425 related articles for article (PubMed ID: 17922888)
1. Hereditary neuropathy with liability to pressure palsies: description of seven patients without known family history.
Beydoun SR; Sykes SN; Ganguly G; Lee TS
Acta Neurol Scand; 2008 Apr; 117(4):266-72. PubMed ID: 17922888
[TBL] [Abstract][Full Text] [Related]
2. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
Li J; Ghandour K; Radovanovic D; Shy RR; Krajewski KM; Shy ME; Nicholson GA
Arch Neurol; 2007 Jul; 64(7):974-8. PubMed ID: 17620487
[TBL] [Abstract][Full Text] [Related]
3. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
Pou Serradell A; Monells J; Téllez MJ; Fossas P; Löfgren A; Meuleman J; Timmerman V; De Jonghe P; Ceuterick C; Martin JJ
Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826
[TBL] [Abstract][Full Text] [Related]
4. Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: a case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade.
Bayrak AO; Battaloglu E; Turker H; Baris I; Oztas G
Brain Dev; 2009 Jun; 31(6):445-8. PubMed ID: 18760885
[TBL] [Abstract][Full Text] [Related]
5. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
Sanahuja J; Franco E; Rojas-García R; Gallardo E; Combarros O; Begué R; Granés P; Illa I
Arch Neurol; 2005 Dec; 62(12):1911-4. PubMed ID: 16344349
[TBL] [Abstract][Full Text] [Related]
6. [A family with hereditary neuropathy with liability to pressure palsies--clinical, electrophysiological, pathological study and DNA analysis].
Kaneko S; Ito H; Kusaka H; Imai T; Yoshikawa H
Rinsho Shinkeigaku; 1994 Jul; 34(7):673-8. PubMed ID: 7955724
[TBL] [Abstract][Full Text] [Related]
7. Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies.
Sutton IJ; Mocroft AP; Lindley VH; Barber RM; Bryon RJ; Winer JB; MacDonald F
Neuromuscul Disord; 2004 Dec; 14(12):804-9. PubMed ID: 15564036
[TBL] [Abstract][Full Text] [Related]
8. Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies.
Li J; Krajewski K; Lewis RA; Shy ME
Muscle Nerve; 2004 Feb; 29(2):205-10. PubMed ID: 14755484
[TBL] [Abstract][Full Text] [Related]
9. Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
Miltenberger-Miltenyi G; Janecke AR; Wanschitz JV; Timmerman V; Windpassinger C; Auer-Grumbach M; Löscher WN
Arch Neurol; 2007 Jul; 64(7):966-70. PubMed ID: 17620486
[TBL] [Abstract][Full Text] [Related]
10. A new single-nucleotide deletion of PMP22 in an HNPP family without recurrent palsies.
Luigetti M; Conte A; Madia F; Mereu ML; Zollino M; Marangi G; Pomponi MG; Liberatore G; Tonali PA; Sabatelli M
Muscle Nerve; 2008 Aug; 38(2):1060-4. PubMed ID: 18642376
[TBL] [Abstract][Full Text] [Related]
11. Overview of hereditary neuropathy with liability to pressure palsies.
Chance PF
Ann N Y Acad Sci; 1999 Sep; 883():14-21. PubMed ID: 10586225
[TBL] [Abstract][Full Text] [Related]
12. A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies.
Zéphir H; Stojkovic T; Latour P; Hurtevent JF; Blankaert F; Vermersch P
Neuromuscul Disord; 2005 Jul; 15(7):493-7. PubMed ID: 15955700
[TBL] [Abstract][Full Text] [Related]
13. Vasculitic neuropathy--electrodiagnostic findings and association with malignancies.
Zivković SA; Ascherman D; Lacomis D
Acta Neurol Scand; 2007 Jun; 115(6):432-6. PubMed ID: 17511855
[TBL] [Abstract][Full Text] [Related]
14. Hereditary neuropathy with liability to pressure palsies mimicking multifocal compression neuropathy.
Lane JE; Foulkes GD; Hope TD; Mayorov VI; Adkison L
J Hand Surg Am; 2001 Jul; 26(4):670-4. PubMed ID: 11466642
[TBL] [Abstract][Full Text] [Related]
15. A rare genetic disorder in the differential diagnosis of the entrapment neuropathies: hereditary neuropathy with liability to pressure palsies.
Koc F; Güzel R; Benlidayi IC; Yerdelen D; Güzel I; Sarica Y
J Clin Rheumatol; 2006 Apr; 12(2):78-82. PubMed ID: 16601541
[TBL] [Abstract][Full Text] [Related]
16. Peripheral neuropathy: the importance of history and examination for correct diagnosis.
Kelly JJ
Rev Neurol Dis; 2005; 2(3):150-3. PubMed ID: 16400316
[TBL] [Abstract][Full Text] [Related]
17. [Recurrent palsies--consider hereditary pressure neuropathy!].
Liedholm LJ
Lakartidningen; 1998 Apr; 95(14):1527-31. PubMed ID: 9564140
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary neuropathy with liability to pressure palsies].
Smith TA; Rasmussen K; Hertz JM
Ugeskr Laeger; 1999 Jun; 161(23):3463-5. PubMed ID: 10388355
[TBL] [Abstract][Full Text] [Related]
19. Pathophysiologic insights into motor axonal function in Kennedy disease.
Vucic S; Kiernan MC
Neurology; 2007 Nov; 69(19):1828-35. PubMed ID: 17984450
[TBL] [Abstract][Full Text] [Related]
20. Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience.
Luigetti M; Del Grande A; Conte A; Lo Monaco M; Bisogni G; Romano A; Zollino M; Rossini PM; Sabatelli M
J Neurol Sci; 2014 Jun; 341(1-2):46-50. PubMed ID: 24726093
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]