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151 related items for PubMed ID: 15897517

  • 1. The electrophysiological profile of hereditary motor and sensory neuropathy-Lom.
    Ishpekova BA, Christova LG, Alexandrov AS, Thomas PK.
    J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):875-8. PubMed ID: 15897517
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary sensorimotor neuropathy in electrophysiological studies].
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Neurol Neurochir Pol; 1998 Jun; 32(2):295-308. PubMed ID: 9760549
    [Abstract] [Full Text] [Related]

  • 3. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
    [Abstract] [Full Text] [Related]

  • 4. [Subclinical lesions of peripheral nervous system in multiple sclerosis patients].
    Pogorzelski R, Baniukiewicz E, Drozdowski W.
    Neurol Neurochir Pol; 2004 Mar; 38(4):257-64. PubMed ID: 15383952
    [Abstract] [Full Text] [Related]

  • 5. Electrophysiological features of POEMS syndrome and chronic inflammatory demyelinating polyneuropathy.
    Guo X, Qin X, Zhang Y, Huang C, Yu G.
    J Clin Neurosci; 2014 Apr; 21(4):587-90. PubMed ID: 24268501
    [Abstract] [Full Text] [Related]

  • 6. Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutation.
    Capasso M, Di Muzio A, Ferrarini M, De Angelis MV, Caporale CM, Lupo S, Cavallaro T, Fabrizi GM, Uncini A.
    Clin Neurophysiol; 2004 Jan; 115(1):64-70. PubMed ID: 14706470
    [Abstract] [Full Text] [Related]

  • 7. Peroneal muscular atrophy with pyramidal features.
    Harding AE, Thomas PK.
    J Neurol Neurosurg Psychiatry; 1984 Feb; 47(2):168-72. PubMed ID: 6707656
    [Abstract] [Full Text] [Related]

  • 8. Subclinical cranial nerve involvement in hereditary motor and sensory neuropathy: a combined conduction study with electrical and magnetic stimulation.
    Kumagai-Eto R, Kaseda Y, Tobimatsu S, Uozumi T, Tsuji S, Nakamura S.
    Clin Neurophysiol; 2004 Jul; 115(7):1689-96. PubMed ID: 15203071
    [Abstract] [Full Text] [Related]

  • 9. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Jul; 31(3-4):207-19. PubMed ID: 8011484
    [Abstract] [Full Text] [Related]

  • 10. Early electrophysiological findings in acute inflammatory demyelinating polyradiculoneuropathy variant of Guillain-Barre syndrome in the Pakistani population - a comparison with global data.
    Wali A, Kanwar D, Khan SA, Khan S.
    J Peripher Nerv Syst; 2017 Dec; 22(4):451-454. PubMed ID: 29091318
    [Abstract] [Full Text] [Related]

  • 11. Facial nerve dysfunction in hereditary motor and sensory neuropathy type I and III.
    Glocker FX, Rösler KM, Linden D, Heinen F, Hess CW, Lücking CH.
    Muscle Nerve; 1999 Sep; 22(9):1201-8. PubMed ID: 10454715
    [Abstract] [Full Text] [Related]

  • 12. [Evaluation of polyneuropathy severity in chronic renal failure patients on continuous ambulatory peritoneal dialysis or on maintenance hemodialysis].
    Janda K, Stompór T, Gryz E, Szczudlik A, Drozdz M, Kraśniak A, Sułowicz W.
    Przegl Lek; 2007 Sep; 64(6):423-30. PubMed ID: 18159852
    [Abstract] [Full Text] [Related]

  • 13. Clinical predominance of proximal upper limb weakness in CMT1A syndrome.
    Auer-Grumbach M, Wagner K, Strasser-Fuchs S, Löscher WN, Fazekas F, Millner M, Hartung HP.
    Muscle Nerve; 2000 Aug; 23(8):1243-9. PubMed ID: 10918262
    [Abstract] [Full Text] [Related]

  • 14. F-wave determination in nerve conduction studies.
    Kimura J.
    Adv Neurol; 1983 Aug; 39():961-75. PubMed ID: 6660130
    [No Abstract] [Full Text] [Related]

  • 15. [Hereditary motor and sensory neuropathy. I. Principles of classification and clinical picture].
    Badurska B, Jedrzejowska H, Ryniewicz B, Drac H.
    Neurol Neurochir Pol; 1986 Aug; 20(1):24-8. PubMed ID: 3012388
    [Abstract] [Full Text] [Related]

  • 16. Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study.
    Auer-Grumbach M, Löscher WN, Wagner K, Petek E, Körner E, Offenbacher H, Hartung HP.
    Brain; 2000 Aug; 123 ( Pt 8)():1612-23. PubMed ID: 10908191
    [Abstract] [Full Text] [Related]

  • 17. Electrophysiological patterns of diabetic polyneuropathy.
    Bagai K, Wilson JR, Khanna M, Song Y, Wang L, Fisher MA.
    Electromyogr Clin Neurophysiol; 2008 Aug; 48(3-4):139-45. PubMed ID: 18551834
    [Abstract] [Full Text] [Related]

  • 18. [Charcot-Marie-Tooth disease. Electromyographic studies in 45 patients].
    Freitas MR, Nascimento OJ, Nevares MT, Escada TM.
    Arq Neuropsiquiatr; 1995 Sep; 53(3-B):552-9. PubMed ID: 8585810
    [Abstract] [Full Text] [Related]

  • 19. Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1.
    Kaku DA, Parry GJ, Malamut R, Lupski JR, Garcia CA.
    Neurology; 1993 Dec; 43(12):2664-7. PubMed ID: 8255473
    [Abstract] [Full Text] [Related]

  • 20. Vitamin B12 deficiency: a clinical and electrophysiological profile.
    Puri V, Chaudhry N, Goel S, Gulati P, Nehru R, Chowdhury D.
    Electromyogr Clin Neurophysiol; 2005 Dec; 45(5):273-84. PubMed ID: 16218195
    [Abstract] [Full Text] [Related]

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