J M Prats

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis et al. · Nature Genetics · 2005 · 264 citations

Life Sciences, Genetics, Neuroscience +12

Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

Christiane Busquets, B. Merinero, Ernst Christensen et al. · Pediatric Research · 2000 · 133 citations

Life Sciences, Genetics, Molecular Genetics +8

<i>LAMA2</i> gene analysis in a cohort of 26 congenital muscular dystrophy patients

Jorge Oliveira, Rosário Santos, Isabel Soares‐Silva et al. · Clinical Genetics · 2008 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

INFANTILE SPASMS TREATED WITH HIGH DOSES OF SODIUM VALPROATE: INITIAL RESPONSE AND FOLLOW‐UP

J M Prats, C Garaízar, Mariano Rua et al. · Developmental Medicine & Child Neurology · 1991 · 57 citations

Medicine, Neurology, Pharmacology +9

Antiepileptic Drugs and Atypical Evolution of Idiopathic Partial Epilepsy

J M Prats, C Garaízar, Marı́a L. Garcı́a-Nieto Psy et al. · Pediatric Neurology · 1998 · 53 citations

Medicine, Pharmacology, Pharmacotherapy +12