Zobrazeno 1 - 10
of 23
pro vyhledávání: '"C, Lozano Giménez"'
Autor:
L. Sánchez Muñoz, L.M.a Villar Gimerans, I. Sánchez Pérez, G. Roy Ariño, A. Carrillo Herranz, C. Lozano Giménez, J. M. Aparicio Meix
Publikováno v:
Anales de Pediatría, Vol 59, Iss 2, Pp 187-189 (2003)
La enfermedad de Rasmussen es un trastorno cerebral inflamatorio, crónico y progresivo que se manifiesta con crisis focales motoras neocorticales resistentes al tratamiento y que culmina en un deterioro grave con hemiparesia, retraso cognitivo y afa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36147da35e45abff12e971d42e1d9736
http://www.sciencedirect.com/science/article/pii/S1695403303787463
http://www.sciencedirect.com/science/article/pii/S1695403303787463
Autor:
A, Carrillo Herranz, I, Sánchez Pérez, J M, Aparicio Meix, C, Lozano Giménez, G, Roy Ariño, L M, Villar Gimerans, L, Sánchez Muñoz
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 59(2)
Rasmussen's disease is an inflammatory, chronic and progressive brain disorder that usually presents with neocortical focal seizures resistant to conventional treatment and culminates in severe deterioration with hemiparesis, cognitive decline and ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3979331e47531746b3aa2c8c09da8fe8
https://pubmed.ncbi.nlm.nih.gov/14987528
https://pubmed.ncbi.nlm.nih.gov/14987528
Publikováno v:
Anales espanoles de pediatria. 52(3)
Cohen syndrome is an autosomal recessive disorder characterized by hypotonia, mental retardation, microcephalia, typical craniofacial features, myopia and chorioretinal dystrophy. The responsible gene has been mapped to chromosome 8q 22 (COH 1). Sinc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85817a8fd3f52293de42ada26d38f95a
https://pubmed.ncbi.nlm.nih.gov/11003912
https://pubmed.ncbi.nlm.nih.gov/11003912
Autor:
A. Carrillo Herranz, I. Sánchez Pérez, J.M. Aparicio Meix, C. Lozano Giménez, G. Roy Ariño, L.M.a Villar Gimerans, L. Sánchez Muñoz
Publikováno v:
Anales de Pediatría, Vol 60, Iss 3, Pp 287-288 (2004)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c3c46b192aca937a9e8d6b8fb29014
http://www.sciencedirect.com/science/article/pii/S1695403304782727
http://www.sciencedirect.com/science/article/pii/S1695403304782727
Publikováno v:
Anales de Pediatría, Vol 58, Iss 2, Pp 199-200 (2003)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396fa87097e6ec0ffb8a97d4b300e17e
http://www.sciencedirect.com/science/article/pii/S1695403303780333
http://www.sciencedirect.com/science/article/pii/S1695403303780333
Autor:
G, Lorenzo Sanz, C, Serna Saugar, A, Quintana Castilla, C, Lozano Giménez, J M, Aparicio Meix
Publikováno v:
Anales espanoles de pediatria. 39(1)
The dysmorphogenic and teratogenic effects of valproic acid, when administered to pregnant women, have been noted in several reports. We report the case of a 3-month-old infant with multiple congenital anomalies, including severe skeletal malformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47d7e9a3eecdedd4adce97981e766035
https://pubmed.ncbi.nlm.nih.gov/8363144
https://pubmed.ncbi.nlm.nih.gov/8363144
Autor:
C. Lozano Giménez, J. M. Aparicio Meix, A. Muñoz Villa, J M Garcia-Sagredo, M Machin Valtueña
Publikováno v:
Journal of Medical Genetics. 24:426-428
Cytogenetic studies carried out in a boy with multiple congenital anomalies showed a partial deletion of the long arm of chromosome 18. The child later developed an extraskeletal Ewing's sarcoma. The possible association of the tumour with 18q- syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821ae46016d6652d92a959899addafc8
https://doi.org/10.1136/jmg.24.7.426
https://doi.org/10.1136/jmg.24.7.426
Publikováno v:
Anales espanoles de pediatria. 9(5)
50 low-birth-weight infants (1,000 g. or less) admitted to an Intensive Care Unit from January 1972 up to December 1974 are evaluated. Obstetrical data maturity and morbidity are compared in order to investigate factors that might predispose survival
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f84b8200c3e8f0fa2a97473fdc7dc6c0
https://pubmed.ncbi.nlm.nih.gov/999093
https://pubmed.ncbi.nlm.nih.gov/999093
Publikováno v:
Anales espanoles de pediatria. 12(2)
A four-year experience with sepsis in the neonate is described. Clinical picture, laboratory data and mortality of 291 newborn, aged 0-28 days, are analyzed. The rise in the incidence of septicemia in the group of newborn with clinical onset within t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0274a8582cd708d2720a9d17a72fa0f1
https://pubmed.ncbi.nlm.nih.gov/426397
https://pubmed.ncbi.nlm.nih.gov/426397
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