Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Salahiddine Saghir"'
Autor:
Brahim El Hasbaoui, Nadia Mebrouk, Salahiddine Saghir, Abdelhkim El Yajouri, Rachid Abilkassem, Aomar Agadr
Publikováno v:
The Pan African Medical Journal, Vol 38, Iss 237 (2021)
Vitamin B12 deficiency in early childhood is an important cause of neurodevelopmental delay and regression. Most of these cases occur in exclusively breast-fed infants of deficient mothers. Symptoms and signs of vitamin B12 deficiency appear between
Externí odkaz:
https://doaj.org/article/2ea963f42f5f4bae86405b2679878377
Autor:
Brahim El Hasbaoui, Zainab Rifai, Salahiddine Saghir, Anas Ayad, Najat Lamalmi, Rachid Abilkassem, Aomar Agadr
Publikováno v:
The Pan African Medical Journal, Vol 38, Iss 188 (2021)
Congenital hepatic fibrosis (CHF) is a rare autosomal recessive disease derived from biliary dysgenesis secondary to ductal plate malformation; it often coexists with Caroli’s disease, von Meyenburg complexes, autosomal dominant polycystic kidney d
Externí odkaz:
https://doaj.org/article/e820d6029e9e4e01908f19f9dabe8cfe
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 127 (2019)
La maladie de Weber-Christian ou panniculite idiopathique est une affection rare, caractérisée par une inflammation du tissu adipeux sous-cutané; il s'agit d'une entité pathologique non spécifique qui reste toujours un sujet de débat et dont l'
Externí odkaz:
https://doaj.org/article/55f3a28b3eda40b5bf1e2054b8a12bda
Autor:
Salahiddine Saghir, Anass Ayad
Publikováno v:
The Pan African Medical Journal, Vol 21, Iss 264 (2015)
Isolated trigonocephaly is a nonsyndromic form of craniosynostosis characterized by the premature fusion of the metopic suture. Incidence is estimated at 1/15,000 births. Males are more frequently affected than females (sex ratio of 2:1) and the freq
Externí odkaz:
https://doaj.org/article/7b53768af5a44dbe8ff416234adbc72c
Publikováno v:
The Pan African Medical Journal, Vol 21, Iss 34 (2015)
Vasa previa is a rare but clinically important obstetrical complication that can be associated with a low-lying placenta or placenta previa. We aim to present one case of vasa previa diagnosed during the placenta examination after the caesarean indic
Externí odkaz:
https://doaj.org/article/29f69d28664f460ab9c9e8a4f6468947
Autor:
Rachid Abilkassem, Aomar Agadr, Brahim El Hasbaoui, Najat Lamalmi, Salahiddine Saghir, Anas Ayad, Zainab Rifai
Publikováno v:
Pan African Medical Journal; Vol. 38 No. 1 (2021)
The Pan African Medical Journal
The Pan African Medical Journal
Congenital hepatic fibrosis (CHF) is a rare autosomal recessive disease derived from biliary dysgenesis secondary to ductal plate malformation; it often coexists with Caroli’s disease, von Meyenburg complexes, autosomal dominant polycystic kidney d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::190fa62e60db81e2f12ca3c7b9e73d22
https://www.ajol.info/index.php/pamj/article/view/237361
https://www.ajol.info/index.php/pamj/article/view/237361
Publikováno v:
The Pan African Medical Journal
We report in this manuscript a case of newborn baby with asymptomatic form of congenital malaria; the screening of the peripheral blood smear of the baby after a positive result in the mother allowed the diagnosis. The authors were permitted through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf48129fa2230affbd6d683f5f407e5d
https://doi.org/10.11604/pamj.2020.35.116.16628
https://doi.org/10.11604/pamj.2020.35.116.16628
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 6, Iss 10, Pp 167-172 (2017)
Primary hyperoxaluria type 1 (PH1) is a metabolic disorder that mainly affects the kidneys. It results from build-up of a substance called oxalate, which normally is filtered through the kidneys and excreted in the urine. In people with PH1, the accu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::778a32db8b9708a47fc331134b472210
http://www.ijmrhs.com/medical-research/primary-hyperoxaluria-case-reports-and-review-of-literature.pdf
http://www.ijmrhs.com/medical-research/primary-hyperoxaluria-case-reports-and-review-of-literature.pdf
Autor:
Salahiddine Saghir, Mounir Moukit, Driss Moussaoui Rahali, Mohammed Dehayni, Rachid Ait Bouhou, Jaouad Kouach
Publikováno v:
Sexually transmitted diseases. 45(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6024b986993e5f87cf76e3017fa1da0c
https://pubmed.ncbi.nlm.nih.gov/29420453
https://pubmed.ncbi.nlm.nih.gov/29420453
Publikováno v:
Clinical Case Reports
Key Clinical Message We describe a case of association of congenital bone abnormalities. It will allow clinicians to look systematically for other skeletal malformations and teach them how to evaluate these cases for the first time. This early screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9328e7f2db94f791c82260f6166cc473
http://europepmc.org/articles/PMC5930189
http://europepmc.org/articles/PMC5930189