Problems in the Diagnosis of Hereditary Galactosaemia-Reference-Cited by-同舟云学术

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Problems in the Diagnosis of Hereditary Galactosaemia

Published:1967-01 Issue:1 Volume:56 Page:85-96
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:Acta Paediatrica

Author:

BRANDT N. J.,TOLSTRUP N.

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1967.tb15347.x/fullpdf

Reference26 articles.

1. A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY

2. 3. N. J. Brandt: To be published.

3. 5. N. J. Brandt: Galaktose-1-fosfat-uridyl-transferase., Thesis , Munksgard, Copenhagen1966 .

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. Unusual Late Neurological Sequelae in Galactosaemia;Developmental Medicine & Child Neurology;2008-11-12

2. Galactosaemia Case for Neonatal Screening Illustrated by Recent Australian Experience;Medical Journal of Australia;1978-10

3. Increased Intracranial Pressure in Galactosemia;Clinical Pediatrics;1976-04

4. Reversibility of Extensive Liver Damage in Galactosemia;Gastroenterology;1975-08

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

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