Sahl Khalid Bedri

Pheochromocytoma cell lines from heterozygous neurofibromatosis knockout mice

James F. Powers, Marian J. Evinger, Panayiotis Tsokas et al. · Cell and Tissue Research · 2000 · 129 citations

Medicine, Histopathology, Neuroendocrine Disorder +7

A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis

Ben J. Gu, Judith Field, Sébastien Dutertre et al. · Human Molecular Genetics · 2015 · 73 citations · Full text

Inflammation, Neurodegenerative Diseases, Molecular Neuroscience +15

Genetic variants are major determinants of CSF antibody levels in multiple sclerosis

An Goris, Ine Pauwels, Marte W. Gustavsen et al. · Brain · 2015 · 67 citations · Full text

Neurogenomics, Neurological Disorder, Genetics +30

Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis

Christina Sundal, Matt Baker, Virginija Danylaité Karrenbauer et al. · European Journal of Neurology · 2014 · 45 citations · Full text

Cerebrospinal fluid oligoclonal immunoglobulin gamma bands and long-term disability progression in multiple sclerosis: a retrospective cohort study

Virginija Danylaité Karrenbauer, Sahl Khalid Bedri, Jan Hillert et al. · Scientific Reports · 2021 · 36 citations · Full text