A. Martínez‐Bermejo

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Primary Degeneration of the Granular Layer of the Cerebellum. A Study of 14 Patients and Review of the Literature

I. Pascual-Castroviejo, S. Pascual-Pascual, A. Martínez-Bermejo, 1994, Neuropediatrics.

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

I. Pascual-Castroviejo, J. García-Peñas, S. Pascual-Pascual, 1996, AJNR. American journal of neuroradiology.

Acute intermittent porphyria: studies of the severe homozygous dominant disease provides insights into the neurologic attacks in acute porphyrias.

T. Naidich, W. Kaufmann, R. Desnick, 2004, Archives of neurology.

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

M. Orozco, J. Gelpí, A. Ribes, 2000, Pediatric Research.

[Management of prolonged convulsive seizures in the community: results of the PERFECT™ study in Spain].

R. Sanchez-Carpintero, A. Martínez-Bermejo, S. Wait, 2014, Anales de pediatria.

Long-Term Use of Oxcarbazepine Oral Suspension in Childhood Epilepsy: Open-Label Study

C. Casas-Fernández, M. Rufo-Campos, A. Martínez‐Bermejo, 2006, Journal of child neurology.

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene

J. Serratosa, J. García-Peñas, P. Gómez-Garre, 2014, Epilepsy Research.

[Narcolepsy with and without cataplexy: an uncommon disabling and unrecognized disease].

M. Merino-Andreu, A. Martínez-Bermejo, A. Martínez‐Bermejo, 2009, Anales de pediatria.

Hypomelanosis of ITO. A study of 76 infantile cases

S. Pascual-Pascual, A. Martínez-Bermejo, J. Arcas, 1998, Brain and Development.

Acute intermittent porphyria: studies of the severe homozygous dominant disease provides insights into the neurologic attacks in acute porphyrias.

T. Naidich, W. Kaufmann, R. Desnick, 2004, Archives of neurology.

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene

J. Serratosa, J. García-Peñas, P. Gómez-Garre, 2014, Epilepsy Research.

[Use of benzodiazepines in prolonged seizures and status epilepticus in the community].

F. Sanmartí, M. Cebollero, F. Sanmartí, 2014, Anales de Pediatría.

Flaccid paraplegia as complication of umbilical artery catheterization.

A. Martínez-Bermejo, R. Escribá, I. Pascual‐Castroviejo, 1993, Pediatric neurology.

Persistence of the Hypoglossal Artery and Partial Agenesis of the Cerebellum

J. López-Terradas, A. Martínez-Bermejo, C. Casas, 1975 .

Identification of a new frameshift mutation (1801delAG) in the ALD gene.

A. Barceló, M. Girós, C. Sarde, 1994, Human molecular genetics.

Hypohidrosis Related to the Administration of Topiramate to Children

A. Martínez-Bermejo, J. Arcas, V. Lopez-Martin, 2001, Epilepsia.