Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Khadija, Belhassan"'
Autor:
Ihssane EL Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Laila Bouguenouch, Imane Samri, Mohammed Iraqui Houssaïni, Karim Ouldim, Samir Atmani
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-7 (2021)
Abstract Background Tetralogy of Fallot is the most prevalent cyanotic congenital heart disease, occurring in 1/3 600 live births. This disorder comprises ventricular septal defect, right ventricular outflow obstruction, over-riding aorta, and right
Externí odkaz:
https://doaj.org/article/2fc64bb9841f4df88cb233028ea67f7d
Autor:
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Khadija Belhassan, Imane Samri, Amal Chaouti, Mohammed Iraqui Houssaïni, Samir Atmani, Karim Ouldim
Publikováno v:
Eurasian Journal of Medicine, Vol 52, Iss 3, Pp 283-287 (2020)
Externí odkaz:
https://doaj.org/article/da99d1801555428da40fb2a3cb55bd72
Autor:
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Imane Samri, Fatima Abdouss, Moulay Abdelilah Melhouf, Mohammed Iraqui Houssaini, Khadija Belhassan, Samir Atmani, Karim Ouldim
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Noonan syndrome (NS) is one of the most common RASopathies, with an autosomal dominant inheritance. This disorder is caused by a range of genes belonging to the RAS-MAP kinase (rat sarcoma viral oncogene homolog/mitogen-activated
Externí odkaz:
https://doaj.org/article/8c81a1981aa24cda858da711a34b2f71
Autor:
Eleanor I. Sams, Jeffrey K. Ng, Victoria Tate, Ying-Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton, Khadija Belhassan, Julie Neidich, Robi D. Mitra, F. Sessions Cole, Patricia Dickson, Jeffrey Milbrandt, Tychele N. Turner
Publikováno v:
HGG Advances, Vol 3, Iss 1, Pp 100081- (2022)
While 9p deletion and duplication syndromes have been studied for several years, small sample sizes and minimal high-resolution data have limited a comprehensive delineation of genotypic and phenotypic characteristics. In this study, we examined gene
Externí odkaz:
https://doaj.org/article/430a1f3c59fe42e7b91d28106053d35a
Autor:
Laila Bouguenouch, Imane Samri, Khadija Belhassan, Hanane Sayel, Meriame Abbassi, Sanae Bennis, Dafr Allah Benajah, Adil Ibrahimi, Afaf Amarti, Karim Ouldim
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 142 (2016)
Le syndrome de Lynch, ou cancer colorectal héréditaire sans polypose ou HNPCC (hereditary non-polyposis colorectal cancer), est la forme la plus fréquente de cancer colorectal héréditaire. Il conduit à une augmentation de la susceptibilité à
Externí odkaz:
https://doaj.org/article/69779e19152e440e8af1490eb9c53989
Autor:
Imane Samri, Samir Atmani, Ihssane El Bouchikhi, Laila Bouguenouch, Moulay Abdelilah Melhouf, Karim Ouldim, Mohammed Iraqui Houssaini, Khadija Belhassan, Fatima Zohra Moufid, Fatima Abdouss
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BackgroundNoonan syndrome (NS) is one of the most common RASopathies, with an autosomal dominant inheritance. This disorder is caused by a range of genes belonging to the RAS-MAP kinase (rat sarcoma viral oncogene homolog/mitogen-activated protein ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b88eba69c8d4e00abdf99178944c6ea
http://link.springer.com/article/10.1186/s43042-020-0047-9
http://link.springer.com/article/10.1186/s43042-020-0047-9
Autor:
Mohammed Iraqui Houssaini, Laila Bouguenouch, Karim Ouldim, Samir Atmani, Khadija Belhassan, Fatima Zohra Moufid, Ihssane El Bouchikhi, Imane Samri
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-7 (2021)
Background Tetralogy of Fallot is the most prevalent cyanotic congenital heart disease, occurring in 1/3 600 live births. This disorder comprises ventricular septal defect, right ventricular outflow obstruction, over-riding aorta, and right ventricul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65d3db7032f998e9a8bd600aa1376d9e
https://doi.org/10.1186/s43042-021-00136-1
https://doi.org/10.1186/s43042-021-00136-1
Autor:
Khadija Belhassan, Jorge L. Granadillo
Genetic disorders account for more than 30% of infant deaths and more than 11% of pediatric hospital admissions in the United States and Canada. The development of genetic testing has enabled the diagnosis of genetic syndromes and the discovery of ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::256dcf87045c736e3e244a918432dc20
https://doi.org/10.1016/b978-0-12-817962-8.00017-2
https://doi.org/10.1016/b978-0-12-817962-8.00017-2
Autor:
Khadija Belhassan, Samir Atmani, Imane Samri, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Ihssane El Bouchikhi, Laila Bouguenouch, Amal Chaouti, Karim Ouldim
Publikováno v:
Eurasian J Med
Eurasian Journal of Medicine, Vol 52, Iss 3, Pp 283-287 (2020)
Eurasian Journal of Medicine, Vol 52, Iss 3, Pp 283-287 (2020)
Objective Atrial septal defect (ASD) is one of the most common types of congenital heart disease (CHD). It is mainly caused by mutations of NK2 homeobox 5, GATA binding protein 4 (GATA4), and myosin heavy chain 6 in non-syndromic cases. This study ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16a6dffb8e2277bea0d397310d506eb1
https://europepmc.org/articles/PMC7651766/
https://europepmc.org/articles/PMC7651766/
Autor:
Mohamed Iraqui Houssaini, Laila Bouguenouch, Karim Ouldim, Bahia Bennani, Laila Chbani, Fatima Zahra Moufid, Ihssane El Bouchikhi, Mohamed Sekal, Khadija Belhassan
Publikováno v:
Genetic Testing and Molecular Biomarkers. 22:492-497
Lynch syndrome (LS) is an autosomal dominant disorder characterized by early age of onset and increased risk of developing extracolonic tumors. Molecular diagnosis of LS requires identification of germline mutations in one of the Mismatch Repair (MMR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ec5c8fede2f12d225079f07c395c8f
https://doi.org/10.1089/gtmb.2018.0067
https://doi.org/10.1089/gtmb.2018.0067