Nadia Serbati
Casablanca, Morocco
Last Updated: 09/26/2026
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Found 12 publications
Bardet-Biedl syndrome: a rare cause of end-stage kidney disease. Case report.
Journal: Annals of medicine and surgery (2012)
Published: November 07, 2024
Lynch syndrome or hereditary non polyposis colorectal cancer (HNPCC) in a moroccan family: Case report.
Journal: Annals of medicine and surgery (2012)
Published: December 23, 2020
Trisomy 18 or postnatal Edward´s syndrome: descriptive study conducted at the University Hospital Center of Casablanca and literature review
Journal: The Pan African medical journal
Published: September 22, 2020
13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report.
Journal: Annals of medicine and surgery (2012)
Published: September 22, 2020
The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease.
Journal: BMC research notes
Published: May 16, 2018
Polymorphisms in oxidative pathway related genes and susceptibility to inflammatory bowel disease.
Journal: World journal of gastroenterology
Published: March 25, 2017
Genetic Polymorphisms of Multidrug Resistance Gene-1 (MDR1/ABCB1) and Glutathione S-Transferase Gene and the Risk of Inflammatory Bowel Disease among Moroccan Patients.
Journal: Mediators of inflammation
Published: May 29, 2015
NOD2/CARD15 gene influences disease behaviour but not IBD susceptibility in a Moroccan population.
Journal: The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
Published: April 25, 2015
Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms: New data and a meta-analysis.
Journal: BMC gastroenterology
Published: June 22, 2014
IL23R and ATG16L1 variants in Moroccan patients with inflammatory bowel disease.
Journal: BMC research notes
Published: April 24, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026