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Genetic aspects of sodium channelopathy in small fiber neuropathyHOEIJMAKERS, Jgj; MERKIES, Isj; GERRITS, M. M et al.Clinical genetics. 2012, Vol 82, Num 4, pp 351-358, issn 0009-9163, 8 p.Article

Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathyPARK, Susanna B; LIN, Cindy S.-Y; KRISHNAN, Arun V et al.Brain. 2009, Vol 132, pp 2712-2723, issn 0006-8950, 12 p., 10Article

ALTERED FUNCTIONAL EXPRESSION OF PURKINJE CELL CALCIUM CHANNELS PRECEDES MOTOR DYSFUNCTION IN TOTTERING MICEERICKSON, M. A; HABURCAK, M; SMUKLER, L et al.Neuroscience. 2007, Vol 150, Num 3, pp 547-555, issn 0306-4522, 9 p.Article

Cardiac sodium channel Nav1.5 and its associated proteinsABRIEL, H.Archives des maladies du coeur et des vaisseaux. 2007, Vol 100, Num 9, pp 787-793, issn 0003-9683, 7 p.Article

The primary periodic paralyses : diagnosis, pathogenesis and treatmentVENANCE, S. L; CANNON, S. C; FIALHO, D et al.Brain. 2006, Vol 129, pp 8-17, issn 0006-8950, 10 p., 1Article

Andersen-tawil syndrome : Prospective cohort analysis and expansion of the phenotypeYOON, G; OBEROI, S; TRISTANI-FIROUZI, M et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 4, pp 312-321, issn 1552-4825, 10 p.Article

Channelopathies: Summary of the hot topic keynotes sessionMAGBY, Jason P; NEAL, April P; ATCHISON, William D et al.Neurotoxicology (Park Forest South). 2011, Vol 32, Num 5, pp 661-665, issn 0161-813X, 5 p.Article

Brugada syndrome: a review of the literatureSHEIKH, Azeem S; RANJAN, Kula.Clinical medicine. 2014, Vol 14, Num 5, pp 482-489, issn 1470-2118, 8 p.Article

Altered synaptic transmission at olfactory and vomeronasal nerve terminals in mice lacking N-type calcium channel Cav2.2WEISS, Jan; PYRSKI, Martina; WEISSGERBER, Petra et al.European journal of neuroscience (Print). 2014, Vol 40, Num 9-10, pp 3422-3435, issn 0953-816X, 14 p.Article

HCN4 SUBUNIT EXPRESSION IN FAST-SPIKING INTERNEURONS OF THE RAT SPINAL CORD AND HIPPOCAMPUSHUGHES, D. I; BOYLE, K. A; KINNON, C. M et al.Neuroscience. 2013, Vol 237, pp 7-18, issn 0306-4522, 12 p.Article

Early- and late-onset inherited erythromelalgia: genotype―phenotype correlationCHONGYANG HAN; DIB-HAJJ, Sulayman D; ZHIMIAO LIN et al.Brain. 2009, Vol 132, pp 1711-1722, issn 0006-8950, 12 p., 7Article

Kidney-specific upregulation of vitamin D3 target genes in CIC-5 KO miceMARITZEN, T; RICKHEIT, G; SCHMITT, A et al.Kidney international. 2006, Vol 70, Num 1, pp 79-87, issn 0085-2538, 9 p.Article

Gain-of-function mutations in sodium channel Nav1.9 in painful neuropathyJIANYING HUANG; CHONGYANG HAN; MERKIES, Ingemar S. J et al.Brain. 2014, Vol 137, pp 1627-1642, issn 0006-8950, 16 p., 6Article

TREATMENT OF HYPOKALEMIC PERIODIC PARALYSIS WITH TOPIRAMATEFIORE, Darren M; STROBER, Jonathan B.Muscle & nerve. 2011, Vol 43, Num 1, pp 127-129, issn 0148-639X, 3 p.Article

Genetics of cardiomyopathy and channelopathyBEZZINA, Connie R.Heart and metabolism. 2008, Num 41, pp 5-10, issn 1566-0338, 6 p.Article

Paroxysmal Dyskinesias in MiceSHIRLEY, Thomas L; RAO, Lekha M; HESS, Ellen J et al.Movement disorders. 2008, Vol 23, Num 2, pp 259-264, issn 0885-3185, 6 p.Article

Up-regulation of slow K+ channels in peripheral motor axons : a transcriptional channelopathy in multiple sclerosisNG, Karl; HOWELLS, James; POLLARD, John D et al.Brain. 2008, Vol 131, pp 3062-3071, issn 0006-8950, 10 p., 11Article

Antidystonic effects of Kv7 (KCNQ) channel openers in the dfsz mutant, an animal model of primary paroxysmal dystoniaRICHTER, A; SANDER, S. E; RUNDFELDT, C et al.British journal of pharmacology. 2006, Vol 149, Num 6, pp 747-753, issn 0007-1188, 7 p.Article

In vivo loss of slow potassium channel activity in individuals with benign familial neonatal epilepsy in remissionTOMLINSON, Susan E; BOSTOCK, Hugh; GRINTON, Bronwyn et al.Brain. 2012, Vol 135, pp 3144-3152, issn 0006-8950, 9 p., 10Article

Deletion mutation of sodium channel NaV1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitabilityXIAOYANG CHENG; DIB-HAJJ, Sulayman D; TYRRELL, Lynda et al.Brain. 2011, Vol 134, pp 1972-1986, issn 0006-8950, 15 p., 7Article

SODIUM AND CHLORIDE CHANNELOPATHIES WITH MYOSITIS: COINCIDENCE OR CONNECTION?MATTHEWS, Emma; MILLER, James A. L; MACLEOD, Malcolm R et al.Muscle & nerve. 2011, Vol 44, Num 2, pp 283-288, issn 0148-639X, 6 p.Article

Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavα1S-subunitPIRONE, Antonella; SCHREDELSEKER, Johann; TULUC, Petronel et al.American journal of physiology. Cell physiology. 2010, Vol 68, Num 6, issn 0363-6143, C1345-C1354Article

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neuronsDIB-HAJJ, S. D; RUSH, A. M; CUMMINS, T. R et al.Brain. 2005, Vol 128, pp 1847-1854, issn 0006-8950, 8 p., 8Article

Molecular basis of Mendelian idiopathic epilepsiesROBINSON, Robert; GARDINER, Mark.Annals of medicine (Helsinki). 2004, Vol 36, Num 2, pp 89-97, issn 0785-3890, 9 p.Article

Dysfunction of the brain calcium channel Cav2.1 in absence epilepsy and episodic ataxiaIMBRICI, Paola; JAFFE, Stephen L; EUNSON, Louise H et al.Brain. 2004, Vol 127, pp 2682-2692, issn 0006-8950, 11 p., 12Article

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