Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents-Reference-Cited by-同舟云学术

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Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents

Published:1976-05 Issue:5 Volume:88 Page:814-818
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Aylsworth Arthur S.,Taylor Harold A.,Stuart Carole M.,Thomas George H.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. A generalised storage disorder resembling Hurler's syndrome;Öckerman;Lancet,1967

2. Mannosidosis: A clinical and histopathologic study;Kjellman;J Pediatr,1967

3. Urinary mannose in mannosidosis;Nordén;J Pediatr,1973

4. Mannosidosis: Clinical, fine-structural and biochemical findings in three cases;Autio;Acta Paediatr Scand,1973

5. Mannosidosis;Gehler,1975

Cited by 28 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. Alfa-mannosidosis: Frequent Symptoms in Rare Patient;Current Pediatrics;2023-01-21

2. Intellectual functioning in alpha‐mannosidosis;JIMD Reports;2019-09-21

3. Cognitive profile and activities of daily living: 35 patients with alpha-mannosidosis;Journal of Inherited Metabolic Disease;2015-05-28

4. Alpha-mannosidosis;Orphanet Journal of Rare Diseases;2008-07-23

5. Mannosidosis: two brothers with different degrees of disease severity;Clinical Genetics;2008-04-23

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