Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M D Mora-Ramírez"'
Publikováno v:
Revista de neurologia. 73(4)
Joubert syndrome is produced by an alteration of the ciliary proteins essential for the structure and function of neurons and organs such as the kidneys, liver, sight, and hearing. Some 34 mutations are currently known.Calculate the incidence / preva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9c87ff32ca019d005464ecd921c4661
https://pubmed.ncbi.nlm.nih.gov/35484703
https://pubmed.ncbi.nlm.nih.gov/35484703
Publikováno v:
Revista de neurologia. 71(10)
Epileptic status represents the most frequent neurological emergency in pediatrics. Prolonged febrile seizures represent the most common etiology. Our objective is to update its epidemiology and analyze its evolutionary consequences.Observational ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a950ec677fc081fec267f779fd7c7ce5
https://pubmed.ncbi.nlm.nih.gov/33145747
https://pubmed.ncbi.nlm.nih.gov/33145747
Autor:
L, Aguilera-Nieto, J, Ferrero-Turrión, M D, Mora-Ramírez, R, Calvo-Medina, C, Ruiz-García, J M, Ramos-Fernández
Publikováno v:
Revista de neurologia. 71(2)
Dyskinesia of the ADCY5 mutation is a rare movement-onset disorder in childhood. It is characterized by isolated chorea movements or associated with myoclonus and dystonia affecting the limbs, neck and face. The low number of patients and families st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0675e4231485f8cca4ce80e24ef183ee
https://pubmed.ncbi.nlm.nih.gov/32627162
https://pubmed.ncbi.nlm.nih.gov/32627162
Publikováno v:
Revista de Neurología. 73:115
Introduccion. El sindrome de Joubert se produce por una alteracion de las proteinas ciliares esenciales para la estructura y la funcion de neuronas y organos como los rinones, el higado, la retina y el oido. Se conocen unas 34 mutaciones en la actual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c70d615950e7812670c0361ffd75e15e
https://doi.org/10.33588/rn.7304.2021066
https://doi.org/10.33588/rn.7304.2021066
Publikováno v:
Revista de Neurología. 71:365
Introduccion. El estado epileptico representa la emergencia neurologica mas frecuente en pediatria. Las convulsiones febriles prolongadas representan la etiologia mas frecuente. Nuestro objetivo es actualizar su epidemiologia y analizar sus consecuen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9775f217cd5882cdcaaf965d26162785
https://doi.org/10.33588/rn.7110.2020306
https://doi.org/10.33588/rn.7110.2020306
Autor:
A C, Rodríguez-Barrionuevo, M A, Caballero-Morales, M P, Delgado-Marqués, M D, Mora-Ramírez, J, Martínez-Antón
Publikováno v:
Revista de neurologia. 26(154)
The childhood opsoclonus-myoclonus or Kinsbourne syndrome, is a uncommon process, of acute or subacute beginning, which affects infant and children. It's course is characterized by opsoclonus, polimyoclonias and cerebellar ataxia. The disease is freq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::339cfa2346afc2d1c23b9960cbf4a379
https://pubmed.ncbi.nlm.nih.gov/9658467
https://pubmed.ncbi.nlm.nih.gov/9658467
Autor:
A C, Rodríguez-Barrionuevo, E, Bauzano-Poley, M P, Delgado-Marqués, M D, Mora-Ramírez, E, Tosina-García
Publikováno v:
Revista de neurologia. 26(150)
Between 369 cases of benign partial epilepsy of the childhood with Rolandic spikes (BECRS) diagnosed in our hospital, we have been able to study three patients that have presented a neurophysiological and clinical presentation that was compatible wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1464bc042e5cf28d057af654e1a4e53a
https://pubmed.ncbi.nlm.nih.gov/9563088
https://pubmed.ncbi.nlm.nih.gov/9563088