The use of amino acid supplements in inherited metabolic disease

Journal of Inherited Metabolic Disease - Tập 29 Số 2-3 - Trang 279-280 - 2006
John H. Walter1, Anita MacDonald2
1Willink Biochemical Genetics Units, RMCH, Manchester, UK
2Birmingham Children's Hospital, United Kingdom

Tóm tắt

SummaryAmino acid supplements are recognized to be essential for the management of a number of inherited metabolic disorders but their use in some other conditions is more controversial.

Từ khóa


Tài liệu tham khảo

10.1002/ana.410440219

10.1016/S1096-7192(03)00078-7

10.1212/01.WNL.0000151976.60624.01

KolkerS GarbadeSF GreenbergCR et al (2006)Natural history outcome and treatment efficacy in children and adults with glutaryl‐CoA dehydrogenase deficiency.Pediatr Res(in press).

Matsuo S, 1995, Efficacy of tryptophan for the treatment of nonketotic hyperglycinemia: a new therapeutic approach for modulating the N‐methyl‐d‐aspartate receptor, Pediatrics, 95, 142, 10.1542/peds.95.1.142

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Thông tin xuất bản

Journal of Inherited Metabolic Disease

Tập 29 Số 2-3

279-280

Thông tin tác giả