Parry G - Search Results

1

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.

Brown KA, Janjua AH, Karbani G, Parry G, Noble A, Crockford G, Bishop DT, Newton VE, Markham AF, Mueller RF. Brown KA, et al. Among authors: parry g. Hum Mol Genet. 1996 Jan;5(1):169-73. doi: 10.1093/hmg/5.1.169. Hum Mol Genet. 1996. PMID: 8789457

2

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF. Campbell DA, et al. Among authors: parry g. J Med Genet. 1997 Dec;34(12):1015-7. doi: 10.1136/jmg.34.12.1015. J Med Genet. 1997. PMID: 9429146 Free PMC article.

3

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.

Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, Mueller RF, Leigh IM. Kelsell DP, et al. Among authors: parry g. Nature. 1997 May 1;387(6628):80-3. doi: 10.1038/387080a0. Nature. 1997. PMID: 9139825

4

Paraneoplastic vasculitic neuropathy related to carcinoid tumor.

Ashok Muley S, Brown K, Parry GJ. Ashok Muley S, et al. J Neurol. 2008 Jul;255(7):1085-7. doi: 10.1007/s00415-008-0825-7. Epub 2008 May 6. J Neurol. 2008. PMID: 18458858 No abstract available.

5

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.

Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, Hong M, Simmons Z, Bird TD, Chance PF, Hannibal MC. Landsverk ML, et al. Among authors: parry gj. Hum Mol Genet. 2009 Apr 1;18(7):1200-8. doi: 10.1093/hmg/ddp014. Epub 2009 Jan 12. Hum Mol Genet. 2009. PMID: 19139049 Free PMC article.

6

Sensory neuropathy with low-dose pyridoxine.

Parry GJ, Bredesen DE. Parry GJ, et al. Neurology. 1985 Oct;35(10):1466-8. doi: 10.1212/wnl.35.10.1466. Neurology. 1985. PMID: 2993949

7

Diabetic neuropathy.

Gominak S, Parry GJ. Gominak S, et al. Adv Neurol. 2002;88:99-109. Adv Neurol. 2002. PMID: 11908239 Review. No abstract available.

8

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy.

Collie AM, Landsverk ML, Ruzzo E, Mefford HC, Buysse K, Adkins JR, Knutzen DM, Barnett K, Brown RH Jr, Parry GJ, Yum SW, Simpson DA, Olney RK, Chinnery PF, Eichler EE, Chance PF, Hannibal MC. Collie AM, et al. Among authors: parry gj. J Med Genet. 2010 Sep;47(9):601-7. doi: 10.1136/jmg.2009.072348. Epub 2009 Nov 25. J Med Genet. 2010. PMID: 19939853

9

Relative utility of different electrophysiologic techniques in the evaluation of brachial plexopathies.

Aminoff MJ, Olney RK, Parry GJ, Raskin NH. Aminoff MJ, et al. Among authors: parry gj. Neurology. 1988 Apr;38(4):546-50. doi: 10.1212/wnl.38.4.546. Neurology. 1988. PMID: 2832784

10

Annual league tables of mortality in neonatal intensive care units: longitudinal study. International Neonatal Network and the Scottish Neonatal Consultants and Nurses Collaborative Study Group.

Parry GJ, Gould CR, McCabe CJ, Tarnow-Mordi WO. Parry GJ, et al. BMJ. 1998 Jun 27;316(7149):1931-5. doi: 10.1136/bmj.316.7149.1931. BMJ. 1998. PMID: 9641927 Free PMC article.

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