Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Víctor Clemente Mendoza Rojas"'
Autor:
Ana María Puentes Ortiz, Leidis Aurora Acevedo Cardoso, Jeimi Yurani Suspes Cruz, Luis Eduardo Franco Ospina, Clara Inés Vargas Castellanos, Gustavo Adolfo Contreras García, Víctor Clemente Mendoza Rojas
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 19, Iss , Pp 100072- (2021)
Objective: To report a Buschke-Ollendorff syndrome case with disproportionate short stature and literature review; recognizing this clinical entity as an infrequent bone dysplasia, which requires a cautious clinical evaluation, bearing in mind not to
Externí odkaz:
https://doaj.org/article/1535151b787e478e901dff309ae7cf1c
Publikováno v:
Salud UIS, Vol 46, Iss 1, Pp 65-70 (2014)
Introducción: El hipertiroidismo es una patología tiroidea poco frecuente en neonatos, relacionada con el antecedente materno de enfermedad de Graves, y por lo tanto con el paso transplacentario de inmunoglobulinas estimulantes del receptor de TSH.
Externí odkaz:
https://doaj.org/article/b99b53d61eca41b294730fd63df200a4
Publikováno v:
Salud UIS, Vol 45, Iss 2, Pp 57-63 (2013)
La cetoacidosis diabética se debe a un estado de deficiencia de insulina. Los criterios bioquímicos que la definen son: hiperglucemia > 200 mg/dl, acidosis metabólica con pH sanguíneo < 7.3 o bicarbonato < 15 mmol/L, cetonemia intensa con cetonur
Externí odkaz:
https://doaj.org/article/5f3b372d0b88437fa98b9129e0a9aee5
Publikováno v:
MedUNAB, Vol 8, Iss 2, Pp 146-150 (2005)
Abnormal uterine hemorrhage is the presence ofexcessive and prolonged menstrual bleeding during various consecutivemenstrual cycles. In most cases its origin is endometrial.It’s the second cause for gynecological consultation, only precededby leuco
Externí odkaz:
https://doaj.org/article/e044d8441a8e40fda91c5e447b5cf8be
Publikováno v:
Revista de la Facultad de Medicina, Vol 70, Iss 4 (2021)
Introduction: Hyperinsulinism/hyperammonemia syndrome (HI/HA) is a rare genetic disease caused by the activation of mutations in the GLUD1 gene. It is characterized by recurrent symptomatic hypoglycemic episodes, poor tolerance to fasting, and requir
Externí odkaz:
https://doaj.org/article/13c0cfd7be344e1c8343fbbbdc91a721
Publikováno v:
Revista de la Facultad de Medicina, Vol 68, Iss 1 (2020)
Introduction: Premature pubarche occurs in girls before the age of 8 or boys before the age of 9 and is a sign of precocious puberty associated with increased growth acceleration. Precocious puberty can be caused, among others, by nonclassic congenit
Externí odkaz:
https://doaj.org/article/c678e7d22db84aed87138b5adfe55417
Publikováno v:
Pediatric endocrinology, diabetes, and metabolism. 25(4)
Introduction Hypoglycaemia is frequent in premature infants and can generate neurological alterations. There is controversy concerning exposure to antenatal corticosteroids for pulmonary maturation and hypoglycaemia. Aim of the study To evaluate whet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e40bc28c98c1230bfc31d700d6d65c2
https://pubmed.ncbi.nlm.nih.gov/32270971
https://pubmed.ncbi.nlm.nih.gov/32270971
Publikováno v:
IATREIA. 31:305-311
Introduccion: la hiperplasia suprarrenal congenita por deficiencia de 11-beta-Hidroxilasa es una enfermedad autosomica recesiva poco frecuente, y en estadios avanzados sus complicaciones cardiovasculares exigen un manejo aun mas complejo. Presentacio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8bc246a8610f74949b0fb4fb9e770d4
https://doi.org/10.17533/udea.iatreia.v31n3a09
https://doi.org/10.17533/udea.iatreia.v31n3a09
Publikováno v:
Revista de la Facultad de Medicina. 70:e93016
Introducción. El síndrome hiperinsulinismo/hiperamoniemia (HI/HA) es una enfermedad genética rara causada por la activación de mutaciones en el gen GLUD1. Este síndrome se caracteriza por hipoglucemias sintomáticas recurrentes, poca tolerancia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b8fdec3dccea836217700370a7f8e39
https://doi.org/10.15446/revfacmed.v70n4.93016
https://doi.org/10.15446/revfacmed.v70n4.93016
Autor:
Carlos Arturo Gómez-Tarazona, Víctor Manuel Mora-Bautista, Víctor Clemente Mendoza-Rojas, Katherine Pinzón-Mantilla, Gustavo Adolfo Contreras-García, John Freddy Martínez-Paredes, Alba Lucía Calderón-Rojas, Gerardo Mantilla-Mora, Luis Alfonso Díaz-Martínez
Publikováno v:
Colombia Médica : CM
In preterm newborn, problems with the interpretation of 17-OHP may occur.Evaluate 17-OHP values in healthy preterm newborns until they reach the corrected gestational age.Longitudinal study of 36 preterm infants with 17-OHP evaluation using ELISA fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630d74d715e97edb426f20680e7f68c0
https://doi.org/10.25100/cm.v48i4.2893
https://doi.org/10.25100/cm.v48i4.2893