Hypothyroidism in late-onset Pompe disease

PURPOSE: In Pompe disease, a deficiency of acid α-glucosidase enzyme activity leads to pathologic accumulation of glycogen in tissues. Phenotype heterogeneity in Pompe includes an infantile form and late-onset forms (juvenile- and adult-onset forms). Symptoms common to all phenotypes include progres...

Descripción completa

Detalles Bibliográficos
Autores principales: Schneider, Joseph, Burmeister, Lynn A., Rudser, Kyle, Whitley, Chester B., Jarnes Utz, Jeanine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932620/
https://www.ncbi.nlm.nih.gov/pubmed/27408821
http://dx.doi.org/10.1016/j.ymgmr.2016.06.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932620/
https://www.ncbi.nlm.nih.gov/pubmed/27408821
http://dx.doi.org/10.1016/j.ymgmr.2016.06.002

Ejemplares similares