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Items: 1 to 50 of 113

1.

Genetic predisposition in anti-LGI1 and anti-NMDA receptor encephalitis.

Mueller SH, Färber A, Prüss H, Melzer N, Golombeck KS, Kümpfel T, Thaler F, Elisak M, Lewerenz J, Kaufmann M, Sühs KW, Ringelstein M, Kellinghaus C, Bien CG, Kraft A, Zettl UK, Ehrlich S, Handreka R, Rostásy K, Then Bergh F, Faiss JH, Lieb W, Franke A, Kuhlenbäumer G, Wandinger KP, Leypoldt F; German Network for Research on Autoimmune Encephalitis (GENERATE).

Ann Neurol. 2018 Apr;83(4):863-869. doi: 10.1002/ana.25216.

PMID:
29572931
2.

[Genetics of tremor].

Kuhlenbäumer G, Hopfner F.

Nervenarzt. 2018 Apr;89(4):416-422. doi: 10.1007/s00115-017-0478-9. Review. German.

PMID:
29327099
3.

c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia.

Shalash AS, Rösler TW, Müller SH, Salama M, Deuschl G, Müller U, Opladen T, Petersen BS, Franke A, Hopfner F, Kuhlenbäumer G, Höglinger GU.

Neurol Genet. 2017 Nov 1;3(6):e197. doi: 10.1212/NXG.0000000000000197. eCollection 2017 Dec.

4.

Gut microbiota in Parkinson disease in a northern German cohort.

Hopfner F, Künstner A, Müller SH, Künzel S, Zeuner KE, Margraf NG, Deuschl G, Baines JF, Kuhlenbäumer G.

Brain Res. 2017 Jul 15;1667:41-45. doi: 10.1016/j.brainres.2017.04.019. Epub 2017 May 12.

PMID:
28506555
5.

Topography of essential tremor.

Chen W, Hopfner F, Szymczak S, Granert O, Müller SH, Kuhlenbäumer G, Deuschl G.

Parkinsonism Relat Disord. 2017 Jul;40:58-63. doi: 10.1016/j.parkreldis.2017.04.012. Epub 2017 Apr 20.

PMID:
28442304
6.

Genome-wide association study in essential tremor identifies three new loci.

Müller SH, Girard SL, Hopfner F, Merner ND, Bourassa CV, Lorenz D, Clark LN, Tittmann L, Soto-Ortolaza AI, Klebe S, Hallett M, Schneider SA, Hodgkinson CA, Lieb W, Wszolek ZK, Pendziwiat M, Lorenzo-Betancor O, Poewe W, Ortega-Cubero S, Seppi K, Rajput A, Hussl A, Rajput AH, Berg D, Dion PA, Wurster I, Shulman JM, Srulijes K, Haubenberger D, Pastor P, Vilariño-Güell C, Postuma RB, Bernard G, Ladwig KH, Dupré N, Jankovic J, Strauch K, Panisset M, Winkelmann J, Testa CM, Reischl E, Zeuner KE, Ross OA, Arzberger T, Chouinard S, Deuschl G, Louis ED, Kuhlenbäumer G, Rouleau GA.

Brain. 2016 Dec;139(Pt 12):3163-3169. Epub 2016 Oct 20.

7.

Knowledge gaps and research recommendations for essential tremor.

Hopfner F, Haubenberger D, Galpern WR, Gwinn K, Van't Veer A, White S, Bhatia K, Adler CH, Eidelberg D, Ondo W, Stebbins GT, Tanner CM, Helmich RC, Lenz FA, Sillitoe RV, Vaillancourt D, Vitek JL, Louis ED, Shill HA, Frosch MP, Foroud T, Kuhlenbäumer G, Singleton A, Testa CM, Hallett M, Elble R, Deuschl G.

Parkinsonism Relat Disord. 2016 Dec;33:27-35. doi: 10.1016/j.parkreldis.2016.10.002. Epub 2016 Oct 4. Review.

8.

Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy.

Verdura E, Hervé D, Bergametti F, Jacquet C, Morvan T, Prieto-Morin C, Mackowiak A, Manchon E, Hosseini H, Cordonnier C, Girard-Buttaz I, Rosenstingl S, Hagel C, Kuhlenbaümer G, Leca-Radu E, Goux D, Fleming L, Van Agtmael T, Chabriat H, Chapon F, Tournier-Lasserve E.

Ann Neurol. 2016 Nov;80(5):741-753. doi: 10.1002/ana.24782. Epub 2016 Oct 19.

PMID:
27666438
9.

Early- and late-onset essential tremor patients represent clinically distinct subgroups.

Hopfner F, Ahlf A, Lorenz D, Klebe S, Zeuner KE, Kuhlenbäumer G, Deuschl G.

Mov Disord. 2016 Oct;31(10):1560-1566. doi: 10.1002/mds.26708.

PMID:
27384030
10.

Early-onset parkinsonism due to compound heterozygous POLG mutations.

Rempe T, Kuhlenbäumer G, Krüger S, Biskup S, Matschke J, Hagel C, Deuschl G, van Eimeren T.

Parkinsonism Relat Disord. 2016 Aug;29:135-7. doi: 10.1016/j.parkreldis.2016.04.020. Epub 2016 Apr 27. No abstract available.

PMID:
27185166
11.

Alpha synuclein and crystallin expression in human lens in Parkinson's disease.

Klettner A, Richert E, Kuhlenbäumer G, Nölle B, Bhatia KP, Deuschl G, Roider J, Schneider SA.

Mov Disord. 2016 Apr;31(4):600-1. doi: 10.1002/mds.26557. Epub 2016 Feb 16. Review. No abstract available.

PMID:
26880170
12.

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.

Klein KM, Pendziwiat M, Cohen R, Appenzeller S, de Kovel CG, Rosenow F, Koeleman BP, Kuhlenbäumer G, Sheintuch L, Veksler R, Friedman A, Afawi Z, Helbig I.

J Neurol. 2016 Jan;263(1):11-6. doi: 10.1007/s00415-015-7921-2. Epub 2015 Oct 12.

PMID:
26459092
13.

Validation of the QUEST for German-speaking countries.

Hopfner F, Nebel A, Lyons KE, Tröster AI, Kuhlenbäumer G, Deuschl G, Martinez-Martin P.

Int J Neurosci. 2016;126(2):127-34. doi: 10.3109/00207454.2015.1077241. Epub 2015 Aug 25.

PMID:
26327253
14.

Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution.

Berse T, Rolfes K, Barenberg J, Dutke S, Kuhlenbäumer G, Völker K, Winter B, Wittig M, Knecht S.

Front Behav Neurosci. 2015 Jul 28;9:196. doi: 10.3389/fnbeh.2015.00196. eCollection 2015.

15.

Testing for alcohol sensitivity of tremor amplitude in a large cohort with essential tremor.

Hopfner F, Erhart T, Knudsen K, Lorenz D, Schneider SA, Zeuner KE, Deuschl G, Kuhlenbäumer G.

Parkinsonism Relat Disord. 2015 Aug;21(8):848-51. doi: 10.1016/j.parkreldis.2015.05.005. Epub 2015 May 14.

PMID:
26002382
16.

Mutations in HTRA2 are not a common cause of familial classic ET.

Hopfner F, Müller SH, Lorenz D, Appenzeller S, Klebe S, Deuschl G, Kuhlenbäumer G.

Mov Disord. 2015 Jul;30(8):1149-50. doi: 10.1002/mds.26252. Epub 2015 May 13. No abstract available.

PMID:
25970799
17.

Determinants of platelet-leukocyte aggregation and platelet activation in stroke.

Schmalbach B, Stepanow O, Jochens A, Riedel C, Deuschl G, Kuhlenbäumer G.

Cerebrovasc Dis. 2015;39(3-4):176-80. doi: 10.1159/000375396. Epub 2015 Feb 26.

PMID:
25720421
18.

The impact of rare variants in FUS in essential tremor.

Hopfner F, Stevanin G, Müller SH, Mundwiller E, Bungeroth M, Durr A, Pendziwiat M, Anheim M, Schneider SA, Tittmann L, Klebe S, Lorenz D, Deuschl G, Brice A, Kuhlenbäumer G.

Mov Disord. 2015 Apr 15;30(5):721-4. doi: 10.1002/mds.26145. Epub 2015 Jan 28.

PMID:
25631824
19.

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

Debette S, Kamatani Y, Metso TM, Kloss M, Chauhan G, Engelter ST, Pezzini A, Thijs V, Markus HS, Dichgans M, Wolf C, Dittrich R, Touzé E, Southerland AM, Samson Y, Abboud S, Béjot Y, Caso V, Bersano A, Gschwendtner A, Sessa M, Cole J, Lamy C, Medeiros E, Beretta S, Bonati LH, Grau AJ, Michel P, Majersik JJ, Sharma P, Kalashnikova L, Nazarova M, Dobrynina L, Bartels E, Guillon B, van den Herik EG, Fernandez-Cadenas I, Jood K, Nalls MA, De Leeuw FE, Jern C, Cheng YC, Werner I, Metso AJ, Lichy C, Lyrer PA, Brandt T, Boncoraglio GB, Wichmann HE, Gieger C, Johnson AD, Böttcher T, Castellano M, Arveiler D, Ikram MA, Breteler MM, Padovani A, Meschia JF, Kuhlenbäumer G, Rolfs A, Worrall BB; International Stroke Genetics Consortium, Ringelstein EB, Zelenika D, Tatlisumak T, Lathrop M, Leys D, Amouyel P, Dallongeville J; CADISP Group.

Nat Genet. 2015 Jan;47(1):78-83. doi: 10.1038/ng.3154. Epub 2014 Nov 24.

20.

Giant Axonal Neuropathy.

Kuhlenbäumer G, Timmerman V, Bomont P.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2003 Jan 9 [updated 2014 Oct 9].

21.

Differential aggregation properties of alpha-synuclein isoforms.

Bungeroth M, Appenzeller S, Regulin A, Völker W, Lorenzen I, Grötzinger J, Pendziwiat M, Kuhlenbäumer G.

Neurobiol Aging. 2014 Aug;35(8):1913-9. doi: 10.1016/j.neurobiolaging.2014.02.009. Epub 2014 Feb 19.

PMID:
24629672
22.

Genetics of essential tremor: meta-analysis and review.

Kuhlenbäumer G, Hopfner F, Deuschl G.

Neurology. 2014 Mar 18;82(11):1000-7. doi: 10.1212/WNL.0000000000000211. Epub 2014 Feb 14. Review.

PMID:
24532269
23.

Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules.

Bai X, Bowen JR, Knox TK, Zhou K, Pendziwiat M, Kuhlenbäumer G, Sindelar CV, Spiliotis ET.

J Cell Biol. 2013 Dec 23;203(6):895-905.

24.

Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus.

Goldberg-Stern H, Aharoni S, Afawi Z, Bennett O, Appenzeller S, Pendziwiat M, Kuhlenbäumer G, Basel-Vanagaite L, Shuper A, Korczyn AD, Helbig I.

J Child Neurol. 2014 Feb;29(2):221-6. doi: 10.1177/0883073813509016. Epub 2013 Nov 20.

PMID:
24257433
25.

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.

Suls A, Jaehn JA, Kecskés A, Weber Y, Weckhuysen S, Craiu DC, Siekierska A, Djémié T, Afrikanova T, Gormley P, von Spiczak S, Kluger G, Iliescu CM, Talvik T, Talvik I, Meral C, Caglayan HS, Giraldez BG, Serratosa J, Lemke JR, Hoffman-Zacharska D, Szczepanik E, Barisic N, Komarek V, Hjalgrim H, Møller RS, Linnankivi T, Dimova P, Striano P, Zara F, Marini C, Guerrini R, Depienne C, Baulac S, Kuhlenbäumer G, Crawford AD, Lehesjoki AE, de Witte PA, Palotie A, Lerche H, Esguerra CV, De Jonghe P, Helbig I; EuroEPINOMICS RES Consortium.

Am J Hum Genet. 2013 Nov 7;93(5):967-75. doi: 10.1016/j.ajhg.2013.09.017. Epub 2013 Oct 24.

26.

Rare variants in ANO3 are not a susceptibility factor in essential tremor.

Hopfner F, Bungeroth M, Pendziwiat M, Tittmann L, Deuschl G, Schneider SA, Kuhlenbäumer G.

Parkinsonism Relat Disord. 2014 Jan;20(1):134-5. doi: 10.1016/j.parkreldis.2013.09.022. Epub 2013 Sep 27. No abstract available.

PMID:
24094724
27.

The role of SCARB2 as susceptibility factor in Parkinson's disease.

Hopfner F, Schulte EC, Mollenhauer B, Bereznai B, Knauf F, Lichtner P, Zimprich A, Haubenberger D, Pirker W, Brücke T, Peters A, Gieger C, Kuhlenbäumer G, Trenkwalder C, Winkelmann J.

Mov Disord. 2013 Apr;28(4):538-40. doi: 10.1002/mds.25349. Epub 2013 Feb 13.

PMID:
23408458
28.

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.

Klebe S, Golmard JL, Nalls MA, Saad M, Singleton AB, Bras JM, Hardy J, Simon-Sanchez J, Heutink P, Kuhlenbäumer G, Charfi R, Klein C, Hagenah J, Gasser T, Wurster I, Lesage S, Lorenz D, Deuschl G, Durif F, Pollak P, Damier P, Tison F, Durr A, Amouyel P, Lambert JC, Tzourio C, Maubaret C, Charbonnier-Beaupel F, Tahiri K, Vidailhet M, Martinez M, Brice A, Corvol JC; French Parkinson's Disease Genetics Study Group; International Parkinson's Disease Genomics Consortium (IPDGC).

J Neurol Neurosurg Psychiatry. 2013 Jun;84(6):666-73. doi: 10.1136/jnnp-2012-304475. Epub 2013 Feb 13.

29.

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

Appenzeller S, Schulte C, Thier S, Hopfner F, Pendziwiat M, Papengut F, Klein C, Hagenah J, Kasten M, Srulijes K, Berg D, Gasser T, Singleton A, Deuschl G, Kuhlenbäumer G.

Mov Disord. 2013 Aug;28(9):1305-6. doi: 10.1002/mds.25330. Epub 2013 Feb 6. No abstract available.

30.

Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations.

Appenzeller S, Helbig I, Stephani U, Häusler M, Kluger G, Bungeroth M, Müller S, Kuhlenbäumer G, van Baalen A.

Dev Med Child Neurol. 2012 Dec;54(12):1144-8. doi: 10.1111/j.1469-8749.2012.04435.x. Epub 2012 Oct 15.

31.

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.

Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng YC, Fornage M, Ikram MA, Malik R, Bevan S, Thorsteinsdottir U, Nalls MA, Longstreth W, Wiggins KL, Yadav S, Parati EA, Destefano AL, Worrall BB, Kittner SJ, Khan MS, Reiner AP, Helgadottir A, Achterberg S, Fernandez-Cadenas I, Abboud S, Schmidt R, Walters M, Chen WM, Ringelstein EB, O'Donnell M, Ho WK, Pera J, Lemmens R, Norrving B, Higgins P, Benn M, Sale M, Kuhlenbäumer G, Doney AS, Vicente AM, Delavaran H, Algra A, Davies G, Oliveira SA, Palmer CN, Deary I, Schmidt H, Pandolfo M, Montaner J, Carty C, de Bakker PI, Kostulas K, Ferro JM, van Zuydam NR, Valdimarsson E, Nordestgaard BG, Lindgren A, Thijs V, Slowik A, Saleheen D, Paré G, Berger K, Thorleifsson G; Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2), Hofman A, Mosley TH, Mitchell BD, Furie K, Clarke R, Levi C, Seshadri S, Gschwendtner A, Boncoraglio GB, Sharma P, Bis JC, Gretarsdottir S, Psaty BM, Rothwell PM, Rosand J, Meschia JF, Stefansson K, Dichgans M, Markus HS; International Stroke Genetics Consortium.

Lancet Neurol. 2012 Nov;11(11):951-62. doi: 10.1016/S1474-4422(12)70234-X. Epub 2012 Oct 5. Erratum in: Lancet Neurol. 2015 Aug;14(8):788.

32.

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.

Helgadottir A, Gretarsdottir S, Thorleifsson G, Holm H, Patel RS, Gudnason T, Jones GT, van Rij AM, Eapen DJ, Baas AF, Tregouet DA, Morange PE, Emmerich J, Lindblad B, Gottsäter A, Kiemeny LA, Lindholt JS, Sakalihasan N, Ferrell RE, Carey DJ, Elmore JR, Tsao PS, Grarup N, Jørgensen T, Witte DR, Hansen T, Pedersen O, Pola R, Gaetani E, Magnadottir HB, Wijmenga C, Tromp G, Ronkainen A, Ruigrok YM, Blankensteijn JD, Mueller T, Wells PS, Corral J, Soria JM, Souto JC, Peden JF, Jalilzadeh S, Mayosi BM, Keavney B, Strawbridge RJ, Sabater-Lleal M, Gertow K, Baldassarre D, Nyyssönen K, Rauramaa R, Smit AJ, Mannarino E, Giral P, Tremoli E, de Faire U, Humphries SE, Hamsten A, Haraldsdottir V, Olafsson I, Magnusson MK, Samani NJ, Levey AI, Markus HS, Kostulas K, Dichgans M, Berger K, Kuhlenbäumer G, Ringelstein EB, Stoll M, Seedorf U, Rothwell PM, Powell JT, Kuivaniemi H, Onundarson PT, Valdimarsson E, Matthiasson SE, Gudbjartsson DF, Thorgeirsson G, Quyyumi AA, Watkins H, Farrall M, Thorsteinsdottir U, Stefansson K.

J Am Coll Cardiol. 2012 Aug 21;60(8):722-9. doi: 10.1016/j.jacc.2012.01.078.

33.

No association between NOD2 variants and Parkinson's disease.

Appenzeller S, Thier S, Papengut F, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Schreiber S, Deuschl G, Kuhlenbäumer G.

Mov Disord. 2012 Aug;27(9):1191-2. doi: 10.1002/mds.25059. Epub 2012 Jul 13. No abstract available.

PMID:
22807259
34.

Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.

Thier S, Lorenz D, Nothnagel M, Poremba C, Papengut F, Appenzeller S, Paschen S, Hofschulte F, Hussl AC, Hering S, Poewe W, Asmus F, Gasser T, Schöls L, Christensen K, Nebel A, Schreiber S, Klebe S, Deuschl G, Kuhlenbäumer G.

Neurology. 2012 Jul 17;79(3):243-8. doi: 10.1212/WNL.0b013e31825fdeed. Epub 2012 Jul 3.

35.

No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients.

Richter J, Appenzeller S, Ammerpohl O, Deuschl G, Paschen S, Brüggemann N, Klein C, Kuhlenbäumer G.

Mov Disord. 2012 Apr;27(4):590-1. doi: 10.1002/mds.24907. Epub 2012 Jan 19. No abstract available.

PMID:
22262231
36.

GABA(A) receptor- and GABA transporter polymorphisms and risk for essential tremor.

Thier S, Kuhlenbäumer G, Lorenz D, Nothnagel M, Nebel A, Christensen K, Schreiber S, Deuschl G, Klebe S.

Eur J Neurol. 2011 Aug;18(8):1098-100. doi: 10.1111/j.1468-1331.2010.03308.x. Epub 2010 Dec 22.

PMID:
21749575
37.

The outer arterial wall layers are primarily affected in spontaneous cervical artery dissection.

Völker W, Dittrich R, Grewe S, Nassenstein I, Csiba L, Herczeg L, Borsay BA, Robenek H, Kuhlenbäumer G, Ringelstein EB.

Neurology. 2011 Apr 26;76(17):1463-71. doi: 10.1212/WNL.0b013e318217e71c. Epub 2011 Mar 23.

PMID:
21430296
38.

Novel genomic techniques open new avenues in the analysis of monogenic disorders.

Kuhlenbäumer G, Hullmann J, Appenzeller S.

Hum Mutat. 2011 Feb;32(2):144-51. doi: 10.1002/humu.21400. Review.

PMID:
21280146
39.

Hereditary and non-hereditary microangiopathies in the young. An up-date.

Ringelstein EB, Kleffner I, Dittrich R, Kuhlenbäumer G, Ritter MA.

J Neurol Sci. 2010 Dec 15;299(1-2):81-5. doi: 10.1016/j.jns.2010.08.037. Epub 2010 Sep 18. Review.

PMID:
20851424
40.

Arterial elongation ("redundancy") is not a feature of spontaneous cervical artery dissection.

Dittrich R, Nassenstein I, Harms S, Maintz D, Heindel W, Kuhlenbäumer G, Ringelstein EB.

J Neurol. 2011 Feb;258(2):250-4. doi: 10.1007/s00415-010-5737-7. Epub 2010 Sep 10.

PMID:
20830592
41.

Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura.

Jung A, Huge A, Kuhlenbäumer G, Kempt S, Seehafer T, Evers S, Berger K, Marziniak M.

J Neural Transm (Vienna). 2010 Nov;117(11):1253-60. doi: 10.1007/s00702-010-0468-6. Epub 2010 Aug 26.

PMID:
20740293
42.

LINGO1 is not associated with Parkinson's disease in German patients.

Klebe S, Thier S, Lorenz D, Nothnagel M, Schreiber S, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Deuschl G, Kuhlenbäumer G.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1173-8. doi: 10.1002/ajmg.b.31085.

PMID:
20468067
43.

Chlamydia pneumoniae infection and Alzheimer's disease: a connection to remember?

Shima K, Kuhlenbäumer G, Rupp J.

Med Microbiol Immunol. 2010 Nov;199(4):283-9. doi: 10.1007/s00430-010-0162-1. Epub 2010 May 6. Review.

PMID:
20445987
44.

LINGO1 polymorphisms are associated with essential tremor in Europeans.

Thier S, Lorenz D, Nothnagel M, Stevanin G, Dürr A, Nebel A, Schreiber S, Kuhlenbäumer G, Deuschl G, Klebe S.

Mov Disord. 2010 Apr 30;25(6):717-23. doi: 10.1002/mds.22887.

PMID:
20310002
45.

Hereditary amyloidosis of the Finnish type in a German family: clinical and electrophysiological presentation.

Lüttmann RJ, Teismann I, Husstedt IW, Ringelstein EB, Kuhlenbäumer G.

Muscle Nerve. 2010 May;41(5):679-84. doi: 10.1002/mus.21534.

PMID:
20229579
46.

Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.

Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G.

Am J Hum Genet. 2010 Jan;86(1):83-7. doi: 10.1016/j.ajhg.2009.12.003.

47.

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

Gudbjartsson DF, Holm H, Gretarsdottir S, Thorleifsson G, Walters GB, Thorgeirsson G, Gulcher J, Mathiesen EB, Njølstad I, Nyrnes A, Wilsgaard T, Hald EM, Hveem K, Stoltenberg C, Kucera G, Stubblefield T, Carter S, Roden D, Ng MC, Baum L, So WY, Wong KS, Chan JC, Gieger C, Wichmann HE, Gschwendtner A, Dichgans M, Kuhlenbäumer G, Berger K, Ringelstein EB, Bevan S, Markus HS, Kostulas K, Hillert J, Sveinbjörnsdóttir S, Valdimarsson EM, Løchen ML, Ma RC, Darbar D, Kong A, Arnar DO, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2009 Aug;41(8):876-8. doi: 10.1038/ng.417. Epub 2009 Jul 13.

48.

Functional gene variants of the serotonin-synthesizing enzyme tryptophan hydroxylase 2 in migraine.

Marziniak M, Kienzler C, Kuhlenbäumer G, Sommer C, Mössner R.

J Neural Transm (Vienna). 2009 Jul;116(7):815-9. doi: 10.1007/s00702-009-0236-7. Epub 2009 May 12.

PMID:
19434366
49.

MRI features of pontine autosomal dominant microangiopathy and leukoencephalopathy (PADMAL).

Ding XQ, Hagel C, Ringelstein EB, Buchheit S, Zeumer H, Kuhlenbäumer G, Appenzeller S, Fiehler J.

J Neuroimaging. 2010 Apr;20(2):134-40. doi: 10.1111/j.1552-6569.2008.00336.x. Epub 2009 Jan 29.

PMID:
19187480
50.

Sensitivity of neurovascular ultrasound for the detection of spontaneous cervical artery dissection.

Nebelsieck J, Sengelhoff C, Nassenstein I, Maintz D, Kuhlenbäumer G, Nabavi DG, Ringelstein EB, Dittrich R.

J Clin Neurosci. 2009 Jan;16(1):79-82. doi: 10.1016/j.jocn.2008.04.005. Epub 2008 Nov 18.

PMID:
19017557

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