D. H’Mida

A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.

N. Drouot, M. Koenig, M. Gribaa, 2007, Brain : a journal of neurology.

Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines.

M. Gribaa, A. Saâd, H. Elghezal, 2008, Placenta.

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

Ali Saad, G. Comi, M. Gribaa, 2011, Journal of Human Genetics.

Multiple Self-Healing Palmoplantar Carcinoma: A Familial Predisposition to Skin Cancer with Primary Palmoplantar and Conjunctival Lesions

B. Merriman, G. Stevanin, M. Gribaa, 2014, The Journal of investigative dermatology.

PHACES syndrome associated with carcinoid endobronchial tumor

N. Mama, K. Tlili-Graiess, M. Yacoubi, 2014, Pediatric Radiology.

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.

M. Gribaa, T. B. Lazreg, A. Saâd, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

A. Saâd, B. Sriha, L. Boussofara, 2021, Human genomics.