I. Castroviejo

发表

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

M. T. Medina, J. Mani, G. Fong, 1998, American journal of human genetics.

Hypoxanthine and xanthine transport through the blood-brain barrier in hypoxanthine phosphoribosyltransferase (HPRT) deficiency.

I. Castroviejo, J. Puig, F. Mateos, 1988, Advances in experimental medicine and biology.

Bilateral Thrombosis of the Middle Cerebral Artery in a Child Aged 14 Months

I. Castroviejo, J. Larrauri, 1971, Developmental medicine and child neurology.

Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.

M. T. Medina, J. Sainz, P. Shah, 1999, Advances in neurology.

Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.

M. T. Medina, I. Castroviejo, G. Pineda, 2006, Brain : a journal of neurology.

Spondylo‐thoracic Dysplasia in Three Sisters

I. Castroviejo, F. Castillo, T. Rodríguez-Costa, 1973, Developmental medicine and child neurology.

[The cerebrospinal fluid in normal premature infants].

I. Castroviejo, E. Roldán, L. G. Coviella, 1968, Revista portuguesa de pediatria e puericultura.

Further delineation of neuropsychiatric findings in Tatton-Brown-Rahman syndrome due to disease-causing variants in DNMT3A: seven new patients

Miguel Ángel Martínez, N. Rahman, Pablo I Alarcón, 2019, European Journal of Human Genetics.

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

Colin A. Johnson, S. Nelson, B. Merriman, 2011, Nature Genetics.

Suprasellar arachnoid cysts in children report of three cases

I. Castroviejo, C. González, M. G. Blázquez, 2005, Acta Neurochirurgica.

The Prosencephalies: Morphology, Neuroradiological Appearances and Differential Diagnosis

I. Castroviejo, A. Brun, F. Probst, 1979 .

Occipital Osteodiastasis A Rare Complication in Cephalic Delivery

I. Castroviejo, M. Roche, A. Vélez, 1990, Acta paediatrica Scandinavica.

Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map.

K. Yamakawa, P. Shah, I. Castroviejo, 2000, Genomics.

Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24

K. Yamakawa, P. Shah, I. Castroviejo, 1999, Epilepsy Research.

Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features.

M. T. Medina, I. Castroviejo, G. Pineda, 2005, Advances in neurology.

In Memoriam. Manuel R. Gómez (1928-2006)

I. Castroviejo, 2006 .