Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sanaa Nassereddine"'
Autor:
Sara Benchikh, Amale Bousfiha, Adil El Hamouchi, Somda Georgina Charlene Soro, Abderrahim Malki, Sanaa Nassereddine
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Chronic myelogenous leukemia (CML) is a type of blood cancer that affects hematopoietic stem cells and is often characterized by the presence of the Philadelphia chromosome. The Philadelphia chromosome encodes for a protein with h
Externí odkaz:
https://doaj.org/article/7de3f157706743d3a7547965d656b650
Autor:
Sanaa Nassereddine, Rachida Habbal, Yaya Kassogue, Ait Boujmia Oum Kaltoum, Korchi Farah, Haraka Majda, Abou Elfath Rhizlane, Sellama Nadifi, Hind Dehbi
Publikováno v:
Annals of Human Biology, Vol 48, Iss 7-8, Pp 585-589 (2021)
Background Essential hypertension (EH) results from a complex interaction between environmental factors and an individual’s genetic background. Aim To assess the relationship between polymorphisms in GSTM1 and GSTT1 and the risk of EH. Subjects and
Externí odkaz:
https://doaj.org/article/4b799d203c724600a5aee317ea2bbc0f
Autor:
Sanaa Nassereddine, Hind Hassani Idrissi, Rachida Habbal, Rhizlane Abouelfath, Farah Korch, Majda Haraka, Adnane Karkar, Sellama Nadifi
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-8 (2018)
Abstract Background Hypertension is a multifactorial disease involving both environmental and genetic Factros. G894 T eNOS polymorphism has been suggested to be responsible for reduced NO synthesis, and EH development. The objective of our case-contr
Externí odkaz:
https://doaj.org/article/870a51b533eb4d6fa6f6ff9b9df19fa1
Autor:
Sanaa, Nassereddine, Rachida, Habbal, Yaya, Kassogue, Ait Boujmia Oum, Kaltoum, Korchi, Farah, Haraka, Majda, Abou Elfath, Rhizlane, Sellama, Nadifi, Hind, Dehbi
Publikováno v:
Annals of human biology. 48(7-8)
Essential hypertension (EH) results from a complex interaction between environmental factors and an individual's genetic background.To assess the relationship between polymorphisms inA multiplex-PCR was used to identify the genotypic profiles ofThe f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5d880c6d6cbcfe5ff58525930d7932a9
https://pubmed.ncbi.nlm.nih.gov/35132887
https://pubmed.ncbi.nlm.nih.gov/35132887
Autor:
Zouhair Elkarhat, Boutaina Belkady, Jamila Aboulfaraj, Latifa Zarouf, Sanaa Nassereddine, Boubker Nasser, Hassan Rouba, Hicham Charoute, Chadli Elbakay, Abdelhamid Barakat, Lunda Razoki
Publikováno v:
American Journal of Medical Genetics Part A. 179:1516-1524
The aim of the present study was to determine the frequency and nature of chromosomal abnormalities involved in patients with the clinical spectrum of ambiguous genitalia (AG), amenorrhea, and Turner phenotype, in order to compare them with those rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8636077a4fdab41cb4edf25ddd1c2c81
https://doi.org/10.1002/ajmg.a.61257
https://doi.org/10.1002/ajmg.a.61257
Autor:
Sanaa Nassereddine, Zouhair Elkarhat, Chadli Elbakay, Latifa Zarouf, Zineb Kindil, Abdelhamid Barakat, Jamila Aboulfaraj, Hassan Rouba, Boubker Nasser, Lunda Razoki
Publikováno v:
Journal of Assisted Reproduction and Genetics. 36:499-507
PURPOSE: The aim of this study is to evaluate the frequency and nature of chromosomal abnormalities in Moroccan couples with recurrent spontaneous miscarriage (RSM). In addition, the data were compared with those reported elsewhere in order to give a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::738e81d855665a4100ccf776107f2861
https://doi.org/10.1007/s10815-018-1373-4
https://doi.org/10.1007/s10815-018-1373-4
Autor:
Rachida Habbal, Sanaa Nassereddine, Sellama Nadifi, Majda Haraka, Hind Hassani Idrissi, Rhizlane Abouelfath, Farah Korch, Adnane Karkar
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-8 (2018)
BMC Medical Genetics
BMC Medical Genetics
Background Hypertension is a multifactorial disease involving both environmental and genetic Factros. G894 T eNOS polymorphism has been suggested to be responsible for reduced NO synthesis, and EH development. The objective of our case-control study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4be40b6ba8958c8702ef36529dc3239c
http://link.springer.com/article/10.1186/s12881-018-0638-1
http://link.springer.com/article/10.1186/s12881-018-0638-1
Autor:
Loubna Amehdare, Abderraouf Hilali, Hayat Talbi, Sanaa Nassereddine, Hanane Houmaid, Chadli El Bekkay
Publikováno v:
Open Journal of Genetics. :15-22
Purpose: A proportion of cases with repeated abortion are caused by chromosomal abnormality in one of the parents. The purpose of this study was to assess the frequency and nature of chromosomal aberrations that contribute to the occurrence of recurr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794c04d7cb31a8b42dac3362df60340d
https://doi.org/10.4236/ojgen.2018.82002
https://doi.org/10.4236/ojgen.2018.82002
Autor:
Sanaa Nassereddine, Boutaina Belkady, Lamiae Elkhattabi, Zouhair Elkarhat, Abdelhamid Barakat, Latifa Zarouf, Lunda Razoki, Rachida Cadi, Hassan Rouba, Jamila Aboulfaraj
Publikováno v:
Human Heredity. 83:274-282
Background: Intellectual disability (ID) has been defined as a considerably reduced ability to understand new or complex information and to learn new skills. It is associated with life-long intellectual and adaptive functioning impairments that have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::874bff940cf24d7d376b35a57cd7df94
https://doi.org/10.1159/000499710
https://doi.org/10.1159/000499710
Publikováno v:
IBRO Reports. 6:S373-S374
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7264c939efc74938a29db861dd72114
https://doi.org/10.1016/j.ibror.2019.07.1187
https://doi.org/10.1016/j.ibror.2019.07.1187