Inherited Metabolic Disorders: Galactosemia-Reference-Cited by-同舟云学术

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Inherited Metabolic Disorders: Galactosemia

Published:1963 Issue: Volume: Page:1-68
ISSN:0065-2423
Container-title:Advances in Clinical Chemistry
language:
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Author:

Woolf L.I.

Publisher

Elsevier

Reference176 articles.

1. Defect in uptake of galactose-1-phosphate into liver nucleotides in congenital galactosemia;Anderson;Science,1957

2. A specific enzymatic assay for the diagnosis of congenital galactosemia. I. The consumption test;Anderson;J. Lab. Clin. Med.,1957

3. A study of the linkage of phosphorus to protein in phosphoglucomutase;Anderson;Arch. Biochem. Biophys.,1957

4. Congenital galactosaemia. Report of a case;Arthurton;Brit. Med. J.,1954

5. A case of congenital cirrhosis of the liver with renal tubular defects akin to those in the Fanconi syndrome;Baber;Arch. Disease Childhood,1956

Cited by 8 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. Microencapsulated Charcoal Hemoperfusion for Galactosemia;Artificial Kidney, Artificial Liver, and Artificial Cells;1978

2. Galaktosämie;Erbliche Defekte des Kohlenhydrat-, Aminosäuren- und Proteinstoffwechsels;1974

3. Biochemical Neurological Disease in Children;Biochemical Aspects of Nervous Diseases;1972

4. Effect of galactose on energy and phospholipid metabolism in the chick brain;Archives of Biochemistry and Biophysics;1969

5. Neurologie et neuropathologie du syndrome de lowe;Journal of the Neurological Sciences;1966-07

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