Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Samir, Atmani"'
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:
Sara, Himri, Bouchra, Oumokhtar, Angéla, Filankembo kava, Samira, El Fakir, Nehemie, Nzoyikorera, Samir, Atmani
Publikováno v:
In Clinical Epidemiology and Global Health December 2020 8(4):1062-1066
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
Publikováno v:
Annals of medicine and surgery (2012). 84
•Developmental Care contributes to improving the quality of neonatal life.•Professionals must develop multidisciplinary approaches to clinical practice.•This research identified a low level of knowledge and practice in Developmental Care.•Sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08aac8056842c3843c6df42fc8bce5eb
https://pubmed.ncbi.nlm.nih.gov/36582915
https://pubmed.ncbi.nlm.nih.gov/36582915
Autor:
Mohammed El-Azami-El-Idrissi, Mounia Lakhdar-Idrissi, Sanae Chaouki, Samir Atmani, Abdelhak Bouharrou, Moustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 53 (2016)
Recurrent respiratory tract infections are one of the most frequent reasons for pediatric visits and hospitalization. Causes of this pathology are multiple ranging from congenital to acquired and local to general. Immune deficiencies are considered a
Externí odkaz:
https://doaj.org/article/5714298cfec240dcb9fc09c0b6e27918
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:
Sanaa Krich, Kawtar Inani, Mariame Meziane, Fatima Zohta Souilmi, Samir Atmani, Mustapha Hida, Taoufik Harmouch, Afaf Amarti, Fatima Zohra Mernissi
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 419 (2015)
Le lupus érythémateux systémique (LES) juvénile est une connectivite rare, d'évolution plus sévère que chez l'adulte. Les cas familiaux sont exceptionnels. Il s'agissait de deux familles (5 patients atteints), chez qui on a objectivé un LES j
Externí odkaz:
https://doaj.org/article/bc76e6a48cff449984ba76595a262c26
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 3 (2015)
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal re
Externí odkaz:
https://doaj.org/article/1e01905510a24508a6c227fc09efdd23
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Multicentric Castleman’s disease is a rare benign and unexplained lymphoproliferative disorder that is extremely uncommon in children. It presents with fever, systemic symptoms, generalized lymphadenopathy, and laboratory markers of inflammation. I
Externí odkaz:
https://doaj.org/article/d0d4830799e54825ab971c0261b3d25d