PubMed for id: 330880

Year	Number of Results
1983	1
1988	1
1991	1
1992	1
1993	1
1994	3
1995	3
1996	4
1997	1
1998	1
1999	2
2000	1
2001	1
2002	2
2003	4
2004	1
2005	3
2007	1
2011	1
2013	1
2014	2
2023	0

1

Clinical and neurophysiologic characterization of an European family with hereditary sensory neuropathy, paroxysmal cough and gastroesophageal reflux.

Barros P, Morais H, Santos C, Roriz J, Coutinho P. Barros P, et al. Arq Neuropsiquiatr. 2014 Apr;72(4):269-72. doi: 10.1590/0004-282x20140014. Arq Neuropsiquiatr. 2014. PMID: 24760089 Free article.

2

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3.

Kornak U, Mademan I, Schinke M, Voigt M, Krawitz P, Hecht J, Barvencik F, Schinke T, Gießelmann S, Beil FT, Pou-Serradell A, Vílchez JJ, Beetz C, Deconinck T, Timmerman V, Kaether C, De Jonghe P, Hübner CA, Gal A, Amling M, Mundlos S, Baets J, Kurth I. Kornak U, et al. Brain. 2014 Mar;137(Pt 3):683-92. doi: 10.1093/brain/awt357. Epub 2014 Jan 22. Brain. 2014. PMID: 24459106

3

Charcot-Marie-Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplication.

Speevak MD, Farrell SA. Speevak MD, et al. Eur J Med Genet. 2013 Oct;56(10):566-9. doi: 10.1016/j.ejmg.2013.06.004. Epub 2013 Jun 25. Eur J Med Genet. 2013. PMID: 23811036

4

Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene.

Taioli F, Cabrini I, Cavallaro T, Simonati A, Testi S, Fabrizi GM. Taioli F, et al. J Peripher Nerv Syst. 2011 Mar;16(1):59-64. doi: 10.1111/j.1529-8027.2011.00319.x. J Peripher Nerv Syst. 2011. PMID: 21504504

5

New mutation of the MPZ gene in a family with the Dejerine-Sottas disease phenotype.

Floroskufi P, Panas M, Karadima G, Vassilopoulos D. Floroskufi P, et al. Muscle Nerve. 2007 May;35(5):667-9. doi: 10.1002/mus.20703. Muscle Nerve. 2007. PMID: 17143884

6

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. Brain. 2005 Dec;128(Pt 12):2797-810. doi: 10.1093/brain/awh653. Brain. 2005. PMID: 16311270

7

Co-segregation of LMNA and PMP22 gene mutations in the same family.

Pegoraro E, Gavassini BF, Benedetti S, Menditto I, Zara G, Padoan R, Mostacciuolo ML, Ferrari M, Angelini C. Pegoraro E, et al. Neuromuscul Disord. 2005 Dec;15(12):858-62. doi: 10.1016/j.nmd.2005.08.008. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288874

8

Marked phenotypic variation in a family with a new myelin protein zero mutation.

Szabo A, Züchner S, Siska E, Mechler F, Molnar MJ. Szabo A, et al. Neuromuscul Disord. 2005 Nov;15(11):760-3. doi: 10.1016/j.nmd.2005.07.006. Epub 2005 Sep 28. Neuromuscul Disord. 2005. PMID: 16198109

9

Phenotypic clustering in MPZ mutations.

Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J. Shy ME, et al. Brain. 2004 Feb;127(Pt 2):371-84. doi: 10.1093/brain/awh048. Epub 2004 Jan 7. Brain. 2004. PMID: 14711881 Review.

10

Dominantly inherited peripheral neuropathies.

Vallat JM. Vallat JM. J Neuropathol Exp Neurol. 2003 Jul;62(7):699-714. doi: 10.1093/jnen/62.7.699. J Neuropathol Exp Neurol. 2003. PMID: 12901697 Review.

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

36 results

Results by year