These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 8393091)

  • 1. Hereditary neuropathy with liability to pressure palsies: a clinical, electroneurophysiological and morphological study.
    Verhagen WI; Gabreëls-Festen AA; van Wensen PJ; Joosten EM; Vingerhoets HM; Gabreëls FJ; de Graaf R
    J Neurol Sci; 1993 Jun; 116(2):176-84. PubMed ID: 8393091
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary neuropathy with liability to pressure palsies in childhood.
    Gabreëls-Festen AA; Gabreëls FJ; Joosten EM; Vingerhoets HM; Renier WO
    Neuropediatrics; 1992 Jun; 23(3):138-43. PubMed ID: 1322507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Uncompacted myelin in hereditary neuropathy with liability to pressure palsies with the 17 p11.2 deletion.
    Jedrzejowska H; Fidziańska A; Kochański A
    Folia Neuropathol; 1999; 37(4):220-6. PubMed ID: 10705641
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial neuropathy with liability to pressure palsies. Report of a case.
    Jedrzejowska H; Hausmanowa-Petrusewicz I
    Ital J Neurol Sci; 1981 Aug; 2(3):229-36. PubMed ID: 6281213
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion.
    Kim SM; Chung KW; Choi BO; Yoon ES; Choi JY; Park KD; Sunwoo IN
    Exp Mol Med; 2004 Feb; 36(1):28-35. PubMed ID: 15031668
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies.
    Sander S; Ouvrier RA; McLeod JG; Nicholson GA; Pollard JD
    J Neurol Neurosurg Psychiatry; 2000 Apr; 68(4):483-8. PubMed ID: 10727485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary neuropathy with liability to pressure palsies. Report of two families and review of the literature.
    Meier C; Moll C
    J Neurol; 1982; 228(2):73-95. PubMed ID: 6185651
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects.
    Behse F; Buchthal F; Carlsen F; Knappeis GG
    Brain; 1972; 95(4):777-94. PubMed ID: 4345910
    [No Abstract]   [Full Text] [Related]  

  • 9. Hereditary pressure-sensitive neuropathy: demonstration of "tomacula" in motor nerve fibers.
    Oda K; Miura H; Shibasaki H; Endo C; Kakigi R; Kuroda Y; Tanaka K
    J Neurol Sci; 1990 Sep; 98(2-3):139-48. PubMed ID: 1700806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tomaculous neuropathy: hereditary predisposition to pressure palsies.
    Fewings JD; Blumbergs PC; Mukherjee TM; Hallpike JF
    Aust N Z J Med; 1985 Oct; 15(5):598-603. PubMed ID: 3004403
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
    Eirís-Punal J; Vidal-Lijó M; Barros-Angueira F; Lopez-Fernández MJ; Pintos-Martínez E; Beiras-Iglesias A; Castro-Gago M
    Rev Neurol; 2000 Sep 16-30; 31(6):506-10. PubMed ID: 11055050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies.
    Umehara F; Kiwaki T; Yoshikawa H; Nishimura T; Nakagawa M; Matsumoto W; Hashimoto K; Izumo S; Arimura Y; Arimura K
    J Neurol Sci; 1995 Nov; 133(1-2):173-6. PubMed ID: 8583222
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary neuropathy with liability to pressure palsies. A contribution to the differential diagnosis of multiplex mononeuropathy].
    Grehl H; Moll C; Meier C
    Dtsch Med Wochenschr; 1987 Feb; 112(7):254-8. PubMed ID: 3028748
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentation.
    Andreadou E; Yapijakis C; Paraskevas GP; Stavropoulos P; Karadimas C; Zis VP; Davaki P; Karandreas N; Rentzos M; Tsakanikas C; Vassilopoulos D; Papageorgiou C
    J Neurol; 1996 Mar; 243(3):225-30. PubMed ID: 8936351
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Multiple exercise-related mononeuropathy with abdominal colic.
    Trockel U; Schröder JM; Reiners KH; Toyka KV; Goerz G; Freund HJ
    J Neurol Sci; 1983; 60(3):431-42. PubMed ID: 6313866
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies.
    Schenone A; Nobbio L; Mandich P; Bellone E; Abbruzzese M; Aymar F; Mancardi GL; Windebank AJ
    Neurology; 1997 Feb; 48(2):445-9. PubMed ID: 9040736
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities.
    Gouider R; LeGuern E; Emile J; Tardieu S; Cabon F; Samid M; Weissenbach J; Agid Y; Bouche P; Brice A
    Neurology; 1994 Dec; 44(12):2250-2. PubMed ID: 7991107
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Neuropathy associated with acrodermatitis chronica atrophicans. Clinical and morphological features.
    Kristoferitsch W; Sluga E; Graf M; Partsch H; Neumann R; Stanek G; Budka H
    Ann N Y Acad Sci; 1988; 539():35-45. PubMed ID: 2847621
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.