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Journal Abstract Search

167 related items for PubMed ID: 1857496

  • 21. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993; 31(3-4):207-19. PubMed ID: 8011484
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  • 23. [Congenital hereditary motor and sensory neuropathy].
    Routon MC, Robain O, Mayer M, Jardin L, Ponsot G.
    Rev Neurol (Paris); 1991; 147(8-9):577-85. PubMed ID: 1962067
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  • 24. Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.
    Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B.
    J Neuropathol Exp Neurol; 2008 Nov; 67(11):1097-102. PubMed ID: 18957892
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  • 25. [Hereditary motor and sensory neuropathy type III. Case report and review of the literature].
    Haverkamp F, Behring B.
    Klin Padiatr; 1995 Nov; 207(1):24-7. PubMed ID: 7885014
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  • 26. The status of HMSN type III.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    Neuromuscul Disord; 1994 Jan; 4(1):63-9. PubMed ID: 8173353
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  • 27. Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.
    Gregory R, Thomas PK, King RH, Hallam PL, Malcolm S, Hughes RA, Harding AE.
    Ann Neurol; 1993 Jun; 33(6):649-52. PubMed ID: 8498845
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  • 28. Sensory-motor hereditary neuropathy with early onset. A case report.
    Malandrini A, De Stefano N, Dotti MT, Vecchione V, Federico A.
    Acta Neurol (Napoli); 1993 Apr; 15(2):81-6. PubMed ID: 8328327
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  • 31. Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex.
    Umehara F, Takenaga S, Nakagawa M, Takahashi K, Izumo S, Matsumuro K, Sakota S, Nishimura T, Yoshikawa H, Osame M.
    Acta Neuropathol; 1993 Apr; 86(6):602-8. PubMed ID: 8310815
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  • 32. Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases.
    Hong SM, Ha H, Suh JH, Kim KK, Khang SK, Ro JY, Park SH.
    J Korean Med Sci; 2000 Apr; 15(2):211-6. PubMed ID: 10803700
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  • 33. A novel MPZ gene mutation in congenital neuropathy with hypomyelination.
    Kochanski A, Drac H, Kabzińska D, Ryniewicz B, Rowińska-Marcińska K, Nowakowski A, Hausmanowa-Petrusewicz I.
    Neurology; 2004 Jun 08; 62(11):2122-3. PubMed ID: 15184631
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  • 34. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF.
    Brain; 1990 Dec 08; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
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  • 35. Phenotypic clustering in MPZ mutations.
    Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J.
    Brain; 2004 Feb 08; 127(Pt 2):371-84. PubMed ID: 14711881
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  • 38. Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.
    Vital A, Vital C, Julien J, Fontan D.
    Acta Neuropathol; 1992 Feb 08; 84(4):433-6. PubMed ID: 1441924
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  • 39. Giant axonal neuropathy in a child with insulin-dependent diabetes mellitus.
    Hoffman WH, Carroll JE, Perry GY, Hartlage PL, Kaminer SJ, Flowers NC, Oh SJ, Kelly DR.
    J Child Neurol; 1995 May 08; 10(3):250-3. PubMed ID: 7642902
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