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Journal Abstract Search
306 related items for PubMed ID: 31536037
1. Pain and small-fiber affection in hereditary neuropathy with liability to pressure palsies (HNPP). Dukefoss TT, Kleggetveit IP, Helås T, Jørum E. Scand J Pain; 2019 Dec 18; 20(1):61-68. PubMed ID: 31536037 [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 28; 48(10):1572-1582. PubMed ID: 38432886 [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 28; 158(5 Pt 1):579-88. PubMed ID: 12072826 [Abstract] [Full Text] [Related]
4. Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation. Yurrebaso I, Casado OL, Barcena J, Perez de Nanclares G, Aguirre U. Neuromuscul Disord; 2014 Jan 28; 24(1):56-62. PubMed ID: 24239057 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion. Hong YH, Kim M, Kim HJ, Sung JJ, Kim SH, Lee KW. Acta Neurol Scand; 2003 Nov 28; 108(5):352-8. PubMed ID: 14616306 [Abstract] [Full Text] [Related]
7. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy. Chance PF. Neuromolecular Med; 2006 Nov 28; 8(1-2):159-74. PubMed ID: 16775374 [Abstract] [Full Text] [Related]
8. Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion. Pabón Meneses RM, Azcona Ganuza G, Urriza Mena J, Ibiricu Yanguas A, Gila Useros L, García de Gurtubay I. Neurologia (Engl Ed); 2022 May 28; 37(4):243-249. PubMed ID: 35595399 [Abstract] [Full Text] [Related]
9. [Analysis of the clinical, electrophysiological and genetic features of a family affected with hereditary neuropathy with liability to pressure palsies]. Qi F, Che F. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb 28; 32(1):31-5. PubMed ID: 25636095 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies. Andersson PB, Yuen E, Parko K, So YT. Neurology; 2000 Jan 11; 54(1):40-4. PubMed ID: 10636123 [Abstract] [Full Text] [Related]
12. 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 11; 25(9):693-8. PubMed ID: 26189194 [Abstract] [Full Text] [Related]
13. Frequency of hereditary neuropathy with liability to pressure palsies (HNPP) due to 17p11.2 deletion in a Korean newborn population. Park JE, Noh SJ, Oh M, Cho DY, Kim SY, Ki CS. Orphanet J Rare Dis; 2018 Mar 15; 13(1):40. PubMed ID: 29544507 [Abstract] [Full Text] [Related]
14. 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 15; 20(2):79-85. PubMed ID: 26110377 [Abstract] [Full Text] [Related]
15. Peripheral neuropathy in diabetes: it's not always what it looks like. Maltese G, Tan SV, Bruno E, Brackenridge A, Thomas S. Diabet Med; 2018 Oct 15; 35(10):1457-1459. PubMed ID: 29862581 [Abstract] [Full Text] [Related]
16. 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 29; 36(1):28-35. PubMed ID: 15031668 [Abstract] [Full Text] [Related]
17. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy. Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A. Muscle Nerve; 1998 Dec 29; 21(12):1686-91. PubMed ID: 9843070 [Abstract] [Full Text] [Related]
18. [Hereditary neuropathy with liability to pressure palsies caused by 17p11.2 chromosome deletion]. Dorobek M, Szmidt-Sałkowska E, Drac H, Hardin A, Kwieciński H. Neurol Neurochir Pol; 1999 Dec 29; 33(1):177-85. PubMed ID: 10399735 [Abstract] [Full Text] [Related]
19. 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 15; 341(1-2):46-50. PubMed ID: 24726093 [Abstract] [Full Text] [Related]
20. [A case of hereditary neuropathy with liability to pressure palsies (HNPP) with diabetes mellitus]. Yasuda T, Hakusui S, Ando T, Yanagi T, Yamamoto M, Sobue G. No To Shinkei; 1996 Aug 15; 48(8):747-51. PubMed ID: 8797209 [Abstract] [Full Text] [Related] Page: [Next] [New Search]