Pollard JD - Search Results

1

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

Silburn PA, Nicholson GA, Teh BT, Blair IP, Pollard JD, Nolan PJ, Larsson C, Boyle RS. Silburn PA, et al. Among authors: pollard jd. Neurology. 1998 Apr;50(4):1067-73. doi: 10.1212/wnl.50.4.1067. Neurology. 1998. PMID: 9566396

2

Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1).

Sander S, Nicholson GA, Ouvrier RA, McLeod JG, Pollard JD. Sander S, et al. Among authors: pollard jd. Muscle Nerve. 1998 Feb;21(2):217-25. doi: 10.1002/(sici)1097-4598(199802)21:2<217::aid-mus9>3.0.co;2-e. Muscle Nerve. 1998. PMID: 9466597

3

Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies.

Sander S, Ouvrier RA, McLeod JG, Nicholson GA, Pollard JD. Sander S, et al. Among authors: pollard jd. J Neurol Neurosurg Psychiatry. 2000 Apr;68(4):483-8. doi: 10.1136/jnnp.68.4.483. J Neurol Neurosurg Psychiatry. 2000. PMID: 10727485 Free PMC article.

4

Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.

Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD. Spring PJ, et al. Among authors: pollard jd. Brain. 2005 Dec;128(Pt 12):2797-810. doi: 10.1093/brain/awh653. Brain. 2005. PMID: 16311270

5

Peripheral neuropathies of infancy.

Wilmshurst JM, Pollard JD, Nicholson G, Antony J, Ouvrier R. Wilmshurst JM, et al. Among authors: pollard jd. Dev Med Child Neurol. 2003 Jun;45(6):408-14. doi: 10.1017/s0012162203000768. Dev Med Child Neurol. 2003. PMID: 12785442 Free article.

6

A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24.

Kok C, Kennerson ML, Spring PJ, Ing AJ, Pollard JD, Nicholson GA. Kok C, et al. Among authors: pollard jd. Am J Hum Genet. 2003 Sep;73(3):632-7. doi: 10.1086/377591. Epub 2003 Jul 17. Am J Hum Genet. 2003. PMID: 12870133 Free PMC article.

7

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B. Vallat JM, et al. Among authors: pollard jd. J Neuropathol Exp Neurol. 2008 Nov;67(11):1097-102. doi: 10.1097/NEN.0b013e31818b6cbc. J Neuropathol Exp Neurol. 2008. PMID: 18957892

8

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.

Nicholson GA, Valentijn LJ, Cherryson AK, Kennerson ML, Bragg TL, DeKroon RM, Ross DA, Pollard JD, McLeod JG, Bolhuis PA, et al. Nicholson GA, et al. Among authors: pollard jd. Nat Genet. 1994 Mar;6(3):263-6. doi: 10.1038/ng0394-263. Nat Genet. 1994. PMID: 8012388

9

Vasculitis confined to peripheral nerves.

Davies L, Spies JM, Pollard JD, McLeod JG. Davies L, et al. Among authors: pollard jd. Brain. 1996 Oct;119 ( Pt 5):1441-8. doi: 10.1093/brain/119.5.1441. Brain. 1996. PMID: 8931569

10

Spinal root and plexus hypertrophy in chronic inflammatory demyelinating polyneuropathy.

Duggins AJ, McLeod JG, Pollard JD, Davies L, Yang F, Thompson EO, Soper JR. Duggins AJ, et al. Among authors: pollard jd. Brain. 1999 Jul;122 ( Pt 7):1383-90. doi: 10.1093/brain/122.7.1383. Brain. 1999. PMID: 10388803

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