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Journal Abstract Search

428 related items for PubMed ID: 15052618

  • 21. Leukodystrophy presenting as acute-onset polyradiculoneuropathy.
    Dubey R, Chakrabarty B, Gulati S, Sharma MC, Deopujari S, Baheti N, Santosh V, Pai G, Kabra M.
    Pediatr Neurol; 2014 Jun; 50(6):616-8. PubMed ID: 24685010
    [Abstract] [Full Text] [Related]

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  • 23. Clinical outcome in four children with metachromatic leukodystrophy treated by bone marrow transplantation.
    Malm G, Ringdén O, Winiarski J, Gröndahl E, Uyebrant P, Eriksson U, Håkansson H, Skjeldal O, Månsson JE.
    Bone Marrow Transplant; 1996 Jun; 17(6):1003-8. PubMed ID: 8807106
    [Abstract] [Full Text] [Related]

  • 24. Conduction block in hereditary neuropathy with susceptibility to pressure palsies.
    Sellman MS, Mayer RF.
    Muscle Nerve; 1987 Sep; 10(7):621-5. PubMed ID: 3477693
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  • 26. Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.
    Yiu EM, Burns J, Ryan MM, Ouvrier RA.
    J Peripher Nerv Syst; 2008 Sep; 13(3):236-41. PubMed ID: 18844790
    [Abstract] [Full Text] [Related]

  • 27. A study of genetic leukodystrophies in Chinese children.
    Wang PJ, Wang TZ, Shen YZ.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1992 Sep; 33(1):44-58. PubMed ID: 1626451
    [Abstract] [Full Text] [Related]

  • 28. Juvenile-onset metachromatic leukodystrophy: biochemical and electrophysiologic studies.
    Clark JR, Miller RG, Vidgoff JM.
    Neurology; 1979 Mar; 29(3):346-3. PubMed ID: 36575
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  • 30. [Metachromatic leukodystrophy: an exceptional cause of dementia in the adult].
    Pérez Sempere A, Martínez Menéndez B, Villaverde Amundaraín FJ, Rodríguez Vallejo A, Togores Veguero J, Portera Sánchez A.
    Neurologia; 1992 May; 7(5):114-6. PubMed ID: 1389290
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  • 32. Familial, demyelinating sensory and motor polyneuropathy with conduction block.
    Scelsa SN.
    Muscle Nerve; 2010 Apr; 41(4):558-62. PubMed ID: 19941344
    [Abstract] [Full Text] [Related]

  • 33. Hereditary and acquired polyneuropathies. Electrophysiologic aspects.
    Miller RG.
    Neurol Clin; 1985 Aug; 3(3):543-56. PubMed ID: 2413343
    [Abstract] [Full Text] [Related]

  • 34. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul; 13(7):586-92. PubMed ID: 2388657
    [Abstract] [Full Text] [Related]

  • 35. Late infantile metachromatic leucodystrophy in two siblings.
    Koul RL, Gururaj A, Chacko AP, Elbualy MS, Bhusnurmath SR, Chand P.
    Indian Pediatr; 1994 Jun; 31(6):694-8. PubMed ID: 7896397
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  • 36. Multifocal motor neuropathy with conduction block: Distribution of demyelination and axonal degeneration.
    Vucic S, Black K, Chong PS, Cros D.
    Clin Neurophysiol; 2007 Jan; 118(1):124-30. PubMed ID: 17095292
    [Abstract] [Full Text] [Related]

  • 37. Conduction slowing, conduction block and temporal dispersion in demyelinating, dysmyelinating and axonal neuropathies: Electrophysiology meets pathology.
    Uncini A, Cavallaro T, Fabrizi GM, Manganelli F, Vallat JM.
    J Peripher Nerv Syst; 2024 Jun; 29(2):135-160. PubMed ID: 38600691
    [Abstract] [Full Text] [Related]

  • 38. Progressive demyelinating polyneuropathy after hematopoietic cell transplantation in metachromatic leukodystrophy: a case series.
    Beerepoot S, Boelens JJ, Lindemans C, de Witte MA, Nierkens S, Vrancken AFJE, van der Knaap MS, Bugiani M, Wolf NI.
    J Neurol; 2024 Jul; 271(7):4028-4038. PubMed ID: 38564053
    [Abstract] [Full Text] [Related]

  • 39. The visual system in myelin disorders. Human and animal myelin disorders: neurophysiological diagnostic methods.
    Guérit JM.
    Bull Soc Belge Ophtalmol; 1983 Nov; 208 Pt 1():267-85. PubMed ID: 6675814
    [No Abstract] [Full Text] [Related]

  • 40. Long-term outcomes after allogeneic hematopoietic stem cell transplantation for metachromatic leukodystrophy: the largest single-institution cohort report.
    Boucher AA, Miller W, Shanley R, Ziegler R, Lund T, Raymond G, Orchard PJ.
    Orphanet J Rare Dis; 2015 Aug 07; 10():94. PubMed ID: 26245762
    [Abstract] [Full Text] [Related]

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