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PUBMED FOR HANDHELDS

Journal Abstract Search


141 related items for PubMed ID: 9481654

  • 21. Total Hip Arthroplasty in Dyggve-Melchior-Clausen Syndrome: Literature Review and Case Report.
    Yacoubian V, Cutter B, Alvarado C.
    Arthroplast Today; 2024 Jun; 27():101402. PubMed ID: 38741921
    [Abstract] [Full Text] [Related]

  • 22. [Dyggve-Melchior-Clausen syndrome].
    Kondoh T, Matsumoto T.
    Ryoikibetsu Shokogun Shirizu; 2000 Jun; (30 Pt 5):175-6. PubMed ID: 11057185
    [No Abstract] [Full Text] [Related]

  • 23. Chiari osteotomy.
    Katz JF.
    Isr J Med Sci; 1980 Apr; 16(4):333-7. PubMed ID: 7390787
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  • 24. Chiari pelvic osteotomy in the management of developmental hip dysplasia: a long term follow-up.
    Rozkydal Z, Kovanda M.
    Bratisl Lek Listy; 2003 Apr; 104(1):7-13. PubMed ID: 12830990
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  • 25. The Chiari osteotomy in the older child with congenital hip subluxation and acetabular dysplasia.
    Katz JF.
    Orthopedics; 1978 Apr; 1(2):109-13. PubMed ID: 724230
    [Abstract] [Full Text] [Related]

  • 26. Management of progressive genu varum in a patient with Dyggve-Melchior-Clausen syndrome.
    Kenis V, Baindurashvili A, Melchenko E, Grill F, Al Kaissi A.
    Ger Med Sci; 2011 Apr; 9():Doc25. PubMed ID: 21966286
    [Abstract] [Full Text] [Related]

  • 27. Atlantoaxial instability in Dyggve-Melchior-Clausen syndrome. Case report and review of the literature.
    Kandziora F, Neumann L, Schnake KJ, Khodadadyan-Klostermann C, Rehart S, Haas NP, Mittlmeier T.
    J Neurosurg; 2002 Jan; 96(1 Suppl):112-7. PubMed ID: 11795698
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  • 29. Dyggve-Melchior-Clausen syndrome with increased pipecolic acid in plasma and urine.
    Roesel RA, Carroll JE, Rizzo WB, van der Zalm T, Hahn DA.
    J Inherit Metab Dis; 1991 Jan; 14(6):876-80. PubMed ID: 1779646
    [Abstract] [Full Text] [Related]

  • 30. A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review.
    Elalaoui SC, Mariam T, Ilham R, Yassamine D, Abdelaziz S.
    Indian J Hum Genet; 2011 May; 17(2):97-9. PubMed ID: 22090722
    [Abstract] [Full Text] [Related]

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  • 34. New autosomal recessive syndrome of mental retardation, epilepsy, short stature, and skeletal dysplasia.
    Gurrieri F, Sammito V, Bellussi A, Neri G.
    Am J Med Genet; 1992 Oct 01; 44(3):315-20. PubMed ID: 1488978
    [No Abstract] [Full Text] [Related]

  • 35. Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia): morphological findings in the growth plate of the iliac crest.
    Nakamura K, Kurokawa T, Nagano A, Nakamura S, Taniguchi K, Hamazaki M.
    Am J Med Genet; 1997 Oct 03; 72(1):11-7. PubMed ID: 9295067
    [Abstract] [Full Text] [Related]

  • 36. Dyggve-Melchior-Clausen syndrome: novel splice mutation with atlanto-axial subluxation.
    Khalifa O, Imtiaz F, Al-Sakati N, Al-Manea K, Verloes A, Al-Owain M.
    Eur J Pediatr; 2011 Jan 03; 170(1):121-6. PubMed ID: 20865280
    [Abstract] [Full Text] [Related]

  • 37. Congenital dislocation of the hip. A re-appraisal of the upper age limit for treatment.
    Vallamshetla VR, Mughal E, O'Hara JN.
    J Bone Joint Surg Br; 2006 Aug 03; 88(8):1076-81. PubMed ID: 16877609
    [Abstract] [Full Text] [Related]

  • 38. Behavior of the proximal femur during the treatment of congenital dysplasia of the hip: a clinical long-term study.
    Rejholec M, Stryhal F.
    J Pediatr Orthop; 1991 Aug 03; 11(4):506-13. PubMed ID: 1860953
    [Abstract] [Full Text] [Related]

  • 39. A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family.
    Bakar A, Shams S, Bibi N, Ullah A, Ahmad W, Jelani M, Muthaffar OY, Abdulkareem AA, Abujamel TS, Haque A, Naseer MI, Khan B.
    Genes (Basel); 2023 Feb 17; 14(2):. PubMed ID: 36833437
    [Abstract] [Full Text] [Related]

  • 40. A homozygous nonsense variant in DYM underlies Dyggve-Melchior-Clausen syndrome associated with ectodermal features.
    Abdullah, Shah PW, Nawaz S, Hussain S, Ullah A, Basit S, Ahmad W.
    Mol Biol Rep; 2020 Sep 17; 47(9):7083-7088. PubMed ID: 32886330
    [Abstract] [Full Text] [Related]


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