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Items: 1 to 50 of 117

1.

[Reduce obstacles, promote health-healthcare access for undocumented migrants within a pilot project in Lower Saxony, Germany (2016-2018)].

Mylius M, Dreesman J, Zühlke C, Mertens E.

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2019 Aug;62(8):927-934. doi: 10.1007/s00103-019-02972-4. German.

PMID:
31201447
2.

Investigation of femtosecond laser induced ripple formation on copper for varying incident angle.

Zuhlke CA, Tsibidis GD, Anderson T, Stratakis E, Gogos G, Alexander DR.

AIP Adv. 2018;8(1):015212. doi: 10.1063/1.5020029. Epub 2018 Jan 10.

3.

Effects of Femtosecond Laser Surface Processed Nanoparticle Layers on Pool Boiling Heat Transfer Performance.

Kruse C, Lucis M, Shield JE, Anderson T, Zuhlke C, Alexander D, Gogos G, Ndao S.

J Therm Sci Eng Appl. 2018 Jun;10(3). pii: 031009. doi: 10.1115/1.4038763. Epub 2018 Mar 28.

4.

Formation of aggregated nanoparticle spheres through femtosecond laser surface processing.

Tsubaki AT, Koten MA, Lucis MJ, Zuhlke C, Ianno N, Shield JE, Alexander DR.

Appl Surf Sci. 2017 Oct 15;419:778-787. doi: 10.1016/j.apsusc.2017.05.094. Epub 2017 May 12.

5.

Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy.

Tunc S, Tadic V, Zühlke C, Hellenbroich Y, Brüggemann N.

Neurology. 2018 Jan 16;90(3):142-143. doi: 10.1212/WNL.0000000000004833. No abstract available.

PMID:
29335306
6.

Micro/nanostructures formation by femtosecond laser surface processing on amorphous and polycrystalline Ni60Nb40.

Peng E, Tsubaki A, Zuhlke CA, Wang M, Bell R, Lucis MJ, Anderson TP, Alexander DR, Gogos G, Shield JE.

Appl Surf Sci. 2017 Feb 28;396:1170-1176. doi: 10.1016/j.apsusc.2016.11.107. Epub 2016 Nov 15.

7.

Growth mechanisms of multiscale, mound-like surface structures on titanium by femtosecond laser processing.

Peng E, Bell R, Zuhlke CA, Wang M, Alexander DR, Gogos G, Shield JE.

J Appl Phys. 2017;122(13). pii: 133108. doi: 10.1063/1.4990709. Epub 2017 Oct 4.

8.

Secondary pool boiling effects.

Kruse C, Tsubaki A, Zuhlke C, Anderson T, Alexander D, Gogos G, Ndao S.

Appl Phys Lett. 2016;108. pii: 051602. doi: 10.1063/1.4941081. Epub 2016 Feb 1.

9.

Experimental explanation of the formation mechanism of surface mound-structures by femtosecond laser on polycrystalline Ni60Nb40.

Peng E, Tsubaki A, Zuhlke CA, Wang M, Bell R, Lucis MJ, Anderson TP, Alexander DR, Gogos G, Shield JE.

Appl Phys Lett. 2016;108(3). pii: 031602. doi: 10.1063/1.4939983. Epub 2016 Jan 19.

10.

Spinocerebellar ataxia 28: a novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing.

Zühlke C, Mikat B, Timmann D, Wieczorek D, Gillessen-Kaesbach G, Bürk K.

Cerebellum Ataxias. 2015 Dec 16;2:19. doi: 10.1186/s40673-015-0038-7. eCollection 2015.

11.

Enhanced pool-boiling heat transfer and critical heat flux on femtosecond laser processed stainless steel surfaces.

Kruse CM, Anderson T, Wilson C, Zuhlke C, Alexander D, Gogos G, Ndao S.

Int J Heat Mass Transf. 2015 Mar;82:109-116. doi: 10.1016/j.ijheatmasstransfer.2014.11.023. Epub 2014 Nov 28.

12.

[The catastrophic antiphospholipid antibody syndrome: case report and review of the literature].

Hüwel J, Zühlke C, Kostopoulos P, Mann C, Hamann GF.

Nervenarzt. 2015 Feb;86(2):205-9. doi: 10.1007/s00115-015-4263-3. Review. German. No abstract available.

PMID:
25637082
13.

Self‑propelled droplets on heated surfaces with angled self‑assembled micro/nanostructures.

Kruse C, Somanas I, Anderson T, Wilson C, Zuhlke C, Alexander D, Gogos G, Ndao S.

Microfluid Nanofluidics. 2015;18(5-6):1417-1424. doi: 10.1007/s10404-014-1540-6. Epub 2015 Jan 9.

14.

Psychosis Complicating Friedreich Ataxia.

Ganos C, Schöttle D, Zühlke C, Münchau A.

Mov Disord Clin Pract. 2014 Nov 28;2(1):84-85. doi: 10.1002/mdc3.12115. eCollection 2015 Mar. No abstract available.

15.
16.

A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.

Bürk K, Kaiser FJ, Tennstedt S, Schöls L, Kreuz FR, Wieland T, Strom TM, Büttner T, Hollstein R, Braunholz D, Plaschke J, Gillessen-Kaesbach G, Zühlke C.

Eur J Med Genet. 2014 Apr;57(5):207-11. doi: 10.1016/j.ejmg.2014.01.005. Epub 2014 Jan 29.

PMID:
24486772
17.

Pathophysiology and treatment options in trigeminal meningoceles.

Preuss M, Steinhoff A, Zühlke CJ, Schulz D, Stein M, Nestler U, Christophis P.

J Neurol Surg Rep. 2013 Dec;74(2):81-7. doi: 10.1055/s-0033-1348955. Epub 2013 Jul 12.

18.

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Doss S, Lohmann K, Seibler P, Arns B, Klopstock T, Zühlke C, Freimann K, Winkler S, Lohnau T, Drungowski M, Nürnberg P, Wiegers K, Lohmann E, Naz S, Kasten M, Bohner G, Ramirez A, Endres M, Klein C.

J Neurol. 2014 Jan;261(1):207-12. doi: 10.1007/s00415-013-7177-7. Epub 2013 Nov 8.

PMID:
24202787
19.

Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14.

Ganos C, Zittel S, Minnerop M, Schunke O, Heinbokel C, Gerloff C, Zühlke C, Bauer P, Klockgether T, Münchau A, Bäumer T.

Cerebellum. 2014 Feb;13(1):89-96. doi: 10.1007/s12311-013-0522-7.

PMID:
24030789
20.

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations.

Elsayed SM, Heller R, Thoenes M, Zaki MS, Swan D, Elsobky E, Zühlke C, Ebermann I, Nürnberg G, Nürnberg P, Bolz HJ.

Eur J Hum Genet. 2014 Feb;22(2):286-8. doi: 10.1038/ejhg.2013.150. Epub 2013 Jul 10.

21.

Extraordinary shifts of the Leidenfrost temperature from multiscale micro/nanostructured surfaces.

Kruse C, Anderson T, Wilson C, Zuhlke C, Alexander D, Gogos G, Ndao S.

Langmuir. 2013 Aug 6;29(31):9798-806. doi: 10.1021/la401936w. Epub 2013 Jul 23.

PMID:
23799305
22.

Formation of multiscale surface structures on nickel via above surface growth and below surface growth mechanisms using femtosecond laser pulses.

Zuhlke CA, Anderson TP, Alexander DR.

Opt Express. 2013 Apr 8;21(7):8460-73. doi: 10.1364/OE.21.008460.

23.

Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13).

Bürk K, Strzelczyk A, Reif PS, Figueroa KP, Pulst SM, Zühlke C, Oertel WH, Hamer HM, Rosenow F.

Int J Neurosci. 2013 Apr;123(4):278-82. doi: 10.3109/00207454.2012.755180. Epub 2013 Jan 29.

PMID:
23215817
24.

Traumatic left lateral C2 epiphysiorhexis in a 3-year-old girl--a case report.

Preuss M, Zühlke CJ, Hahn A, Stein M, Nestler U.

Eur J Pediatr Surg. 2011 Dec;21(6):412-4. doi: 10.1055/s-0031-1286253. Epub 2011 Oct 5. No abstract available.

PMID:
21976231
25.

Influence of WC-Co substrate pretreatment on diamond film deposition by laser-assisted combustion synthesis.

Veillère A, Guillemet T, Xie ZQ, Zuhlke CA, Alexander DR, Silvain JF, Heintz JM, Chandra N, Lu YF.

ACS Appl Mater Interfaces. 2011 Apr;3(4):1134-9. doi: 10.1021/am101271b. Epub 2011 Apr 11.

PMID:
21462974
26.

Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic.

Edener U, Bernard V, Hellenbroich Y, Gillessen-Kaesbach G, Zühlke C.

J Neurol. 2011 Jul;258(7):1223-7. doi: 10.1007/s00415-011-5905-4. Epub 2011 Jan 26.

PMID:
21267591
27.

Progressive biological behavior of a dysembryoplastic neuroepithelial tumor.

Preuss M, Nestler U, Zühlke CJ, Kuchelmeister K, Neubauer BA, Jödicke A.

Pediatr Neurosurg. 2010;46(4):294-8. doi: 10.1159/000320729. Epub 2010 Dec 30.

PMID:
21196795
28.

[Clinical details and genetics of recessive ataxias].

Zühlke C, Kreuz F, Bürk K.

Nervenarzt. 2011 Apr;82(4):447-8, 450-8. doi: 10.1007/s00115-010-3079-4. Review. German.

PMID:
20640395
29.

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K.

Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857.

PMID:
20589871
30.

Self assembled nanoparticle aggregates from line focused femtosecond laser ablation.

Zuhlke CA, Alexander DR, Bruce JC 3rd, Ianno NJ, Kamler CA, Yang W.

Opt Express. 2010 Mar 1;18(5):4329-39. doi: 10.1364/OE.18.004329.

PMID:
20389444
31.

Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation.

Edener U, Wöllner J, Hehr U, Kohl Z, Schilling S, Kreuz F, Bauer P, Bernard V, Gillessen-Kaesbach G, Zühlke C.

Eur J Hum Genet. 2010 Aug;18(8):965-8. doi: 10.1038/ejhg.2010.40. Epub 2010 Mar 31.

32.

EMQN Best Practice Guidelines for molecular genetic testing of SCAs.

Sequeiros J, Martindale J, Seneca S, Giunti P, Kämäräinen O, Volpini V, Weirich H, Christodoulou K, Bazak N, Sinke R, Sulek-Piatkowska A, Garcia-Planells J, Davis M, Frontali M, Hämäläinen P, Wieczorek S, Zühlke C, Saraiva-Pereira ML, Warner J, Leguern E, Thonney F, Quintáns Castro B, Jonasson J, Storm K, Andersson A, Ravani A, Correia L, Silveira I, Alonso I, Martins C, Pinto Basto J, Coutinho P, Perdigão A, Barton D, Davis M; European Molecular Quality Genetics Network.

Eur J Hum Genet. 2010 Nov;18(11):1173-6. doi: 10.1038/ejhg.2010.8. Epub 2010 Feb 24. No abstract available. Erratum in: Eur J Hum Genet. 2010 Nov;18(11):1176-7. multiple author names added.

33.

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Reetz K, Lencer R, Hagenah JM, Gaser C, Tadic V, Walter U, Wolters A, Steinlechner S, Zühlke C, Brockmann K, Klein C, Rolfs A, Binkofski F.

Cerebellum. 2010 Jun;9(2):210-7. doi: 10.1007/s12311-009-0150-4.

PMID:
20016963
34.

Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.

Bernard V, Minnerop M, Bürk K, Kreuz F, Gillessen-Kaesbach G, Zühlke C.

BMC Med Genet. 2009 Sep 11;10:87. doi: 10.1186/1471-2350-10-87.

35.

Isolation and in vitro cultivation turns cells from exocrine human pancreas into multipotent stem-cells.

Rapoport DH, Schicktanz S, Gürleyik E, Zühlke C, Kruse C.

Ann Anat. 2009 Nov;191(5):446-58. doi: 10.1016/j.aanat.2009.07.002. Epub 2009 Jul 21.

PMID:
19716277
36.

Multiple cardiac metastases from a malignant melanoma causing consecutive pulmonary embolism.

Machnick S, Butz T, van Bracht M, Zühlke C, Plehn G, Yeni H, Meissner A, Trappe HJ.

Herz. 2009 Aug;34(5):410-1. doi: 10.1007/s00059-009-3253-2. No abstract available.

PMID:
19711037
37.

Ataxia with oculomotor apraxia type 2: novel mutations in six patients with juvenile age of onset and elevated serum alpha-fetoprotein.

Bernard V, Stricker S, Kreuz F, Minnerop M, Gillessen-Kaesbach G, Zühlke C.

Neuropediatrics. 2008 Dec;39(6):347-50. doi: 10.1055/s-0029-1214424. Epub 2009 Jun 30.

PMID:
19569000
38.

Missense exchanges in the TTBK2 gene mutated in SCA11.

Edener U, Kurth I, Meiner A, Hoffmann F, Hübner CA, Bernard V, Gillessen-Kaesbach G, Zühlke C.

J Neurol. 2009 Nov;256(11):1856-9. doi: 10.1007/s00415-009-5209-0. Epub 2009 Jun 17.

PMID:
19533200
39.

Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic.

Hellenbroich Y, Bernard V, Zühlke C.

J Neurol. 2008 Apr;255(4):612-3. doi: 10.1007/s00415-008-0771-4. Epub 2008 Feb 25. No abstract available.

PMID:
18293026
40.

Investigation of recessive ataxia loci in patients with young age of onset.

Zühlke C, Bernard V, Gillessen-Kaesbach G.

Neuropediatrics. 2007 Aug;38(4):207-9.

PMID:
18058631
41.

Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17.

Gao R, Matsuura T, Coolbaugh M, Zühlke C, Nakamura K, Rasmussen A, Siciliano MJ, Ashizawa T, Lin X.

Eur J Hum Genet. 2008 Feb;16(2):215-22. Epub 2007 Nov 28.

42.

Screening of the SPTBN2 (SCA5) gene in German SCA patients.

Zühlke C, Bernard V, Dalski A, Lorenz P, Mitulla B, Gillessen-Kaesbach G, Bürk K.

J Neurol. 2007 Dec;254(12):1649-52. Epub 2007 Oct 25.

PMID:
17940722
43.

[Disproportionate shortening of left ventricular diastolic duration in patients with dilated cardiomyopathy].

Plehn G, Vormbrock J, Zühlke C, Christ M, Perings C, Perings S, Trappe HJ, Meissner A.

Med Klin (Munich). 2007 Sep 15;102(9):707-13. German.

PMID:
17879008
44.

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.

Zühlke C, Bürk K.

Cerebellum. 2007;6(4):300-7. doi: 10.1080/14734220601136177. Epub 2007 Jan 19. Review.

PMID:
17853080
45.

Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).

Hübner J, Sprenger A, Klein C, Hagenah J, Rambold H, Zühlke C, Kömpf D, Rolfs A, Kimmig H, Helmchen C.

Neurology. 2007 Sep 11;69(11):1160-8.

PMID:
17846415
46.

Homozygous myotonic dystrophy: clinical findings in two patients and review of the literature.

Zühlke C, Roeder E, Purmann S, Wieczorek D, Curry C, Loustalet C, Hellenbroich Y, Richardt HH, Gillessen-Kaesbach G.

Am J Med Genet A. 2007 Sep 1;143A(17):2058-61. Review. No abstract available.

PMID:
17663477
47.

[Genetics of oculocutaneous albinism].

Zühlke C, Stell A, Käsmann-Kellner B.

Ophthalmologe. 2007 Aug;104(8):674-80. Review. German.

PMID:
17646993
48.

Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.

Hagenah J, Reetz K, Zühlke C, Rolfs A, Binkofski F, Klein C.

Neurology. 2007 Jun 12;68(24):2157; author reply 2157-8. No abstract available.

PMID:
17562842
49.

Polymorphisms in the genes for oculocutaneous albinism type 1 and type 4 in the German population.

Zühlke C, Criée C, Gemoll T, Schillinger T, Kaesmann-Kellner B.

Pigment Cell Res. 2007 Jun;20(3):225-7. No abstract available.

PMID:
17516931
50.

Demonstration of a nanoparticle-based optical diode.

Alexander D, Bruce J 3rd, Zuhlke C, Koch B, Rudebusch R, Deogun J, Hamza H.

Opt Lett. 2006 Jul 1;31(13):1957-9.

PMID:
16770397

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