Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Naima, Erreimi"'
Autor:
Ahmed Bouhouche, Omar Askander, Hicham Charoute, Mouna Sabib, Abdeljalil El Quessar, Amine El Hassani, Naima Erreimi
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 28, Iss , Pp 100144- (2023)
Introduction: In humans, there is considerable individual variability in ethanol metabolism, and these differences have been partially attributed to genetic variability at the ADH locus at 4q22-23, where seven genes are found. They encode ADH enzymes
Externí odkaz:
https://doaj.org/article/128eb9956a514944882c508dfe0c2a06
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
Publikováno v:
Asia Pacific Journal of Medical Toxicology, Vol 3, Iss 4, Pp 173-175 (2014)
Background: Closantel is a veterinary drug used as anthelmintic for ruminants while it is contraindicated for humans. This report describes a rare case of blindness, increased liver enzymes and coagulopathy following closantel poisoning. Case report:
Externí odkaz:
https://doaj.org/article/df37fb25bc1445bbb13b7bd3ead78f19
Publikováno v:
Scholars Journal of Applied Medical Sciences. :541-544
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3521495e6925031ba58012d3e962dd7b
https://doi.org/10.36347/sjams.2020.v08i02.036
https://doi.org/10.36347/sjams.2020.v08i02.036
Autor:
Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui, Lamiae Belayachi, Naima El Hafidi, Houyam Hardizi, Elmostafa El Fahime, Naima Erreimi, Abdelhamid Barakat, Mohammed Khattab, Fouad Seghrouchni, Amine El Hassani
Publikováno v:
BioMed Research International.
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6629c4f900704ce4490b6c7d341067b
Autor:
Ahmed, Bouhouche, Yasmin, Tabache, Omar, Askander, Hicham, Charoute, Nada, Mesnaoui, Lamiae, Belayachi, Naima, El Hafidi, Houyam, Hardizi, Elmostafa, El Fahime, Naima, Erreimi, Abdelhamid, Barakat, Mohammed, Khattab, Fouad, Seghrouchni, Amine, El Hassani
Publikováno v:
BioMed research international. 2022
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa98e7b3587364832a77cf6901efd6b4
https://pubmed.ncbi.nlm.nih.gov/35281597
https://pubmed.ncbi.nlm.nih.gov/35281597
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 18 (2015)
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it's one of the rare genetic diseases for which therapy is now available. The purpose of this work is to study the epidemiological features of the disease an
Externí odkaz:
https://doaj.org/article/2930500426f7452fa3a6cee0d0e4be8c
Publikováno v:
The Pan African Medical Journal, Vol 17, Iss 63 (2014)
Malignant Infantile Osteopetrosis (MIOP) is a rare genetic disorder due to osteoclast abnormal activity.We report a thirteen month-old male patient, diagnosed as MIOP while investigating the cause of hepatosplenomegaly associated with hydrocephalus.
Externí odkaz:
https://doaj.org/article/e303034d4a0c46a39a34f97eea447a5e
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
Publikováno v:
The Pan African Medical Journal
Pan African Medical Journal; Vol 20, No 1 (2015)
The Pan African Medical Journal, Vol 20, Iss 18 (2015)
Pan African Medical Journal; Vol 20, No 1 (2015)
The Pan African Medical Journal, Vol 20, Iss 18 (2015)
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it's one of the rare genetic diseases for which therapy is now available. The purpose of this work is to study the epidemiological features of the disease an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::934bb3369cd0c8dbd69f416b74c259c7
https://doi.org/10.11604/pamj.2015.20.18.4112
https://doi.org/10.11604/pamj.2015.20.18.4112