King RH - Search Results

1

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: king rh. Ann Neurol. 2004 Oct;56(4):586-90. doi: 10.1002/ana.20281. Ann Neurol. 2004. PMID: 15455439

2

Coexistent hereditary and inflammatory neuropathy.

Ginsberg L, Malik O, Kenton AR, Sharp D, Muddle JR, Davis MB, Winer JB, Orrell RW, King RH. Ginsberg L, et al. Among authors: king rh. Brain. 2004 Jan;127(Pt 1):193-202. doi: 10.1093/brain/awh017. Epub 2003 Nov 7. Brain. 2004. PMID: 14607795

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: king rh. Ann Neurol. 2001 Apr;49(4):521-5. Ann Neurol. 2001. PMID: 11310631

4

Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin.

Houlden H, King RH, Wood NW, Thomas PK, Reilly MM. Houlden H, et al. Among authors: king rh. Brain. 2001 May;124(Pt 5):907-15. doi: 10.1093/brain/124.5.907. Brain. 2001. PMID: 11335693

5

The nerve biopsy: indications, technical aspects, and contribution.

King R, Ginsberg L. King R, et al. Handb Clin Neurol. 2013;115:155-70. doi: 10.1016/B978-0-444-52902-2.00009-6. Handb Clin Neurol. 2013. PMID: 23931779 Review.

6

Pathological findings in a patient with ventilatory failure and chronic inflammatory demyelinating polyneuropathy.

Kimber TE, Orrell RW, King RH, Ginsberg L. Kimber TE, et al. Among authors: king rh. J Peripher Nerv Syst. 2003 Mar;8(1):13-6. doi: 10.1046/j.1529-8027.2003.03003.x. J Peripher Nerv Syst. 2003. PMID: 12678549

7

Brachial plexus hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy.

Bradley LJ, Wilhelm T, King RH, Ginsberg L, Orrell RW. Bradley LJ, et al. Among authors: king rh. Neuromuscul Disord. 2006 Feb;16(2):126-31. doi: 10.1016/j.nmd.2005.11.006. Epub 2006 Jan 19. Neuromuscul Disord. 2006. PMID: 16427285

8

Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons.

Schapira AH, Cleeter MW, Muddle JR, Workman JM, Cooper JM, King RH. Schapira AH, et al. Among authors: king rh. Ann Neurol. 2006 Aug;60(2):253-5. doi: 10.1002/ana.20934. Ann Neurol. 2006. PMID: 16862591

9

The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy.

Houlden H, Laura M, Ginsberg L, Jungbluth H, Robb SA, Blake J, Robinson S, King RH, Reilly MM. Houlden H, et al. Among authors: king rh. Neuromuscul Disord. 2009 Apr;19(4):264-9. doi: 10.1016/j.nmd.2009.01.006. Epub 2009 Mar 9. Neuromuscul Disord. 2009. PMID: 19272779

10

Peripheral nerve granuloma in a patient with tuberculosis.

Orrell RW, King RH, Bowler JV, Ginsberg L. Orrell RW, et al. Among authors: king rh. J Neurol Neurosurg Psychiatry. 2002 Dec;73(6):769-71. doi: 10.1136/jnnp.73.6.769. J Neurol Neurosurg Psychiatry. 2002. PMID: 12438489 Free PMC article.

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