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There are 9108 results for: content related to: Genetic aspects of sodium channelopathy in small fiber neuropathy

  1. You have free access to this content
    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

    Article first published online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01942.x

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    Potential causes for the non-Newtonian rheology of crystal-bearing magmas

    Geochemistry, Geophysics, Geosystems

    Volume 12, Issue 5, May 2011, Yolanda Deubelbeiss, Boris J. P. Kaus, James A. D. Connolly and Luca Caricchi

    Article first published online : 17 MAY 2011, DOI: 10.1029/2010GC003485

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    Pharmacogenetics of pain and analgesia

    Clinical Genetics

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

    Article first published online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01936.x

  4. 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

    Article first published online : 5 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01905.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

    Article first published online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01923.x

  6. Genetic heterogeneity in Pakistani microcephaly families

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 446–451, M Sajid Hussain, S Marriam Bakhtiar, M Farooq, I Anjum, E Janzen, M Reza Toliat, H Eiberg, KW Kjaer, N Tommerup, AA Noegel, P Nürnberg, SM Baig and L Hansen

    Article first published online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01932.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

    Article first published online : 22 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01941.x

  8. 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

    Article first published online : 29 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01900.x

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    Twin studies of pain

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 331–340, CS Nielsen, GP Knudsen and ÓA Steingrímsdóttir

    Article first published online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01938.x

  10. The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p.S358L mutation in TMEM43

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 321–331, KA Hodgkinson, SP Connors, N Merner, A Haywood, T-L Young, WJ McKenna, B Gallagher, F Curtis, AS Bassett and PS Parfrey

    Article first published online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01919.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

    Article first published online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01943.x

  12. Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 457–461, NA Hanchard, DR Murdock, PL Magoulas, M Bainbridge, D Muzny, YQ Wu, M Wang, AL McGuire, JR Lupski, RA Gibbs and CW Brown

    Article first published online : 11 SEP 2012, DOI: 10.1111/j.1399-0004.2012.01951.x

  13. Primary care physicians' knowledge of and experience with pharmacogenetic testing

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 388–394, SB Haga, W Burke, GS Ginsburg, R Mills and R Agans

    Article first published online : 3 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01908.x

  14. Gene therapy for primary immunodeficiencies

    Clinical Genetics

    A. Fischer, S. Hacein-Bey Abina, F. Touzot and M. Cavazzana

    Article first published online : 23 MAR 2015, DOI: 10.1111/cge.12576

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    The emerging era of pharmacogenomics: current successes, future potential, and challenges

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 21–28, J.W. Lee, F. Aminkeng, A.P. Bhavsar, K. Shaw, B.C. Carleton, M.R. Hayden and C.J.D. Ross

    Article first published online : 9 MAY 2014, DOI: 10.1111/cge.12392

  16. Germline RAD51C mutations in ovarian cancer susceptibility

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 332–336, F Coulet, A Fajac, C Colas, M Eyries, A Dion-Minière, R Rouzier, S Uzan, J-P Lefranc, M Carbonnel, F Cornelis, A Cortez and F Soubrier

    Article first published online : 23 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01917.x

  17. Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 439–445, S Jahnavi, V Poovazhagi, V Mohan, D Bodhini, P Raghupathy, A Amutha, P Suresh Kumar, P Adhikari, M Shriraam, T Kaur, AK Das, J Molnes, PR Njolstad, R Unnikrishnan and V Radha

    Article first published online : 20 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01939.x

  18. Genotype–phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 422–431, SG Mehta, M Khare, R Ramani, GDJ Watts, M Simon, KE Osann, S Donkervoort, E Dec, A Nalbandian, J Platt, M Pasquali, A Wang, T Mozaffar, CD Smith and VE Kimonis

    Article first published online : 4 OCT 2012, DOI: 10.1111/cge.12000

  19. Mutation analysis of the STRA6 gene in isolated and non-isolated anophthalmia/microphthalmia

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 244–250, N Chassaing, N Ragge, A Kariminejad, A Buffet, S Ghaderi-Sohi, J Martinovic and P Calvas

    Article first published online : 4 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01904.x

  20. Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 359–364, S Stuckless, J Green, L Dawson, B Barrett, MO Woods, E Dicks and PS Parfrey

    Article first published online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01929.x