Nyhan, Inherited Metabolic Disease: A Clinical Approach.Hoffman G. Inherited metabolic diseases: a clinical approach. 2 nd ed. Philadelphia: Lippincott William & Wilkins; 2004.Hoffman GF, Zschocke J, Nyhan WL. Inherited metabolic diseases; A clinical approach. Heidelberg: Springer-Verlag; 2010....
网络释义 1. 遗传性代谢病 遗传代谢缺陷病,目前又称遗传性代谢病(inherited metabolic diseases)或先天性代谢缺陷病(inborn erros of metabolism),是指人 … www.chinagan.com|基于3个网页 2. 遗传代谢病 代谢病,metabolic... ... )inherited metabolic diseases遗传代谢病) metabolic diseases 代谢病 ... ...
Inherited Metabolic Diseases 作者: Hoffmann, Georg F. (EDT)/ Nyhan, Willian L./ Zschocke, Johannes/ Kahler, Stephen G./ Mayatepek, Ertan/ Hoffmann, Georg F.出版社: Lippincott Williams & Wilkins出版年: 2001-9页数: 448定价: 276.00元
1)inherited metabolic diseases遗传代谢病 1.Clinical application of hematopoietic stem cell transplantation in the treatment of childhoodinherited metabolic diseases;造血干细胞移植在遗传代谢病治疗中的应用 2.Clinical features and analysis ofinherited metabolic diseasesin neonatal intensive care unit;新生儿重症监...
Many inherited metabolic diseases affect the liver in neonates, children, or adults. The histopathologic changes are diverse and may be acute or chronic. They can be considered primary (when the injury is from the cytopathic effect of an accumulated metabolite) or secondary (e.g., an infection...
Currently, very few studies on long-term follow up of health outcomes and health-care utilization of children with inherited metabolic disorders identified through newborn screening are available. In this project, we analyzed acute care utilization for c
1 cases showed only elevated carnitine level and 2 cases showed decreased amino acid levels.Conclusions:Preliminary screening for inherited metabolic diseases in 88 cases of high-risk infants through laboratory and clinical analysis indicated that the incidence of inherited metabolic disease in Qinghai ...
Inherited metabolic diseases mimicking hereditary spastic paraplegia (HSP): a chance for treatment Hélio A. G. Teive Carlos Henrique F. Camargo Renato P. Munhoz neurogenetics (2022) Late Onset Subacute Profound Biotinidase Deficiency Caused by a Novel Homozygous Variant c.466-3T>G in the BTD...
对丢失的恐惧,因此它能够并且应该被珍惜,因此不想要错过,当它时是,来到2011年! [translate] aearly screening of congenital inherited metabolic diseases 早期的掩护先天遗传的新陈代谢的疾病 [translate] 英语翻译 日语翻译 韩语翻译 德语翻译 法语翻译 俄语翻译 阿拉伯语翻译 西班牙语翻译 葡萄牙语翻译 意大利语翻译...
This excellent and very readable book consisting of 10 chapters (321 pages) guides you on a logical and fascinating journey from the basic principles of metabolic disorders, their clinical presentation, laboratory investigations and finally to their treatment. The complexity of the presentation of metab...