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Doença neurodegenerativa rara: itinerário de portadores de doença de huntington em busca de diagnóstico e tratamento / Rare neurodegenerative disease: itinerary of huntington disease carriers in search of diagnosis and treatment

机译：罕见的神经退行性疾病：亨廷顿疾病运营商行程寻找诊断和治疗/罕见神经退行性疾病：亨廷顿病携带者的行程寻求诊断和治疗

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José Juliano Cedaro; Vivian Susi de Assis Canizares; Naime Oliveira Ramos; Andonai Krauze de França; Jamaira do Nascimento Xavier; Thaynara Naiane Castro Campelo; Thamyris Lucimar Pastorini Gonçalves; Janaina Gianne Araújo de Medeiros;
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1. Da busca pelo diagnóstico às incertezas do tratamento: desafios do cuidado para as doen?as genéticas raras no Brasil [J] . Jorge Alberto Bernstein?Iriart, Marina Fisher?Nucci, Tatiane Pereira?Muniz, Ciência & Saúde Coletiva . 2019,第10期

机译：寻求诊断治疗的不确定性：对巴西罕见遗传的照顾挑战
2. Doen?as raras: itinerário diagnóstico e terapêutico das famílias de pessoas afetadas [J] . Francine Demontigny, Geisa Dos Santos Luz, Mara Regina Santos Da Silva Acta Paulista de Enfermagem . 2015,第5期

机译：罕见疾病：受影响家庭的诊断和治疗路线
3. Doen?as raras: itinerário diagnóstico e terapêutico das famílias de pessoas afetadas [J] . Francine Demontigny, Geisa Dos Santos Luz, Mara Regina Santos Da Silva Acta Paulista de Enfermagem . 2015,第5期

机译：罕见疾病：受影响家庭的诊断和治疗路线
4. Decision Support Systems in Neurodegenerative Diseases Diagnosis, Treatment and Management [C] . Themis Exarchos International Conference on Brain Function Assessment in Learning . 2020

机译：决策支持系统在神经退行性疾病诊断，治疗和管理中
5. Characterizing the Huntington's disease, Parkinson's disease, and pan-neurodegenerative gene expression signature with RNA sequencing [D] . Labadorf, Adam Thomas 2016

机译：利用RNA测序表征亨廷顿氏病，帕金森氏病和泛神经变性基因表达特征
6. Brain hypometabolism in rare genetic neurodegenerative disease: Niemann-Pick disease type C spinocerebellar ataxia and Huntington disease assessed by FDG PET [O] . Yung Hsiang Kao, Melissa Cheng, Dennis Velakoulis, 2021

机译：稀有遗传神经变性疾病中的脑抑郁症状：Niemann-pick型C型CSpinocerebellar Ataxia和FDG PET评估的亨廷顿病
7. Molecular diagnosis of Huntington disease in Brazilian patients Diagnóstico molecular da doença de Huntington em pacientes brasileiros [O] . TEREZA C. LIMA E SILVA, HELIANE GUERRA SERRA, CARMEN S. BERTUZZO, 2000

机译：巴西患者亨廷顿氏病的分子诊断巴西患者的亨廷顿舞蹈病的分子诊断

Doença neurodegenerativa rara: itinerário de portadores de doença de huntington em busca de diagnóstico e tratamento / Rare neurodegenerative disease: itinerary of huntington disease carriers in search of diagnosis and treatment

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