Hentati A - Search Results

1

Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.

Hentati A, Lamy C, Melki J, Zuber M, Munnich A, de Recondo J. Hentati A, et al. Genomics. 1992 Jan;12(1):155-7. doi: 10.1016/0888-7543(92)90419-s. Genomics. 1992. PMID: 1733853

2

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Hentati A, et al. Among authors: hentati f. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

3

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.

Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S, et al. Hentati A, et al. Among authors: hentati f. Hum Mol Genet. 1994 Oct;3(10):1867-71. doi: 10.1093/hmg/3.10.1867. Hum Mol Genet. 1994. PMID: 7849714

4

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.

Isozumi K, DeLong R, Kaplan J, Deng HX, Iqbal Z, Hung WY, Wilhelmsen KC, Hentati A, Pericak-Vance MA, Siddique T. Isozumi K, et al. Among authors: hentati a. Hum Mol Genet. 1996 Sep;5(9):1377-82. doi: 10.1093/hmg/5.9.1377. Hum Mol Genet. 1996. PMID: 8872481

5

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al. Hentati A, et al. Among authors: hentati f. Nat Genet. 1994 Jul;7(3):425-8. doi: 10.1038/ng0794-425. Nat Genet. 1994. PMID: 7920663

6

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.

Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Among authors: hentati f. Neurogenetics. 1998 Dec;2(1):55-60. doi: 10.1007/s100480050052. Neurogenetics. 1998. PMID: 9933301

7

Molecular genetic basis of familial ALS.

Siddique T, Nijhawan D, Hentati A. Siddique T, et al. Among authors: hentati a. Neurology. 1996 Oct;47(4 Suppl 2):S27-34; discussion S34-5. doi: 10.1212/wnl.47.4_suppl_2.27s. Neurology. 1996. PMID: 8858048 Review.

8

Familial amyotrophic lateral sclerosis.

Siddique T, Hentati A. Siddique T, et al. Among authors: hentati a. Clin Neurosci. 1995-1996;3(6):338-47. Clin Neurosci. 1995. PMID: 9021255 Review.

9

Familial amyotrophic lateral sclerosis.

Siddique T, Nijhawan D, Hentati A. Siddique T, et al. Among authors: hentati a. J Neural Transm Suppl. 1997;49:219-33. doi: 10.1007/978-3-7091-6844-8_23. J Neural Transm Suppl. 1997. PMID: 9266431 Review.

10

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX, et al. Rosen DR, et al. Among authors: hentati a. Nature. 1993 Mar 4;362(6415):59-62. doi: 10.1038/362059a0. Nature. 1993. PMID: 8446170

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

57 results

Search Page

Filters