Reilly M - Search Results

1

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

Bhatia K, Reilly M, Adams D, Davis MB, Hawkes CH, Thomas PK, Said G, Harding AE. Bhatia K, et al. Among authors: reilly m. J Neurol Neurosurg Psychiatry. 1993 Jun;56(6):694-7. doi: 10.1136/jnnp.56.6.694. J Neurol Neurosurg Psychiatry. 1993. PMID: 8509786 Free PMC article.

2

[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence].

Adams D, Reilly M, Harding AE, Said G. Adams D, et al. Among authors: reilly m. Rev Neurol (Paris). 1992;148(12):736-41. Rev Neurol (Paris). 1992. PMID: 1338934 Review. French.

3

A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.

Houlden H, King RH, Hashemi-Nejad A, Wood NW, Mathias CJ, Reilly M, Thomas PK. Houlden H, et al. Among authors: reilly m. Ann Neurol. 2001 Apr;49(4):521-5. Ann Neurol. 2001. PMID: 11310631

4

Clinical and genetic characterization of families with triple A (Allgrove) syndrome.

Houlden H, Smith S, De Carvalho M, Blake J, Mathias C, Wood NW, Reilly MM. Houlden H, et al. Among authors: reilly mm. Brain. 2002 Dec;125(Pt 12):2681-90. doi: 10.1093/brain/awf270. Brain. 2002. PMID: 12429595

5

Microvasculitic paraproteinaemic polyneuropathy and B-cell lymphoma.

Turner MR, Warren JD, Jacobs JM, Groves MJ, Yong K, Honan WP, Thomas PK, Reilly MM. Turner MR, et al. Among authors: reilly mm. J Peripher Nerv Syst. 2003 Jun;8(2):100-7. doi: 10.1046/j.1529-8027.2003.03013.x. J Peripher Nerv Syst. 2003. PMID: 12795714

6

Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.

Lee MJ, Stephenson DA, Groves MJ, Sweeney MG, Davis MB, An SF, Houlden H, Salih MA, Timmerman V, de Jonghe P, Auer-Grumbach M, Di Maria E, Scaravilli F, Wood NW, Reilly MM. Lee MJ, et al. Among authors: reilly mm. Hum Mol Genet. 2003 Aug 1;12(15):1917-25. doi: 10.1093/hmg/ddg198. Hum Mol Genet. 2003. PMID: 12874111

7

Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.

Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R. Pitt M, et al. Among authors: reilly m. Brain. 2003 Dec;126(Pt 12):2682-92. doi: 10.1093/brain/awg278. Epub 2003 Sep 23. Brain. 2003. PMID: 14506069

8

A novel RAB7 mutation associated with ulcero-mutilating neuropathy.

Houlden H, King RH, Muddle JR, Warner TT, Reilly MM, Orrell RW, Ginsberg L. Houlden H, et al. Among authors: reilly mm. Ann Neurol. 2004 Oct;56(4):586-90. doi: 10.1002/ana.20281. Ann Neurol. 2004. PMID: 15455439

9

Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I).

Houlden H, King R, Blake J, Groves M, Love S, Woodward C, Hammans S, Nicoll J, Lennox G, O'Donovan DG, Gabriel C, Thomas PK, Reilly MM. Houlden H, et al. Among authors: reilly mm. Brain. 2006 Feb;129(Pt 2):411-25. doi: 10.1093/brain/awh712. Epub 2005 Dec 19. Brain. 2006. PMID: 16364956

10

New mutations, genotype phenotype studies and manifesting carriers in giant axonal neuropathy.

Houlden H, Groves M, Miedzybrodzka Z, Roper H, Willis T, Winer J, Cole G, Reilly MM. Houlden H, et al. Among authors: reilly mm. J Neurol Neurosurg Psychiatry. 2007 Nov;78(11):1267-70. doi: 10.1136/jnnp.2007.118968. Epub 2007 Jun 19. J Neurol Neurosurg Psychiatry. 2007. PMID: 17578852 Free PMC article.

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

1,884 results

Search Page

Filters