Afif Hentati
Affiliations: | Neurology | University of Chicago, Pritzker School of Medicine |
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| Claire Simon K, Hentati A, Rubin S, et al. (2018) Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care. Multiple Sclerosis Journal - Experimental, Translational and Clinical. 4: 2055217318813736 |
| Tsaousidou MK, Ouahchi K, Warner TT, et al. (2008) Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. American Journal of Human Genetics. 82: 510-5 |
| Yip AG, Dürr A, Marchuk DA, et al. (2003) Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class. Journal of Medical Genetics. 40: e106 |
| Yang Y, Hentati A, Deng HX, et al. (2001) The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nature Genetics. 29: 160-5 |
| Hentati A, Deng HX, Zhai H, et al. (2000) Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 55: 1388-90 |
| Hentati A, Ouahchi K, Pericak-Vance MA, et al. (1998) Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 2: 55-60 |
| Siddique T, Nijhawan D, Hentati A. (1997) Familial amyotrophic lateral sclerosis. Journal of Neural Transmission. Supplementum. 49: 219-33 |
| Ahmed MS, Afsar S, Hentati A, et al. (1997) A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis. Neurology. 48: 258-60 |
| Isozumi K, DeLong R, Kaplan J, et al. (1996) Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31. Human Molecular Genetics. 5: 1377-82 |
| Siddique T, Nijhawan D, Hentati A. (1996) Molecular genetic basis of familial ALS. Neurology. 47: S27-34; discussion S |