Khemissa Bejaoui
Marshfield Clinic(US)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Neurogenetic and Muscular Disorders Research, Cardiomyopathy and Myosin Studies, Endoplasmic Reticulum Stress and Disease
Most-Cited Works
- → Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy(1998)917 cited
- → SPTLC1 is mutated in hereditary sensory neuropathy, type 1(2001)291 cited
- → Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35(1994)205 cited
- → Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14(1995)147 cited
- → Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis(2002)85 cited
- → Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22(1999)29 cited
- → Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus ( ALS2 ) on chromosome 2q33(1998)22 cited
- → What is the risk of permanent disability from a multiple sclerosis relapse?(2010)20 cited
- → Evolution of muscle specific proteins in Werdnig-Hoffman's disease(1992)17 cited