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Journal Abstract Search

215 related items for PubMed ID: 9008488

  • 21. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.
    Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG.
    J Neurol Neurosurg Psychiatry; 1999 Aug; 67(2):174-9. PubMed ID: 10406984
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  • 23. HMSN III phenotype due to homozygous expression of a dominant HMSN II gene.
    Sghirlanzoni A, Pareyson D, Balestrini MR, Bellone E, Berta E, Ciano C, Mandich P, Marazzi R.
    Neurology; 1992 Nov; 42(11):2201-4. PubMed ID: 1436537
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  • 24. Medial dorsal superficial peroneal nerve studies in patients with polyneuropathy and normal sural responses.
    Kushnir M, Klein C, Kimiagar Y, Pollak L, Rabey JM.
    Muscle Nerve; 2005 Mar; 31(3):386-9. PubMed ID: 15508123
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  • 25. Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
    Butinar D, Zidar J, Leonardis L, Popovic M, Kalaydjieva L, Angelicheva D, Sininger Y, Keats B, Starr A.
    Ann Neurol; 1999 Jul; 46(1):36-44. PubMed ID: 10401778
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  • 34. Autosomal dominant HMSN with proximal involvement: new Brazilian cases.
    Patroclo CB, Lino AM, Marchiori PE, Brotto MW, Hirata MT.
    Arq Neuropsiquiatr; 2009 Sep; 67(3B):892-6. PubMed ID: 19838524
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  • 35. Central motor conduction in a family with hereditary motor and sensory neuropathy with pyramidal signs (HMSN V).
    Schnider A, Hess CW, Koppi S.
    J Neurol Neurosurg Psychiatry; 1991 Jun; 54(6):511-5. PubMed ID: 1652623
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  • 36. Practically applicable nerve ultrasound models for the diagnosis of axonal and demyelinating hereditary motor and sensory neuropathies (HMSN).
    Loewenbrück KF, Dittrich M, Böhm J, Klingelhöfer J, Baum P, Schäfer J, Reichmann H, Hermann A, Storch A.
    J Neurol; 2018 Jan; 265(1):165-177. PubMed ID: 29185050
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  • 37. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 39. 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
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