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Clinical Symptoms and laboratory diagnostic Abnormalities in Border Collies with Suspected hereditary juvenile Cobalamin deficiency

机译：疑似遗传性少年钴胺素缺乏症的边境牧羊犬的临床症状和实验室诊断异常

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《Kleintier-Praxis: Archiv fur Kleine Haus- und Nutztiere Sowie Laboratoriums- und Zoo-Tiere》 |2015年第3期|共2页
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Knoepfler;
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正文语种 ger
中图分类动物医学（兽医学）;
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1. Clinical Symptoms and laboratory diagnostic Abnormalities in Border Collies with Suspected hereditary juvenile Cobalamin deficiency [J] . Knoepfler Kleintier-Praxis: Archiv fur Kleine Haus- und Nutztiere Sowie Laboratoriums- und Zoo-Tiere . 2015,第3期

机译：疑似遗传性少年钴胺素缺乏症的边境牧羊犬的临床症状和实验室诊断异常
2. Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C disease: Response to letter "disappearance of congenital noncompaction in hereditary cobalamin-C-deficiency 2.5 years after birth" by J. Finsterer and Claudia St?llberger, DOI 10.1007/s10545-013-9612-4 [J] . TanpaiboonP., VendittiC.P. Journal of inherited metabolic disease . 2013,第6期

机译：Cobalamin C疾病的心室心肌和胎盘积液的失密：J。Finsterer和Claudia St？llberger，DOI 10.1007 / s10545-013-对字母“出生后遗传性钴胺素C缺乏症先天性失密消失消失2.5岁”的回应9612-4
3. Holotranscobalamin in laboratory diagnosis of cobalamin deficiency compared to total cobalamin and methylmalonic acid. [J] . Obeid R, Herrmann W Clinical chemistry and laboratory medicine: CCLM . 2007,第12期

机译：与总钴胺素和甲基丙二酸相比，全反钴胺素在实验室诊断钴胺素缺乏症。
4. FOCUS ON HEREDITARY DISEASES GENETIC PREDISPOSITIONS CLINICAL LABORATORY DIAGNOSTIC APPROACH TO HEREDITARY DISEASES [C] . anonymous American College of Veterinary Internal Medicine Forum . 2008

机译：专注于遗传性疾病与遗传易感性临床和实验室诊断方法对遗传性疾病
5. Treating an N-glycosylation abnormality in airways with a cystic fibrosis transmembrane conductance regulator protein deficiency reduces Pseudomonas aeruginosa colonization; A hallmark symptom of cystic fibrosis [D] . Martino, Ashley Thomas 2007

机译：用囊性纤维化跨膜电导调节蛋白缺乏治疗气道N-糖基化异常可减少铜绿假单胞菌定植；囊性纤维化的典型症状
6. Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene [O] . Stephan M. Tanner, Zhongyuan Li, James D. Perko, 2005

机译：内在因子基因突变引起的遗传性少年钴胺素缺乏症
7. Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene [O] . Tanner, Stephan M., Li, Zhongyuan, Perko, James D., 2005

机译：内在因子基因突变引起的遗传性少年钴胺素缺乏症
8. Increased Heat Sensitivity of Red Blood Cells in Hereditary Elliptocytosis with Acquired Cobalamin (Vitamin B12) Deficiency [R] . Schoomaker, E. B., Butler, W. M., Diehl, L. F. 1981

机译：获得性维生素B12（维生素B12）缺乏对遗传性椭圆形细胞增多症中红细胞的热敏感性增加

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