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Journal Abstract Search

251 related items for PubMed ID: 26189194

  • 1. Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update.
    Chrestian N, McMillan H, Poulin C, Campbell C, Vajsar J.
    Neuromuscul Disord; 2015 Sep; 25(9):693-8. PubMed ID: 26189194
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  • 2. Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy.
    Potulska-Chromik A, Sinkiewicz-Darol E, Ryniewicz B, Lipowska M, Kabzińska D, Kochański A, Kostera-Pruszczyk A.
    Muscle Nerve; 2014 Dec; 50(6):914-8. PubMed ID: 24668782
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  • 3. Mutational analysis of Greek patients with suspected hereditary neuropathy with liability to pressure palsies (HNPP): a 15-year experience.
    Karadima G, Koutsis G, Raftopoulou M, Karletidi KM, Zambelis T, Karandreas N, Panas M.
    J Peripher Nerv Syst; 2015 Jun; 20(2):79-85. PubMed ID: 26110377
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  • 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 27; 43(1):97. PubMed ID: 29078790
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  • 5. [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 27; 158(5 Pt 1):579-88. PubMed ID: 12072826
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  • 7. A Case of Severe Early-Onset Neuropathy Caused by a Compound Heterozygous Deletion of the PMP22 Gene: Clinical and Neurographic Aspects.
    D'Arrigo S, Tessarollo V, Taroni F, Baratta S, Pantaleoni C, Schiaffi E, Ciano C.
    Neuropediatrics; 2020 Jun 27; 51(3):173-177. PubMed ID: 31784971
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  • 10. Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.
    Beydoun SR, Cho J.
    J Clin Neuromuscul Dis; 2013 Sep 27; 15(1):28-33. PubMed ID: 23965407
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  • 11. Hereditary Neuropathy With Liability to Pressure Palsies: Diverse Phenotypes in Childhood.
    Harada Y, Puwanant A, Herrmann DN.
    J Clin Neuromuscul Dis; 2016 Dec 27; 18(2):79-83. PubMed ID: 27861220
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  • 12. A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: the value of complete electrodiagnostic testing.
    Bulusu S, McMillan HJ.
    Am J Electroneurodiagnostic Technol; 2011 Sep 27; 51(3):183-90. PubMed ID: 21988036
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  • 13. 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 28; 48(10):1572-1582. PubMed ID: 38432886
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  • 14. Proximal arm weakness is the most common presentation in young Korean soldiers diagnosed as having hereditary neuropathy with liability to pressure palsy (HNPP).
    Kim KE, Yeom J.
    J R Army Med Corps; 2016 Oct 28; 162(5):352-354. PubMed ID: 26462743
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  • 15. Hereditary neuropathy with liability to pressure palsy: a brief review with a case report.
    Rana AQ, Masroor MS.
    Int J Neurosci; 2012 Mar 28; 122(3):119-23. PubMed ID: 22023293
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  • 16. Hereditary neuropathy with liability to pressure palsies.
    Attarian S, Fatehi F, Rajabally YA, Pareyson D.
    J Neurol; 2020 Aug 28; 267(8):2198-2206. PubMed ID: 30989370
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  • 17. Hereditary neuropathy with liability to pressure palsies. Diagnosis in the first family (1947) confirmed.
    Koehler PJ, Baas F.
    J Peripher Nerv Syst; 2012 Dec 28; 17(4):412-3. PubMed ID: 23279343
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  • 18. A Case of Apoplexy Attack-Like Neuropathy due to Hereditary Neuropathy with Liability to Pressure Palsies in a Patient Diagnosed with Chronic Cerebral Infarction.
    Hachisuka A, Matsushima Y, Hachisuka K, Saeki S.
    J Stroke Cerebrovasc Dis; 2016 Jun 28; 25(6):e83-5. PubMed ID: 27080157
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  • 19. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
    Chance PF.
    Neuromolecular Med; 2006 Jun 28; 8(1-2):159-74. PubMed ID: 16775374
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  • 20. A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP.
    Benquey T, Fockens E, Kouton L, Delmont E, Martini N, Levy N, Attarian S, Bonello-Palot N.
    J Neuromuscul Dis; 2020 Jun 28; 7(4):505-510. PubMed ID: 32538861
    [Abstract] [Full Text] [Related]

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