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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

104 related items for PubMed ID: 3802679

  • 41.
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  • 43. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.
    Srp Arh Celok Lek; 1999; 127(1-2):21-7. PubMed ID: 10377836
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  • 44. [Strumpell's disease in childhood].
    Popov'ian MD, Dubinskaia EE, Allaverdova RA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(10):29-32. PubMed ID: 7180276
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  • 45. Hereditary spastic paraplegia.
    Charkabarti AK, Lloyd GH, Johnson SC.
    J Indian Med Assoc; 1977 Oct 01; 69(7):141-6. PubMed ID: 611148
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  • 51. [Oculo-dental-digital dysplasia: report of a case with spastic paraplegia].
    Nivelon-Chevallier A, Audry D, Audry F, Dumas R.
    J Genet Hum; 1981 Jun 01; 29(2):171-9. PubMed ID: 6276501
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  • 53. [Classical Strumpell-Lorrain disease in a father and congenital diplegia in his son].
    Christodorescu D.
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977 Jun 01; 22(3):235-8. PubMed ID: 303794
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  • 54. Spastic paraplegia associated with brachydactyly and cone shaped epiphyses.
    Fitzsimmons JS, Guilbert PR.
    J Med Genet; 1987 Nov 01; 24(11):702-5. PubMed ID: 3430547
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  • 55. [Four cases with congenital factor XII (Hageman factor) deficiency (author's transl)].
    Morishima Y, Kamiya T, Ogata K, Takamatsu J, Ishiguro J.
    Rinsho Ketsueki; 1977 Oct 01; 18(10):1246-52. PubMed ID: 592500
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