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Revista De Neurologia
|
July 26, 2014
[Diploid/triploid mosaicism: a variable but characteristic phenotype]
Daniel Natera-De Benito, Pilar Poo, Esther Gean, et al.
Cerebellum (London, England)
|
May 27, 2009
Cerebellar hemorrhage in a patient with propionic acidemia
Daniel Velasco-Sánchez, Lilianne Gómez-Lopez, María Antonia Vilaseca, et al.
Expert Review of Neurotherapeutics
|
June 21, 2015
Clinical, etiological and therapeutic aspects of cerebral folate deficiency
Marta Molero-Luis, Mercedes Serrano, Maria M O'Callaghan, et al.
Annals of Neurology
|
November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspects
Angels García-Cazorla, Daniel Rabier, Guy Touati, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 11, 2008
Efficacy of rasburicase in hyperuricemia secondary to Lesch-Nyhan syndrome
Ana Roche, Belén Pérez-Dueñas, Juan Antonio Camacho, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 21, 2006
Determination of 5-methyltetrahydrofolate in cerebrospinal fluid of paediatric patients: reference values for a paediatric population
Aida Ormazabal, Angels García-Cazorla, Belén Pérez-Dueñas, et al.
Developmental Medicine and Child Neurology
|
March 5, 2004
White matter alterations associated with chromosomal disorders
Angels García-Cazorla, Anna Sans, Miguel Baquero, et al.
Pediatric Neurology
|
October 18, 2015
Efficacy of the Ketogenic Diet for the Treatment of Refractory Childhood Epilepsy: Cerebrospinal Fluid Neurotransmitters and Amino Acid Levels
Andrea Sariego-Jamardo, Angels García-Cazorla, Rafael Artuch, et al.
Clinical Biochemistry
|
March 15, 2011
Folate analysis for the differential diagnosis of profound cerebrospinal fluid folate deficiency
Aida Ormazábal, Belén Perez-Dueñas, Cristina Sierra, et al.
JIMD Reports
|
February 23, 2013
5-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense Changes
Eduardo Calpena, Mercedes Casado, Dolores Martínez-Rubio, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 62) with videos related to
Sort By:
Page
of 7
Revista De Neurologia
|
July 26, 2014
[Diploid/triploid mosaicism: a variable but characteristic phenotype]
Daniel Natera-De Benito, Pilar Poo, Esther Gean, et al.
Cerebellum (London, England)
|
May 27, 2009
Cerebellar hemorrhage in a patient with propionic acidemia
Daniel Velasco-Sánchez, Lilianne Gómez-Lopez, María Antonia Vilaseca, et al.
Expert Review of Neurotherapeutics
|
June 21, 2015
Clinical, etiological and therapeutic aspects of cerebral folate deficiency
Marta Molero-Luis, Mercedes Serrano, Maria M O'Callaghan, et al.
Annals of Neurology
|
November 10, 2005
Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspects
Angels García-Cazorla, Daniel Rabier, Guy Touati, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 11, 2008
Efficacy of rasburicase in hyperuricemia secondary to Lesch-Nyhan syndrome
Ana Roche, Belén Pérez-Dueñas, Juan Antonio Camacho, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 21, 2006
Determination of 5-methyltetrahydrofolate in cerebrospinal fluid of paediatric patients: reference values for a paediatric population
Aida Ormazabal, Angels García-Cazorla, Belén Pérez-Dueñas, et al.
Developmental Medicine and Child Neurology
|
March 5, 2004
White matter alterations associated with chromosomal disorders
Angels García-Cazorla, Anna Sans, Miguel Baquero, et al.
Pediatric Neurology
|
October 18, 2015
Efficacy of the Ketogenic Diet for the Treatment of Refractory Childhood Epilepsy: Cerebrospinal Fluid Neurotransmitters and Amino Acid Levels
Andrea Sariego-Jamardo, Angels García-Cazorla, Rafael Artuch, et al.
Clinical Biochemistry
|
March 15, 2011
Folate analysis for the differential diagnosis of profound cerebrospinal fluid folate deficiency
Aida Ormazábal, Belén Perez-Dueñas, Cristina Sierra, et al.
JIMD Reports
|
February 23, 2013
5-Oxoprolinuria in Heterozygous Patients for 5-Oxoprolinase (OPLAH) Missense Changes
Eduardo Calpena, Mercedes Casado, Dolores Martínez-Rubio, et al.
Page
of 7