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Results: 1 to 20 of 91

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1.

Idiopathic small fiber neuropathy: phenotype, etiologies, and the search for fabry disease.

Samuelsson K, Kostulas K, Vrethem M, Rolfs A, Press R.

J Clin Neurol. 2014 Apr;10(2):108-18. doi: 10.3988/jcn.2014.10.2.108. Epub 2014 Apr 23.

2.

Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young.

De Brabander I, Yperzeele L, Ceuterick-De Groote C, Brouns R, Baker R, Belachew S, Delbecq J, De Keulenaer G, Dethy S, Eyskens F, Fumal A, Hemelsoet D, Hughes D, Jeangette S, Nuytten D, Redondo P, Sadzot B, Sindic C, Sheorajpanday R, Thijs V, Van Broeckhoven C, De Deyn PP.

Clin Neurol Neurosurg. 2013 Jul;115(7):1088-93. doi: 10.1016/j.clineuro.2012.11.003. Epub 2012 Dec 4.

PMID:
23219219
3.

Gain of function Naν1.7 mutations in idiopathic small fiber neuropathy.

Faber CG, Hoeijmakers JG, Ahn HS, Cheng X, Han C, Choi JS, Estacion M, Lauria G, Vanhoutte EK, Gerrits MM, Dib-Hajj S, Drenth JP, Waxman SG, Merkies IS.

Ann Neurol. 2012 Jan;71(1):26-39. doi: 10.1002/ana.22485. Epub 2011 Jun 22.

PMID:
21698661
4.

Non-length dependent small fiber neuropathy. a prospective case series.

Gemignani F, Giovanelli M, Vitetta F, Santilli D, Bellanova MF, Brindani F, Marbini A.

J Peripher Nerv Syst. 2010 Mar;15(1):57-62. doi: 10.1111/j.1529-8027.2010.00252.x.

PMID:
20433606
5.

Mutations of the GLA gene in young patients with stroke: the PORTYSTROKE study--screening genetic conditions in Portuguese young stroke patients.

Baptista MV, Ferreira S, Pinho-E-Melo T, Carvalho M, Cruz VT, Carmona C, Silva FA, Tuna A, Rodrigues M, Ferreira C, Pinto AA, Leitão A, Gabriel JP, Calado S, Oliveira JP, Ferro JM; PORTuguese Young STROKE Investigators.

Stroke. 2010 Mar;41(3):431-6. doi: 10.1161/STROKEAHA.109.570499. Epub 2010 Jan 28.

6.

Impaired small fiber conduction in patients with Fabry disease: a neurophysiological case-control study.

Üçeyler N, Kahn AK, Kramer D, Zeller D, Casanova-Molla J, Wanner C, Weidemann F, Katsarava Z, Sommer C.

BMC Neurol. 2013 May 24;13:47. doi: 10.1186/1471-2377-13-47.

7.

Cryptogenic stroke and small fiber neuropathy of unknown etiology in patients with alpha-galactosidase A -10T genotype.

Schelleckes M, Lenders M, Guske K, Schmitz B, Tanislav C, Ständer S, Metze D, Katona I, Weis J, Brand SM, Duning T, Brand E.

Orphanet J Rare Dis. 2014 Nov 26;9:178. doi: 10.1186/s13023-014-0178-5.

8.

The value of skin biopsy with recording of intraepidermal nerve fiber density and quantitative sensory testing in the assessment of small fiber involvement in patients with different causes of polyneuropathy.

Nebuchennykh M, Løseth S, Lindal S, Mellgren SI.

J Neurol. 2009 Jul;256(7):1067-75. doi: 10.1007/s00415-009-5065-y. Epub 2009 Mar 1. Erratum in: J Neurol. 2009 Jun;256(6):1034.

PMID:
19252773
9.

Elevated proinflammatory cytokine expression in affected skin in small fiber neuropathy.

Uçeyler N, Kafke W, Riediger N, He L, Necula G, Toyka KV, Sommer C.

Neurology. 2010 Jun 1;74(22):1806-13. doi: 10.1212/WNL.0b013e3181e0f7b3.

PMID:
20513817
10.

The diagnostic criteria for small fibre neuropathy: from symptoms to neuropathology.

Devigili G, Tugnoli V, Penza P, Camozzi F, Lombardi R, Melli G, Broglio L, Granieri E, Lauria G.

Brain. 2008 Jul;131(Pt 7):1912-25. doi: 10.1093/brain/awn093. Epub 2008 Jun 4.

11.

Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study.

Tanislav C, Kaps M, Rolfs A, Böttcher T, Lackner K, Paschke E, Mascher H, Laue M, Blaes F.

Eur J Neurol. 2011 Apr;18(4):631-6. doi: 10.1111/j.1468-1331.2010.03227.x. Epub 2010 Sep 23.

PMID:
20860754
12.

Utility of skin biopsy in management of small fiber neuropathy.

Boruchow SA, Gibbons CH.

Muscle Nerve. 2013 Dec;48(6):877-82. doi: 10.1002/mus.23859. Epub 2013 Sep 11.

PMID:
23553795
13.

Small fiber dysfunction predominates in Fabry neuropathy.

Dütsch M, Marthol H, Stemper B, Brys M, Haendl T, Hilz MJ.

J Clin Neurophysiol. 2002 Dec;19(6):575-86.

PMID:
12488789
14.

Sjögren Syndrome-Associated Small Fiber Neuropathy: Characterization From a Prospective Series of 40 Cases.

Sène D, Cacoub P, Authier FJ, Haroche J, Créange A, Saadoun D, Amoura Z, Guillausseau PJ, Lefaucheur JP.

Medicine (Baltimore). 2013 Aug 26. [Epub ahead of print]

PMID:
23982054
15.

Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability.

Han C, Hoeijmakers JG, Ahn HS, Zhao P, Shah P, Lauria G, Gerrits MM, te Morsche RH, Dib-Hajj SD, Drenth JP, Faber CG, Merkies IS, Waxman SG.

Neurology. 2012 May 22;78(21):1635-43. doi: 10.1212/WNL.0b013e3182574f12. Epub 2012 Apr 25.

PMID:
22539570
16.

Value of the oral glucose tolerance test in the evaluation of chronic idiopathic axonal polyneuropathy.

Hoffman-Snyder C, Smith BE, Ross MA, Hernandez J, Bosch EP.

Arch Neurol. 2006 Aug;63(8):1075-9. Epub 2006 Jun 12.

PMID:
16769858
17.

Microneurographic evaluation of sympathetic activity in small fiber neuropathy.

Liguori R, Giannoccaro MP, Di Stasi V, Pizza F, Cortelli P, Baruzzi A, Montagna P, Donadio V.

Clin Neurophysiol. 2011 Sep;122(9):1854-9. doi: 10.1016/j.clinph.2011.02.024. Epub 2011 Mar 23.

PMID:
21435945
18.

Contribution of QSART to the diagnosis of small fiber neuropathy.

Thaisetthawatkul P, Fernandes Filho JA, Herrmann DN.

Muscle Nerve. 2013 Dec;48(6):883-8. doi: 10.1002/mus.23891. Epub 2013 Oct 4.

PMID:
23649502
19.

Autonomic neuropathy in Fabry disease: a prospective study using the Autonomic Symptom Profile and cardiovascular autonomic function tests.

Biegstraaten M, van Schaik IN, Wieling W, Wijburg FA, Hollak CE.

BMC Neurol. 2010 Jun 7;10:38. doi: 10.1186/1471-2377-10-38.

20.

Association of HLA DQB1 0602 in sarcoidosis patients with small fiber neuropathy.

Voorter CE, Drent M, Hoitsma E, Faber KG, van den Berg-Loonen EM.

Sarcoidosis Vasc Diffuse Lung Dis. 2005 Jun;22(2):129-32.

PMID:
16053028
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