Soto-Quintana M.
103
Coauthors
18
Documentos
Volumen de publicaciones por año
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Año de publicación | Num. Publicaciones |
---|---|
1997 | 1 |
1998 | 2 |
1999 | 3 |
2001 | 1 |
2003 | 4 |
2004 | 2 |
2005 | 1 |
2008 | 2 |
2009 | 1 |
2010 | 1 |
Publicaciones por áreas de conocimiento
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Área de conocimiento | Num. Publicaciones |
---|---|
Genética | 14 |
Patología | 4 |
Cáncer | 4 |
Medicamento | 4 |
Inmunología | 2 |
Obstetricia | 2 |
Pediatría | 1 |
Estudios de género | 1 |
Ginecología | 1 |
Biología del desarrollo | 1 |
Publicaciones por áreas temáticas
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Área temática | Num. Publicaciones |
---|---|
Enfermedades | 17 |
Ginecología, obstetricia, pediatría, geriatría | 7 |
Fisiología humana | 7 |
Anatomía humana, citología, histología | 2 |
Medicina y salud | 2 |
Bioquímica | 2 |
Principales fuentes de datos
Origen | Num. Publicaciones |
---|---|
Scopus | 18 |
Google Scholar | 16 |
RRAAE | 0 |
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Coautores destacados por número de publicaciones
Coautor | Num. Publicaciones |
---|---|
Francisco Álvarez-Nava | 18 |
Urdaneta K. | 5 |
Rojas-Atencio A.E. | 5 |
Prieto-Carrasquero M. | 4 |
González S. | 3 |
Martínez M.C. | 3 |
Álvarez Z. | 3 |
Borjas L. | 3 |
Lanes R. | 3 |
González-Ferrer S. | 2 |
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Publicaciones del autor
Diagnosis and management of patients with sex differentiation disorders: experience at the Unit of Medical Genetics of the University of Zulia, Maracaibo, Venezuela
ArticleAbstract: Abnormalities of sexual differentiation (ASD) represent a group of entities, heterogeneous in theirPalabras claves:Autores:Francisco Álvarez-Nava, González-Ferrer S., Soto-Quintana M.Fuentes:googlescopusComplete androgen insensitivity syndrome: Clinical and anatomopathological findings in 23 patients
ArticleAbstract: Complete Androgen Insensitivity Syndrome (CAIS) is a type of Male Pseudohermaphroditism due to a defPalabras claves:androgen receptor, Male pseudohermaphroditism, primary amenorrhea, Testicular feminization, Testicular tissueAutores:Francisco Álvarez-Nava, González S., Martinez C., Prieto-Carrasquero M., Soto-Quintana M.Fuentes:googlescopusFISH and PCR analyses in three patients with 45,X/46,X,idic(Y) karyotype: Clinical and pathologic spectrum
ArticleAbstract: Objective. - To delineate the phenotypic spectrum (clinical and gonadal features) from patients withPalabras claves:45,X/46,X,idic(Y), Molecular analysis, SRY gene, Testicular developmentAutores:Álvarez Z., Francisco Álvarez-Nava, Martínez M.C., Prieto-Carrasquero M., Soto-Quintana M.Fuentes:googlescopusFemale pseudohermaphroditism with phallic urethra in the offspring of a mother with an adrenal tumor
ArticleAbstract: Background: Female pseudohermaphroditism is a disorder in which 46,XX females with ovaries do not dePalabras claves:Differential Diagnosis, Female pseudohermaphroditism, Maternal adrenal tumorAutores:Álvarez Z., Francisco Álvarez-Nava, Lanes R., Soto-Quintana M., Temponi A.Fuentes:googlescopusHigh incidence of Y-chromosome microdeletions in gonadal tissues from patients with 45,X/46,XY gonadal dysgenesis
ArticleAbstract: A higher incidence of Y-chromosome microdeletions was found on gonadal DNA than on peripheral bloodPalabras claves:Autores:Francisco Álvarez-Nava, Pineda L., Puerta H., Soto-Quintana M., Temponi A.Fuentes:googlescopus