Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases

Detalles Bibliográficos
Autores principales: Vasanwala, Rashida, Yap, Fabian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Poster Presentation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850457/
http://dx.doi.org/10.1186/1687-9856-2013-S1-P126
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author Vasanwala, Rashida
Yap, Fabian
author_facet Vasanwala, Rashida
Yap, Fabian
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spelling pubmed-38504572013-12-16 Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases Vasanwala, Rashida Yap, Fabian Int J Pediatr Endocrinol Poster Presentation BioMed Central 2013 2013-10-03 /pmc/articles/PMC3850457/ http://dx.doi.org/10.1186/1687-9856-2013-S1-P126 Text en Copyright © 2013 Vasanwala and Yap; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Presentation
Vasanwala, Rashida
Yap, Fabian
Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title_full Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title_fullStr Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title_full_unstemmed Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title_short Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
title_sort congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. clinical and biochemical findings in two cases
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850457/
http://dx.doi.org/10.1186/1687-9856-2013-S1-P126
work_keys_str_mv AT vasanwalarashida congenitaladrenalhypoplasiaglycerolkinasedeficiencyandmyopathyconditionrequiringpromptidentificationclinicalandbiochemicalfindingsintwocases
AT yapfabian congenitaladrenalhypoplasiaglycerolkinasedeficiencyandmyopathyconditionrequiringpromptidentificationclinicalandbiochemicalfindingsintwocases

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