Search Results

There are 11830 results for: content related to: PS: Pain and sodium channels

  1. 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

    Article first published online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01937.x

  2. 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

  3. 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

  4. 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

  5. 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

  6. MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype–phenotype study

    Clinical Genetics

    Volume 84, Issue 6, December 2013, Pages: 539–545, P Makrythanasis, BW van Bon, M Steehouwer, B Rodríguez-Santiago, M Simpson, P Dias, BM Anderlid, P Arts, M Bhat, B Augello, E Biamino, EMHF Bongers, M del Campo, I Cordeiro, AM Cueto-González, I Cuscó, C Deshpande, E Frysira, L Izatt, R Flores, E Galán, B Gener, C Gilissen, SM Granneman, J Hoyer, HG Yntema, CM Kets, DA Koolen, CL Marcelis, A Medeira, L Micale, S Mohammed, SA de Munnik, A Nordgren, S Psoni, W Reardon, N Revencu, T Roscioli, M Ruiterkamp-Versteeg, HG Santos, J Schoumans, JHM Schuurs-Hoeijmakers, MC Silengo, L Toledo, T Vendrell, I van der Burgt, B van Lier, C Zweier, A Reymond, RC Trembath, L Perez-Jurado, J Dupont, BBA de Vries, HG Brunner, JA Veltman, G Merla, SE Antonarakis and A Hoischen

    Article first published online : 26 APR 2013, DOI: 10.1111/cge.12081

  7. Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 20–30, TB Rasmussen, J Hansen, PH Nissen, J Palmfeldt, S Dalager, UB Jensen, WY Kim, L Heickendorff, H Mølgaard, HK Jensen, KE Sørensen, UT Baandrup, P Bross and J Mogensen

    Article first published online : 3 DEC 2012, DOI: 10.1111/cge.12056

  8. 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

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

  9. You have free access to this content
    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

  10. 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

  11. 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

  12. You have free access to this content
    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

  13. 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

  14. 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

  15. Phenotype–genotype correlations in patients with Marinesco–Sjögren syndrome

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 74–84, F. Ezgu, P. Krejci, S. Li, C. de Sousa, J.M. Graham Jr, I. Hansmann, W. He, K. Porpora, D. Wand, W. Wertelecki, A. Schneider and W.R. Wilcox

    Article first published online : 30 JUL 2013, DOI: 10.1111/cge.12230

  16. The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 401–410, M. Ruggieri, A. Polizzi, A. Spalice, V. Salpietro, R. Caltabiano, V. D'Orazi, P. Pavone, C. Pirrone, G. Magro, N. Platania, S. Cavallaro, M. Muglia and F. Nicita

    Article first published online : 22 NOV 2014, DOI: 10.1111/cge.12498

  17. An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 337–344, Y Hilhorst-Hofstee, AJHA Scholte, MEB Rijlaarsdam, A van Haeringen, LJ Kroft, M Reijnierse, CAL Ruivenkamp, MIM Versteegh, G Pals and MH Breuning

    Article first published online : 21 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01931.x

  18. You have free access to this content
    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

  19. Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability

    Clinical Genetics

    Volume 84, Issue 6, December 2013, Pages: 507–521, P Callier, B Aral, N Hanna, S Lambert, H Dindy, C Ragon, M Payet, G Collod-Beroud, V Carmignac, MA Delrue, C Goizet, N Philip, T Busa, Y Dulac, I Missotte, Y Sznajer, A Toutain, C Francannet, A Megarbane, S Julia, T Edouard, P Sarda, J Amiel, S Lyonnet, V Cormier-Daire, B Gilbert, A Jacquette, D Heron, P Collignon, D Lacombe, F Morice-Picard, PS Jouk, V Cusin, M Willems, E Sarrazin, K Amarof, C Coubes, MC Addor, H Journel, E Colin, P Khau Van Kien, C Baumann, B Leheup, D Martin- Coignard, M Doco-Fenzy, A Goldenberg, G Plessis, J Thevenon, L Pasquier, S Odent, P Vabres, F Huet, N Marle, AL Mosca- Boidron, F Mugneret, S Gauthier, C Binquet, C Thauvin-Robinet, G Jondeau, C Boileau and L Faivre

    Article first published online : 18 MAR 2013, DOI: 10.1111/cge.12094

  20. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 345–351, N Hoppman-Chaney, K Wain, PR Seger, DW Superneau and JC Hodge

    Article first published online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01925.x