Publications by authors named "Sakka R"

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A recipe for a disaster: food, climate change, and cancer.
Leticia M Nogueira, Rand Sakka, Christine Jovanovic

Cancer Causes Control· October 2025

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Portraying the full picture of Neurofibromatosis-Noonan syndrome: a systematic review of literature.
Omeyma Trimeche, Rania Sakka, Ekram Hajji, Abdelmouhaymen Missaoui, Bilel Ben Amor

J Med Genet· January 2025

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Phenotypic variability and management of patients with mosaic monosomy X and Y chromosome material: a case series.
Myriam Ben Fredj, Marwa Messaoud, Sabrine Ben Youssef, Salma Mani, Syrine Laaribi

Ital J Pediatr· May 2024

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An unusual familial Xp22.12 microduplication including EIF1AX: A novel candidate dosage-sensitive gene for premature ovarian insufficiency.
Rim Sakka, Fatma Abdelhedi, Hanen Sellami, Bruno Pichon, Yosra Lajmi

Eur J Med Genet· November 2022

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Relationship between nuclear DNA fragmentation, mitochondrial DNA damage and standard sperm parameters in spermatozoa of infertile patients with leukocytospermia.
Rihab Derbel, Hanen Sellami, Rim Sakka, Ahlem Ben Slima, Ilyess Mkaddem

J Gynecol Obstet Hum Reprod· May 2021

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Mandibuloacral dysplasia type A in five tunisian patients.
Sakka R, Marmouch H, Trabelsi M, Achour A, Golli M

Eur J Med Genet· February 2021

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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.
Saida Lahbib, Mediha Trabelsi, Hamza Dallali, Rania Sakka, Rym Bourourou

Mol Biol Rep· August 2019

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Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation.
Rania Sakka, Bahri Mahjoub, Emna Kerkeni, Amina Werdani, Raoudha Boussoffara

Pediatr Blood Cancer· September 2018

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Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome.
Nehla Ghedira, Arnaud Lagarde, Karim Ben Ameur, Sahar Elouej, Rania Sakka

BMC Pediatr· August 2018

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Duodenal Atresia Associated with Apple Peel Atresia and Situs Inversus Abdominus: A Case Report.
H Ben Hamida, R Hadj Salem, K Ben Ameur, A Rassas, F Z Chioukh

J Neonatal Surg· October 2016

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Sanjad-Sakati syndrome in a Tunisian child.
E Kerkeni, R Sakka, S Sfar, S Bouaziz, N Ghedira

Arch Pediatr· September 2015

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[Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family].
Rania Sakka, Emna Kerkeni, Myriam Chaabouni, Fatma Zohra Chioukh, Sofiène Ben Amor

Tunis Med· March 2015

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