Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M P, Martínez Escribano"'
Autor:
M P, Martínez Escribano, J, Sierra Sirvent, J, Mengual Gil, J, Membrado Granizo, C, Loris Pablo
Publikováno v:
Anales espanoles de pediatria. 21(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ad055220b23115090d831b6f1b0f4e8
https://pubmed.ncbi.nlm.nih.gov/6529032
https://pubmed.ncbi.nlm.nih.gov/6529032
Autor:
C, Loris Pablo, M J, Oliván del Cacho, M, Heras Gironella, J, Sierra Sirvant, M P, Martínez Escribano, C, Izaguirre Zugazaga, J, Lázaro Castillo, A, March
Publikováno v:
Anales espanoles de pediatria. 19(5)
Classically it is considered that vital prognosis of Lesch-Nyhan syndrome depends on renal affectation secondary to uric nephropathy. A case of Lesch-Nyhan syndrome treated with Allopurinol is described which presented multiple and bilateral renal st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e05c0090c3d8b661a58edbade25e459b
https://pubmed.ncbi.nlm.nih.gov/6660658
https://pubmed.ncbi.nlm.nih.gov/6660658
Autor:
J F, Sierra Sirvent, M P, Martínez Escribano, M J, Oliván Del Cacho, M, Heras Gironella, M J, Ríos Mitchell, C, Loris Pablo
Publikováno v:
Anales espanoles de pediatria. 20(2)
Authors describe a case of newborn whose malformations of genitourinary tract of abdominal muscles deficiency and renal dysplasia make it very compatible with Prune-Belly Syndrome. The case it is exceptionally interesting because it is a female subje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95a8b39c7b995baa1b7c7de09d245279
https://pubmed.ncbi.nlm.nih.gov/6712024
https://pubmed.ncbi.nlm.nih.gov/6712024
Autor:
M J, Oliván del Cacho, M, Heras Gironella, J, Sierra Sirvent, M P, Martínez Escribano, C, Izaguirre Zugazaga, L, Plaza Mas, C, Loris Pablo
Publikováno v:
Anales espanoles de pediatria. 19(1)
This report describes the first pediatric case of chronic renal failure as a complication of infectious mononucleosis in a 3 1/2 year old girl. The clinical features were marked at onset by proteinuria and later by nephrotic syndrome. The evolution t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::572c811f3f4219bd3dca2a37f86be9b3
https://pubmed.ncbi.nlm.nih.gov/6638711
https://pubmed.ncbi.nlm.nih.gov/6638711