-
1
-
-
77953124434
-
Sodium channel Na v 1.7 immunoreactivity in painful human dental pulp and burning mouth syndrome
-
K. Beneng, T. Renton, Z. Yilmaz, Y. Yiangou, and P. Anand Sodium channel Na v 1.7 immunoreactivity in painful human dental pulp and burning mouth syndrome BMC Neurosci 11 2010 71
-
(2010)
BMC Neurosci
, vol.11
, pp. 71
-
-
Beneng, K.1
Renton, T.2
Yilmaz, Z.3
Yiangou, Y.4
Anand, P.5
-
2
-
-
58149326824
-
Inherited neuronal ion channelopathies: New windows on complex neurological diseases
-
W.A. Catterall, S. Dib-Hajj, M.H. Meisler, and D. Pietrobon Inherited neuronal ion channelopathies: new windows on complex neurological diseases J Neurosci 28 2008 11768 11777
-
(2008)
J Neurosci
, vol.28
, pp. 11768-11777
-
-
Catterall, W.A.1
Dib-Hajj, S.2
Meisler, M.H.3
Pietrobon, D.4
-
3
-
-
33845901486
-
An SCN9A channelopathy causes congenital inability to experience pain
-
DOI 10.1038/nature05413, PII NATURE05413
-
J.J. Cox, F. Reimann, A.K. Nicholas, G. Thornton, E. Roberts, K. Springell, G. Karbani, H. Jafri, J. Mannan, Y. Raashid, L. Al-Gazali, H. Hamamy, E.M. Valente, S. Gorman, R. Williams, D.P. McHale, J.N. Wood, F.M. Gribble, and C.G. Woods An SCN9A channelopathy causes congenital inability to experience pain Nature 444 2006 894 898 (Pubitemid 46024997)
-
(2006)
Nature
, vol.444
, Issue.7121
, pp. 894-898
-
-
Cox, J.J.1
Reimann, F.2
Nicholas, A.K.3
Thornton, G.4
Roberts, E.5
Springell, K.6
Karbani, G.7
Jafri, H.8
Mannan, J.9
Raashid, Y.10
Al-Gazali, L.11
Hamamy, H.12
Valente, E.M.13
Gorman, S.14
Williams, R.15
McHale, D.P.16
Wood, J.N.17
Gribble, F.M.18
Woods, C.G.19
-
4
-
-
65249182753
-
Congenital insensitivity to pain
-
N. Danziger, and J.C. Willer Congenital insensitivity to pain Rev Neurol (Paris) 165 2009 129 136
-
(2009)
Rev Neurol (Paris)
, vol.165
, pp. 129-136
-
-
Danziger, N.1
Willer, J.C.2
-
5
-
-
23444443202
-
v1.7 in familial erythromelalgia induces bursting of sensory neurons
-
DOI 10.1093/brain/awh514
-
S.D. Dib-Hajj, A.M. Rush, T.R. Cummins, F.M. Hisama, S. Novella, L. Tyrrell, L. Marshall, and S.G. Waxman Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons Brain 128 2005 1847 1854 (Pubitemid 41373656)
-
(2005)
Brain
, vol.128
, Issue.8
, pp. 1847-1854
-
-
Dib-Hajj, S.D.1
Rush, A.M.2
Cummins, T.R.3
Hisama, F.M.4
Novella, S.5
Tyrrell, L.6
Marshall, L.7
Waxman, S.G.8
-
6
-
-
36849036949
-
Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders
-
DOI 10.1172/JCI33297
-
J.P. Drenth, and S.G. Waxman Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders J Clin Invest 117 2007 3603 3609 (Pubitemid 350224065)
-
(2007)
Journal of Clinical Investigation
, vol.117
, Issue.12
, pp. 3603-3609
-
-
Drenth, J.P.H.1
Waxman, S.G.2
-
7
-
-
38549181857
-
Interpreting the Clinical Importance of Treatment Outcomes in Chronic Pain Clinical Trials: IMMPACT Recommendations
-
DOI 10.1016/j.jpain.2007.09.005, PII S1526590007008991
-
R.H. Dworkin, D.C. Turk, K.W. Wyrwich, D. Beaton, C.S. Cleeland, J.T. Farrar, J.A. Haythornthwaite, M.P. Jensen, R.D. Kerns, D.N. Ader, N. Brandenburg, L.B. Burke, D. Cella, J. Chandler, P. Cowan, R. Dimitrova, R. Dionne, S. Hertz, A.R. Jadad, N.P. Katz, H. Kehlet, L.D. Kramer, D.C. Manning, C. McCormick, M.P. McDermott, H.J. McQuay, S. Patel, L. Porter, S. Quessy, B.A. Rappaport, C. Rauschkolb, D.A. Revicki, M. Rothman, K.E. Schmader, B.R. Stacey, J.W. Stauffer, T. Von Stein, R.E. White, J. Witter, and S. Zavisic Interpreting the clinical importance of treatment outcomes in chronic pain clinical trials: IMMPACT recommendations J Pain 9 2008 105 121 (Pubitemid 351147828)
-
(2008)
Journal of Pain
, vol.9
, Issue.2
, pp. 105-121
-
-
Dworkin, R.H.1
Turk, D.C.2
Wyrwich, K.W.3
Beaton, D.4
Cleeland, C.S.5
Farrar, J.T.6
Haythornthwaite, J.A.7
Jensen, M.P.8
Kerns, R.D.9
Ader, D.N.10
Brandenburg, N.11
Burke, L.B.12
Cella, D.13
Chandler, J.14
Cowan, P.15
Dimitrova, R.16
Dionne, R.17
Hertz, S.18
Jadad, A.R.19
Katz, N.P.20
Kehlet, H.21
Kramer, L.D.22
Manning, D.C.23
McCormick, C.24
McDermott, M.P.25
McQuay, H.J.26
Patel, S.27
Porter, L.28
Quessy, S.29
Rappaport, B.A.30
Rauschkolb, C.31
Revicki, D.A.32
Rothman, M.33
Schmader, K.E.34
Stacey, B.R.35
Stauffer, J.W.36
Von Stein, T.37
White, R.E.38
Witter, J.39
Zavisic, S.40
more..
-
8
-
-
0034578738
-
Defining the clinically important difference in pain outcome measures
-
J.T. Farrar, R.K. Portenoy, J.A. Berlin, J.L. Kinman, and B.L. Strom Defining the clinically important difference in pain outcome measures Pain 88 2000 287 294
-
(2000)
Pain
, vol.88
, pp. 287-294
-
-
Farrar, J.T.1
Portenoy, R.K.2
Berlin, J.A.3
Kinman, J.L.4
Strom, B.L.5
-
9
-
-
67650090921
-
A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia
-
T.Z. Fischer, E.S. Gilmore, M. Estacion, E. Eastman, S. Taylor, M. Melanson, S.D. Dib-Hajj, and S.G. Waxman A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia Ann Neurol 65 2009 733 741
-
(2009)
Ann Neurol
, vol.65
, pp. 733-741
-
-
Fischer, T.Z.1
Gilmore, E.S.2
Estacion, M.3
Eastman, E.4
Taylor, S.5
Melanson, M.6
Dib-Hajj, S.D.7
Waxman, S.G.8
-
10
-
-
77949896163
-
Familial pain syndromes from mutations of the NaV1.7 sodium channel
-
T.Z. Fischer, and S.G. Waxman Familial pain syndromes from mutations of the NaV1.7 sodium channel Ann NY Acad Sci 1184 2010 196 207
-
(2010)
Ann NY Acad Sci
, vol.1184
, pp. 196-207
-
-
Fischer, T.Z.1
Waxman, S.G.2
-
11
-
-
34247874778
-
v1.7 gene underlie congenital indifference to pain in multiple human populations
-
DOI 10.1111/j.1399-0004.2007.00790.x
-
Y.P. Goldberg, J. MacFarlane, M.L. MacDonald, J. Thompson, M.P. Dube, M. Mattice, R. Fraser, C. Young, S. Hossain, T. Pape, B. Payne, C. Radomski, G. Donaldson, E. Ives, J. Cox, H.B. Younghusband, R. Green, A. Duff, E. Boltshauser, G.A. Grinspan, J.H. Dimon, B.G. Sibley, G. Andria, E. Toscano, J. Kerdraon, D. Bowsher, S.N. Pimstone, M.E. Samuels, R. Sherrington, and M.R. Hayden Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations Clin Genet 71 2007 311 319 (Pubitemid 46690905)
-
(2007)
Clinical Genetics
, vol.71
, Issue.4
, pp. 311-319
-
-
Goldberg, Y.P.1
Macfarlane, J.2
Macdonald, M.L.3
Thompson, J.4
Dube, M.P.5
Mattice, M.6
Fraser, R.7
Young, C.8
Hossain, S.9
Pape, T.10
Payne, B.11
Radomski, C.12
Donaldson, G.13
Ives, E.14
Cox, J.15
Younghusband, H.B.16
Green, R.17
Duff, A.18
Boltshauser, E.19
Grinspan, G.A.20
Dimon, J.H.21
Sibley, B.G.22
Andria, G.23
Toscano, E.24
Kerdraon, J.25
Bowsher, D.26
Pimstone, S.N.27
Samuels, M.E.28
Sherrington, R.29
Hayden, M.R.30
more..
-
13
-
-
77950429077
-
Pain perception is altered by a nucleotide polymorphism in SCN9A
-
F. Reimann, J.J. Cox, I. Belfer, L. Diatchenko, D.V. Zaykin, D.P. McHale, J.P. Drenth, F. Dai, J. Wheeler, F. Sanders, L. Wood, T.X. Wu, J. Karppinen, L. Nikolajsen, M. Mannikko, M.B. Max, C. Kiselycznyk, M. Poddar, R.H. Te Morsche, S. Smith, D. Gibson, A. Kelempisioti, W. Maixner, F.M. Gribble, and C.G. Woods Pain perception is altered by a nucleotide polymorphism in SCN9A Proc Natl Acad Sci USA 107 2010 5148 5153
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 5148-5153
-
-
Reimann, F.1
Cox, J.J.2
Belfer, I.3
Diatchenko, L.4
Zaykin, D.V.5
McHale, D.P.6
Drenth, J.P.7
Dai, F.8
Wheeler, J.9
Sanders, F.10
Wood, L.11
Wu, T.X.12
Karppinen, J.13
Nikolajsen, L.14
Mannikko, M.15
Max, M.B.16
Kiselycznyk, C.17
Poddar, M.18
Te Morsche, R.H.19
Smith, S.20
Gibson, D.21
Kelempisioti, A.22
Maixner, W.23
Gribble, F.M.24
Woods, C.G.25
more..
-
14
-
-
34548426549
-
Nav1.7, its mutations, and the syndromes that they cause
-
DOI 10.1212/01.wnl.0000268068.02343.37, PII 0000611420070807000002
-
S.G. Waxman Nav1.7, its mutations, and the syndromes that they cause Neurology 69 2007 505 507 (Pubitemid 47357256)
-
(2007)
Neurology
, vol.69
, Issue.6
, pp. 505-507
-
-
Waxman, S.G.1
-
15
-
-
12144288410
-
Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia
-
Y. Yang, Y. Wang, S. Li, Z. Xu, H. Li, L. Ma, J. Fan, D. Bu, B. Liu, Z. Fan, G. Wu, J. Jin, B. Ding, X. Zhu, and Y. Shen Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia J Med Genet 41 2004 171 174 (Pubitemid 38333793)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.3
, pp. 171-174
-
-
Yang, Y.1
Wang, Y.2
Li, S.3
Xu, Z.4
Li, H.5
Ma, L.6
Fan, J.7
Bu, D.8
Liu, B.9
Fan, Z.10
Wu, G.11
Jin, J.12
Ding, B.13
Zhu, X.14
Shen, Y.15
-
16
-
-
51549108121
-
Voltage-gated sodium channel expression in rat and human epidermal keratinocytes: Evidence for a role in pain
-
P. Zhao, T.P. Barr, Q. Hou, S.D. Dib-Hajj, J.A. Black, P.J. Albrecht, K. Petersen, E. Eisenberg, J.P. Wymer, F.L. Rice, and S.G. Waxman Voltage-gated sodium channel expression in rat and human epidermal keratinocytes: evidence for a role in pain Pain 139 2008 90 105
-
(2008)
Pain
, vol.139
, pp. 90-105
-
-
Zhao, P.1
Barr, T.P.2
Hou, Q.3
Dib-Hajj, S.D.4
Black, J.A.5
Albrecht, P.J.6
Petersen, K.7
Eisenberg, E.8
Wymer, J.P.9
Rice, F.L.10
Waxman, S.G.11
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