J Campos-Castelló

Congenital muscular dystrophy and cerebral CT scan anomalies

Bernard Échenne, M Arthuis, C. Billard et al. · Journal of the Neurological Sciences · 1986 · 62 citations

Medicine, Pediatrics, Radiology +12

Efficacy and Tolerability of Lacosamide in the Concomitant Treatment of 130 Patients Under 16 Years of Age with Refractory Epilepsy

C Casas-Fernández, A Martínez-Bermejo, M Rufo-Campos et al. · Drugs in R&D · 2012 · 53 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +16

Aicardi–Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

Sabine Fauré, Isabelle Bordelais, Catherine M. Marquette et al. · Clinical Genetics · 1999 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

[Rett syndrome: 50 years' history of a still not well known condition].

J Campos-Castelló, Daniel Martı́n Fernández-Mayoralas, Nuria Muñoz-Jareño et al. · PubMed · 2007 · 12 citations

Life Sciences, Genetics, Neurology +17

Biotinidase deficiency: result of treatment with biotin from age 12 years

E Casado de Frías, J Campos-Castelló, J Careaga Maldonado et al. · European Journal of Paediatric Neurology · 1997 · 11 citations

Life Sciences, Biochemistry, Pediatrics +7