-
1
-
-
77953684015
-
Sodium channels in normal and pathological pain
-
20367448 10.1146/annurev-neuro-060909-153234 1:CAS:528:DC%2BC3cXhsFartrrP This comprehensive review summarizes the knowledge on the different types of voltage-gated sodium channels and their function in normal and pathologic conditions
-
SD Dib-Hajj TR Cummins JA Black SG Waxman 2010 Sodium channels in normal and pathological pain Annu Rev Neurosci 33 325 347 20367448 10.1146/annurev- neuro-060909-153234 1:CAS:528:DC%2BC3cXhsFartrrP This comprehensive review summarizes the knowledge on the different types of voltage-gated sodium channels and their function in normal and pathologic conditions
-
(2010)
Annu Rev Neurosci
, vol.33
, pp. 325-347
-
-
Dib-Hajj, S.D.1
Cummins, T.R.2
Black, J.A.3
Waxman, S.G.4
-
2
-
-
77949896163
-
Familial pain syndromes from mutations of the NaV1.7 sodium channels
-
20146699 10.1111/j.1749-6632.2009.05110.x 1:CAS:528:DC%2BC3cXivVegtLc%3D
-
TZ Fischer SG Waxman 2010 Familial pain syndromes from mutations of the NaV1.7 sodium channels Ann N Y Acad Sci 1184 196 207 20146699 10.1111/j.1749-6632.2009.05110.x 1:CAS:528:DC%2BC3cXivVegtLc%3D
-
(2010)
Ann N y Acad Sci
, vol.1184
, pp. 196-207
-
-
Fischer, T.Z.1
Waxman, S.G.2
-
3
-
-
71149115257
-
Structure-function studies on the voltage-gated sodium channel
-
19747894 10.1016/j.bbamem.2009.08.017 1:CAS:528:DC%2BD1MXhtlWitrzE The article clarifies the relations between the molecular structure and physiologic function of VGSC
-
H Duclohier 2009 Structure-function studies on the voltage-gated sodium channel Biochim Biophys Acta 1788 11 2374 2379 19747894 10.1016/j.bbamem.2009. 08.017 1:CAS:528:DC%2BD1MXhtlWitrzE The article clarifies the relations between the molecular structure and physiologic function of VGSC
-
(2009)
Biochim Biophys Acta
, vol.1788
, Issue.11
, pp. 2374-2379
-
-
Duclohier, H.1
-
4
-
-
0033694833
-
From ionic currents to molecular mechanisms: The structure and function of voltage-gated sodium channels
-
10798388 10.1016/S0896-6273(00)81133-2 1:CAS:528:DC%2BD3cXjtFSksbY%3D
-
WA Catterall 2000 From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels Neuron 26 13 25 10798388 10.1016/S0896-6273(00)81133-2 1:CAS:528:DC%2BD3cXjtFSksbY%3D
-
(2000)
Neuron
, vol.26
, pp. 13-25
-
-
Catterall, W.A.1
-
5
-
-
0021123234
-
Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence
-
DOI 10.1038/312121a0
-
M Noda T Shimizu T Tanabe, et al. 1984 Primary structure of Electrophorus Electricus sodium channel deduced from cDNA sequence Nature 312 121 127 6209577 10.1038/312121a0 1:CAS:528:DyaL2MXntlCgug%3D%3D (Pubitemid 14000075)
-
(1984)
Nature
, vol.312
, Issue.5990
, pp. 121-127
-
-
Noda, M.1
Shimizu, S.2
Tanabe, T.3
-
6
-
-
0037264170
-
Overview of the voltage-gated sodium channel family
-
DOI 10.1186/gb-2003-4-3-207
-
FH Yu WA Catterall 2003 Overview of the volatage-gated sodium channel superfamily Genome Biol 4 207 214 12620097 10.1186/gb-2003-4-3-207 (Pubitemid 36546590)
-
(2003)
Genome Biology
, vol.4
, Issue.3
, pp. 207
-
-
Yu, F.H.1
Catterall, W.A.2
-
7
-
-
0029838677
-
Structure and function of voltage-dependent sodium channels: Comparison of brain II and cardiac isoforms
-
HA Fozzard DA Hanck 1996 Structure and function of voltage-dependent sodium channels: Comparison of brain II and cardiac isoforms Physiol Rev 76 887 926 8757791 1:CAS:528:DyaK28XltVags7o%3D (Pubitemid 26286081)
-
(1996)
Physiological Reviews
, vol.76
, Issue.3
, pp. 887-926
-
-
Fozzard, H.A.1
Hanck, D.A.2
-
8
-
-
29844438166
-
International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels
-
DOI 10.1124/pr.57.4.4
-
WA Catterall AL Goldin SG Waxman 2005 International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels Pharmacol Rev 57 397 409 16382098 10.1124/pr.57.4.4 1:CAS:528:DC%2BD28XhtFWgu74%3D (Pubitemid 43036431)
-
(2005)
Pharmacological Reviews
, vol.57
, Issue.4
, pp. 397-409
-
-
Catterall, W.A.1
Goldin, A.L.2
Waxman, S.G.3
-
9
-
-
0030608445
-
Spinal sensory neurons express multiple sodium channel α-subunit mRNAs
-
DOI 10.1016/S0169-328X(96)00163-5, PII S0169328X96001635
-
JA Black SD Dib-Hajj K McNabola, et al. 1996 Spinal sensory neurons express multiple sodium channel alpha-subunit mRNA Brain Res. Mol Brain Res 43 117 131 9037525 10.1016/S0169-328X(96)00163-5 1:CAS:528:DyaK28XmvFemsbY%3D (Pubitemid 27042398)
-
(1996)
Molecular Brain Research
, vol.43
, Issue.1-2
, pp. 117-131
-
-
Black, J.A.1
Dib-Hajj, S.2
McNabola, K.3
Jeste, S.4
Rizzo, M.A.5
Kocsis, J.D.6
Waxman, S.G.7
-
10
-
-
0031840375
-
Rescue of α-SNS sodium channel expression in small dorsal root ganglion neurons after axotomy by nerve growth factor in vivo
-
SD Dib-Hajj JA Black TR Cummins, et al. 1998 Rescue of alpha-SNS sodium channel expression in small root ganglion neurons after axonotomy by nerve growth factor in vivo J Neurophysiol 79 2668 2676 9582237 1:CAS:528: DyaK1cXjsF2it7Y%3D (Pubitemid 28261650)
-
(1998)
Journal of Neurophysiology
, vol.79
, Issue.5
, pp. 2668-2676
-
-
Dib-Hajj, S.D.1
Black, J.A.2
Cummins, T.R.3
Kenney, A.M.4
Kocsis, J.D.5
Waxman, S.G.6
-
12
-
-
0027933696
-
Type III sodium channel mRNA is expressed in embryonic but not adult spinal sensory neurons, and is reexpressed following axotomy
-
SG Waxman JD Kocsis JA Black 1994 Type III sodium channel mRNA is expressed in embryonic but not adult spinal sensory neurons, and is reexpressed following axotomy J Neurophysiol 72 466 470 7965028 1:CAS:528:DyaK2cXmvFOksLk%3D (Pubitemid 24233666)
-
(1994)
Journal of Neurophysiology
, vol.72
, Issue.1
, pp. 466-470
-
-
Waxman, S.G.1
Kocsis, J.D.2
Black, J.A.3
-
13
-
-
39149136856
-
Mutation of sodium channel SCN3A in patients with cryptogenic pediatric partial epilepsy
-
10.1016/j.neulet.2007.12.064 1:CAS:528:DC%2BD1cXitlerurk%3D
-
KD Holland JA Kearney TA Glauser, et al. 2008 Mutation of sodium channel SCN3A in patients with cryptogenic pediatric partial epilepsy Neusci Lett 433 65 70 10.1016/j.neulet.2007.12.064 1:CAS:528:DC%2BD1cXitlerurk%3D
-
(2008)
Neusci Lett
, vol.433
, pp. 65-70
-
-
Holland, K.D.1
Kearney, J.A.2
Glauser, T.A.3
-
14
-
-
0035977980
-
Comparative distribution of voltage-gated sodium channel proteins in human brain
-
DOI 10.1016/S0169-328X(00)00289-8, PII S0169328X00002898
-
WR Whitaker RL Faull HJ Waldvogel, et al. 2001 Comparative distribution of voltage-gated sodium channel proteins in human brain Mol Brain Res 88 37 53 11295230 10.1016/S0169-328X(00)00289-8 1:CAS:528:DC%2BD3MXisVWgsr8%3D (Pubitemid 32274258)
-
(2001)
Molecular Brain Research
, vol.88
, Issue.1-2
, pp. 37-53
-
-
Whitaker, W.R.J.1
Faull, R.L.M.2
Waldvogel, H.J.3
Plumpton, C.J.4
Emson, P.C.5
Clare, J.J.6
-
15
-
-
0033363999
-
The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways
-
DOI 10.1038/9195
-
AN Akopian V Souslova S England, et al. 1999 The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways Nat Neurosci 2 541 548 10448219 10.1038/9195 1:CAS:528:DyaK1MXjsFSis78%3D (Pubitemid 30491235)
-
(1999)
Nature Neuroscience
, vol.2
, Issue.6
, pp. 541-548
-
-
Akopian, A.N.1
Souslova, V.2
England, S.3
Okuse, K.4
Ogata, N.5
Ure, J.6
Smith, A.7
Kerr, B.J.8
McMahon, S.B.9
Boyce, S.10
Hill, R.11
Stanfa, L.C.12
Dickenson, A.H.13
Wood, J.N.14
-
16
-
-
0032240731
-
Two sodium channels contribute to the TTX-R sodium current in primary sensory neurons
-
10196578 10.1038/3652 1:CAS:528:DyaK1MXitVCgsb4%3D
-
S Tate S Benn C Hick, et al. 1998 Two sodium channels contribute to the TTX-R sodium current in primary sensory neurons Nat Neurosci 1 653 655 10196578 10.1038/3652 1:CAS:528:DyaK1MXitVCgsb4%3D
-
(1998)
Nat Neurosci
, vol.1
, pp. 653-655
-
-
Tate, S.1
Benn, S.2
Hick, C.3
-
17
-
-
33845631301
-
v1.9 is an effector of peripheral inflammatory pain hypersensitivity
-
DOI 10.1523/JNEUROSCI.4015-06.2006
-
F Amaya H Wang M Costigan, et al. 2006 The voltage-gated sodium channel Nav1.9 is an effector of peripheral inflammatory pain hypersensitivity J Neuroscoi 26 12852 12860 10.1523/JNEUROSCI.4015-06.2006 1:CAS:528: DC%2BD2sXhs1Ciug%3D%3D (Pubitemid 44954605)
-
(2006)
Journal of Neuroscience
, vol.26
, Issue.50
, pp. 12852-12860
-
-
Amaya, F.1
Wang, H.2
Costigan, M.3
Allchorne, A.J.4
Hatcher, J.P.5
Egerton, J.6
Stean, T.7
Morisset, V.8
Grose, D.9
Gunthorpe, M.J.10
Chessell, I.P.11
Tate, S.12
Green, P.J.13
Woolf, C.J.14
-
18
-
-
42949160614
-
V1.9 in a distinct population of dorsal root ganglia innervating the rat knee joint in a model of chronic inflammatory joint pain
-
DOI 10.1016/j.ejpain.2007.09.001, PII S1090380107006490
-
IT Strickland JC Martindale PL Woodhams, et al. 2008 Changes in the expression of Nav1.7, Nav1.8 and Nav1.9 in a distinct population of dorsal root ganglia innervating the rat knee joint in a model of chronic inflammatory joint pain Eur J Pain 12 564 572 17950013 10.1016/j.ejpain.2007.09.001 1:CAS:528:DC%2BD1cXlvVSls7k%3D (Pubitemid 351615304)
-
(2008)
European Journal of Pain
, vol.12
, Issue.5
, pp. 564-572
-
-
Strickland, I.T.1
Martindale, J.C.2
Woodhams, P.L.3
Reeve, A.J.4
Chessell, I.P.5
McQueen, D.S.6
-
19
-
-
3042791018
-
v 1.7 and 1.8 sodium channels associated with complete freund's adjuvant-induced inflammation in rat
-
DOI 10.1016/j.jpain.2004.04.005, PII S152659000400762X
-
HJ Guold 3rd JD England RD Soignier, et al. 2004 Ibuprofen blocks changes in Nav1.7 and 1.8 sodium channels associated with complete freund's adjuvant-induced inflammation in rat J pain 5 270 280 10.1016/j.jpain.2004.04. 005 (Pubitemid 38859681)
-
(2004)
Journal of Pain
, vol.5
, Issue.5
, pp. 270-280
-
-
Gould III, H.J.1
England, J.D.2
Soignier, R.D.3
Nolan, P.4
Minor, L.D.5
Liu, Z.P.6
Levinson, S.R.7
Paul, D.8
-
20
-
-
4344670206
-
v 1.7 (PN1) in acute and inflammatory pain
-
DOI 10.1073/pnas.0404915101
-
MA Nassar LC Stirling G Forlani, et al. 2004 Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain Proc Natl Acad Sci USA 101 12706 12711 15314237 10.1073/pnas.0404915101 1:CAS:528:DC%2BD2cXnsVent7k%3D (Pubitemid 39122087)
-
(2004)
Proceedings of the National Academy of Sciences of the United States of America
, vol.101
, Issue.34
, pp. 12706-12711
-
-
Nassar, M.A.1
Stirling, L.C.2
Forlani, G.3
Baker, M.D.4
Matthewst, E.A.5
Dickenson, A.H.6
Wood, J.N.7
-
21
-
-
0033955244
-
Immunolocalization of SNS/PN3 and NaN/SNS2 sodium channels in human pain states
-
DOI 10.1016/S0304-3959(99)00251-1, PII S0304395999002511
-
K Coward C Plumpton P Facer, et al. 2000 Immunolocalization of SNS/PN3 and NaN/SNS2 sodium channels in human pain states Pain 85 41 50 10692601 10.1016/S0304-3959(99)00251-1 1:CAS:528:DC%2BD3cXht1Oitrk%3D (Pubitemid 30110742)
-
(2000)
Pain
, vol.85
, Issue.1-2
, pp. 41-50
-
-
Coward, K.1
Plumpton, C.2
Facer, P.3
Birch, R.4
Carlstedt, T.5
Tate, S.6
Bountra, C.7
Anand, P.8
-
22
-
-
58149232445
-
Multiple sodium channel isoforms and mitogen-activated protein kinases are present in painful human neuromas
-
19107992 10.1002/ana.21527
-
JA Black L Nikolajsen K Kroner, et al. 2008 Multiple sodium channel isoforms and mitogen-activated protein kinases are present in painful human neuromas Ann Neurol 64 644 653 19107992 10.1002/ana.21527
-
(2008)
Ann Neurol
, vol.64
, pp. 644-653
-
-
Black, J.A.1
Nikolajsen, L.2
Kroner, K.3
-
23
-
-
0027497442
-
Hereditary erythermalgia and acquired erythromelalgia [3]
-
DOI 10.1002/ajmg.1320450426
-
PJ Van Genderen JJ Michiels P Drenth 1993 Hereditary erythermalgia and acquired erythromelalgia Am J Med Genet 45 530 532 8465864 10.1002/ajmg. 1320450426 (Pubitemid 23029653)
-
(1993)
American Journal of Medical Genetics
, vol.45
, Issue.4
, pp. 530-532
-
-
Van Genderen, P.J.J.1
Michiels, J.J.2
Drenth, J.P.H.3
Finley, W.H.4
Lindsey Jr., J.R.5
Fine, J.-D.6
Dixon, G.A.7
Burbank, M.K.8
-
24
-
-
0034014898
-
Natural history of erythromelalgia: Presentation and outcome in 168 patients
-
MD Davis WM O'Fallon RS Rogers III 2000 Rooke TW: Natural history of erythromelalgia: presentation and outcome in 168 patients Arch Dermatol 136 330 336 10724194 10.1001/archderm.136.3.330 1:STN:280:DC%2BD3c7os1Oruw%3D%3D (Pubitemid 30149105)
-
(2000)
Archives of Dermatology
, vol.136
, Issue.3
, pp. 330-336
-
-
Davis, M.D.P.1
O'Fallon, W.M.2
Rogers III, R.S.3
Rooke, T.W.4
-
25
-
-
0020684659
-
Autonomic innervation of the skin in primary erythermalgia
-
DOI 10.1001/archderm.119.1.65
-
H Uno F Parker 1983 Autonomic innervation of the skin in primary erythermalgia Arch Dermatol 119 65 71 6336930 10.1001/archderm.1983. 01650250069020 1:STN:280:DyaL3s%2FpvFemsw%3D%3D (Pubitemid 13224229)
-
(1983)
Archives of Dermatology
, vol.119
, Issue.1
, pp. 65-71
-
-
Uno, H.1
Parker, F.2
-
26
-
-
28244468409
-
Erythermalgia: Molecular basis for an inherited pain syndrome
-
DOI 10.1016/j.molmed.2005.10.004, PII S1471491405002315
-
SG Waxman S Dib-Hajj 2005 Erythermalgia: molecular basis for an inherited pain syndrome Trends Mol Med 11 555 562 16278094 10.1016/j.molmed.2005.10.004 1:CAS:528:DC%2BD2MXht1Omsr3K (Pubitemid 41713997)
-
(2005)
Trends in Molecular Medicine
, vol.11
, Issue.12
, pp. 555-562
-
-
Waxman, S.G.1
Dib-Hajj, S.2
-
27
-
-
12144288410
-
Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia
-
Y Yang Y Wang S Li, et al. 2004 Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia J Med Gen 41 171 174 10.1136/jmg.2003.012153 1:CAS:528:DC%2BD2cXjtFCgsrw%3D (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
-
28
-
-
23444443202
-
v1.7 in familial erythromelalgia induces bursting of sensory neurons
-
DOI 10.1093/brain/awh514
-
SD Dib-Hajj AM Rush TR Cummins, et al. 2005 Gain-of-function mutation in NaV1.7 in familial erythromelalgia induces bursting of sensory neurons Brain 128 1847 1854 15958509 10.1093/brain/awh514 1:STN:280:DC%2BD2MzntF2mtw%3D%3D (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
-
29
-
-
20544476041
-
SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels
-
DOI 10.1111/j.0022-202X.2005.23737.x
-
JP Drenth RH te Morsche G Guillet, et al. 2005 SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels J Invest Dermatol 124 1333 1338 15955112 10.1111/j.0022-202X.2005.23737.x 1:CAS:528:DC%2BD2MXlvF2ktb4%3D (Pubitemid 40847424)
-
(2005)
Journal of Investigative Dermatology
, vol.124
, Issue.6
, pp. 1333-1338
-
-
Drenth, J.P.H.1
Te Morsche, R.H.M.2
Guillet, G.3
Taieb, A.4
Kirby, R.L.5
Jansen, J.B.M.J.6
-
30
-
-
0030041548
-
A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons
-
DOI 10.1038/379257a0
-
AN Akopian L Sivilotti JN Wood 1996 A tetrodotoxin-resistant voltage-gated sodium channel expressed by sensory neurons Nature 379 257 262 8538791 10.1038/379257a0 1:CAS:528:DyaK28Xmtl2nsg%3D%3D (Pubitemid 26025211)
-
(1996)
Nature
, vol.379
, Issue.6562
, pp. 257-262
-
-
Akopian, A.N.1
Sivilotti, L.2
Wood, J.N.3
-
31
-
-
67650090921
-
A novel NaV1.7 mutation producing carbamazepine-responsive erythromelalgia
-
10.1002/ana.21678
-
TZ Fischer M Gilmore M Estacion, et al. 2009 A novel NaV1.7 mutation producing carbamazepine-responsive erythromelalgia Ann Neurol 65 773 741 10.1002/ana.21678
-
(2009)
Ann Neurol
, vol.65
, pp. 773-741
-
-
Fischer, T.Z.1
Gilmore, M.2
Estacion, M.3
-
32
-
-
61949316005
-
Mexiletine-responsive erythromelalgia due to a new NaV1.7 mutation showing use-dependent current fall-off
-
19162012 10.1016/j.expneurol.2008.12.012 1:CAS:528:DC%2BD1MXjsVOjt7k%3D
-
JS Choi L Zhang SD Dib-Hajj, et al. 2009 Mexiletine-responsive erythromelalgia due to a new NaV1.7 mutation showing use-dependent current fall-off Exp Neurol 216 383 389 19162012 10.1016/j.expneurol.2008.12.012 1:CAS:528:DC%2BD1MXjsVOjt7k%3D
-
(2009)
Exp Neurol
, vol.216
, pp. 383-389
-
-
Choi, J.S.1
Zhang, L.2
Dib-Hajj, S.D.3
-
33
-
-
45949089884
-
Compound heterozygosity in sodium channel Nav 1.7 in a family with hereditary erythermalgia
-
DOI 10.1186/1744-8069-4-21
-
ME Samuels RH te Morsche ME Lynch JP Drenth 2008 Compound heterozigosity in sodium channel NaV1.7 in a family with hereditary erythermalgia Mol Pain 4 21 18518989 10.1186/1744-8069-4-21 (Pubitemid 351891442)
-
(2008)
Molecular Pain
, vol.4
, pp. 21
-
-
Samuels, M.E.1
Te Morsche, R.H.M.2
Lynch, M.E.3
Drenth, J.P.H.4
-
34
-
-
73549101494
-
A sodium channel gene SCN9A polymorphism that increases nociceptor excitability
-
20033988 10.1002/ana.21895 1:CAS:528:DC%2BC3cXhtlamsLY%3D
-
M Estacion TP Harry JS Choi, et al. 2009 A sodium channel gene SCN9A polymorphism that increases nociceptor excitability Ann Neurol 66 862 866 20033988 10.1002/ana.21895 1:CAS:528:DC%2BC3cXhtlamsLY%3D
-
(2009)
Ann Neurol
, vol.66
, pp. 862-866
-
-
Estacion, M.1
Harry, T.P.2
Choi, J.S.3
-
35
-
-
64549097605
-
Primary erythromelalgia: Efficacy of oxcarbazepine
-
19361700 10.1016/j.annder.2008.10.032 1:STN:280:DC%2BD1M3ntlChtg%3D%3D
-
S Skali Dahbi K Zuohair B Moutawakil, et al. 2009 Primary erythromelalgia: efficacy of oxcarbazepine Ann Dermatol Venereol 136 337 340 19361700 10.1016/j.annder.2008.10.032 1:STN:280:DC%2BD1M3ntlChtg%3D%3D
-
(2009)
Ann Dermatol Venereol
, vol.136
, pp. 337-340
-
-
Skali Dahbi, S.1
Zuohair, K.2
Moutawakil, B.3
-
36
-
-
0037701447
-
Traitement de l'erythermalgie familiale par l'association lidocaïne-mexilétine
-
E Legroux-Crespel B Sassolas G Guillet, et al. 2003 Treatment of familial erythermalgia with the association of lidocaine and mexiletine Ann Dermatol Venereol 130 429 433 12843854 1:STN:280:DC%2BD3szhtlSnsw%3D%3D (Pubitemid 36723273)
-
(2003)
Annales de Dermatologie et de Venereologie
, vol.130
, Issue.4
, pp. 429-433
-
-
Legroux-Crespel, E.1
Sassolas, B.2
Guillet, G.3
Kupfer, I.4
Dupre, D.5
Misery, L.6
-
37
-
-
72549113013
-
Treatment with carbamazepine and gabapentine of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in the SCN9A gene, encoding a voltage-gated sodium channel
-
19549232 10.1111/j.1365-2230.2009.03355.x 1:STN:280: DC%2BC3c%2FhtVGhtg%3D%3D
-
J Natkunarajah D Atherton F Elmslie, et al. 2009 Treatment with carbamazepine and gabapentine of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in the SCN9A gene, encoding a voltage-gated sodium channel Clin Exp Dermatol 34 e640 e642 19549232 10.1111/j.1365-2230.2009.03355.x 1:STN:280:DC%2BC3c%2FhtVGhtg%3D%3D
-
(2009)
Clin Exp Dermatol
, vol.34
-
-
Natkunarajah, J.1
Atherton, D.2
Elmslie, F.3
-
38
-
-
34548414786
-
Rectal, ocular and submandibular pain
-
1:STN:280:DyaG1M%2Fms1ejtQ%3D%3D
-
R Hayden M Grossman 1959 Rectal, ocular and submandibular pain Am J Dis Child 97 479 482 1:STN:280:DyaG1M%2Fms1ejtQ%3D%3D
-
(1959)
Am J Dis Child
, vol.97
, pp. 479-482
-
-
Hayden, R.1
Grossman, M.2
-
39
-
-
34548446384
-
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)
-
DOI 10.1212/01.wnl.0000268065.16865.5f, PII 0000611420070807000012
-
CR Fertleman CD Ferrie J Aicardi, et al. 2007 Paroxysmal extreme pain disorder (previously familial rectal pain syndrome) Neurology 69 586 595 17679678 10.1212/01.wnl.0000268065.16865.5f 1:STN:280:DC%2BD2svmt1SntA%3D%3D (Pubitemid 47357266)
-
(2007)
Neurology
, vol.69
, Issue.6
, pp. 586-595
-
-
Fertleman, C.R.1
Ferrie, C.D.2
Aicardi, J.3
Bednarek, N.A.F.4
Eeg-Olofsson, O.5
Elmslie, F.V.6
Griesemer, D.A.7
Goutieres, F.8
Kirkpatrick, M.9
Malmros, I.N.O.10
Pollitzer, M.11
Rossiter, M.12
Roulet-Perez, E.13
Schubert, R.14
Smith, V.V.15
Testard, H.16
Wong, V.17
Stephenson, J.B.P.18
-
40
-
-
33847168937
-
SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
-
DOI 10.1016/j.neuron.2006.10.006, PII S0896627306008051
-
CR Fertleman MD Baker KA Parker, et al. 2006 SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes Neuron 52 767 774 17145499 10.1016/j.neuron.2006.10.006 1:CAS:528:DC%2BD28XhtlCgu7fJ (Pubitemid 44828442)
-
(2006)
Neuron
, vol.52
, Issue.5
, pp. 767-774
-
-
Fertleman, C.R.1
Baker, M.D.2
Parker, K.A.3
Moffatt, S.4
Elmslie, F.V.5
Abrahamsen, B.6
Ostman, J.7
Klugbauer, N.8
Wood, J.N.9
Gardiner, R.M.10
Rees, M.11
-
41
-
-
53349171632
-
Paroxysmal extreme pain disorder M1627K mutation in human NaV1.7 renders DRG neurons hyperexcitable
-
18803825 10.1186/1744-8069-4-37
-
SD Dib-Hajj M Estacion BW Jarecki, et al. 2008 Paroxysmal extreme pain disorder M1627K mutation in human NaV1.7 renders DRG neurons hyperexcitable Mol Pain 4 37 18803825 10.1186/1744-8069-4-37
-
(2008)
Mol Pain
, vol.4
, pp. 37
-
-
Dib-Hajj, S.D.1
Estacion, M.2
Jarecki, B.W.3
-
43
-
-
79251569257
-
NaV1.7 mutations associated with paroxysmal extreme pain disorder, but not erythromelalgia, enhance NaV β4 peptide-mediated resurgent sodium currents
-
21115638 10.1113/jphysiol.2010.200915 1:CAS:528:DC%2BC3MXksFOltbw%3D
-
JW Theile BW Jarecki AD Piekarz TR Cummins 2011 NaV1.7 mutations associated with paroxysmal extreme pain disorder, but not erythromelalgia, enhance NaV β4 peptide-mediated resurgent sodium currents J Physiol 589 597 608 21115638 10.1113/jphysiol.2010.200915 1:CAS:528:DC%2BC3MXksFOltbw%3D
-
(2011)
J Physiol
, vol.589
, pp. 597-608
-
-
Theile, J.W.1
Jarecki, B.W.2
Piekarz, A.D.3
Cummins, T.R.4
-
44
-
-
58149154859
-
NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders
-
v1.7mutaion causing mixed IEM-PEPD phenotype, suggesting that these two syndromes are a physiologic continuum
-
v1.7mutaion causing mixed IEM-PEPD phenotype, suggesting that these two syndromes are a physiologic continuum
-
(2008)
J Neurosci
, vol.28
, pp. 11079-11088
-
-
Estacion, M.1
Dib-Hajj, S.D.2
Benke, P.J.3
-
45
-
-
78751582171
-
Chronic non-paroxysmal neuropathic pain - Novel mutation in the sodium channel SCN9A gene
-
21094958 10.1016/j.jns.2010.10.006 1:CAS:528:DC%2BC3MXmsFeqtA%3D%3D This is the first description of a patient with NaV1.7 mutation causing non-paroxysmal chronic painful syndrome
-
R Dabby M Sadeh R Gilad, et al. 2011 Chronic non-paroxysmal neuropathic pain - novel mutation in the sodium channel SCN9A gene J Neurol Sci 301 90 92 21094958 10.1016/j.jns.2010.10.006 1:CAS:528:DC%2BC3MXmsFeqtA%3D%3D This is the first description of a patient with NaV1.7 mutation causing non-paroxysmal chronic painful syndrome
-
(2011)
J Neurol Sci
, vol.301
, pp. 90-92
-
-
Dabby, R.1
Sadeh, M.2
Gilad, R.3
-
47
-
-
0000282772
-
A case of congenital pure analgesia
-
10.1097/00005053-193206000-00002
-
G Dearborn 1932 A case of congenital pure analgesia J Nerv Ment dis 75 612 615 10.1097/00005053-193206000-00002
-
(1932)
J Nerv Ment Dis
, vol.75
, pp. 612-615
-
-
Dearborn, G.1
-
48
-
-
33845901486
-
An SCN9A channelopathy causes congenital inability to experience pain
-
DOI 10.1038/nature05413, PII NATURE05413
-
JJ Cox F Reimann AK Nicholas, et al. 2006 An SCN9A channelopathy causes congenital inability to experience pain Nature 444 894 898 17167479 10.1038/nature05413 1:CAS:528:DC%2BD28XhtlShtrzM (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
-
49
-
-
34548419652
-
A stop codon mutation in SCN9A causes lack of pain sensation
-
DOI 10.1093/hmg/ddm160
-
S Ahmad L Dahllund AB Eriksson, et al. 2007 A stop codon mutation in SCN9A causes lack of pain sensation Hum Mol Genet 16 2114 2121 17597096 10.1093/hmg/ddm160 1:CAS:528:DC%2BD2sXpvVWqt7o%3D (Pubitemid 47354894)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.17
, pp. 2114-2121
-
-
Ahmad, S.1
Dahllund, L.2
Eriksson, A.B.3
Hellgren, D.4
Karlsson, U.5
Lund, P.-E.6
Meijer, I.A.7
Meury, L.8
Mills, T.9
Moody, A.10
Morinville, A.11
Morten, J.12
O'Donnell, D.13
Raynoschek, C.14
Salter, H.15
Rouleau, G.A.16
Krupp, J.J.17
-
50
-
-
34247874778
-
v1.7 gene underlie congenital indifference to pain in multiple human populations
-
DOI 10.1111/j.1399-0004.2007.00790.x
-
YP Goldberg J MacFarlane ML MacDonald, et al. 2007 Loss-of-function mutations in the NaV1.7 gene underlie congenital indifference to pain in multiple human populations Clin Genet 71 311 319 17470132 10.1111/j.1399-0004. 2007.00790.x 1:STN:280:DC%2BD2s3mtFSqsg%3D%3D (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..
|