Literature DB >> 6481556

Systemic carnitine deficiency simulating Reye syndrome.

P M Coates, D E Hale, C A Stanley, A M Glasgow.   

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Year:  1984        PMID： 6481556     DOI： 10.1016/s0022-3476(84)80460-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

Review 1.  Interrelationships of liver and brain with special reference to Reye syndrome.

Authors:  J K Brown; H Imam
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

2.  Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.

Authors:  P Steenhout; C Elmer; A Clercx; D Blum; D Gnat; S van Erum; F Vertongen; E Vamos
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.

Authors:  B A Amendt; W J Rhead
Journal:  J Clin Invest       Date:  1985-09       Impact factor: 14.808

4.  Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.

Authors:  I Tein; D C De Vivo; D Ranucci; S DiMauro
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

Review 5.  Clinical characteristics of primary carnitine deficiency: A structured review using a case-by-case approach.

Authors:  Loek L Crefcoeur; Gepke Visser; Sacha Ferdinandusse; Frits A Wijburg; Mirjam Langeveld; Barbara Sjouke
Journal:  J Inherit Metab Dis       Date:  2022-02-03       Impact factor: 4.750
  5 in total

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