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Journal Abstract Search

130 related items for PubMed ID: 2291397

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  • 3. Phe 84 deletion of the PMP22 gene associated with hereditary motor and sensory neuropathy HMSN III with multiple cranial neuropathy: clinical, neurophysiological and magnetic resonance imaging findings.
    Yener GG, Guiochon-Mantel A, Obuz F, Baklan B, Oztürk V, Kovanlikaya I, Cakmur R, Genç A.
    J Neurol; 2001 Mar; 248(3):193-6. PubMed ID: 11355152
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  • 4. Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM).
    Müller HD, Mugler M, Ramaekers VT, Schröder JM.
    J Peripher Nerv Syst; 2000 Sep; 5(3):147-57. PubMed ID: 11442171
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  • 7. Congenital hypomyelination neuropathy: glial bundles in cranial and spinal nerve roots.
    Towfighi J.
    Ann Neurol; 1981 Dec; 10(6):570-3. PubMed ID: 7325606
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  • 8. [A case with hereditary motor and sensory neuropathy with multiple cranial nerves involvement].
    Nakamura N, Oka N, Nakamura S, Akiguchi I, Kashii S.
    Rinsho Shinkeigaku; 1995 May; 35(5):516-20. PubMed ID: 7664521
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  • 9. Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family.
    Sekijima Y, Ohara S, Nakagawa S, Tabata K, Yoshida K, Ishigame H, Shimizu Y, Yanagisawa N.
    J Neurol Sci; 1998 Jun 11; 158(1):30-7. PubMed ID: 9667774
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  • 11. Infantile hereditary neuropathy with hypomyelination: report of two siblings with different expressivity.
    Balestrini MR, Cavaletti G, D'Angelo A, Tredici G.
    Neuropediatrics; 1991 May 11; 22(2):65-70. PubMed ID: 1857496
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  • 12. A morphometric study of myelinated fibers in lumbar ventral roots and hypoglossal nerves in motor neuron diseases.
    Kondo A, Nagara H, Sato Y, Koga M, Tateishi J.
    Clin Neuropathol; 1986 May 11; 5(5):217-23. PubMed ID: 3791728
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  • 13. Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers.
    Mancardi GL, Di Rocco M, Schenone A, Veneselli E, Doria M, Abbruzzese M, Tabaton M, Borrone C.
    J Neurol Sci; 1992 Jul 11; 110(1-2):121-30. PubMed ID: 1506851
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  • 14. Spinal and cranial hypertrophic neuropathy in multiple sclerosis.
    Quan D, Pelak V, Tanabe J, Durairaj V, Kleinschmidt-Demasters BK.
    Muscle Nerve; 2005 Jun 11; 31(6):772-9. PubMed ID: 15793846
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  • 15. [Two families of Charcot-Marie-Tooth disease with Adie's pupil, axonal neuropahy and the Thr124Met mutation in the peripheral myelin protein zero gene].
    Misu K, Yoshihara T, Yamamoto M, Hattori N, Nagamatu M, Mukai E, Takegami T, Sobue G.
    Rinsho Shinkeigaku; 2000 Feb 11; 40(2):149-54. PubMed ID: 10835936
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  • 16. Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
    Leonardis L, Zidar J, Popovic M, Timmerman V, Löfgren A, Van Broeckhoven C, Butinar D.
    Pflugers Arch; 2000 Feb 11; 439(3 Suppl):R208-10. PubMed ID: 10653194
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  • 17. Radicular lesions in tuberculous meningitis. A clinicopathological study.
    De Bruyne J, Sieben G, De Reuck J, Vander Eecken H.
    Acta Neurol Belg; 1983 Feb 11; 83(3):117-25. PubMed ID: 6613514
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  • 18. A second family with hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibres, detected in the same geographic area as the first family.
    Santoro L, Barbieri F, Crisci C, Gasparo Rippa P, Manganelli F.
    J Neurol; 1998 Apr 11; 245(4):240-4. PubMed ID: 9591228
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  • 19. Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0.
    Simonati A, Fabrizi GM, Taioli F, Polo A, Cerini R, Rizzuto N.
    J Neurol; 2002 Sep 11; 249(9):1298-302. PubMed ID: 12242557
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  • 20. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature.
    Sonoda K, Sasaki K, Tateishi T, Yamasaki R, Hayashi S, Sakae N, Ohyagi Y, Iwaki T, Kira J.
    J Neurol Sci; 2013 Sep 15; 332(1-2):148-53. PubMed ID: 23849263
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