A Martínez-Bermejo

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 · 132 citations · Full text

Aldehyde Dehydrogenase, Metabolic Disorder, Genetics +6

Hemangiomas of the head, neck, and chest with associated vascular and brain anomalies: a complex neurocutaneous syndrome.

I Pascual-Castroviejo, J. Viaño, Fernando Moreno et al. · PubMed · 1996 · 115 citations · Full text

Hypomelanosis of ITO. A study of 76 infantile cases

I Pascual-Castroviejo, Carmen Roche, A Martínez-Bermejo et al. · Brain and Development · 1998 · 111 citations

Developmental Anomaly, Thumb Hypoplasia, Neurological Disorder +4

Acute Intermittent Porphyria

Constanza Solis, A Martínez-Bermejo, Thomas P. Naidich et al. · Archives of Neurology · 2004 · 100 citations

Hypohidrosis Related to the Administration of Topiramate to Children

Joaquín Arcas, Teresa Ferrer, María C. Roche et al. · Epilepsia · 2001 · 67 citations · Full text