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Patricia Alcaide
Patricia Alcaide
Autonomous University of Madrid
Medicine
Phenotype
Gene
Genetics
Creatine transporter deficiency
2
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14
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Severe anemia in patients with Propionic acidemia is associated with branched-chain amino acid imbalance.
2021
Orphanet Journal of Rare Diseases
Sinziana Stanescu
Amaya Bélanger-Quintana
Borja Manuel Fernández Félix
Francisco Arrieta
Victor Quintero
Maria Soledad Maldonado
Patricia Alcaide
Mercedes Martínez-Pardo
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A new case of creatine transporter deficiency associated with mild clinical phenotype and a novel mutation in the SLC6A8 gene
2010
Developmental Medicine & Child Neurology
Patricia Alcaide
Pilar Rodríguez-Pombo
Pedro Ruiz-Sala
Isaac Ferrer
Pedro Castro
Yolanda Ruíz-Martín
Begoña Merinero
Magdalena Ugarte
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Citations (14)
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