Davis MB - Search Results

1

Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3.

Marques W Jr, Davis MB, Abou-Sleiman PM, Marques VD, Silva WA Jr, Zago MA, Sobreira CS, Barreira AA. Marques W Jr, et al. Among authors: davis mb. Braz J Med Biol Res. 2004 Nov;37(11):1757-62. doi: 10.1590/S0100-879X2004001100022. Epub 2004 Oct 26. Braz J Med Biol Res. 2004. PMID: 15517093 Free article.

2

A family with Friedreich ataxia and onion-bulb formations at sural nerve biopsy.

Barreira AA, Marques Júnior W, Sweeney MG, Davis MB, Chimelli L, Paçó-Larson ML, Wood NW. Barreira AA, et al. Among authors: davis mb. Ann N Y Acad Sci. 1999 Sep 14;883:466-8. Ann N Y Acad Sci. 1999. PMID: 10586275 No abstract available.

3

A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve Biopsy.

Barreira AA, Marques W Jr, Sweeney MG, Davis MB, Chimelli L, Paçó-Larson ML, Wood NW. Barreira AA, et al. Among authors: davis mb. Ann N Y Acad Sci. 1999 Oct;883(1):466-468. doi: 10.1111/j.1749-6632.1999.tb08612.x. Ann N Y Acad Sci. 1999. PMID: 29086964 No abstract available.

4

The phenotypic manifestations of chromosome 17p11.2 duplication.

Thomas PK, Marques W Jr, Davis MB, Sweeney MG, King RH, Bradley JL, Muddle JR, Tyson J, Malcolm S, Harding AE. Thomas PK, et al. Among authors: davis mb. Brain. 1997 Mar;120 ( Pt 3):465-78. doi: 10.1093/brain/120.3.465. Brain. 1997. PMID: 9126058

5

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

Jarman PR, Wood NW, Davis MT, Davis PV, Bhatia KP, Marsden CD, Davis MB. Jarman PR, et al. Among authors: davis mb, davis pv, davis mt. Am J Hum Genet. 1997 Oct;61(4):928-33. doi: 10.1086/514883. Am J Hum Genet. 1997. PMID: 9382105 Free PMC article.

6

DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.

Valente EM, Bentivoglio AR, Cassetta E, Dixon PH, Davis MB, Ferraris A, Ialongo T, Frontali M, Wood NW, Albanese A. Valente EM, et al. Among authors: davis mb. Ann Neurol. 2001 Mar;49(3):362-6. Ann Neurol. 2001. PMID: 11261511

7

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB. Valente EM, et al. Among authors: davis mb. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

8

Linkage analysis with chromosome 9 markers in hereditary essential tremor.

Conway D, Bain PG, Warner TT, Davis MB, Findley LJ, Thompson PD, Marsden CD, Harding AE. Conway D, et al. Among authors: davis mb. Mov Disord. 1993 Jul;8(3):374-6. doi: 10.1002/mds.870080324. Mov Disord. 1993. PMID: 8341306

9

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort.

Davidson G, Murphy S, Polke J, Laura M, Salih M, Muntoni F, Blake J, Brandner S, Davies N, Horvath R, Price S, Donaghy M, Roberts M, Foulds N, Ramdharry G, Soler D, Lunn M, Manji H, Davis M, Houlden H, Reilly M. Davidson G, et al. J Neurol. 2012 Aug;259(8):1673-85. doi: 10.1007/s00415-011-6397-y. J Neurol. 2012. PMID: 22302274 Free PMC article.

10

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Worth PF, Giunti P, Gardner-Thorpe C, Dixon PH, Davis MB, Wood NW. Worth PF, et al. Among authors: davis mb. Am J Hum Genet. 1999 Aug;65(2):420-6. doi: 10.1086/302495. Am J Hum Genet. 1999. PMID: 10417284 Free PMC article.

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