Zobrazeno 1 - 10
of 49
pro vyhledávání: '"C, Loris Pablo"'
Publikováno v:
Anales de Pediatría, Vol 61, Iss 6, Pp 502-508 (2004)
Antecedentes: La hipomagnesemia familiar con hipercalciuria y nefrocalcinosis es una enfermedad rara que sin tratamiento específico suele conducir a insuficiencia renal terminal y que en grado variable presenta alteraciones oculares. La enfermedad s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c361852d48d374b8d50cb3f20216f1
https://doi.org/10.1016/s1695-4033(04)78436-2
https://doi.org/10.1016/s1695-4033(04)78436-2
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 61(6)
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an unusual disease that usually leads to end-stage renal failure. There is no specific treatment and, to a variable degree, patients with this disease present ocular abnormalities. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b392c81da696c8772215056b126ca374
https://pubmed.ncbi.nlm.nih.gov/15574250
https://pubmed.ncbi.nlm.nih.gov/15574250
Autor:
J M, Jiménez-Hereza, M, Heras-Gironella, C, Loris-Pablo, J, Garagorri-Otero, M J, Tardós-Solano
Publikováno v:
Anales espanoles de pediatria. 49(5)
The purpose of this study was to search for risk factors for the evolution reflux nephropathy by comparing the results of the ambulatory blood pressures in a group of children with reflux nephropathy of different degrees.Out-patient blood pressure mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c5101cdc6f2af4318a7594fc2ef0ffb
https://pubmed.ncbi.nlm.nih.gov/9949586
https://pubmed.ncbi.nlm.nih.gov/9949586
Autor:
B, Solsona-Narbón, J A, Castillo Laita, J C, Buñuel Alvarez, J, Elías Pollina, C, Loris Pablo, A, Romo Montejo, J, Esteban Ibarz, E, Bello Andrés
Publikováno v:
Anales espanoles de pediatria. 36(3)
In this paper we report a review of the omphalic pathology that was admitted to our hospital from january 1973 through december 1990. Eleven cases of Beckwith-Wiedemann Syndrome were diagnosed during this period of time. Our eleven cases comply with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::20142b7b310ac3010e3a8c5d57a19a09
https://pubmed.ncbi.nlm.nih.gov/1580425
https://pubmed.ncbi.nlm.nih.gov/1580425
Publikováno v:
Anales espanoles de pediatria. 25(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5673fac7dc82518bbf38191d91b3a1bd
https://pubmed.ncbi.nlm.nih.gov/2948434
https://pubmed.ncbi.nlm.nih.gov/2948434
Publikováno v:
Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica. 1(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e90da6c545d350d957ae4bcbe3f682fc
https://pubmed.ncbi.nlm.nih.gov/3153198
https://pubmed.ncbi.nlm.nih.gov/3153198
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:
T, Arana Navarro, P, Puyuelo del Val, L, Plaza Mas, J, Sánchez García, M, Heras Gironella, C, Loris Pablo
Publikováno v:
Anales espanoles de pediatria. 30(4)
We report two cases of eosinophilic cystitis in children of 11 months and 11 and a half year of age respectively. The presenting symptoms were the emision of mucosanguinolent filaments in the urine in one case and with lower urinary tract symptoms an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7ac8b0cbd785101bb43e158fe4523f1
https://pubmed.ncbi.nlm.nih.gov/2742240
https://pubmed.ncbi.nlm.nih.gov/2742240
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