Rania Sakka
Monastir, Tunisia
Last Updated: 09/26/2026
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Found 10 publications
Types of genotypes in progressive familial intrahepatic cholestasis and liver transplantation: A meta-analysis of observational studies.
Journal: PloS one
Published: September 07, 2025
Three cases of pediatric adrenocortical carcinoma with intermediate malignant potential: a case report with literature review.
Journal: AME case reports
Published: August 09, 2025
Portraying the full picture of Neurofibromatosis-Noonan syndrome: a systematic review of literature.
Portraying the full picture of Neurofibromatosis-Noonan syndrome: a systematic review of literature.
Journal: Journal of medical genetics
Published: July 23, 2024
Phenotypic variability and management of patients with mosaic monosomy X and Y chromosome material: a case series.
Journal: Italian journal of pediatrics
Published: July 27, 2023
Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family.
Journal: Molecular biology reports
Published: February 28, 2019
Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation.
Journal: Pediatric blood & cancer
Published: December 28, 2017
Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.
Journal: BMC pediatrics
Published: June 14, 2017
Duodenal Atresia Associated with Apple Peel Atresia and Situs Inversus Abdominus: A Case Report.
Journal: Journal of neonatal surgery
Published: July 04, 2016
Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family
Journal: La Tunisie medicale
Published: September 15, 2015
Sanjad-Sakati syndrome in a Tunisian child.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: February 21, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026