Juan José Garcı́a-Peñas

Author

Hospital Infantil Universitario Niño Jesús ORCID

Also Known As

J J Garcia-Penas, J J Garcia-Peñas, J J García-Peñas, J. J. García‐Peñas, J.J García-Peñas, J.J. García-Peñas, Juan Garcı́a-Peñas, Juan J García-Peñas, Juan J. Garcia‐Peñas, Juan J. García-Peñas

Publications

888

Citations

H-Index

Concepts

All Affiliations

Hospital Infantil Universitario Niño Jesús Hospital Universitario Virgen de la Arrixaca Hospital Universitario 12 De Octubre Hospital Universitario La Paz Centre for Biomedical Network Research on Rare Diseases

About

Juan José Garcı́a-Peñas is an author at Hospital Infantil Universitario Niño Jesús specializing in medicine, pediatrics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	12	262
2	Social Sciences	3	3	45
3	Natural Sciences	1	1	29
4	Anatomy	1	1	10
5	Biochemistry	1	1	29

Juan José Garcı́a-Peñas

Publications

666

Citations

H-Index

Page 1

	Year	Citations
Hemangiomas of the head, neck, and chest with associated vascular and brain anomalies: a complex neurocutaneous syndrome. I Pascual-Castroviejo, J. Viaño, Fernando Moreno, PubMed	1996	115
Perampanel in routine clinical use in idiopathic generalized epilepsy: The 12‐month GENERAL study Vicente Villanueva, Javier Montoya, Ascensión Castillo, Epilepsia	2018	111
Incontinentia pigmenti: MR demonstration of brain changes. I Pascual-Castroviejo, M C Roche, M Perez-Romero, PubMed	1994	53
Clinical, polysomnographic and laboratory characteristics of narcolepsy–cataplexy in a sample of children and adolescents Rosa Peraita‐Adrados, Juan José Garcı́a-Peñas, Luz Ruiz-Falcó, Sleep Medicine MedicineLaboratory CharacteristicsPediatrics	2010	46
Emergency implementation of telemedicine for epilepsy in Spain: Results of a survey during SARS-CoV-2 pandemic Estefanía Conde‐Blanco, María Centeno, Ester Tió, Epilepsy & Behavior	2020	45
Clinical heterogeneity associated with mitochondrial DNA depletion in muscle Yolanda Campos, Miguel A. Martı́n, Teresa Garcı́a-Silva, Neuromuscular Disorders Mitochondrial MyopathyMitochondrial FunctionClinical HeterogeneityPhysiologyDna Replication	1998	30
A Nonsense Mutation in the Exon 2 of the 3-Hydroxy- 3-methylglutaryl Coenzyme A Lyase (HL) Gene Producing Three Mature mRNAs Is the Main Cause of 3-Hydroxy-3-methylglutaric Aciduria in European Mediterranean Patients César H. Casale, Núria Casals, Juan Pié, Archives of Biochemistry and Biophysics Mendelian DisorderBiochemistryGenetic DisorderNatural SciencesGenetics	1998	29
Macrophagic Myofasciitis in Childhood: A Controversial Entity Eloy Rivas, Mercedes Gómez, José Ramón Ricoy, Pediatric Neurology Autoimmune DiseasePathogenesisPediatricsTuberculosisInfection Control	2005	28
Nap polygraphic recordings after partial sleep deprivation in patients with suspected epileptic seizures Rosa Peraita‐Adrados, Luis González Gutiérrez-Solana, M.L. Ruiz-Falcó, Neurophysiologie Clinique Sleep DisordersSleepSleep DisorderNeurophysiologyPartial Sleep Deprivation	2001	22
Clinical and genetic features of 13 Spanish patients with KCNQ2 mutations Montesclaros Hortigüela, Ana Fernández‐Marmiesse, Verónica Cantarín, Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologySpanish PatientsPathology	2016	22

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