BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 4309044)

  • 61. Familial parkinsonism with peripheral neuropathy.
    Rohatgi A; Kulshrestha M; Sachdeva S
    J Assoc Physicians India; 2000 Jul; 48(7):752-3. PubMed ID: 11273520
    [No Abstract]   [Full Text] [Related]  

  • 62. [Familial amyloidosis].
    Vinogradova OM; Borisov IA
    Klin Med (Mosk); 1975 Jan; 53(1):31-5. PubMed ID: 1134017
    [No Abstract]   [Full Text] [Related]  

  • 63. [Defective lacrimation in familial amyloid polyneuropathy].
    Okajima T; Nakashima H; Ueno H; Inada K; Okamura R
    Rinsho Shinkeigaku; 1983 Mar; 23(3):247-52. PubMed ID: 6307575
    [No Abstract]   [Full Text] [Related]  

  • 64. The sinoatrial node in familial amyloidosis with polyneuropathy. A clinico-pathological study of nine cases from northern Sweden.
    Eriksson A; Eriksson P; Olofsson BO; Thornell LE
    Virchows Arch A Pathol Anat Histopathol; 1984; 402(3):239-46. PubMed ID: 6322411
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Scalloped pupils in familial amyloid polyneuropathy.
    Rubinow A; Cohen AS
    Arthritis Rheum; 1986 Mar; 29(3):445-7. PubMed ID: 3008766
    [No Abstract]   [Full Text] [Related]  

  • 66. Familial amyloidosis. A histopathological study.
    Tanimura A; Cho T; Shinohara Y; Yamaguchi T; Nakashima A; Okuzono H; Kurinami S; Kitsu T
    Acta Pathol Jpn; 1984 Mar; 34(2):335-44. PubMed ID: 6377820
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Familial amyloidosis of the Finnish type (FAF). A clinical study of 30 patients.
    Kiuru S
    Acta Neurol Scand; 1992 Oct; 86(4):346-53. PubMed ID: 1333716
    [TBL] [Abstract][Full Text] [Related]  

  • 68. [On the mechanism of defective lacrimation in familial amyloid polyneuropathy].
    Okajima T; Inada K; Ueno H; Nakashima H; Okamura R
    Rinsho Shinkeigaku; 1983 May; 23(5):421-6. PubMed ID: 6309454
    [No Abstract]   [Full Text] [Related]  

  • 69. [Ocular manifestations of Corino de Andrade's Portuguese amyloidosis].
    Plane C; Maupetit J; Colnet G; Tournilhac M
    Bull Soc Ophtalmol Fr; 1977 Jan; 77(1):123-5. PubMed ID: 201388
    [No Abstract]   [Full Text] [Related]  

  • 70. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.
    Dyck PJ; Lambert EH
    Arch Neurol; 1968 Jun; 18(6):603-18. PubMed ID: 4297451
    [No Abstract]   [Full Text] [Related]  

  • 71. [Hereditary emyloid neuropathies. Apropos of a French familial case].
    Geraud G; Bes A; D'Arzac P; Sorbara R; Arbus L; Geraud J
    Rev Otoneuroophtalmol; 1977; 49(3):185-200. PubMed ID: 897459
    [No Abstract]   [Full Text] [Related]  

  • 72. Cases with familiar amyloid neuropathy starting of the upper limbs and having hepatic disorder.
    Tsukada K; Ohhashi M; Isobe T; Masuko K
    Jpn J Med; 1987 May; 26(2):243-8. PubMed ID: 3041084
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Pulmonary function in familial amyloidosis with polyneuropathy.
    Olofsson BO
    Acta Med Scand; 1981; 209(5):379-84. PubMed ID: 6264749
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Hypertrophic neuropathy: a report of Dejerine-Sottas disease in two sibs.
    O'Brien MD
    Guys Hosp Rep; 1968; 117(2):79-88. PubMed ID: 4300473
    [No Abstract]   [Full Text] [Related]  

  • 75. Classification of the neuromuscular disorders. Appendix A to the Minutes of the Meeting of the Research Group on Neuromuscular Diseases, held in Montreal, Canada, on 21 September, 1967.
    J Neurol Sci; 1968; 6(1):165-77. PubMed ID: 4296280
    [No Abstract]   [Full Text] [Related]  

  • 76. [Sporadic and familial recurrent truncular paralysis].
    Castaigne P; Brunet P; Sicard JP; Hauw JJ; Henin MD; Dordain G
    Ann Med Interne (Paris); 1975 May; 126(5):361-8. PubMed ID: 179455
    [No Abstract]   [Full Text] [Related]  

  • 77. Molecular genetics of amyloid neuropathy in Europe.
    Benson MD
    Lancet; 1989 May; 1(8648):1203. PubMed ID: 2566762
    [No Abstract]   [Full Text] [Related]  

  • 78. Familial recurrent peripheral neuropathy.
    Saraiva S; Levy JA; JuliĆ£o OF
    Rev Hosp Clin Fac Med Sao Paulo; 1975; 30(2):165-8. PubMed ID: 166425
    [No Abstract]   [Full Text] [Related]  

  • 79. Type I familial amyloid polyneuropathy in a Chinese family.
    Chang CM; Yu YL; Wong M; Ng TH; Woo E; Huang CY
    Acta Neurol Scand; 1989 May; 79(5):391-6. PubMed ID: 2741670
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A clinico-pathological study of chronic hereditary motor neuropathy.
    Matsubara S; Tanabe H
    Acta Neuropathol; 1983; 61(1):43-51. PubMed ID: 6312725
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.