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Journal Abstract Search

189 related items for PubMed ID: 5491443

  • 1. Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred.
    Lebenthal E, Shochet SB, Adam A, Seelenfreund M, Fried A, Najenson T, Sandbank U, Matoth Y.
    Pediatrics; 1970 Dec; 46(6):891-9. PubMed ID: 5491443
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  • 2. Arthrogryposis multiplex congenita in an Arab kindred: update.
    Jaber L, Weitz R, Bu X, Fischel-Ghodsian N, Rotter JI, Shohat M.
    Am J Med Genet; 1995 Jan 30; 55(3):331-4. PubMed ID: 7726232
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  • 3. Electromyographic and histopathologic correlations in arthrogryposis.
    Amick LD, Johnson WW, Smith HL.
    Arch Neurol; 1967 May 30; 16(5):512-23. PubMed ID: 6022533
    [No Abstract] [Full Text] [Related]

  • 4. A new familial arthrogryposis without weakness.
    Daentl DL, Berg BO, Layzer RB, Epstein CJ.
    Neurology; 1974 Jan 30; 24(1):55-60. PubMed ID: 4855665
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  • 5. [Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].
    Tangheroni W, Cao A, Cianchetti C, Calisti L.
    Minerva Pediatr; 1974 Jun 23; 26(22):1125-45. PubMed ID: 4276719
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  • 13. [Restoration of elbow joint flexion using pectoral muscle transfer in patients with arthrogryposis multiplex congenita. Part I: surgical method, rehabilitation and clinical results].
    Chomiak J, Dungl P.
    Acta Chir Orthop Traumatol Cech; 2002 Jun 23; 69(6):333-43. PubMed ID: 12587494
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  • 15. [Electrophysiological, chemical and histological findings in collagen diseases (author's transl)].
    Sitzer G, Rolf L, Windgassen K, Themann H.
    Nervenarzt; 1982 Apr 23; 53(4):187-92. PubMed ID: 7099300
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  • 16. Identification of three novel ECEL1 mutations in three families with distal arthrogryposis type 5D.
    Shaheen R, Al-Owain M, Khan AO, Zaki MS, Hossni HA, Al-Tassan R, Eyaid W, Alkuraya FS.
    Clin Genet; 2014 Jun 23; 85(6):568-72. PubMed ID: 23829171
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  • 20. Neuropathologic aspects of arthrogryposis multiplex congenita.
    Banker BQ.
    Clin Orthop Relat Res; 1985 Apr 23; (194):30-43. PubMed ID: 3978931
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