Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Alarabe Alarabe, A."'
Autor:
Arnáez Solís, J., Ortega Molina, M., Cervera Bravo, A., Roa Francia, M.A., Alarabe Alarabe, A., Gómez Vázquez, M.ªJ.
Publikováno v:
In Anales de Pediatria 2005 62(3):221-228
Autor:
M. Ortega Molina, A. Cervera Bravo, María J Gómez Vázquez, J. Arnáez Solís, M A Roa Francia, A Alarabe Alarabe
Publikováno v:
Anales de Pediatría, Vol 62, Iss 3, Pp 221-228 (2005)
Introducción: El síndrome torácico agudo (neumonía y/o infarto pulmonar) es una causa importante de morbimortalidad en la drepanocitosis. Objetivo: Revisar la sintomatología y el manejo de estos episodios en nuestro medio y estudiar las posibles
Hiperferritinemia aislada en un lactante sano: síndrome hereditario de hiperferritinemia y cataratas
Autor:
A Alarabe Alarabe, A. Cervera Bravo, M. Sebastián Planas, M.J. Avilés Egea, A. Díez Sáenz, A. Balas Pérez
Publikováno v:
Anales de Pediatría, Vol 52, Iss 3, Pp 267-270 (2000)
Se describe el caso de un lactante varón con hallazgo casual de hiperferritinemia a los 3 meses, a través del cual se llegó al diagnóstico en varios familiares de 3 generaciones de síndrome hereditario de hiperferritinemia y cataratas, con una n
[Evaluation of twenty-three episodes of acute thoracic syndrome in patients with sickle cell anemia]
Autor:
J, Arnáez Solís, M, Ortega Molina, A, Cervera Bravo, M A, Roa Francia, A, Alarabe Alarabe, María J, Gómez Vázquez
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 62(3)
Acute thoracic syndrome (pneumonia and/or lung infarction) is a significant cause of morbidity and mortality in sickle cell anemia.To review the clinical manifestations, management and outcome of episodes of acute thoracic syndrome in our hospital.We
Autor:
A, Cervera Bravo, M, Sebastían Planas, A, Alarabe Alarabe, A, Díez Sáenz, M J, Avilés Egea, A, Balas Pérez
Publikováno v:
Anales espanoles de pediatria. 52(3)
The case of a male infant who was found to have hyperferritinemia was made at the age of 3 months is described. The patient and several members of his family from three generations were diagnosed with hereditary hyperferritinemia-cataract syndrome wi
Autor:
Cervera Bravo A; Servicio de Pediatría, Hospital de Móstoles, Madrid., Sebastían Planas M, Alarabe Alarabe A, Díez Sáenz A, Avilés Egea MJ, Balas Pérez A
Publikováno v:
Anales espanoles de pediatria [An Esp Pediatr] 2000 Mar; Vol. 52 (3), pp. 267-70.
Publikováno v:
Journal of Perinatal Medicine; Oct2015 Supplement, Vol. 43, p1300-1364, 64p
Lexical borrowing is the living proof of impact of languages and cultures on each other, even when there are ethnical or ideological differences darkening or preventing acknowledgment of these facts, not only by common people, but even by established
Autor:
Karoline P. Cook
During the sixteenth and seventeenth centuries, Spanish authorities restricted emigration to the Americas to those who could prove they had been Catholic for at least three generations. In doing so, they hoped to instill religious orthodoxy in the co
Autor:
Gregory J. Anderson, Gordon D. McLaren
Iron Physiology and Pathophysiology in Humans provides health professionals in many areas of research and practice with the most up-to-date and well-referenced volume on the importance of iron as a nutrient and its role in health and disease. This im