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There are 65317 results for: content related to: Twin studies of pain

  1. You have free access to this content
    Pharmacogenetics of pain and analgesia

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 321–330, MT Smith and A Muralidharan

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01936.x

  2. You have free access to this content
    Genetic aspects of sodium channelopathy in small fiber neuropathy

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 351–358, JGJ Hoeijmakers, ISJ Merkies, MM Gerrits, SG Waxman and CG Faber

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01937.x

  3. You have free access to this content
    From mouse to humans: discovery of the CACNG2 pain susceptibility gene

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 311–320, J Nissenbaum

    Version of Record online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01924.x

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    Opioid genetics: the key to personalized pain control?

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 301–310, R Branford, J Droney and JR Ross

    Version of Record online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01923.x

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    Drosophila as a tool for studying the conserved genetics of pain

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 359–366, G Milinkeviciute, C Gentile and G Gregory Neely

    Version of Record online : 22 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01941.x

  6. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 285–294, K. Rai, R. Pilarski, C.M. Cebulla and M.H. Abdel-Rahman

    Version of Record online : 14 JUL 2015, DOI: 10.1111/cge.12630

  7. Genetics of human Bardet–Biedl syndrome, an updates

    Clinical Genetics

    Volume 90, Issue 1, July 2016, Pages: 3–15, S.A. Khan, N. Muhammad, M.A. Khan, A. Kamal, Z.U. Rehman and S. Khan

    Version of Record online : 9 FEB 2016, DOI: 10.1111/cge.12737

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    Recommendations for the predictive genetic test in Huntington's disease

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 221–231, R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, RA Roos and Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network

    Version of Record online : 29 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01900.x

  9. Nature or nurture in low back pain? Results of a systematic review of studies based on twin samples

    European Journal of Pain

    Volume 17, Issue 7, August 2013, Pages: 957–971, P.H. Ferreira, P. Beckenkamp, C.G. Maher, J.L. Hopper and M.L. Ferreira

    Version of Record online : 20 JAN 2013, DOI: 10.1002/j.1532-2149.2012.00277.x

  10. Fabry disease in children: agalsidase-beta enzyme replacement therapy

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 432–438, L Borgwardt, U Feldt-Rasmussen, AK Rasmussen, M Ballegaard and A Meldgaard Lund

    Version of Record online : 27 SEP 2012, DOI: 10.1111/j.1399-0004.2012.01947.x

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    Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 341–350, Y Indo

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01943.x

  12. Prenatal diagnosis of congenital myopathies and muscular dystrophies

    Clinical Genetics

    D. Massalska, J.G. Zimowski, J. Bijok, A. Kucińska-Chahwan, A. Łusakowska, G. Jakiel and T. Roszkowski

    Version of Record online : 2 JUN 2016, DOI: 10.1111/cge.12801

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    Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 367–373, YP Goldberg, SN Pimstone, R Namdari, N Price, C Cohen, RP Sherrington and MR Hayden

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01942.x

  14. Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 251–256, SK Holman, T Morgan, G Baujat, V Cormier-Daire, T-J Cho, M Lees, J Samanich, D Tapon, HD Hove, A Hing, R Hennekam and SP Robertson

    Version of Record online : 5 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01905.x

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    Genetics of the corneal endothelial dystrophies: an evidence-based review

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 109–119, A J Aldave, J Han and R F Frausto

    Version of Record online : 10 JUN 2013, DOI: 10.1111/cge.12191

  16. Polydactyly: phenotypes, genetics and classification

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 203–212, S. Malik

    Version of Record online : 18 OCT 2013, DOI: 10.1111/cge.12276

  17. The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 303–314, FC Connell, K Gordon, G Brice, V Keeley, S Jeffery, PS Mortimer, S Mansour and P Ostergaard

    Version of Record online : 27 JUN 2013, DOI: 10.1111/cge.12173

  18. The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers

    Clinical Genetics

    Volume 85, Issue 1, January 2014, Pages: 7–15, C Borreani, S Manoukian, E Bianchi, C Brunelli, B Peissel, A Caruso, G Morasso and MA Pierotti

    Version of Record online : 5 NOV 2013, DOI: 10.1111/cge.12298

  19. Molecular cytogenetics: recent developments and applications in cancer

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 315–325, K Das and P Tan

    Version of Record online : 6 AUG 2013, DOI: 10.1111/cge.12229

  20. National mutation study among Danish patients with hereditary haemorrhagic telangiectasia

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 123–133, P.M. Tørring, K. Brusgaard, L.B. Ousager, P.E. Andersen and A.D. Kjeldsen

    Version of Record online : 3 OCT 2013, DOI: 10.1111/cge.12269