Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rana Aa Mahmoud"'
Autor:
Idoia Martínez de LaPiscina, Rana AA Mahmoud, Kay-Sara Sauter, Isabel Esteva, Milagros Alonso, Ines Costa, Jose Manuel Rial-Rodriguez, Amaia Rodríguez-Estévez, Amaia Vela, Luis Castano, Christa E. Flück
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 22, p 8554 (2020)
Variants of NR5A1 are often found in individuals with 46,XY disorders of sex development (DSD) and manifest with a very broad spectrum of clinical characteristics and variable sex hormone levels. Such complex phenotypic expression can be due to the i
Externí odkaz:
https://doaj.org/article/2bb1eafc7a2f441f9424248c71a6a3e7
Autor:
Amaia Rodríguez-Estévez, Luis Castaño, Amaia Vela, Milagros Alonso, Idoia Martínez de LaPiscina, Christa E. Flück, Jose Manuel Rial-Rodriguez, Ines Costa, Isabel Esteva, Rana Aa Mahmoud, Kay-Sara Sauter
Publikováno v:
Martínez de LaPiscina, Idoia; Mahmoud, Rana Aa; Sauter, Kay-Sara; Esteva, Isabel; Alonso, Milagros; Costa, Ines; Rial-Rodriguez, Jose Manuel; Rodríguez-Estévez, Amaia; Vela, Amaia; Castano, Luis; Flück, Christa E. (2020). Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1. International journal of molecular sciences, 21(22) MDPI 10.3390/ijms21228554
Addi. Archivo Digital para la Docencia y la Investigación
instname
International Journal of Molecular Sciences, Vol 21, Iss 8554, p 8554 (2020)
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
International Journal of Molecular Sciences
Volume 21
Issue 22
Addi. Archivo Digital para la Docencia y la Investigación
instname
International Journal of Molecular Sciences, Vol 21, Iss 8554, p 8554 (2020)
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
International Journal of Molecular Sciences
Volume 21
Issue 22
Variants of NR5A1 are often found in individuals with 46,XY disorders of sex development (DSD) and manifest with a very broad spectrum of clinical characteristics and variable sex hormone levels. Such complex phenotypic expression can be due to the i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e664dc1ec32426a9b1bacbd811c7a12c
https://boris.unibe.ch/150407/1/ijms-21-08554.pdf
https://boris.unibe.ch/150407/1/ijms-21-08554.pdf
Autor:
Rasha T. Hamza, Tarek M. Kamal, Nermine H. Amr, Farida El-Baz Mohamed, Rana Aa Mahmoud, A. M. Youssef
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 1, Pp 67-73 (2017)
Egyptian Journal of Medical Human Genetics; Vol 18, No 1 (2017); 67-73
Egyptian Journal of Medical Human Genetics; Vol 18, No 1 (2017); 67-73
Background: Melanocortinergic system represents a known system involved in the central regulation of body weight with the central proopiomelanocortin (POMC) neurons forming a potent anorexigenic network. Polymorphisms in the POMC gene locus are assoc
Autor:
Rana Aa Mahmoud, Eman Ahmed Zaky
Publikováno v:
Journal Clinical Psychiatry and Cognitive Psychology.
Tuberous sclerosis complex is a disorder that affects many systems of the body including the central nervous system, the cardiovascular system, the skin, the kidneys, the lungs, and the retina. Much neuropsychiatric comorbidity is recorded in individ