Zobrazeno 1 - 10
of 49
pro vyhledávání: '"C, Mosquera Tenreiro"'
Autor:
C. Mosquera Tenreiro, A. Rodríguez Fernández, I. Riaño Galán, C. Rodríguez Dehli, F. Ariza Hevia, E. García López, J. Fernández Toral
Publikováno v:
Anales de Pediatría, Vol 73, Iss 3, Pp 132-137 (2010)
Resumen: Introducción: Las fisuras labiales y palatinas son los defectos congénitos faciales más frecuentes. Objetivo: Conocer la frecuencia de estos defectos en Asturias y realizar una descripción clinicoepidemiológica de sus anomalías asociad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::875a40ca75332bd0005fd69668e85c38
https://doi.org/10.1016/j.anpedi.2009.07.013
https://doi.org/10.1016/j.anpedi.2009.07.013
Autor:
C. Rodríguez Dehli, E. Suárez Menéndez, F. Ariza Hevia, I. Riaño Galán, C. Mosquera Tenreiro, E. García López, C. Moro Bayón
Publikováno v:
Anales de Pediatría, Vol 72, Iss 4, Pp 250-256 (2010)
Resumen: Introducción: Los defectos oculares congénitos (DOC) pueden originar importante discapacidad. Objetivo: El objetivo de este estudio fue conocer la prevalencia total de los DOC en Asturias, su tendencia y realizar una descripción de su for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::633882feeb8df2640940c4bbc5b90ce4
http://www.sciencedirect.com/science/article/pii/S169540331000069X
http://www.sciencedirect.com/science/article/pii/S169540331000069X
Autor:
J. Fernández Toral, F. Ariza Hevia, I. Riaño Galán, E. Suárez Menéndez, C. Mosquera Tenreiro, A. Rodríguez Fernández, E. García López, A. Franganillo Fernández, C. Moro Bayón
Publikováno v:
Anales de Pediatría, Vol 52, Iss 4, Pp 362-368 (2000)
Objetivo: Conocer la prevalencia y forma de presentación clínicade los defectos por reducción de extremidades en la poblaciónasturiana. Pacientes y métodos: Estudio de niños con defectos de reducción de extremidadesentre los 91.300 nacidos viv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc815429c30e949240f83401f355fa0b
https://doi.org/10.1016/s1695-4033(00)77358-9
https://doi.org/10.1016/s1695-4033(00)77358-9
Autor:
I, Riaño Galán, C, Rodríguez Dehli, E, García López, C, Moro Bayón, E, Suárez Menéndez, F, Ariza Hevia, C, Mosquera Tenreiro
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 72(4)
Congenital ocular anomalies (COAs) can produce serious disability.The purpose of this investigation was to assess the prevalence of COAs, their trends and to describe the associated malformations and syndromes in a geographically defined population.D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::405ed77d8bd8cd7f7dbe72e55f518d5a
https://pubmed.ncbi.nlm.nih.gov/20199894
https://pubmed.ncbi.nlm.nih.gov/20199894
Autor:
C, Rodríguez Dehli, F, Ariza Hevia, I, Riaño Galán, C, Moro Bayón, E, Suárez Menéndez, C, Mosquera Tenreiro, E, García López
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 71(6)
Congenital heart diseases (CHDs) are the most common type of birth defect.The purpose of this investigation was to assess the prevalence and trends of CHDs, and to describe the associated malformations and syndromes or sequences in a geographically d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::155576647e9adf71db58b578e05237ca
https://pubmed.ncbi.nlm.nih.gov/19819200
https://pubmed.ncbi.nlm.nih.gov/19819200
Autor:
C, Rodríguez Dehli, C, Mosquera Tenreiro, E, García López, J, Fernández Toral, A, Rodríguez Fernández, I, Riaño Galán, F, Ariza Hevia
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 73(3)
Cleft lip and palate (oral clefts) are the most common congenital facial defects.To assess the prevalence of oral clefts and to describe the associated malformations in a geographically defined population.Data from the Asturias Registry of Congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b3465e79d62ec805642d45578321f79d
https://pubmed.ncbi.nlm.nih.gov/19726251
https://pubmed.ncbi.nlm.nih.gov/19726251
Autor:
Loane, Maria, Dolk, Helen, Morris, Joan, EUROCAT working group. Collaborators(23) Haeusler, Martin, Nelen, Vera, Barišić, Ingeborg, Garne, Ester, de Vigan, Catherine, Doray, Berenice, Queisser-Luft, Annette, Poetzsch, Simone, O'Mahony, Mary, McDonnell, B, Roche BA, Calzolari, Eliza, Pierini, Anna, Gatt, Miriam, de Walle, Heruien, Latos-Bielenska, Anna, Dias C, Mosquera- Tenreiro C, Salvador, Joaquin, Portillo, Isabel, Addor, Marie-Claude, Boyd, Patricia, Tucker, David
OBJECTIVES: To determine the excess risk of non- chromosomal congenital anomaly (NCA) among teenage mothers and older mothers. DESIGN AND SETTING: Population-based prevalence study using data from EUROCAT congenital anomaly registers in 23 regions of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e529b918e31ae915fce98e3602c8d143
https://www.bib.irb.hr/453855
https://www.bib.irb.hr/453855
Autor:
I, Riaño Galán, J, Fernández Toral, E, García López, C, Moro Bayón, C, Mosquera Tenreiro, A, Rodríguez Fernández, E, Suárez Menéndez, F, Ariza Hevia, A, Franganillo Fernández
Publikováno v:
Anales espanoles de pediatria. 52(4)
To determine the prevalence and clinical presentation of limb reduction defects in Asturias (Spain).Among the 92300 newborns, stillbirths and induced abortions for congenital defects surveyed by the Registry of Congenital Defects in Asturias (populat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7d32ce280d6bb560a727d7f1afe26387
https://pubmed.ncbi.nlm.nih.gov/11003927
https://pubmed.ncbi.nlm.nih.gov/11003927
Autor:
J, Salvador Peral, S, García-Miñaur Rica, M R, Caballín Fernández, C, Mosquera Tenreiro, N, Baena Díez, E, García López, V, Castro Laiz, M, Guitart Feluibadaló, E, Gabau Vila, A, Plasència Taradach
Publikováno v:
Anales espanoles de pediatria. 48(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a356922d375b51250763452f1202857
https://pubmed.ncbi.nlm.nih.gov/9662839
https://pubmed.ncbi.nlm.nih.gov/9662839
Autor:
C, Mosquera Tenreiro, J, Fernández Toral, J, Espinosa Pérez, E, García López, M, González-Rico, C, Moro Bayón, I, Riaño Galán, A, Rodríguez Fernández, E, Suárez Menéndez, F, Ariza Hevia
Publikováno v:
Gaceta sanitaria. 10(53)
To determine the frequency of Down Syndrome (DS) in Asturias and the prenatal diagnosis impact on the birth prevalence of this chromosomal anomaly.The analysed data came from the Registry of Congenital Defects of Asturias (1990-1993) and from a retro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0ca6086e586bf399806462868826d54
https://pubmed.ncbi.nlm.nih.gov/8755157
https://pubmed.ncbi.nlm.nih.gov/8755157