Evolución secular y por autonomías de la frecuencia de tratamientos de fertilidad, partos múltiples y cesáreas en España ML Martínez-Frías, E Bermejo, E Rodríguez-Pinilla, G Dequino, ... Med Clin (Barc) 124 (4), 132-9, 2005 | 86* | 2005 |
Consumo de tabaco durante el embarazo en España: análisis por años, comunidades autónomas y características maternas ML Martínez-Frías, E Rodríguez-Pinilla, E Bermejo Med Clin (Barc) 124 (3), 86-92, 2005 | 67 | 2005 |
FRECUENCIA DE ANOMALÍAS CONGÉNITAS EN ESPAÑA: VIGILANCIA EPIDEMIOLÓGICA EN EL ECEMC EN EL PERIODO 1980 2007 E Bermejo, L Cuevas, J Mendioroz | 52* | |
Proximal partial 5p trisomy resulting from a maternal (19; 5) insertion I Lorda‐Sánchez, M Urioste, A Villa, MC Carrascosa, MS Vásquez, ... American journal of medical genetics 68 (4), 476-480, 1997 | 38 | 1997 |
Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement A Fernández-Marmiesse, MC Carrascosa-Romero, BA Ponce, ... Neuromuscular Disorders 27 (2), 188-192, 2017 | 35 | 2017 |
X-chromosome-linked ichthyosis associated to epilepsy, hyperactivity, autism and mental retardation, due to the Xp22. 31 microdeletion]. MC Carrascosa-Romero, J Suela, B Alfaro-Ponce, AJ Cepillo-Boluda Revista de neurologia 54 (4), 241, 2012 | 24 | 2012 |
Incidencia de las epilepsias y síndromes epilépticos de la infancia en la provincia de Albacete IO Ramírez, MH Rodríguez, JMA Meix, CC Romero An Esp Pediatr 51 (2), 154-158, 1999 | 24 | 1999 |
Neonatal lupus erythematosus with multisystem organ involvement preceding cutaneous lesions E Fonseca, F Contreras, E García-Frías, MC Carrascosa Lupus 1 (1), 49, 1991 | 24 | 1991 |
A new severe mutation in the SLC5A7 gene related to congenital myasthenic syndrome type 20 JM Pardal-Fernández, MC Carrascosa-Romero, S Álvarez, ... Neuromuscular Disorders 28 (10), 881-884, 2018 | 23 | 2018 |
GM1-gangliosidosis presenting as nonimmune hydrops fetalis: a case report MJ Tasso, A Martinez-Gutierrez, C Carrascosa, S Vazquez, R Tebar Walter de Gruyter, Berlin/New York 24 (5), 445-449, 1996 | 23 | 1996 |
Congenital gingival hyperplasia in a neonate with foetal valproate syndrome M Rodríguez-Vázquez, MC Carrascosa-Romero, JM Pardal-Fernández, ... Neuropediatrics 38 (05), 251-252, 2007 | 19 | 2007 |
Priapism and Fabry disease: a case report J García-Consuegra, M Padrón, E Jaureguizar, C Carrascosa, J Ramos European journal of pediatrics 149 (7), 500-501, 1990 | 17 | 1990 |
Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c. 125C> T mutation in ASAH1 BG Giráldez, R Guerrero-López, L Ortega-Moreno, A Verdú, ... Neuromuscular Disorders 25 (3), 222-224, 2015 | 16 | 2015 |
Tobacco smoking during pregnancy in Spain: an analysis according to years, autonomous communities and maternal characteristics ML Martínez-Frías, E Rodríguez-Pinilla, E Bermejo Medicina Clinica 124 (3), 86-92, 2005 | 16 | 2005 |
Pericentric inversions of chromosome 4: report of a new family and review of the literature A Villa, M Urioste, MC Carrascosa, S Vazquez, A Martinez, ... Clinical genetics 48 (5), 255-260, 1995 | 16 | 1995 |
The comorbidity of ADHD and Autism Spectrum Disorders (ASDs) in community preschoolers MC Carrascosa-Romero, C De Cabo-De La Vega ADHD-New Directions in Diagnosis and Treatment, 109-162, 2015 | 12 | 2015 |
A 2.84 Mb deletion at 21q22. 11 in a patient clinically diagnosed with Marden–Walker syndrome MC Carrascosa‐Romero, J Suela, JM Pardal‐Fernández, ... American Journal of Medical Genetics Part A 161 (9), 2281-2290, 2013 | 11 | 2013 |
Análisis clínico de los recién nacidos con defectos congénitos registrados en el ECEMC: Distribución por etiología y por grupos étnicos ML Martínez-Frías, E Bermejo-Sanchez Instituto de Salud Carlos III (ISCIII). Instituto de Investigación de …, 2009 | 11* | 2009 |
Neonatal viral meningitis. The importance of the polymerase chain reaction in their diagnosis C Marcilla-Vazquez, A Martinez-Gutierrez, MC Carrascosa-Romero, ... Revista de neurologia 67 (12), 484-490, 2018 | 10 | 2018 |
Neurocristopathies: a high incidence of cerebral dysgenesis in patients with Hirschsprung's disease MC Carrascosa-Romero, MS Fernandez-Cordoba, J Gonzalvez-Pinera, ... Revista de Neurologia 45 (12), 707-712, 2007 | 10 | 2007 |