeth Berry-Kravis;Isabel Fernandez-Carvajal;Sultana MH Faradz;Khaled Amiri;Huda Shaheen;Roberta Polli;Luis Murillo-Bonilla;Gabriel de Jesus Silva Arevalo;Patricia Cogram;Alessandra Murgia;Flora Tassone
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- AGG interruptions FMR1 allele CGG repeat expansion ethnicity;
6.Addictive substances may induce a rapid neurological deterioration in fragile X-associated tremor ataxia syndrome: A report of two cases

机译：上瘾的物质可能会导致脆性X相关性震颤共济失调综合征快速神经系统恶化：2例病例报告
- 作者：Zukhrofi Muzar;Patrick E. Adams;Andrea Schneider;Randi J. Hagerman;Reymundo Lozano
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Substance abuse neurological deterioration FXTAS premutation opiates;
7.Parent-delivered touchscreen intervention for children with fragile X syndrome

机译：父母为脆性X综合征儿童提供的触摸屏干预
- 作者：María Díez-Juan;Andrea Schneider;Tiffany Phillips;Reymundo Lozano;Flora Tassone;Marjorie Solomon;Randi J. Hagerman
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第4期
- Touchscreen devices educational applications parent training innovative therapy;
8.The current status of orphan drug development in Europe and the US

机译：欧美孤儿药物开发的现状
- 作者：Anthony K Hall;Marilyn R Carlson
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- Rare diseases orphan drugs orphan designation patient organisations;
9.Human Mendelian diseases related to abnormalities of the RNA exosome or its cofactors

机译：与RNA外泌体或其辅因子异常有关的人类孟德尔疾病
- 作者：Alexandre Fabre;Catherine Badens
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- Syndromic diarrhea tricho-hepato-enteric syndrome RNA exosome Ponto-cerebellar hypoplasia type 1 EXOSC3 TTC37 SKIV2L;
10.Effects of targeted modulation of miR-762 on expression of the IFITM5 gene in Saos-2 cells

机译：靶向调节miR-762对Saos-2细胞中IFITM5基因表达的影响
- 作者：Xinkai Mo;Yanqin Lu;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- IFITM5 gene miR-762 mineralization target gene;
11.Auditory processing disorders associated with a case of Kartagners syndrome

机译：与Kartagener综合征有关的听觉加工障碍
- 作者：Jain Saransh;Dwarkanath Mysore Vikas
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- Kartagners syndrome primary ciliary dyskinesia auditory processing psychoacoustics;
12.Pulmonary nocardiosis in patients with connective tissue disease: A report of two cases

机译：结缔组织病患者的肺性心肌病：两例报告
- 作者：Shinya Hagiwara;Hiroto Tsuboi;Chihiro Hagiya;Masahiro Yokosawa;Tomoya Hirota;Hiroshi Ebe;Hiroyuki Takahashi;Hiroshi Ogishima;Hiromitsu Asashima;Yuya Kondo;Naoto Umeda;Takeshi Suzuki;Shigemi Hitomi;Isao Matsumoto;Takayuki Sumida
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- Connective tissue disease immunosuppressive therapy nocardia pulmonary nocardiosis;
13.Anti-cytokine treatment for Takayasu arteritis: State of the art

机译：Takayasu动脉炎的抗细胞因子治疗：最新技术
- 作者：Enrico Tombetti;Maria Chiara Di Chio;Silvia Sartorelli;Enrica Bozzolo;Maria Grazia Sabbadini;Angelo A. Manfredi;Elena Baldissera
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第1期
- Takayasu arteritis tumor necrosis factor (TNF) tocilizumab angioplasty surgery;
14.Current treatment of atypical hemolytic uremic syndrome

机译：非典型溶血性尿毒症综合征的当前治疗
- 作者：Bernard S. Kaplan;Rebecca L. Ruebner;Joann M. Spinale;Lawrence Copelovitch
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第2期
- Alternate pathway of complement atypical hemolytic uremic syndrome DGPE deficiency eculizumab hemolytic uremic syndrome S. pneumoniae hemolytic uremic syndrome Cbl deficiency thrombotic microangiopathy;
15.Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressiva

机译：骨化性增生症的手和颈椎的放射学特征
- 作者：Kenichi Mishima;Hiroshi Kitoh;Nobuhiko Haga;Yasuharu Nakashima;Junji Kamizono;Takenobu Katagiri;Takafumi Susami;Masaki Matsushita;Naoki Ishiguro
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第2期
- Fibrodysplasia ossificans progressiva early diagnosis radiographic characteristics;
16.Seizures caused by pyridoxine (vitamin B6) deficiency in adults: A case report and literature review

机译：成人吡ido醇（维生素B6）缺乏引起的癫痫发作：一例病例报告及文献复习
- 作者：Yisha Tong
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第2期
- Adult literature review pyridoxine seizure vitamin B6;
17.Histiocytic meningioma: A distinctive subtype of meningioma?

机译：组织细胞性脑膜瘤：脑膜瘤的独特亚型？
- 作者：Liqiong Liu;Jonathan Stone;Joan T. Hoffpauir;Zhenggang Xiong
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第2期
- Meningioma Histiocyte Brain tumor;
18.Iron deficiency ischaemic strokes and right-to-left shunts: From pulmonary arteriovenous malformations to patent foramen ovale?

机译：铁缺乏症缺血性中风和从右向左分流：从肺动静脉畸形到卵圆孔未闭？
- 作者：Claire L. Shovlin
- 期刊名称：《Intractable Rare Diseases Research》 | 2014年第2期
- Iron deficiency 5HT (5 hydroxytryptamine serotonin) right-to-left shunt pulmonary capillary filter paradoxical embolism patent foramen ovale platelet aggregation;
19.Alzheimers Disease and Prion Protein

机译：阿尔茨海默氏病和Pri蛋白
- 作者：Jiayi Zhou;Bingqian Liu
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- PRNP gene protein misfolding N1 fragment Fyn kinase long-term potentiation (LTP);
20.Advances in research on and diagnosis and treatment of achondroplasia in China

机译：中国软骨发育不良的研究与诊治进展
- 作者：Yao Wang;Zeying Liu;Zhenxing Liu;Heng Zhao;Xiaoyan Zhou;Yazhou Cui;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Rare diseases gene mutation chondrodystrophia fetalis chondrodystrophic dwarfism;
21.Melorheostosis and a review of the literature in China

机译：髓鞘造血术和中国文献综述
- 作者：Chi Zhang;Wenda Dai;Yi Yang;Qi Tang;Zhenjun Yao
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Melorheostosis sclerosing bone dysplasia developmental anomalies bone sclerosis China;
22.Serum levels of leptin receptor in patients with systemic sclerosis

机译：系统性硬化症患者的血清瘦素受体水平
- 作者：Yukimi Ohyoshi;Takamitsu Makino;Masatoshi Jinnin;Wakana Nakayama;Satoshi Fukushima;Yuji Inoue;Hironobu Ihn
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Leptin receptor systemic sclerosis scleroderma spectrum disorder ELISA;
23.A comparative proteomics study on matrix vesicles of osteoblast-like Saos-2 and U2-OS cells

机译：成骨样Saos-2和U2-OS细胞基质囊泡的比较蛋白质组学研究
- 作者：Liang Jiang;Yazhou Cui;Jing Luan;Xiaoyan Zhou;Xiaoying Zhou;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Matrix vesicle osteoblasts mineralization proteomics;
24.Clinicopathological subclassification of biliary cystic tumors: Report of 4 cases with a review of the literature

机译：胆囊性肿瘤的临床病理分类：4例报告并文献复习
- 作者：Suguru Yamashita;Nobutaka Tanaka;Michiro Takahashi;Shojiro Hata;Yukihiro Nomura;Kenji Ooe;Yoshio Suzuki
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Biliary cystic tumors ovarian mesenchymal stroma luminal communication with bile duct;
25.Necessity of cooperation with government on publication of scientific research results for intractable diseases

机译：与政府合作发表关于顽固性疾病的科学研究成果的必要性
- 作者：Yoshinori Inagaki;Peipei Song
- 期刊名称：《Intractable Rare Diseases Research》 | 2013年第2期
- Intractable diseases rare diseases orphan drugs governmental supports;
26.Access to orphan drugs in the Middle East: Challenge and perspective

机译：中东获取孤儿药物的挑战与前景
- 作者：Ziyad S. Almalki;Abdullah K. Alahmari;Jeff J. Guo;Christina M.L. Kelton
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Orphan drug rare disease genetic disorder Middle East;
27.Peripheral stimulation in treating Parkinsons disease: Is it a realistic idea or a romantic whimsicality?

机译：外周刺激治疗帕金森氏病：是现实的想法还是浪漫的异想天开？
- 作者：Tetsuya Asakawa;Huan Fang;Zhen Hong;Kenji Sugiyama;Takao Nozaki;Hiroki Namba
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Parkinsons disease deep brain stimulation peripheral stimulation dorsal column acupuncture somatosensory system;
28.Classification and management of hepatolithiasis: A high-volume single-centers experience

机译：肝结石的分类和管理：高容量单中心的经验
- 作者：Xiaobin Feng;Shuguo Zheng;Feng Xia;Kuansheng Ma;Shuguang Wang;Ping Bie;Jiahong Dong
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Hepatectomy hepatolithiasis classification;
29.The use of cffDNA in fetal sex determination during the first trimester of pregnancy of female DMD carriers

机译：cffDNA在女性DMD携带者妊娠前三个月胎儿性别测定中的应用
- 作者：Dong Wu;Qiaofang Hou;Tao Li;Yan Chu;Qiannan Guo;Bing Kang;Shixiu Liao
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Cell-free fetal DNA (cffDNA) non-invasive prenatal diagnostic (NIPD) Duchenne muscular dystrophy (DMD) fetal sex determination;
30.Study and analysis of the state of rare disease research in Shandong Province China

机译：中国山东省罕见病研究状况的研究与分析
- 作者：Heng Zhao;Yazhou Cui;Xiaoyan Zhou;Jingxiang Pang;Xiumei Zhang;Shuangqing Xu;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Rare diseases awareness survey descriptive analysis;
31.Henoch-Schönlein purpura associated with a neuroblastoma: Report of one case and a review of the literature

机译：Henoch-Schönlein紫癜与神经母细胞瘤相关：1例报告并文献复习
- 作者：Qiaoli Dong;Shanshan Cao;Hongwen Zhang;Hui Geng
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第4期
- Henoch-Schönlein purpura (HSP) neuroblastoma malignancy;
32.Intractable and rare diseases research

机译：难治性罕见病研究
- 作者：Wei Tang;Masatoshi Makuuchi
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
33.Rare diseases orphan drugs and their regulation in Asia: Current status and future perspectives

机译：亚洲的罕见病孤儿药及其监管：现状和未来展望
- 作者：Peipei Song;Jianjun Gao;Yoshinori Inagaki;Norihiro Kokudo;Wei Tang
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Orphan diseases orphan drugs legislation incentives reimbursement;
34.Rare diseases research in China: Opportunities challenges and solutions

机译：中国的罕见病研究：机遇挑战和解决方案
- 作者：Jinxiang Han;Yazhou Cui;Xiaoyan Zhou
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Rare disease China development epidemiology;
35.Primary sclerosing cholangitis as an intractable disease

机译：原发性硬化性胆管炎为难治性疾病
- 作者：Sumihito Tamura;Yasuhiko Sugawara;Norihiro Kokudo
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Primary sclerosing cholangitis (PSC) living donor liver transplantation (LDLT) deceased donor liver transplantation (DDLT) Japan;
36.Unusual causes of upper gastrointestinal bleeding: Review of Chinese literature

机译：上消化道出血的异常原因：中国文献综述
- 作者：Wei Zhang;Eliakim Manda;Ming Qiu
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Upper gastrointestinal bleeding unusual cause China;
37.The etiologies of new cases of cerebral venous sinus thrombosis reported in the past year

机译：过去一年新报告的脑静脉窦血栓形成的病因
- 作者：Ran Meng;Xunming Ji;Xiaoying Wang;Yuchuan Ding
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Cerebral venous sinus thrombosis etiology;
38.Identification of a germline mutation in the HRPT2 gene in a Chinese family with parathyroid carcinomas

机译：中国甲状旁腺癌家庭HRPT2基因种系突变的鉴定
- 作者：Mei Zhang;Qin Li;Lili Zhang;Rongzhan Fu;Yulong Wang;Shouhua Chen;Kai Yuan;He Gu;Yazhou Cui
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Familial parathyroid tumor hyperparathyroidism HRPT2;
39.Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis

机译：X连锁青少年视网膜裂隙症中国家庭中RS1基因的突变。
- 作者：Qiaofang Hou;Yan Chu;Qiannan Guo;Dong Wu;Shixiu Liao
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- X-linked juvenile retinoschisis polymerase chain reaction frameshift mutation foveal schisis;
40.Chronic intestinal pseudo-obstruction due to lymphocytic intestinal leiomyositis: Case report and literature review

机译：淋巴细胞性肠平滑肌炎引起的慢性肠假性阻塞：病例报告及文献复习
- 作者：Keiichi Uchida;Kohei Otake;Mikihiro Inoue;Yuhki Koike;Kohei Matsushita;Toshimitsu Araki;Yoshiki Okita;Koji Tanaka;Katsunori Uchida;Noriko Yodoya;Shotaro Iwamoto;Katsuhiro Arai;Masato Kusunoki
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Chronic intestinal pseudo-obstruction (CIPO) pseudo-obstruction leiomyositis intestine;
41.Imaging diagnosis of hepatic ectopic pregnancy: A report of one case

机译：肝异位妊娠的影像学诊断：一例报告
- 作者：Chenglin Wang;Lin Cheng;Ziqin Zhang;Zhidong Yuan
- 期刊名称：《Intractable Rare Diseases Research》 | 2012年第1期
- Hepatic ectopic pregnancy ultrasound computed tomography magnetic resonance imaging;
42.A basic understanding of mucopolysaccharidosis: Incidence clinical features diagnosis and management

机译：粘多糖贮积病的基本理解：发病率临床特征诊断和治疗
- 作者：Jing Zhou;Jing Lin;Wing Ting Leung;Ling Wang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- mucopolysaccharidosis;
- symptom;
- diagnosis;
- treatment;
43.Advances in stem cell therapy for the treatment of Peyronies disease

机译：干细胞治疗佩罗尼氏病的研究进展
- 作者：Mohamad Moussa;Mohamad Abou Chakra;Yasmin Moussa
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- Peyronies disease;
- stem cell;
- adipose stem cells;
- fibrosis;
- regeneration;
44.Comprehensive bioinformatic analysis of Wnt1 and Wnt1-associated diseases

机译：Wnt1和Wnt1相关疾病的综合生物信息学分析
- 作者：Chuanming Peng;Yanqin Lu;Xiuzhi Ren;Yanzhou Wang;Shie Zhang;Mei Chen;Junlong Liu;Fengling Fang;Tianyou Li;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
45.TXNDC5 protects synovial fibroblasts of rheumatoid arthritis from the detrimental effects of endoplasmic reticulum stress

机译：TXNDC5保护类风湿关节炎的滑膜成纤维细胞免受内质网应激的不利影响
- 作者：Qiqi Lu;Jinguang Wang;Xiumei Zhang;Ruisong Tian;Li Qiao;Luna Ge;Jihong Pan;Lin Wang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- TXNDC5;
- endoplasmic reticulum stress;
- rheumatoid arthritis;
46.Identification and clinical implications of a novel pathogenic variant in the GJB2 gene causes autosomal recessive non-syndromic hearing loss in a consanguineous Iranian family

机译：GJB2基因中新型致病变异的鉴定和临床意义导致近亲伊朗家庭中的常染色体隐性非综合征性听力损失
- 作者：Mahbobeh Koohiyan
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- autosomal recessive non-syndromic hearing loss;
47.Health assessment of patients with achondroplasia pseudoachondroplasia and rickets based on 3D non-linear diagnostics

机译：基于3D非线性诊断的软骨发育不全假软骨发育不全和病患者的健康评估
- 作者：Jian Zhang;Yanqin Lu;Yanzhou Wang;Tianyou Li;Chuanming Peng;Shie Zhang;Qingxia Gao;Wei Li;Chunshang Liu;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- achondroplasia;
- pseudoachondroplasia;
- rickets;
- health assessment;
- 3-D non-linear scanning technology;
48.Replication study of four keloid-associated polymorphisms in patients of European descent - a single centre study

机译：欧洲血统患者中四种与瘢痕loid相关的多态性的复制研究-单中心研究
- 作者：Andrzej Dmytrzak;Agnieszka Boroń;Beata Łoniewska;Jeremy S.C. Clark;Mariusz Kaczmarczyk;Andrzej Ciechanowicz
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- association study;
- genetic polymorphism;
- Caucasians;
- keloid;
49.Minor blood group incompatibility due to blood groups other than Rh(D) leading to hemolytic disease of fetus and newborn: a need for routine antibody screening during pregnancy

机译：由于Rh（D）以外的其他血型导致的轻微血型不合导致胎儿和新生儿溶血性疾病：怀孕期间需要常规抗体筛查
- 作者：Anika Agrawal;Karamalla Saddam Hussain;Ajay Kumar
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
50.A brief introduction to Chinas new Drug Administration Law and its impact on medications for rare diseases

机译：中国新版药品管理法及其对罕见病用药的影响简介
- 作者：Yueqiang Wang;Duo Chen;Jiangjiang He
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Drug Administration Law;
- characteristics of legislation;
- implementation of the law;
- rare disease;
- orphan drug;
51.Characterization of a novel pathogenic variation c.1237TG in the FZD4 gene presenting new inheritance from an Iranian individual suffering vitreoretinopathy

机译：FZD4基因中新的致病变异c.1237T G的表征呈现出来自患有玻璃体视网膜病变的伊朗个体的新遗传
- 作者：Mina Zamani;Gholamreza Shariati;Tahereh Seifi;Alireza Sedaghat;Hamid Galehdari
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- exome sequencing;
- FZD4;
- vitreoretinopathy;
- autosomal recessive;
52.Quality of life in refractory generalized myasthenia gravis: A rapid review of the literature

机译：难治性广义重症肌无力患者的生活质量：文献速览
- 作者：Nathaly Garzón-Orjuela;Laura van der Werf;Laura Catalina Prieto-Pinto;Pieralessandro Lasalvia;Camilo Castañeda-Cardona;Diego Rosselli
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Myasthenia gravis;
- refractory generalized myasthenia gravis;
- quality of life;
- generalized myasthenia gravis;
53.Nitrous oxide recreational abuse presenting with myeloneuropathy and mimicking Guillain-Barre syndrome

机译：一氧化二氮娱乐性虐待表现为脊髓神经病并模仿格林-巴利综合征
- 作者：Hussein Algahtani;Bader Shirah;Nawal Abdelghaffar;Osamah Abuhawi;Abdulrahman Alqahtani
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- nitrous oxide;
- recreational abuse;
- myeloneuropathy;
- Guillain-Barre syndrome;
54.Clinical investigation of pituitary incidentalomas: A two-center study

机译：垂体偶发瘤的临床研究：两个中心的研究
- 作者：Kota Ishii;Ichiro Abe;Wataru Kameda;Kaoru Sugimoto;Yusuke Morinaga;Miiko Ito;Yuichi Takashi;Makiko Abe;Yurika Hada;Kaoru Takase;Hideyuki Fujii;Hanako Ohishi;Kentaro Ochi;Yuka Yamao;Midori Minezaki;Tadachika Kudo;Toshio Higashi;Yukihiko Sonoda;Kenichi Ishizawa;Kunihisa Kobayashi
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Pituitary incidentaloma;
- hormonal deficiency;
- pituitary apoplexy;
55.High prevalence of congenital generalized lipodystrophy in Piura Peru

机译：秘鲁皮乌拉的先天性全身性脂肪营养不良患病率高
- 作者：Nelson David Purizaca-Rosillo;Yamalí Elena Benites-Cóndor;Hugo Abarca Barriga;Carlos del Águila Villar;Miguel Chávez Pastor;Littner Franco Palacios;Ricardo Olea Zapata;James Rejas Parodi;Luz Martinez Uceda;Felix Chavesta Velásquez;John Gamarra Vilela;Sebastián Arámbulo Castillo;Amanda Ávila Reyes
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- congenital generalized lipodystrophy;
- rare diseases;
- Peru (Mesh Terms);
56.Coronary artery disease and mesenteric artery stenosis - Two sides of the same coin? - Long term prospective analysis

机译：冠状动脉疾病和肠系膜动脉狭窄-同一枚硬币的两个侧面？ -长期前瞻性分析
- 作者：Gautham Krishnamurthy;Aravind Menon;Kumaresan Kannan;Suhasini Prakash;A Rajendran;Darwin Philips
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Mesenteric ischemia;
- coronary artery disease;
- angiography;
- chronic mesenteric ischemia;
- mesenteric artery stenosis;
57.Multiphasic acute disseminated encephalomyelitis and differential with early onset multiple sclerosis

机译：多相急性弥漫性脑脊髓炎和早期发作的多发性硬化症的鉴别
- 作者：Arla Cinderella Stokes Brackett;Otto Jesus Hernández-Fustes;Carlos Arteaga Rodríguez;Olga Judith Hernandez Fustes
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第1期
- multiple Sclerosis;
- multiphasic acute disseminated encephalomyelitis;
- childhood;
58.Medical students knowledge and opinions about rare diseases: A case study from Poland

机译：医学生对罕见病的知识和见解：以波兰为例
- 作者：Jan Domaradzki;Dariusz Walkowiak
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Rare diseases;
- medical education;
- medical students knowledge;
59.Microglia express TMEM119 in the brains of Nasu-Hakola disease

机译：小胶质细胞在Nasu-Hakola疾病的大脑中表达TMEM119
- 作者：Jun-ichi Satoh;Yoshihiro Kino;Motoaki Yanaizu;Tsuyoshi Ishida;Yuko Saito
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Alzheimers disease;
- disease-associated microglia (DAM);
- microglia;
- Nasu-Hakola disease;
- TMEM119;
60.Malignant transformation of hepatic adenoma complicated by rupture and hemorrhage: An extremely rare clinical entity

机译：肝腺瘤恶性转化并发破裂和出血：极为罕见的临床实体
- 作者：Rishi Philip Mathew;Florin Manolea;Safwat Girgis;Vimal Patel;Gavin Low
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Hepatic adenoma;
- inflammatory adenoma;
- hepatocellular carcinoma;
- oral contraceptive pill;
- hemorrhage;
- malignant transformation;
61.Management of cyclical pelvic pain by multiple ultrasound-guided superior hypogastric plexus blocks in a rare case of Mayer- Rokitansky-Küster-Hauser syndrome - A case series of three blocks in a patient

机译：在罕见的Mayer-Rokitansky-Küster-Hauser综合征病例中由多个超声引导下胃下神经丛阻滞治疗盆腔周期性疼痛-患者的三例阻塞病例
- 作者：Mesha Srivastava;Jyotsna Punj
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Superior hypogastric plexus block;
- ultrasound;
- Mayer-Rokitansky-Kuster-Hauser syndrome;
- pelvic pain;
62.A case of recurrent progressive multifocal leukoencephalopathy after human stem cell transplant with detection of John Cunningham virus and human herpesvirus 6 on cerebrospinal fluid treated with Mirtazapine Olanzapine and Foscarnet

机译：一例人干细胞移植后复发性进行性多灶性白质脑病在脑脊液上检测到约翰·坎宁安病毒和人疱疹病毒6型并用米氮平奥氮平和膦甲酸钠治疗
- 作者：Matteo Pasca;Antonella Picchioni;Salvatore Mazzeo;Federica Terenzi;Elio Prestipino;Roberto Fratangelo;Anna Maria Repice;Giovanna Carlucci;Luca Massacesi;Alessandro Barilaro
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Neurovirology;
- human herpesvirus 6;
- CNS infection;
63.Anaplastic glioneuronal tumor with KIAA1549/BRAF fusion

机译：间变性胶质神经胶质瘤与KIAA1549 / BRAF融合
- 作者：Liqiong Liu;Prithvi Narayan;Jay Xiong;Zhenggang Xiong
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Glioneuronal tumor;
64.A curious case of disseminated cysticercosis in an immunocompetent adult

机译：一名具有免疫能力的成年人中发生弥漫性囊尾osis病的奇怪案例
- 作者：Azka Latif;Vikas Kapoor;Brett Weum;Mohsin Mirza;Manasa Velagapudi
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Disseminated;
- cysticercosis;
- immunocompetent;
65.Successful anaesthesia management of a child with hunter syndrome for adenotonsillectomy

机译：亨氏综合征儿童腺扁桃体切除术的成功麻醉管理
- 作者：Jyotsna Punj;Paridhi Kaler;Basavaraj Ankalagi;Arya Prasad;Renu Sinha;Prem Sagar
- 期刊名称：《Intractable Rare Diseases Research》 | 2019年第4期
- Endotracheal intubation;
- hunter syndrome;
- airway;
- C Mac blade;
66.A basic understanding of congenital extrahepatic portosystemic shunt: incidence mechanism complications diagnosis and treatment

机译：先天性肝外门体分流的基本知识：发生率机制并发症诊断和治疗
- 作者：Haowen Tang;Peipei Song;Zhiqiang Wang;Bing Han;Xiangfei Meng;Yingwei Pan;Xuan Meng;Weidong Duan
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- Congenital extrahepatic portosystemic shunt;
- incidence;
- mechanism;
- complications;
- diagnosis;
- treatment;
- review;
67.Update on cystine stones: current and future concepts in treatment

机译：胱氨酸结石的更新：当前和未来的治疗概念
- 作者：Mohamad Moussa;Athanasios G. Papatsoris;Mohamad Abou Chakra;Yasmin Moussa
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- cystinuria;
- urolithiasis;
- novel therapy;
- cystine stone;
- tiopronin;
- D-penicillamine;
68.Performance of matching methods in studies of rare diseases: a simulation study

机译：匹配方法在稀有疾病研究中的性能：模拟研究
- 作者：Irena Cenzer;W. John Boscardin;Karin Berger
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- matching methods;
- propensity score matching;
- small samples;
- rare diseases;
69.Association between antinuclear antibodies (ANA) patterns and extractable nuclear antigens (ENA) in HEp-2 cells in patients with autoimmune diseases in Riyadh Saudi Arabia

机译：沙特阿拉伯利雅得自身免疫性疾病患者HEp-2细胞中抗核抗体（ANA）模式与可提取核抗原（ENA）之间的关联
- 作者：Roua Alsubki;Hajera Tabassum;Hala Alfawaz;Rasha Alaqil;Feda Aljaser;Sabah Ansar;Abdullah Al Jurayyan
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- autoimmune diseases;
- extractable nuclear antigens;
- ANA immunofluorescence;
70.Identification of novel compound heterozygous mutations of the DYNC2H1 gene in a fetus with short-rib thoracic dysplasia 3 with or without polydactyly

机译：鉴定具有或不具有多指的短肋胸廓发育不良3胎儿中DYNC2H1基因的新型复合杂合突变
- 作者：Kaiyue Geng;Kai Mu;Yan Zhao;Jing Luan;Yazhou Cui;Jinxiang Han
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- short-rib thoracic dysplasia 3 with or without polydactyly;
71.Increased CD27 expression in the skins and sera of patients with systemic sclerosis

机译：系统性硬化症患者皮肤和血清中CD27表达增加
- 作者：Yuka Oshikawa;Takamitsu Makino;Miri Nakayama;Soichiro Sawamura;Katsunari Makino;Ikko Kajihara;Jun Aoi;Shinichi Masuguchi;Satoshi Fukushima;Hironobu Ihn
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- CD27;
- tumor necrosis factor (TNF) receptor family;
- systemic sclerosis;
- fibrosis;
72.Reporting one very rare pathogenic variation c.1106GA in POMT2 gene

机译：报告POMT2基因中一种非常罕见的致病性变异c.1106G A
- 作者：Ghazale Mahjoub;Mohammad Ali Faghihi;Maryam Taghdiri
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- dystroglycanopathy;
- alpha-dystroglycan;
- rare mutation;
73.A novel frame shift mutation in STIM1 gene causing primary immunodeficiency

机译：STIM1基因的新型移码突变导致原发性免疫缺陷
- 作者：Dorna Derakhshan;Erfan Taherifard;Ehsan Taherifard;Sarvin Sajedianfard;Ali Derakhshan
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- genetics;
- immunology;
- recurrent infections;
- pediatrics;
74.Fragile X associated neuropsychiatric disorders in a male without FXTAS

机译：没有FXTAS的男性中易碎X相关的神经精神疾病
- 作者：Ana María Cabal-Herrera;Wilmar Saldarriaga-Gil;Maria Jimena Salcedo-Arellano;Randi J Hagerman
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- fragile X mental retardation 1 gene;
- fragile X-associated neuropsychiatric disorders;
- premutation;
- FXAND;
- psychosis;
75.Efficacy of trazodone for treating paroxysmal sympathetic hyperactivity presenting after left temporal subcortical hemorrhage

机译：曲唑酮治疗左颞下皮层出血后阵发性交感神经亢进的疗效
- 作者：Yusuke Morinaga;Kouhei Nii;Hayatsura Hanada;Kimiya Sakamoto;Ritsurou Inoue;Takafumi Mitsutake
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- paroxysmal sympathetic hyperactivity;
- temporal subcortical hemorrhage;
- trazodone;
76.Successful early diagnosis and treatment of non-convulsive status epilepticus-induced Takotsubo syndrome

机译：非惊厥性癫痫发作的Takotsubo综合征的成功早期诊断和治疗
- 作者：Yusuke Morinaga;Kouhei Nii;Kimiya Sakamoto;Ritsurou Inoue;Takafumi Mitsutake;Hayatsura Hanada
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- non-convulsive status epilepticus;
- Takotsubo syndrome;
- trazodone;
77.Food intolerance/malabsorption may occur in rare diseases

机译：在罕见疾病中可能发生食物不耐受/吸收不良
- 作者：Wolfgang J. Schnedl;Manfred Tillich;Michael Schenk;Dietmar Enko;Harald Mangge
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第2期
- primary epiploic appendagitis;
- Gullo syndrome;
- beta-thalassemia minor;
- inferior vena cava anomaly;
- lactose;
- fructose;
- histamine;
78.Cost-effectiveness analysis of enzyme replacement therapy (ERT) for treatment of infantile-onset Pompe disease (IOPD) in the Iranian pharmaceutical market

机译：酶置换疗法（EOPD）在伊朗制药市场中酶替代治疗（EOPD）的成本效益分析
- 作者：Reza Hashempour;Majid Davari;Abolghasem Pourreza;Mohammadreza Alaei;Batoul Ahmadi
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- Myozyme;
- enzyme replacement therapy;
- Pompe disease;
- cost-effectiveness;
- Iran;
79.The challenge of managing comorbidities: a case report of primary Sjogrens syndrome in a patient with acute intermittent porphyria

机译：管理合并症的挑战：急性间歇性卟啉症患者中原发性Sjogren综合征的案例报告
- 作者：Qing Teng;Liyan Ma;Yuelin Ma;Yiran Zhang;Ninglin Kang;Yuanxiang Hu;Songyun Zhang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- acute intermittent porphyria;
- primary Sjogrens syndrome;
- autoimmune disease;
- treatment;
80.An extremely rare combination of acute intermittent porphyria and Turner syndrome

机译：急性间歇性卟啉和特纳综合征的极少数结合
- 作者：Songyun Zhang;Jiahong Wu;Qing Teng;Yiran Zhang;Yuanxiang Hu;Ninglin Kang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- acute intermittent porphyrin (AIP);
- Turner syndrome;
- HMBS gene;
- isochromosome;
- depression;
81.array-CGH revealed gain of Yp11.2 in 49XXXXY and gain of Xp22.33 in 48XXYY karyotypes of two rare klinefelter variants

机译：Array-CGH显示49XXXXY和XP22.33中的XP22.33中的增益XP22.33XXyy Klytypes的两种罕见的KlineFelter变体
- 作者：Somprakash Dhangar;Jagdeeshwar Ghatanatti;Babu Rao Vundinti
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
82.A novel variant c.3706CT p.(Avg 1236Cys) in the ABCA7 gene in a Saudi patient with susceptibility to Alzheimers disease 9

机译：一种新的变异C.3706C T p。（AVG 1236cys）在沙特患者的ABCA7基因中易患阿尔茨海默病9
- 作者：Hussein Algahtani;Bader Shirah;Alhusain Alshareef;Mohammad H. Al-Qahtani;Angham Abdulrahman Abdulkareem;Muhammad Imran Naseer
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- Alzheimer disease;
- dementia;
- mutation;
- Saudi Arabia;
83.Benign adrenal and suprarenal retroperitoneal schwannomas can mimic aggressive adrenal malignancies: case report and review of the literature

机译：良性肾上腺和寄生术和术腹膜肺脉冲施沃马斯可以模仿侵略性的肾上腺恶性肿瘤：案例报告和文献审查
- 作者：Mitchell P. Wilson;Prayash Katlariwala;Jingyang Huang;Gavin Low;Edward Wiebe
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- adrenal;
- schwannoma;
- retroperitoneal;
- suprarenal;
- malignancy;
- nerve;
84.Successful endoscopic biopsy for Primary central nervous system lymphoma of the corpus callosum in the splenium with bilateral visuomotor ataxia

机译：脾脏胼um胼um胼um具有双侧游瓜素瘤的原发性神经系统淋巴瘤成功的内窥镜活组织检查
- 作者：Yusuke Morinaga;Kouhei Nii;Kimiya Sakamoto;Ritsurou Inoue;Takafumi Mitsutake;Hayatsura Hanada;Seiji Haraoka
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- PCNSL;
- DLBCL;
- visuomotor ataxia;
- corpus callosum in the splenium;
- endoscopic biopsy;
85.Pseudohypoparathyroidism presenting with seizures: a case report and literature review

机译：癫痫发作的假核偶转症状：案例报告和文献综述
- 作者：Mostafa Suhail Najim;Riyadh Ali;Mohammed Awad;Asaad Omer
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- hypocalcemia;
- pseudohypoparathyroidism;
- seizures;
86.Tuberculous choroiditis masquerading as sympathetic ophthalmia: a case report

机译：伪装成结块性脉络膜炎作为交感神经眼科目：案例报告
- 作者：Xiaoxu Huang;Xiaolin Qin;Zhengyang Luo;Luoxiang Li;Jianbin Hu
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- ocular tuberculosis;
- sympathetic ophthalmia;
- choroiditis;
87.Cranial intraosseous angiolipoma: case report and literature review

机译：颅骨血管素似似族猿：病例报告和文献综述
- 作者：Katherine M. Morgan;Simon Hanft;Zhenggang Xiong
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- intraosseous angiolipoma;
- calvarium;
- cranium;
- skull bone;
- soft tissue tumor;
88.Comprehensive Rare Disease Care model for screening and diagnosis of rare genetic diseases - an experience of private medical college and hospital South India

机译：综合稀有疾病保健模型用于释放遗传疾病的筛选和诊断 - 南印度私立医学院和医院经验
- 作者：Sathish Raju Nilakantam;Deepa Bhat;M.D. Ravi;(Col) M Dayananda;H. Basavanagowdappa;Jagadish Kumar K
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- Rare/genetic diseases;
- medical genetics;
- model;
- planning;
- public health;
- genetic counseling;
- management;
- interdisciplinary team;
89.An update on microRNAs as potential novel therapeutic targets in testicular germ cell tumors

机译：MicroRNA的更新作为睾丸生殖细胞肿瘤中的潜在新型治疗靶标
- 作者：Marco De Martino;Francesco Esposito;Paolo Chieffi
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第3期
- HMGA1;
- microRNA;
- testicular germ cell tumor (TGCT);
- seminoma;
90.Acute intermittent porphyria: focus on possible mechanisms of acute and chronic manifestations

机译：急性间歇性卟啉：专注于急性和慢性表现的可能机制
- 作者：Yuelin Ma;Qing Teng;Yiran Zhang;Songyun Zhang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- acute intermittent porphyria;
- mechanisms;
- aminolevulinic acid (ALA);
- attack;
91.Recent advances in the epidemiology and genetics of acute intermittent porphyria

机译：急性间歇性卟啉症的流行病学和遗传学的最新进展
- 作者：Liyan Ma;Yu Tian;Chenxing Peng;Yiran Zhang;Songyun Zhang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- acute intermittent porphyria;
- prevalence;
- penetrance;
- genetic traits;
- genotype-phenotype correlation;
- modifying genes;
92.Therapeutic strategies for acute intermittent porphyria

机译：急性间歇性卟啉症的治疗策略
- 作者：Lanlan Zhao;Xinyang Wang;Xiaoning Zhang;Xiantao Liu;Ningzhen Ma;Yiran Zhang;Songyun Zhang
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- acute intermittent porphyria;
- heme;
- carbohydrate loading;
- givosiran (siRNA);
- mRNA therapy;
93.Reactive astrocytes express Aggregatin (

机译：反应性星形胶质细胞表达聚集（
- 作者：Jun-ichi Satoh;Yoshihiro Kino;Motoaki Yanaizu;Tsuyoshi Ishida;Yuko Saito
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- Aggregatin;
- Alzheimers disease;
- amyloid plaque;
- FAM222A;
- Nasu-Hakola disease;
- reactive astrocytes;
94.Two new missense mutations in the protein interaction ASH domain of OCRL1 identified in patients with Lowe syndrome

机译：低成综合征患者蛋白质相互作用灰分中蛋白质相互作用灰域突变的两个新的畸形突变
- 作者：Ana Perdomo-Ramirez;Montserrat Antón-Gamero;Daniela Sakaguchi Rizzo;Amelia Trindade;Elena Ramos-Trujillo;Felix Claverie-Martin
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- OCRL;
95.Genetic variant affecting the myosin light chain 2 related to familial hypertrophic cardiomyopathy

机译：影响肌球蛋白轻链2与家族性肥厚性心肌病相关的遗传变异
- 作者：Wilmar Saldarriaga Gil;Laura Alejandra Ávila Vidal;Manuel Alejandro Vásquez Salguero;Mateo Betancourt Cajiao;Claudia Valencia Peña
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- heart diseases;
- cardiomyopathy;
- hypertrophic;
- familial;
- hypertrophy;
- left ventricle;
96.Primary neuroendocrine carcinoma of the breast: a rare presentation and review of the literature

机译：乳房的原发性神经内分泌癌：对文献的罕见介绍和审查
- 作者：Nikolaos S. Salemis
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- neuroendocrine;
- carcinoma;
- breast;
97.Cortical deafness as a sequela to meningitis: a single case study

机译：皮质耳聋作为脑膜炎的后遗症：单一案例研究
- 作者：Megha Sasidharan;Jinsi Elsa Itty;Ghanta Hinduja;Shabnam Hasna;Deena Priya
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- meningitis;
- pure-tone audiometry;
- late latency response;
98.Primary leiomyoma of the liver in an immunocompetent patient

机译：肝脏初级平滑肌瘤在免疫活性患者中
- 作者：Diego Coletta;Chiara Parrino;Simone Nicosia;Emy Manzi;Giada Pattaro;Andrea Oddi;Marco DAnnibale;Mirella Marino;Gian Luca Grazi
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- liver resection;
- liver leiomyoma;
- liver neoplasm;
- rare liver diseases;
99.A case of coronavirus disease 2019 in acquired immunodeficiency syndrome patient: a case report and review of the literature

机译：预测免疫缺陷综合征患者冠状病毒疾病的病例：案例报告和对文献的审查
- 作者：Abdallah Qasim;Mohamed Mansour;Omar Kousa;Dana Awad;Bader Abuhazeem;Paul Millner;Manasa Velagapudi
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- COVID-19;
- coronavirus;
- HIV;
- AIDS;
- chemotherapy;
- SARS-CoV-2;
- pneumonia;
100.Primary cutaneous follicle center lymphoma of the breast: Management of an exceedingly rare malignancy

机译：乳房的主要皮肤卵泡中心淋巴瘤：管理严重罕见的恶性肿瘤
- 作者：Nikolaos S. Salemis;Nikolaos Koliarakis;Kyriakos Spiliopoulos;Konstantina Kimpouri;Leonidas Marinos
- 期刊名称：《Intractable Rare Diseases Research》 | 2020年第4期
- PCFCL;
- cutaneous;
- lymphoma;
- follicle;
- center;
- breast;