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Journal Abstract Search

132 related items for PubMed ID: 4176659

  • 1. Arthrogryposis multiplex congenita. Report of two cases of a radicular type with familial incidence.
    Peña CE, Miller F, Budzilovich GN, Feigin I.
    Neurology; 1968 Sep; 18(9):926-30. PubMed ID: 4176659
    [No Abstract] [Full Text] [Related]

  • 2. Arthrogryposis multiplex congenita. Simultaneous involvement of peripheral nerve and skeletal muscle.
    Hooshmand H, Martinez AJ, Rosenblum WI.
    Arch Neurol; 1971 Jun; 24(6):561-72. PubMed ID: 5089902
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  • 3. Arthrogryposis multiplex congenita--myopathic type.
    Lebenthal E, Ben-Bassat M, Reisner SH, Seelenfreund M.
    Isr J Med Sci; 1973 Apr; 9(4):463-8. PubMed ID: 4709230
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  • 4. The myopathic variety of arthrogryposis multiplex congenita: a disorder with autosomal recessive inheritance.
    Der Kaloustian VM, Afifi AK, Mire J.
    J Pediatr; 1972 Jul; 81(1):76-82. PubMed ID: 4338386
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  • 9. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg.
    Agapitos M, Georgiou-Theodoropoulou M, Koutselinis A, Papacharalambus N.
    Pediatr Pathol; 1988 Jul; 8(4):409-13. PubMed ID: 2974953
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  • 10. Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
    Valdés-Flores M, Casas-Avila L, Hernández-Zamora E, Kofman S, Hidalgo-Bravo A.
    J Pediatr (Rio J); 2016 Jul; 92(1):58-64. PubMed ID: 26453511
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  • 11. Arthrogryposis multiplex congenita: an autopsy case of a fatal form.
    Imamura M, Yamanaka N, Nakamura F, Oyanagi K.
    Hum Pathol; 1981 Aug; 12(8):699-704. PubMed ID: 7286967
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  • 16. Arthrogryposis multiplex congenita. A case of neurogenic origin.
    Vestermark B.
    Acta Paediatr Scand; 1966 Jan; 55(1):117-20. PubMed ID: 5919469
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  • 17. The syndrome of arthrogryposis multiplex congenita.
    Drachman DB.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):90-7. PubMed ID: 5173748
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  • 18. A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease.
    Nezelof C, Dupart MC, Jaubert F, Eliachar E.
    J Pediatr; 1979 Feb; 94(2):258-60. PubMed ID: 762621
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