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 *

178 related articles for article (PubMed ID: 29137918)

  • 1. Spinobulbar muscular atrophy combined with atypical hereditary neuropathy with liability to pressure palsy.
    Choi K; Ahn SH; Baek SH; Kim JS; Choi SJ; Shin JY; Kim SM; Hong YH; Sung JJ
    J Clin Neurosci; 2018 Feb; 48():90-92. PubMed ID: 29137918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular genetic characteristics of 24 families of hereditary neuropathy with liability to pressure palsy and literature review.
    Cao W; Huang S; Zhao H; Li Z; Zhu X; Liu L; Zhang R
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Oct; 48(10):1572-1582. PubMed ID: 38432886
    [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): report of a family with a new point mutation in PMP22 gene.
    Fusco C; Spagnoli C; Salerno GG; Pavlidis E; Frattini D; Pisani F
    Ital J Pediatr; 2017 Oct; 43(1):97. PubMed ID: 29078790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinal and bulbar muscular atrophy and Charcot-Marie-Tooth type 1A: Co-existence of two rare neuromuscular genetic diseases in the same patient.
    Sagnelli A; Scaioli V; Piscosquito G; Salsano E; Dalla Bella E; Gellera C; Pareyson D
    Neuromuscul Disord; 2015 Oct; 25(10):800-1. PubMed ID: 26298608
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies.
    Moszyńska I; Kabzińska D; Sinkiewicz-Darol E; Kochański A
    Acta Biochim Pol; 2009; 56(4):627-30. PubMed ID: 19830275
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Hereditary neuropathy with liability to pressure palsy.
    Paprocka J; Kajor M; Jamroz E; Jezela-Stanek A; Seeman P; Marszał E
    Folia Neuropathol; 2006; 44(4):290-4. PubMed ID: 17183456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary neuropathy with liability to pressure palsy: an investigation in a rare and large Chinese family.
    He Y; Wu Q; Xu Z; Wang Q; Wang W; Li D; Liu W; He X
    Eur Neurol; 2012; 68(5):322-8. PubMed ID: 23147806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Multiple phenotypic manifestations of X-linked spinobulbar muscular atrophy].
    Vandenberghe N; Bouhour F; Petiot P; Gonnaud PM; Latour P; Broussolle E; Vial C
    Rev Neurol (Paris); 2009 Jan; 165(1):31-7. PubMed ID: 18667219
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary neuropathy with liability to pressure palsies and amyotrophic lateral sclerosis.
    Bhatt A; Farooq MU; Aburashed R; Kassab MY; Majid A; Bhatt S; Naravetla B; Dhaliwal G
    Neurol Sci; 2009 Jun; 30(3):241-5. PubMed ID: 19238316
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.
    Beydoun SR; Cho J
    J Clin Neuromuscul Dis; 2013 Sep; 15(1):28-33. PubMed ID: 23965407
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple tendon transfer for a case of radial nerve palsy in hereditary neuropathy with liability to pressure palsy.
    Palumbo F; Yamamoto M; Hirata H
    Nagoya J Med Sci; 2023 Feb; 85(1):204-210. PubMed ID: 36923620
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CAG repeat polymorphism in the androgen receptor (AR) gene of SBMA patients and a control group.
    Sułek A; Hoffman-Zacharska D; Krysa W; Szirkowiec W; Fidziańska E; Zaremba J
    J Appl Genet; 2005; 46(2):237-9. PubMed ID: 15876692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.
    Young P; Wiebusch H; Stögbauer F; Ringelstein B; Assmann G; Funke H
    Neurology; 1997 Feb; 48(2):450-2. PubMed ID: 9040737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat.
    Grunseich C; Kats IR; Bott LC; Rinaldi C; Kokkinis A; Fox D; Chen KL; Schindler AB; Mankodi AK; Shrader JA; Schwartz DP; Lehky TJ; Liu CY; Fischbeck KH
    Neuromuscul Disord; 2014 Nov; 24(11):978-81. PubMed ID: 25047668
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].
    Degos B; Echaniz-Laguna A; Latour P; Vandenberghe A; Anheim M; Talmant V; Tranchant C
    Rev Neurol (Paris); 2004 Dec; 160(12):1203-6. PubMed ID: 15602369
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.