-
1
-
-
22944490864
-
Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia
-
Burns TM, Te Morsche RH, Jansen JB et al. Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia. Br J Dermatol 2005; 153: 174-177.
-
(2005)
Br J Dermatol
, vol.153
, pp. 174-177
-
-
Burns, T.M.1
Te Morsche, R.H.2
Jansen, J.B.3
-
2
-
-
0036310758
-
An expanding view for the molecular basis of familial periodic paralysis
-
Cannon SC. An expanding view for the molecular basis of familial periodic paralysis. Neuromuscul Disord 2002; 12: 533-543.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 533-543
-
-
Cannon, S.C.1
-
3
-
-
4644268452
-
Electrophysiological properties of mutant Nav 1.7 sodium channels in a painful inherited neuropathy
-
Cummins TR, Dib-Hajj SD, Waxman SG. Electrophysiological properties of mutant Nav 1.7 sodium channels in a painful inherited neuropathy. J Neurosci 2004; 24: 8232-8236.
-
(2004)
J Neurosci
, vol.24
, pp. 8232-8236
-
-
Cummins, T.R.1
Dib-Hajj, S.D.2
Waxman, S.G.3
-
4
-
-
33746898642
-
Histopathologic findings in primary erythromelalgia are nonspecific: Special studies show a decrease in small nerve fiber density
-
Davis MD, Weenig RH, Genebriera J et al. Histopathologic findings in primary erythromelalgia are nonspecific: special studies show a decrease in small nerve fiber density. J Am Acad Dermatol 2006; 55: 519-522.
-
(2006)
J Am Acad Dermatol
, vol.55
, pp. 519-522
-
-
Davis, M.D.1
Weenig, R.H.2
Genebriera, J.3
-
5
-
-
33747600396
-
Between episodes of erythromelalgia: A spectrum of colors
-
Davis MD, Wilkins F, Rooke TW. Between episodes of erythromelalgia: a spectrum of colors. Arch Dermatol 2006; 142: 1085-1086.
-
(2006)
Arch Dermatol
, vol.142
, pp. 1085-1086
-
-
Davis, M.D.1
Wilkins, F.2
Rooke, T.W.3
-
7
-
-
0141960942
-
Erythromelalgia: Vasculopathy, neuropathy, or both? A prospective study of vascular and neurophysiologic studies in erythromelalgia
-
Davis MD, Sandroni P, Rooke TW et al. Erythromelalgia: vasculopathy, neuropathy, or both? A prospective study of vascular and neurophysiologic studies in erythromelalgia. Arch Dermatol 2003; 139: 1337-1343.
-
(2003)
Arch Dermatol
, vol.139
, pp. 1337-1343
-
-
Davis, M.D.1
Sandroni, P.2
Rooke, T.W.3
-
8
-
-
0034014898
-
-
rd et al. Natural history of erythromelalgia: presentation and outcome in 168 patients. Arch Dermatol 2000; 136: 330-336.
-
rd et al. Natural history of erythromelalgia: presentation and outcome in 168 patients. Arch Dermatol 2000; 136: 330-336.
-
-
-
-
9
-
-
23444443202
-
Gain-of-function mutation in Nav 1.7 in familial erythromelalgia induces bursting of sensory neurons
-
Dib-Hajj SD, Rush AM, Cummins TR. Gain-of-function mutation in Nav 1.7 in familial erythromelalgia induces bursting of sensory neurons. Brain 2005; 128: 1847-1854.
-
(2005)
Brain
, vol.128
, pp. 1847-1854
-
-
Dib-Hajj, S.D.1
Rush, A.M.2
Cummins, T.R.3
-
10
-
-
0037440084
-
Sensory and electrophysiological properties of guinea-pig sensory neurones expressing Nav 1.7 (PN1) Na+ channel alpha subunit protein
-
Djouhri L, Newton R, Levinson SR et al. Sensory and electrophysiological properties of guinea-pig sensory neurones expressing Nav 1.7 (PN1) Na+ channel alpha subunit protein. J Physiol 2003; 546: 565-576.
-
(2003)
J Physiol
, vol.546
, pp. 565-576
-
-
Djouhri, L.1
Newton, R.2
Levinson, S.R.3
-
11
-
-
20544476041
-
SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels
-
Drenth JP, te Morsche RH, Guillet G et al. SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. J Invest Dermatol 2005; 124: 1333-1338.
-
(2005)
J Invest Dermatol
, vol.124
, pp. 1333-1338
-
-
Drenth, J.P.1
te Morsche, R.H.2
Guillet, G.3
-
12
-
-
0035023041
-
The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32
-
Drenth JP, Finley WH, Breedveld GJ et al. The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32. Am J Hum Genet 2001; 68: 1277-1282.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1277-1282
-
-
Drenth, J.P.1
Finley, W.H.2
Breedveld, G.J.3
-
14
-
-
0028236198
-
Erythromelalgia and erythermalgia: Diagnostic differentiation
-
Drenth JP, Michiels JJ. Erythromelalgia and erythermalgia: diagnostic differentiation. Int J Dermatol 1994; 33: 393-397.
-
(1994)
Int J Dermatol
, vol.33
, pp. 393-397
-
-
Drenth, J.P.1
Michiels, J.J.2
-
15
-
-
0033784876
-
Channelopathies: Ion channel defects linked to heritable clinical disorders
-
Felix R. Channelopathies: Ion channel defects linked to heritable clinical disorders. J Med Genet 2000; 37: 729-740.
-
(2000)
J Med Genet
, vol.37
, pp. 729-740
-
-
Felix, R.1
-
16
-
-
33644826050
-
Sporadic on-set of erythermalgia: A gain-of-function mutation in Nav1.7
-
Han C, Rush AM, Dib-Hajj SD et al. Sporadic on-set of erythermalgia: a gain-of-function mutation in Nav1.7. Ann Neurol 2006; 59: 553-558.
-
(2006)
Ann Neurol
, vol.59
, pp. 553-558
-
-
Han, C.1
Rush, A.M.2
Dib-Hajj, S.D.3
-
18
-
-
0345689648
-
Prostacyclin reduces symptoms and sympathetic dysfunction in erythromelalgia in a double-blind randomized pilot study
-
Kalgaard OM, Mork C, Kvernebo K. Prostacyclin reduces symptoms and sympathetic dysfunction in erythromelalgia in a double-blind randomized pilot study. Acta Derm Venereol 2003; 83: 442-444.
-
(2003)
Acta Derm Venereol
, vol.83
, pp. 442-444
-
-
Kalgaard, O.M.1
Mork, C.2
Kvernebo, K.3
-
19
-
-
0028985863
-
Structure and functional expression of a new member of the tetrodotoxin-sensitive voltage-activated sodium channel family from human neuroendocrine cells
-
Klugbauer N, Lacinova L, Flockerzi V et al. Structure and functional expression of a new member of the tetrodotoxin-sensitive voltage-activated sodium channel family from human neuroendocrine cells. EMBO J 1995; 14: 1084-1090.
-
(1995)
EMBO J
, vol.14
, pp. 1084-1090
-
-
Klugbauer, N.1
Lacinova, L.2
Flockerzi, V.3
-
20
-
-
0042237710
-
Neurological disorders caused by inherited ion-channel mutations
-
Kullmann DM, Hanna MG. Neurological disorders caused by inherited ion-channel mutations. Lancet Neurol 2002; 1: 157-166.
-
(2002)
Lancet Neurol
, vol.1
, pp. 157-166
-
-
Kullmann, D.M.1
Hanna, M.G.2
-
21
-
-
0023065182
-
Erythromelalgia - pathophysiological and therapeutic aspects. A preliminary report
-
Kvernebo K, Seem E. Erythromelalgia - pathophysiological and therapeutic aspects. A preliminary report. J Oslo City Hosp 1987; 37: 9-12.
-
(1987)
J Oslo City Hosp
, vol.37
, pp. 9-12
-
-
Kvernebo, K.1
Seem, E.2
-
22
-
-
0032823307
-
Voltage-gated ion channels and hereditary disease
-
Lehmann-Horn F, Jurkat-Rott K. Voltage-gated ion channels and hereditary disease. Physiol Rev 1999; 79: 1317-1372.
-
(1999)
Physiol Rev
, vol.79
, pp. 1317-1372
-
-
Lehmann-Horn, F.1
Jurkat-Rott, K.2
-
23
-
-
15744368453
-
Ion channel defects in idiopathic epilepsies
-
Lerche H, Weber YG, Jurkat-Rott K et al. Ion channel defects in idiopathic epilepsies. Curr Pharm Des 2005; 11: 2737-2752.
-
(2005)
Curr Pharm Des
, vol.11
, pp. 2737-2752
-
-
Lerche, H.1
Weber, Y.G.2
Jurkat-Rott, K.3
-
24
-
-
0032956913
-
Impaired skin vasomotor reflexes in patients with erythromelalgia
-
Littleford RC, Khan F, Belch JJ. Impaired skin vasomotor reflexes in patients with erythromelalgia. Clin Sci (Lond) 1999; 96: 507-512.
-
(1999)
Clin Sci (Lond)
, vol.96
, pp. 507-512
-
-
Littleford, R.C.1
Khan, F.2
Belch, J.J.3
-
26
-
-
26444466085
-
Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7
-
Michiels JJ, te Morsche RH, Jansen JB et al. Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7. Arch Neurol 2005; 62: 1587-1590.
-
(2005)
Arch Neurol
, vol.62
, pp. 1587-1590
-
-
Michiels, J.J.1
te Morsche, R.H.2
Jansen, J.B.3
-
27
-
-
0028287711
-
Erythromelalgia and erythermalgia: Lumpers and splitters
-
Michiels JJ, Drenth JP. Erythromelalgia and erythermalgia: lumpers and splitters. Int J Dermatol 1994; 33: 412-413.
-
(1994)
Int J Dermatol
, vol.33
, pp. 412-413
-
-
Michiels, J.J.1
Drenth, J.P.2
-
28
-
-
0002044612
-
On a rare vaso-motor neurosis of the extremities, and on the maladies with which it may be confounded
-
Mitchell SW. On a rare vaso-motor neurosis of the extremities, and on the maladies with which it may be confounded. Am J Med Sci 1878; 76.
-
(1878)
Am J Med Sci
, pp. 76
-
-
Mitchell, S.W.1
-
29
-
-
0033998444
-
Microvascular arteriovenous shunting is a probable pathogenetic mechanism in erythromelalgia
-
Mork C, Asker CL, Salerud EG et al. Microvascular arteriovenous shunting is a probable pathogenetic mechanism in erythromelalgia. J Invest Dermatol 2000; 114: 643-646.
-
(2000)
J Invest Dermatol
, vol.114
, pp. 643-646
-
-
Mork, C.1
Asker, C.L.2
Salerud, E.G.3
-
30
-
-
1842740341
-
The prostaglandin E1 analog misoprostol reduces symptoms and microvascular arteriovenous shunting in erythromelalgia-a double-blind, crossover, placebo-compared study
-
Mork C, Salerud EG, Asker CL et al. The prostaglandin E1 analog misoprostol reduces symptoms and microvascular arteriovenous shunting in erythromelalgia-a double-blind, crossover, placebo-compared study. J Invest Dermatol 2004; 122: 587-593.
-
(2004)
J Invest Dermatol
, vol.122
, pp. 587-593
-
-
Mork, C.1
Salerud, E.G.2
Asker, C.L.3
-
31
-
-
18744372718
-
Reduced skin capillary density during attacks of erythromelalgia implies arteriovenous shunting as pathogenetic mechanism
-
Mørk C, Kvernebo K, Asker CL, Salerud EG. Reduced skin capillary density during attacks of erythromelalgia implies arteriovenous shunting as pathogenetic mechanism. J Invest Dermatol 2002; 119: 949-953.
-
(2002)
J Invest Dermatol
, vol.119
, pp. 949-953
-
-
Mørk, C.1
Kvernebo, K.2
Asker, C.L.3
Salerud, E.G.4
-
32
-
-
4344670206
-
Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain
-
Nassar MA, Stirling LC, Forlani G et al. Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain. Proc Natl Acad Sci USA 2004; 101: 12706-12711.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 12706-12711
-
-
Nassar, M.A.1
Stirling, L.C.2
Forlani, G.3
-
33
-
-
33645100226
-
Combination gel of 1% amitriptyline and 0.5% ketamine to treat refractory erythromelalgia pain: A new treatment option?
-
Sandroni P, Davis MD. Combination gel of 1% amitriptyline and 0.5% ketamine to treat refractory erythromelalgia pain: a new treatment option? Arch Dermatol 2006; 142: 283-286.
-
(2006)
Arch Dermatol
, vol.142
, pp. 283-286
-
-
Sandroni, P.1
Davis, M.D.2
-
34
-
-
12644256626
-
A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia
-
Sangameswaran L, Fish LM, Koch BD et al. A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia. J Biol Chem 1997; 272: 14805-14809.
-
(1997)
J Biol Chem
, vol.272
, pp. 14805-14809
-
-
Sangameswaran, L.1
Fish, L.M.2
Koch, B.D.3
-
35
-
-
0011018095
-
Erythermalgia (erythromelalgia) of the extremities: A syndrome characterized by redness, heat, and pain
-
Smith LA, Allen EV. Erythermalgia (erythromelalgia) of the extremities: a syndrome characterized by redness, heat, and pain. Am Heart J 1938; 16: 175-188.
-
(1938)
Am Heart J
, vol.16
, pp. 175-188
-
-
Smith, L.A.1
Allen, E.V.2
-
36
-
-
85047693453
-
Erythromelalgia as a form of neuropathy
-
Staub DB, Munger BL, Uno H et al. Erythromelalgia as a form of neuropathy Arch Dermatol 1992; 128: 1654-1655.
-
(1992)
Arch Dermatol
, vol.128
, pp. 1654-1655
-
-
Staub, D.B.1
Munger, B.L.2
Uno, H.3
-
37
-
-
0026352188
-
Primary erythromelalgia: The role of skin sympathetic nerve activity
-
Sugiyama Y, Hakusui S, Takahashi A et al. Primary erythromelalgia: the role of skin sympathetic nerve activity. Jpn J Med 1991; 30: 564-567.
-
(1991)
Jpn J Med
, vol.30
, pp. 564-567
-
-
Sugiyama, Y.1
Hakusui, S.2
Takahashi, A.3
-
38
-
-
12644288297
-
Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons
-
Toledo-Aral JJ, Moss BL, He ZJ et al. Identification of PN1, a predominant voltage-dependent sodium channel expressed principally in peripheral neurons. Proc Natl Acad Sci USA 1997; 94: 1527-1532.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 1527-1532
-
-
Toledo-Aral, J.J.1
Moss, B.L.2
He, Z.J.3
-
39
-
-
0020684659
-
Autonomic innervation of the skin in primary erythermalgia
-
Uno H, Parker F. Autonomic innervation of the skin in primary erythermalgia. Arch Dermatol 1983; 119: 65-71.
-
(1983)
Arch Dermatol
, vol.119
, pp. 65-71
-
-
Uno, H.1
Parker, F.2
-
40
-
-
0029847674
-
Erythromelalgia in essential thrombocythemia is characterized by platelet activation and endothelial cell damage but not by thrombin generation
-
Van Genderen PJ, Lucas IS, van Strik R et al. Erythromelalgia in essential thrombocythemia is characterized by platelet activation and endothelial cell damage but not by thrombin generation. Thromb Haemost 1996; 76: 333-338.
-
(1996)
Thromb Haemost
, vol.76
, pp. 333-338
-
-
Van Genderen, P.J.1
Lucas, I.S.2
van Strik, R.3
-
41
-
-
20444408342
-
Erythromelalgia: A hereditary pain syndrome enters the molecular era
-
Waxman SG, Dib-Hajj SD. Erythromelalgia: a hereditary pain syndrome enters the molecular era. Ann Neurol 2005; 57: 785-788.
-
(2005)
Ann Neurol
, vol.57
, pp. 785-788
-
-
Waxman, S.G.1
Dib-Hajj, S.D.2
-
42
-
-
12144288410
-
Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia
-
Yang Y, Wang Y, Li S et al. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. J Med Genet 2004; 41: 171-174.
-
(2004)
J Med Genet
, vol.41
, pp. 171-174
-
-
Yang, Y.1
Wang, Y.2
Li, S.3
|