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Journal Abstract Search

121 related items for PubMed ID: 2636102

  • 21. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 22. [Hereditary diseases accompanied with aberrant catecholamine metabolism, in special reference to catecholamine sensitive periodic fever and familial amyloid polyneuropathy (author's transl)].
    Hayashi A, Suzuki T.
    Tanpakushitsu Kakusan Koso; 1981 Aug; 26(11):1789-97. PubMed ID: 6946522
    [No Abstract] [Full Text] [Related]

  • 23. Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M).
    Lobato L.
    J Nephrol; 2003 Aug; 16(3):438-42. PubMed ID: 12832749
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  • 24. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
    Augustin S, Llige D, Andreu A, González A, Genescà J.
    Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
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  • 26. Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
    Sandgren O, Drugge U, Holmgren G, Sousa A.
    Clin Genet; 1991 Dec; 40(6):452-60. PubMed ID: 1685700
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  • 28. [A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan].
    Minauchi Y, Kohka M, Igata A, Ohkatsu Y.
    Rinsho Shinkeigaku; 1982 Oct; 22(10):918-25. PubMed ID: 6963557
    [No Abstract] [Full Text] [Related]

  • 29. [Orthotopic liver transplantation for familial Portuguese amyloidosis].
    Fournier B, Giostra E, Mentha G, Huber O, Hadengue A, Morel P.
    Schweiz Med Wochenschr Suppl; 1997 Oct; 89():36S-40S. PubMed ID: 9289838
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  • 34. [A late onset familial amyloidotic polyneuropathy (FAP) with a novel variant transthyretin characterized by a basic-for-acidic amino acid substitution (Glu61-->Lys)].
    Yamamoto T, Matsunaga K, Ohnishi A, Nakazato M, Murai Y.
    Rinsho Shinkeigaku; 1996 Sep; 36(9):1065-8. PubMed ID: 8976129
    [Abstract] [Full Text] [Related]

  • 35. [Familial amyloidotic polyneuropathy with a transthyretin variant (Val30-->Leu)].
    Shimizu H, Ishikawa K, Kobayashi H, Murakami T, Nakazato M, Miura K, Atsumi T.
    No To Shinkei; 1996 Feb; 48(2):175-8. PubMed ID: 8865698
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  • 37. Immunohistochemistry of amyloid-related neuropathies.
    Horn U, Goebel HH, Störkel S, Bohl J, Thomas E, Schlote W, Budzilovich G.
    Clin Neuropathol; 1991 Feb; 10(5):237-43. PubMed ID: 1959254
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  • 38. Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety.
    Danon MJ, Carpenter S.
    Neurology; 1985 Aug; 35(8):1226-9. PubMed ID: 3860748
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  • 39. [Late onset of type I familial amyloid neuropathy: results of biopsy from accessory salivary glands].
    Mackowiak A, Stojkovic T, Hurtevent JF, Maurage CA, Vermersch P.
    Rev Neurol (Paris); 1999 Feb; 155(2):155-7. PubMed ID: 10226321
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