CARTAS AL EDITOR
Deficiencia del transportador de glucosa tipo I: una enfermedad neurometabólica tratable
C. Gómez Ladoa,
, M.L. Couce Picob, A. Sánchez-Salmónc, J.M. Pascuald
Autor para correspondencia
gomezlado@yahoo.es
Dra. C. Gómez Lado. Departamento de Pediatría. Servicio de Neuropediatría. Complejo Hospitalario Universitario de Santiago de Compostela. A Choupana, s/n. 15706 Santiago de Compostela. España.
Dra. C. Gómez Lado. Departamento de Pediatría. Servicio de Neuropediatría. Complejo Hospitalario Universitario de Santiago de Compostela. A Choupana, s/n. 15706 Santiago de Compostela. España.
a Servicio de Neurología Pediátrica. Unidad de Trastornos Metabólicos. Hospital Clínico Universitario de Santiago de Compostela. Santiago de Compostela. España
b Servicios de Neonatología. Hospital Clínico Universitario de Santiago de Compostela. Santiago de Compostela. España
c Servicios de Medicina Nuclear. Hospital Clínico Universitario de Santiago de Compostela. Santiago de Compostela. España Neurometabolic Clinic, Departments of Neurology. The University of Texas Southwestern Medical Center. Texas. Estados Unidos
d Servicios de Physiology and Pediatrics The University of Texas Southwestern Medical Center. Texas. Estados Unidos
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Información del artículo
ISSN: 16954033Idioma original: Español
DOI:10.1157/13125831
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