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Pathologie-Biologie|January 8, 2008
[Molecular analysis of the p.Asn 370 Ser mutation in Gaucher disease]A Dandana, S Ferchichi, S Ben Khelifa, et al.La Revue De Medecine Interne|April 26, 2024
[McArdle's disease revealed by acute low back pain]C Langbour, S Nicolas, A Bigot, et al.Journal of Neurodegenerative Diseases|March 8, 2017
Clinical Analysis of Algerian Patients with Pompe DiseaseY Sifi, M Medjroubi, R Froissart, et al.Molecular Genetics and Metabolism Reports|October 21, 2016
30 months follow-up of an early enzyme replacement therapy in a severe Morquio A patient: About one caseJ Do Cao, A Wiedemann, T Quinaux, et al.Neurology|May 29, 2008
Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe diseaseP Laforêt, P Petiot, M Nicolino, et al.Journal of Virology|August 17, 2001
Biochemical characterization of the helper component of Cauliflower mosaic virusE Hebrard, M Drucker, D Leclerc, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 31, 2007
[Mucopolysaccharidosis type I: identification of alpha-L-iduronidase mutations in Tunisian families]L Chkioua, S Khedhiri, Z Jaidane, et al.Annales De Biologie Clinique|March 14, 2007
[Diagnostic strategy of mucopolysaccharidosis type I in Tunisia]L Chkioua, S Ferchichi, S Khedhiri, et al.Annales De Biologie Clinique|November 28, 2007
[Biochemical and molecular diagnosis of Gaucher disease in Tunisia]A Dandana, S Ferchichi, S Khedhiri, et al.Bone Marrow Transplantation|June 11, 2003
Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sourcesG Souillet, N Guffon, I Maire, et al.Pageof 5