PUBLICACIÓN

Trastornos del aprendizaje no verbal:: estudio clínico y tratamiento farmacológico

ACCEDER A LA PUBLICACIÓN: Dialnet

Julián Vaquerizo Madrid, Cristina Cáceres Marzal, M. Ramírez Arenas, Sonia Arias Castro, M. Fernández Carbonero, R. Valverde Palomares

2009 REVISTA DE NEUROLOGIA

Medicine (miscellaneous) (Q3), Neurology (clinical) (Q3)

JCR: 1.234

SJR: 0.29

DOI

10.33588/rn.48s02.2009132

ISSN

0210-0010

AUTORES DE LA UEX

Cristina Cáceres Marzal

OTRAS PUBLICACIONES DE INTERÉS

Zellweger Syndrome. Reports On Two New Cases
Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization
Idiopathic Intracranial Hypertension. Review Of Our Experience In The Last Eight Years (2016-2023)
Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization
Genetic Diagnosis Of Basal Ganglia Disease In Childhood
Clinprior: An Algorithm For Diagnosis And Novel Gene Discovery By Network-Based Prioritization
Genetic Diagnosis Of Basal Ganglia Disease In Childhood
Management And Monitoring Of Patients With Duchenne Disease
Genetic Diagnosis Of Basal Ganglia Disease In Childhood
Management And Monitoring Of Patients With Duchenne Disease
Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma
Management And Monitoring Of Patients With Duchenne Disease
Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma
Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis
Central Nervous System Chemotoxicity During Treatment Of Pediatric Acute Lymphoblastic Leukemia/lymphoma
Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis
Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties
Methotrexate-Induced Subacute Neurotoxicity In A Child With Acute Lymphoblastic Leukemia Carrying Genetic Polymorphisms Related To Folate Homeostasis
Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties
Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico
Idiopathic Focal Epilepsies In Childhood. Diagnostic Difficulties
Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico
Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment
Trastornos Del Aprendizaje No Verbal:: Estudio Clínico Y Tratamiento Farmacológico
Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment
Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Non-Verbal Learning Disorders: A Clinical Study And Pharmacological Treatment
Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Decreased Corneal Opacity And Improved Vision In A Patient With Mucopolysaccharidosis I (Hurler-Scheie) Treated With Enzyme Replacement Therapy (Laronidase, Aldurazyme®)
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Early Response To Idursulfase Treatment In A 3 Year-Old Boy Affected Of Hunter Syndrome
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Holt-Oram Syndrome [4]
Early Mitochondrial Dysfunction In An Infant With Alexander Disease
Holt-Oram Syndrome [4]
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Holt-Oram Syndrome [4]
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Zellweger Syndrome. Reports On Two New Cases
Hair With A Double Crown And Dilatation Of Virchow-Robin Spaces: A Proposal For A New Neurocutaneous Association
Zellweger Syndrome. Reports On Two New Cases
Clinical And Molecular Profiling In Gnao1 Permits Phenotype–genotype Correlation
WEB ACCESIBLE