Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elsy Roxana Geroy Moya"'
Publikováno v:
Revista Finlay, Vol 12, Iss 3, Pp 343-351 (2022)
Neuroectodermal tumors are the main cause of mediastinal tumors. Of these, the ganglioneuroma is the most benign and the least frequent, with an incidence of 1 in 100,000 children. It occurs predominantly in childhood with a mean presentation at age
Externí odkaz:
https://doaj.org/article/6ee935b1d31d4b3182be2ef18b38cd1d
Publikováno v:
Revista Finlay, Vol 11, Iss 1, Pp 106-116 (2021)
Congenital aplasia cutis is a rare and heterogeneous disorder, with an estimated incidence of 1-3 cases per 10,000 births. It can appear in isolation or as part of several polymalformative syndromes, observing autosomal recessive and autosomal domina
Externí odkaz:
https://doaj.org/article/d343e039df4243f495fa385dbf798d01
Autor:
Jan O´neil González Ramos, Nancy González Vales, Eida María Mena Albernal, Elsy Roxana Geroy Moya, Nicolás Ramón Cruz Pérez, Annia Quintana Marrero
Publikováno v:
Revista Finlay, Vol 11, Iss 1, Pp 41-50 (2021)
Background: congenital heart diseases are the most serious congenital anomalies in the newborn, with a great impact on pediatric morbidity and mortality. The most frequent are the interventricular and interatrial communication. Objective: to characte
Externí odkaz:
https://doaj.org/article/95e3165f1b804290a19f19c22ad2958b
Publikováno v:
Revista Finlay, Vol 10, Iss 1, Pp 62-72 (2020)
Marfan syndrome is an autosomal dominant genetic disorder, with a prevalence of 1 every 5,000-10,000 newborns, so it is classified as an uncommon disease. It affects multiple organs and systems; its prognosis is marked by the cardiovascular involveme
Externí odkaz:
https://doaj.org/article/96ba189b247547c59cbadd856191fa6b
Autor:
Elsy Roxana Geroy Moya, María Elena Quiñones Hernández, María Dolores García Suárez, Leidy Sosa Águila, María Ocaña Gil
Publikováno v:
Revista Finlay, Vol 9, Iss 1, Pp 11-19 (2019)
Fundamento: el padecimiento de una enfermedad rara produce dificultades para su diagnóstico oportuno. Su pronóstico ensombrece cuando se asocia a desnutrición. Objetivo: caracterizar a niños y adolescentes con enfermedades raras y desnutrición,
Externí odkaz:
https://doaj.org/article/5fd07adeb55f45fbae11d80df8628f02
Autor:
Elsy Roxana Geroy Moya, María Elena Quiñones Hernández, María Dolores García Suárez, Leidy Sosa Águila, María Ocaña Gil
Publikováno v:
Revista Finlay, Vol 9, Iss 1, Pp 11-19 (2019)
Foundation: suffering an uncommon disease causes difficulties for its timely diagnosis. Their prognosis overshadows when associated with malnutrition. Objective: to characterize children and adolescents with uncommon diseases and malnutrition, assist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::2e450f5a13583f7b1a2e23d18de6b570
http://revfinlay.sld.cu/index.php/finlay/article/view/682
http://revfinlay.sld.cu/index.php/finlay/article/view/682