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Specific changes in conduction velocity recovery cycles of single nociceptors in a patient with erythromelalgia with the I848T gain-of-function mutation of Nav1.7.
Namer B, Ørstavik K, Schmidt R, Kleggetveit IP, Weidner C, Mørk C, Kvernebo MS, Kvernebo K, Salter H, Carr TH, Segerdahl M, Quiding H, Waxman SG, Handwerker HO, Torebjörk HE, Jørum E, Schmelz M. Namer B, et al. Among authors: salter h. Pain. 2015 Sep;156(9):1637-1646. doi: 10.1097/j.pain.0000000000000229. Pain. 2015. PMID: 25993546
SCN10A Mutation in a Patient with Erythromelalgia Enhances C-Fiber Activity Dependent Slowing.
Kist AM, Sagafos D, Rush AM, Neacsu C, Eberhardt E, Schmidt R, Lunden LK, Ørstavik K, Kaluza L, Meents J, Zhang Z, Carr TH, Salter H, Malinowsky D, Wollberg P, Krupp J, Kleggetveit IP, Schmelz M, Jørum E, Lampert A, Namer B. Kist AM, et al. Among authors: salter h. PLoS One. 2016 Sep 6;11(9):e0161789. doi: 10.1371/journal.pone.0161789. eCollection 2016. PLoS One. 2016. PMID: 27598514 Free PMC article.
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia.
Zhang Z, Schmelz M, Segerdahl M, Quiding H, Centerholt C, Juréus A, Carr TH, Whiteley J, Salter H, Kvernebo MS, Ørstavik K, Helås T, Kleggetveit IP, Lunden LK, Jørum E. Zhang Z, et al. Among authors: salter h. Scand J Pain. 2014 Oct 1;5(4):217-225. doi: 10.1016/j.sjpain.2014.09.002. Scand J Pain. 2014. PMID: 29911575 Free article.
A stop codon mutation in SCN9A causes lack of pain sensation.
Ahmad S, Dahllund L, Eriksson AB, Hellgren D, Karlsson U, Lund PE, Meijer IA, Meury L, Mills T, Moody A, Morinville A, Morten J, O'donnell D, Raynoschek C, Salter H, Rouleau GA, Krupp JJ. Ahmad S, et al. Among authors: salter h. Hum Mol Genet. 2007 Sep 1;16(17):2114-21. doi: 10.1093/hmg/ddm160. Epub 2007 Jun 27. Hum Mol Genet. 2007. PMID: 17597096
Possible allelic structure of IgG2a and IgG2c in mice.
Zhang Z, Goldschmidt T, Salter H. Zhang Z, et al. Among authors: salter h. Mol Immunol. 2012 Mar;50(3):169-71. doi: 10.1016/j.molimm.2011.11.006. Epub 2011 Dec 15. Mol Immunol. 2012. PMID: 22177661
APOE genotypes and disease severity in multiple sclerosis.
Masterman T, Zhang Z, Hellgren D, Salter H, Anvret M, Lilius L, Lannfelt L, Hillert J. Masterman T, et al. Among authors: salter h. Mult Scler. 2002 Apr;8(2):98-103. doi: 10.1191/1352458502ms787oa. Mult Scler. 2002. PMID: 11990879
CTLA4 dimorphisms and the multiple sclerosis phenotype.
Masterman T, Ligers A, Zhang Z, Hellgren D, Salter H, Anvret M, Hillert J. Masterman T, et al. Among authors: salter h. J Neuroimmunol. 2002 Oct;131(1-2):208-12. doi: 10.1016/s0165-5728(02)00274-6. J Neuroimmunol. 2002. PMID: 12458054
76 results