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Journal Abstract Search

165 related items for PubMed ID: 6299869

  • 1. The nosology of genetic peripheral neuropathies in Swedish children.
    Hagberg B, Westerberg B.
    Dev Med Child Neurol; 1983 Feb; 25(1):3-18. PubMed ID: 6299869
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  • 5. Hereditary motor and sensory neuropathies in Swedish children. I. Prevalence and distribution by disability groups.
    Hagberg B, Westerberg B.
    Acta Paediatr Scand; 1983 May; 72(3):379-83. PubMed ID: 6576612
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  • 6. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 8. Pooled European series of hereditary peripheral neuropathies in infancy and childhood. A "correspondence work shop" report of the European Federation of Child Neurology Societies (EFCNS).
    Hagberg B, Lyon G.
    Neuropediatrics; 1981 Feb; 12(1):9-17. PubMed ID: 6265822
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  • 9. Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family.
    Berciano J, Combarros O, Figols J, Calleja J, Cabello A, Silos I, Coria F.
    Brain; 1986 Oct; 109 ( Pt 5)():897-914. PubMed ID: 3022865
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  • 10. Chronic inflammatory demyelinating polyneuropathy in two siblings.
    Gabreëls-Festen AA, Hageman AT, Gabreëls FJ, Joosten EM, Renier WO, Weemaes CM, ter Laak HJ.
    J Neurol Neurosurg Psychiatry; 1986 Feb; 49(2):152-6. PubMed ID: 3456424
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  • 17. Hereditary sensory neuropathy with spastic paraplegia.
    Cavanagh NP, Eames RA, Galvin RJ, Brett EM, Kelly RE.
    Brain; 1979 Mar; 102(1):79-94. PubMed ID: 218673
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