Infantile free sialuria without lysosomal storage-Reference-Cited by-同舟云学术

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Infantile free sialuria without lysosomal storage

Published:1987-01 Issue:1 Volume:3 Page:40-43
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Roesel R.August,Byrne Katharyn M.,Hommes Frits,Trefz Jill,Kelloes Cathy,Nelson Anne M.,Carroll James E.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Salla disease: A new lysosomal storage disorder;Aula;Arch Neurol,1979

2. Salla disease: A new lysosomal storage disorder with disturbed sialic acid metabolism;Renlund;Neurology,1983

3. Clinical and laboratory diagnosis of Salla disease in infancy and childhood;Renlund;J Pediatr,1984

4. Sialic acid storage disease with sialuria: Clinical and biochemical features in the severe infantile type;Stevenson;Pediatrics,1983

5. Infantile form of sialic storage disorder: Clinical, ultrastructural and biochemical studies in two siblings;Tondeur;Eur J Pediatr,1982

Cited by 2 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. Infantile sialic acid storage disease: Biochemical studies;American Journal of Medical Genetics;1995-07-31

2. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

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