Related Experiment Videos
[Effect of consanguinity on certain hereditary-degenerative spinocerebellar diseases in Tunisia]
La Tunisie Medicale
|January 1, 1985
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
[Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families].
Journal francais d'ophtalmologie·2006
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.
Neuromuscular disorders : NMD·2003
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.
European journal of neurology·2001
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.
Neuromuscular disorders : NMD·2001
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.
Neuromuscular disorders : NMD·2000
Andes Hantavirus at FIFA World Cup 2026: No vaccine, no protocol, no time.
La Tunisie medicale·2026
Chronic pain among patients treated for breast cancer: Prevalence and associates factors.
La Tunisie medicale·2026
Predictive factors of hemoptysis recurrence after hospital discharge.
La Tunisie medicale·2026
LRP12 CGG Repeat Expansions in Patients With Adult-Onset Non-5q Spinal Muscular Atrophy.
Neurology. Genetics·2026
[National Protocol for the Diagnosis and Management of Stickler syndrome: Summary for the attending physician].
Journal francais d'ophtalmologie·2026
Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.
bioRxiv : the preprint server for biology·2026
Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.
bioRxiv : the preprint server for biology·2026
Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.
bioRxiv : the preprint server for biology·2026