Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gonzalo Mateo-Martínez"'
Autor:
Obdulia Sánchez‐Lijarcio, Delia Yubero, Fátima Leal, María L. Couce, Luis González Gutiérrez‐Solana, Eduardo López‐Laso, Àngels García‐Cazorla, Leticia Pías‐Peleteiro, Begoña de Azua Brea, Salvador Ibáñez‐Micó, Gonzalo Mateo‐Martínez, Monica Troncoso‐Schifferli, Scarlet Witting‐Enriquez, Magdalena Ugarte, Rafael Artuch, Belén Pérez
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
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Glucose transporter 1 deficiency syndrome (GLUT1DS) is a neurometabolic disorder caused by haploinsufficiency of the GLUT1 glucose transporter (encoded by SLC2A1) leading to defective glucose transport across the blood–brain barrier. This work desc
Autor:
Vincenzo Lupo, Samuel I. Pascual-Pascual, M. Gutiérrez-Molina, Carmen Espinós, Gonzalo Mateo-Martínez, Paula Sancho, Eduardo Calpena, Gema Arriola-Pereda
Publikováno v:
Journal of Child Neurology. 30:1544-1548
Early-onset hereditary motor and sensory neuropathies are rare diseases representing a broad clinical and genetic spectrum. Without a notable familial history, the clinical diagnosis is complicated because acquired causes of peripheral neuropathy, su
Autor:
María Jesús García Mazario, Francisco José Martín Gómez, Fatima Olalla Nadal, Angélica Andrés Bartolomé, Beatriz Blazquez Arrabal, Gonzalo Mateo Martínez, Gema Arriola Pereda
Publikováno v:
European Journal of Paediatric Neurology. 21:e201