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Journal Abstract Search

130 related items for PubMed ID: 4338386

  • 1. 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
    [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
    [No Abstract] [Full Text] [Related]

  • 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
    [No Abstract] [Full Text] [Related]

  • 4. Arthrogryposis multiplex congenita: neurogenic type with autosomal recessive inheritance.
    Rosenmann A, Arad I.
    J Med Genet; 1974 Mar; 11(1):91-4. PubMed ID: 4837288
    [Abstract] [Full Text] [Related]

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  • 6. Neuropathologic aspects of arthrogryposis multiplex congenita.
    Banker BQ.
    Clin Orthop Relat Res; 1985 Apr; (194):30-43. PubMed ID: 3978931
    [Abstract] [Full Text] [Related]

  • 7. [Arthogryposis multiplex congenita. Presentation of 5 cases].
    Corradini HB, Albuquerque Diniz EM, Araujo Ramos JL, Costa Vaz FA.
    Rev Hosp Clin Fac Med Sao Paulo; 1979 Feb; 34(1):28-33. PubMed ID: 224441
    [No Abstract] [Full Text] [Related]

  • 8. Arthrogryposis multiplex congenita: spectrum of pathologic changes.
    Banker BQ.
    Hum Pathol; 1986 Jul; 17(7):656-72. PubMed ID: 3721492
    [Abstract] [Full Text] [Related]

  • 9. Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex.
    Yuill GM, Lynch PG.
    J Neurol Neurosurg Psychiatry; 1974 Mar; 37(3):316-23. PubMed ID: 4364274
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. CT-scanning of skeletal muscle in arthrogryposis multiplex congenita.
    Roscam Abbing PJ, Hageman G, Willemse J.
    Brain Dev; 1985 Sep; 7(5):484-91. PubMed ID: 4083384
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  • 13. Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait.
    Tiemann C, Bührer C, Burwinkel B, Wirtenberger M, Hoehn T, Hübner C, van Landeghem FK, Stoltenburg G, Obladen M.
    Am J Med Genet A; 2005 Aug 30; 137(2):125-9. PubMed ID: 16059941
    [Abstract] [Full Text] [Related]

  • 14. EMG and needle muscle biopsy studies in arthrogryposis multiplex congenita.
    Strehl E, Vanasse M, Brochu P.
    Neuropediatrics; 1985 Nov 30; 16(4):225-7. PubMed ID: 4080098
    [Abstract] [Full Text] [Related]

  • 15. 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 Nov 30; 92(1):58-64. PubMed ID: 26453511
    [Abstract] [Full Text] [Related]

  • 16. Neurogenic arthrogryposis multiplex congenita: clinical and muscle biopsy findings.
    Adams C, Becker LE, Murphy EG.
    Pediatr Neurosci; 1988 Nov 30; 14(2):97-102. PubMed ID: 3251214
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  • 18. 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
    [No Abstract] [Full Text] [Related]

  • 19. Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system.
    Illum N, Reske-Nielsen E, Skovby F, Askjaer SA, Bernsen A.
    Neuropediatrics; 1988 Nov 30; 19(4):186-92. PubMed ID: 3205375
    [Abstract] [Full Text] [Related]

  • 20. Arthrogryposis multiplex congenita due to congenital myasthenia.
    Smit LM, Barth PG.
    Dev Med Child Neurol; 1980 Jun 30; 22(3):371-4. PubMed ID: 6446471
    [Abstract] [Full Text] [Related]

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