M. Sebai

发表

A novel WFS1 variant associated with severe diabetic retinopathy in Wolfram syndrome type 1

C. Rouzier, L. Ben Jemaa, H. Jilani, 2022, Ophthalmic genetics.

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

J. Beygo, A. Saâd, K. Buiting, 2021, Molecular genetics & genomic medicine.

Surgical Management of Spinal Tuberculosis

M. Madkour, K. A. Al Moutaery, K. Moutaery, 2004 .

The Identification of Large Rearrangements Involving Intron 2 of the CDH1 Gene in BRCA1/2 Negative and Breast Cancer Susceptibility

I. Bièche, R. Lidereau, F. Vialard, 2022, Genes.

Evaluation of radiological investigations in spinal tuberculosis

M. Sebai, Karim Arabi, M. Chakaki, 1992, International Orthopaedics.

Bifacetal dislocation following tuberculosis of the cervical spine

M. Sebai, Karim Arabi, 1991 .

Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I

S. Richard, R. Lidereau, D. Stoppa-Lyonnet, 2021, Human mutation.

A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report

A. Rolfs, H. Jilani, S. Hizem, 2022, Clinical case reports.

Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3.

F. Bilan, H. Jilani, S. Hizem, 2023, Ophthalmic genetics.