Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Fatima Zohra Moufid"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100067- (2023)
Externí odkaz:
https://doaj.org/article/ea56d1436bf64c29aa6b15c9e47502ed
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:
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
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
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:
Laila Bouguenouch, Ihssane El Bouchikhi, Samir Atmani, Khadija Belhassan, Fatima Zohra Moufid, Mohamed Bouhrim, Mohammed Iraqui Houssaini, Imane Samri, Karim Ouldim
Publikováno v:
African Health Sciences
African Health Sciences; Vol 18, No 4 (2018); 922-930
African Health Sciences; Vol 18, No 4 (2018); 922-930
Background: Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart defect (CHD) with an incidence of 1/3600 live births. This disorder was associated with mutations in the transcription factors involved in cardiogenesis, like Nk2 home
Autor:
Mohammed Iraqui Houssaini, Samir Atmani, Ihssane El Bouchikhi, Khadija Belhassan, Karim Ouldim, Fatima Zohra Moufid, Laila Bouguenouch, Imane Samri
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 3, Iss 4, Pp 133-142 (2016)
International Journal of Pediatrics and Adolescent Medicine, Vol 3, Iss 4, Pp 133-142 (2016)
Noonan syndrome is a common autosomal dominant disorder characterized by short stature, congenital heart disease and facial dysmorphia with an incidence of 1/1000 to 2500 live births. Up to now, several genes have been proven to be involved in the di
Autor:
Mohammed Iraqui Houssaini, Khadija Belhassan, Ihssane El-Bouchikhi, Samir Atmani, Karim Ouldim, Fatima Zohra Moufid
Publikováno v:
The Turkish journal of pediatrics. 59(5)
Atrioventricular septal defect is a complex congenital heart defects (CHD) with a prevalence of approximately 4% of all CHDs. Transitional form of atrio-ventricular septal defect (tAVSD) associates ostium primum atrial septal defect, common atriovent