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There are 7786124 results for: content related to: Sclerosteosis: report of a case in a black African man

  1. Osteochondrodysplasias in South Africa

    American Journal of Medical Genetics

    Volume 63, Issue 1, 3 May 1996, Pages: 7–11, Peter Beighton

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960503)63:1<7::AID-AJMG4>3.0.CO;2-V

  2. A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population

    American Journal of Medical Genetics

    Volume 110, Issue 2, 15 June 2002, Pages: 144–152, Karen Staehling-Hampton, Sean Proll, Bryan W. Paeper, Lei Zhao, Patrick Charmley, Analisa Brown, Jessica C. Gardner, David Galas, Randall C. Schatzman, Peter Beighton, Socrates Papapoulos, Herman Hamersma and Mary E. Brunkow

    Version of Record online : 16 APR 2002, DOI: 10.1002/ajmg.10401

  3. The syndromic status of sclerosteosis and van Buchem disease

    Clinical Genetics

    Volume 25, Issue 2, February 1984, Pages: 175–181, P. Beighton, A. Barnard, H. Hamersma and A. van der Wouden

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1984.tb00481.x

  4. You have free access to this content
    Van Buchem disease: Clinical, biochemical, and densitometric features of patients and disease carriers

    Journal of Bone and Mineral Research

    Volume 28, Issue 4, April 2013, Pages: 848–854, Antoon H van Lierop, Neveen AT Hamdy, Martje E van Egmond, Egbert Bakker, Freek G Dikkers and Socrates E Papapoulos

    Version of Record online : 18 MAR 2013, DOI: 10.1002/jbmr.1794

  5. Dominantly inherited craniodiaphyseal dysplasia: A new craniotubular dysplasia

    Clinical Genetics

    Volume 30, Issue 5, November 1986, Pages: 381–391, B. Schaefer, S. Stein, D. Oshman, O. Rennert, G. Thurnau, J. Wall, J. Bodensteiner and O. Brown

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1986.tb01895.x

  6. You have free access to this content
    First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin function

    Human Mutation

    Volume 31, Issue 7, July 2010, Pages: E1526–E1543, Elke Piters, Cavit Culha, Martiene Moester, Rutger Van Bezooijen, Dirk Adriaensen, Thomas Mueller, Stella Weidauer, Karen Jennes, Fenna de Freitas, Clemens Löwik, Jean-Pierre Timmermans, Wim Van Hul and Socrates Papapoulos

    Version of Record online : 10 MAY 2010, DOI: 10.1002/humu.21274

  7. The natural history of sclerosteosis

    Clinical Genetics

    Volume 63, Issue 3, March 2003, Pages: 192–197, H Hamersma, J Gardner and P Beighton

    Version of Record online : 12 APR 2003, DOI: 10.1034/j.1399-0004.2003.00036.x

  8. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)

    American Journal of Medical Genetics Part A

    Volume 119A, Issue 3, 15 June 2003, Pages: 386–390, Athanasios I. Tsirikos, Dan E. Mason, Charles I. Scott Jr and Wei-Ning Chang

    Version of Record online : 25 FEB 2003, DOI: 10.1002/ajmg.a.20061

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    High serum sclerostin predicts the occurrence of osteoporotic fractures in postmenopausal women: The center of excellence for osteoporosis research study

    Journal of Bone and Mineral Research

    Volume 27, Issue 12, December 2012, Pages: 2592–2602, Mohammed-Salleh M Ardawi, Abdulrahim A Rouzi, Sharifa A Al-Sibiani, Nawal S Al-Senani, Mohammed H Qari and Shaker A Mousa

    Version of Record online : 19 NOV 2012, DOI: 10.1002/jbmr.1718

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    Wnt but Not BMP Signaling Is Involved in the Inhibitory Action of Sclerostin on BMP-Stimulated Bone Formation

    Journal of Bone and Mineral Research

    Volume 22, Issue 1, January 2007, Pages: 19–28, Rutger L van Bezooijen, J Peter Svensson, Daniël Eefting, Annemieke Visser, Geertje van der Horst, Marcel Karperien, Paul HA Quax, Harry Vrieling, Socrates E Papapoulos, Peter ten Dijke and Clemens WGM Löwik

    Version of Record online : 9 OCT 2006, DOI: 10.1359/jbmr.061002

  11. Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997

    American Journal of Medical Genetics

    Volume 77, Issue 1, 28 April 1998, Pages: 31–37, Peter Beighton, Anne De Paepe, Beat Steinmann, Petros Tsipouras and Richard J. Wenstrup

    Version of Record online : 6 JAN 1999, DOI: 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO;2-O

  12. Prevalence of joint hypermobility in Kuwait

    International Journal of Rheumatic Diseases

    Khaled Al-Jarallah, Diaa Shehab, Munirah T. Al-Jaser, Khaled M. Al-Azemi, Fatma F. Wais, Ahmed M. Al-Saleh, Abdulhadi S. Al-Ajmi, Hamad A. Al-Omairah, Mini Abraham and Prem N. Sharma

    Version of Record online : 20 DEC 2014, DOI: 10.1111/1756-185X.12556

  13. General joint laxity in 1845 Swedish school children of different ages: age- and gender-specific distributions

    Acta Paediatrica

    Volume 93, Issue 9, September 2004, Pages: 1202–1206, A Jansson, T Saartok, S Werner and P Renström

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2004.tb02749.x

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    Patients with sclerosteosis and disease carriers: Human models of the effect of sclerostin on bone turnover

    Journal of Bone and Mineral Research

    Volume 26, Issue 12, December 2011, Pages: 2804–2811, Antoon H van Lierop, Neveen AT Hamdy, Herman Hamersma, Rutger L van Bezooijen, Jon Power, Nigel Loveridge and Socrates E Papapoulos

    Version of Record online : 21 NOV 2011, DOI: 10.1002/jbmr.474

  15. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): Clinical and radiological findings in a guatemalan patient

    American Journal of Medical Genetics

    Volume 59, Issue 2, 6 November 1995, Pages: 234–237, Joyce M. Bradburn and Bryan D. Hall

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320590222

  16. Chapter 88. Sclerosing Bone Disorders

    Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism

    , Pages: 411–423, 2009

    Published Online : 23 DEC 2009, DOI: 10.1002/9780470623992.ch88

  17. You have full text access to this OnlineOpen article
    Epidemiology of generalized joint laxity (hypermobility) in fourteen-year-old children from the UK: A population-based evaluation

    Arthritis & Rheumatism

    Volume 63, Issue 9, September 2011, Pages: 2819–2827, Jacqui Clinch, Kevin Deere, Adrian Sayers, Shea Palmer, Chris Riddoch, Jonathan H. Tobias and Emma M. Clark

    Version of Record online : 31 AUG 2011, DOI: 10.1002/art.30435

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    Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibody

    Journal of Bone and Mineral Research

    Volume 26, Issue 1, January 2011, Pages: 19–26, Desmond Padhi, Graham Jang, Brian Stouch, Liang Fang and Edward Posvar

    Version of Record online : 30 JUN 2010, DOI: 10.1002/jbmr.173

  19. The Ehlers-Danlos Syndrome

    Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects, Second Edition

    Beat Steinmann, Peter M. Royce, Andrea Superti-Furga, Pages: 431–523, 2003

    Published Online : 30 APR 2003, DOI: 10.1002/0471221929.ch9

  20. Phenotypic discriminants in the Waardenburg syndrome

    Clinical Genetics

    Volume 41, Issue 4, April 1992, Pages: 181–188, Ingrid Winsbip and Peter Brighton

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1992.tb03660.x