author-photo

Khemissa Bejaoui

Harvard University

14

Papers

1492

Citations

Citation Trend

Filter By

Papers (10) Sort By

Journal Conference Others

Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis.

2002 Journal of Clinical Investigation
Show All
- Source
- Cite
- Save
Citations (79)
SPTLC1 is mutated in hereditary sensory neuropathy, type 1

2001 Nature Genetics
Show All
- Source
- Cite
- Save
Citations (236)
Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

1999 Neurology
Show All
- Source
- Cite
- Save
Citations (22)
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes.

1998 Neurogenetics
Show All
- Source
- Cite
- Save
Citations (11)
Physical mapping of the Miyoshi myopathy/LGMD2B locus on chromosome 2p13

1997 Neuromuscular Disorders
Show All
- Source
- Cite
- Save
Citations (0)
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

1995 Neurology
Show All
- Source
- Cite
- Save
Citations (130)
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.

1994 Muscle & Nerve
Show All
- Source
- Cite
- Save
Citations (8)
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

1994 Nature Genetics
Show All
- Source
- Cite
- Save
Citations (185)
Evolution of muscle specific proteins in Werdnig-Hoffman's disease

1992 Journal of the Neurological Sciences
Show All
- Source
- Cite
- Save
Citations (13)
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome

1991 Journal of the Neurological Sciences
Show All
- Source
- Cite
- Save
Citations (12)