Intermittent Branched Chain Ketonuria-Reference-Cited by-同舟云学术

Intermittent Branched Chain Ketonuria

Published:1971-04 Issue:1-6 Volume:4 Page:52-58
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Irwin W.C.,Martel S.B.,Goluboff N.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference16 articles.

1. A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance;Menkes;Pediatrics,1954

2. Diagnosis of maple syrup urine disease (branched chain ketoaciduria) by in vitro study of peripheral leukocyte;Dancis;Pediatrics,1963

3. Clinical and biochemical observations on an apparently nonfatal variant of branched-chain ketoaciduria (maple syrup urine disease);Morris;Pediatrics,1961

4. Intermittent branched-chain ketonuria;Dancis;New Eng. J. Med.,1967

5. Late-onset branched-chain ketoaciduria (Mapple syrup urine disease);Morris;J. Lancet,1966

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Screening Newborns for Multiple Organic Acidurias in Dried Filter Paper Urine Samples: Method Development;Pediatric Research;1991-10

2. Newborn Screening for Maple Syrup Urine Disease (Branched-Chain Ketoaciduria);Neonatal Screening for Inborn Errors of Metabolism;1980

3. Thiamine-responsive intermittent branched-chain ketoaciduria;The Journal of Pediatrics;1979-04

4. Substrate specificity and stabilization by thiamine pyrophosphate of rat liver branched chain α-ketoacid dehydrogenase;Biochemical Medicine;1978-02

5. Maple syrup urine disease: Branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts;Biochemical Genetics;1976-08