2011

Lin J, Lemke C, Redies C, Yan X, Mix E, Rolfs A, Luo J.
ADAM17 overexpression promotes angiogenesis by increasing blood vessel sproutin and pericyte number during brain microvessel development
Int J Dev Biol. 2011;55(10-12):961-8.

Morgan PJ, Liedmann A, Hübner R, Hovakimyan M, Rolfs A, Frech MJ
Human neural progenitor cells show functional neuronal differentiation and regional preference after engraftment onto hippocampal slice cultures.
Stem Cells Dev. 2011. [Epub ahead of print]

Hovakimyan M, Petersen J, Maass F, Reichard M, Witt M, Lukas J, Stachs O, Guthoff R, Rolfs A, Wree A.
Corneal alterations during combined therapy with cyclodextrin/ allopregnanolone and miglustat in a knock-out mouse model of NPC1 disease.
PLoS One. 2011;6(12):e28418. Epub 2011 Dec 6.

Brüggemann N, Külper W, Hagenah J, Bauer P, Pattaro C, Tadic V, Lohnau T, Winkler S, Tönnies H, Sprenger A, Pramstaller P, Rolfs A, Siebert R, Riess O, Vieregge P, Lohmann K, Klein C.
Autosomal dominant Parkinson's disease in a large German pedigree.
Acta Neurol Scand. 2011 Nov 23. [Epub ahead of print]

Arif B, Grünewald A, Fatima A, Ramirez A, Ali A, Brüggemann N, Würfel J, Rolfs A, Lohmann K, Malik A, Klein C, Naz S.
An unusual neurological syndrome of crawling git, dystonia, pyramidal signs, and limited speech.
Mov Disord. 2011 Oct;26(12):2279-83. Epub 2011 Sep 23.

Yan X, Lukas J, Witt M, Wree A, Hübner R, Frech M, Köhling R, Rolfs A, Luo J.
Decreased expression of myelin gene regulatory factor in Niemann-Pick type C 1 mouse.
Metab Brain Dis. 2011 Sep 21. [Epub ahead of print]

Markus A, Yan X, Rolfs A, Luo J.
Quantitative and dynamic expression profile of premature and active forms of the regional ADAM proteins during chicken brain development.
Cell Mol Biol Lett. 2011 Sep;16(3):431-51. Epub 2011 Jul 18.

Hovakimyan M, Stachs O, Reichard M, Mascher H, Lukas J, Frech MJ, Guthoff R, Witt M, Rolfs A, Wree A.
Morphological alterations of the cornea in the mouse model of niemann-pick disease type c1.
Cornea. (2011) Jul; 30(7):796-803.

Yan X, Lin J, Rolfs A, Luo J.
Differential expression of the ADAMs in developing chicken retina
Develop. Growth Differ. (2011) Jun; 53, 726-739

Fong CY, Rolfs A, Schwarzbraun T, Klein C, O'Callaghan FJ.
Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation
Eur J Paediatr Neurol. (2011) May; 15(3):271-5. Epub 2011 Feb 12.

Yan X, Lin J, Markus A, Rolfs A, Luo J.
Regional expression of ADAM19 during chicken embryonic development
Develop. Growth Differ. (2011) Apr; 53, 333-346

Tanislav C, Kaps M, Rolfs A, Böttcher T, Lackner K, Paschke E, Mascher H, Laue M, Blaes F.
Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot study.
Eur J Neurol. (2011) Apr; 18(4):631-6. Epub 2010 Sep 23.

Al-Maawali A, Rolfs A, Klingenhaeger M, Yoon G.
Hereditary spastic paraplegia associated with axonal neuropathy: A novel mutation of SPG3A in a large family
J Clin Neuromuscul Dis. (2011) Mar; 12(3):143-6.

Hermann A, Reuner U, Ziethe G, Bräuer A, Gölnitz U, Rolfs A, Ricci C.
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene.
Amyotroph Lateral Scler. (2011) Mar 17. [Epub ahead of print]

Lazarova NE, Usunoffa KG, Schmitt O, Itzev DE, Rolfs A, Wree A
Amygdalotrigeminal projection in the rat: An anterograde tracing study
Annals of Anatomy 193 (2011) Mar; 118–126

Rolfs A, Martus P, Heuschmann PU, Grittner U, Holzhausen M, Tatlisumak T, Böttcher T, Fazekas F, Enzinger C, Ropele S, Schmidt R, Riess O, Norrving B; sifap1 Investigators.
Protocol and methodology of the Stroke in Young Fabry Patients (sifap1) study: a prospective multicenter European study of 5,024 young stroke patients aged 18-55 years.
Cerebrovasc Dis. (2011) Feb; 31(3):253-62. Epub 2010 Dec 21.

Fellgiebel A, Keller I, Martus P, Ropele S, Yakushev I, Böttcher T, Fazekas F, Rolfs A.
Basilar artery diameter is a potential screening tool for Fabry disease in young stroke patients.
Cerebrovasc Dis. (2011) Feb; 31(3):294-9. Epub 2010 Dec 22.

Tanislav C, Feustel A, Franzen W, Wüsten O, Schneider C, Reichenberger F, Rolfs A, Sieweke N.
Persistent increase in cardiac troponin I in Fabry disease: a case report.
BMC Cardiovasc Disord. (2011) Jan 31; 11:6.

Lange C, Mix E, Frahm J, Glass Ä, Müller J, Schmitt O, Schmöle AC, Klemm K, Ortinau S, Hübner R, Frech MJ, Wree A, Rolfs A.
Small molecule GSK-3 inhibitors increase neurogenesis of human neural
progenitor cells
Neuroscience Letters 488 (2011) Jan; 36–40

Reetz K, Kleiman A, Klein C, Lencer R, Zuehlke C, Brockmann K, Rolfs A, Binkofski F.
CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM study.
PLoS One. (2011) Jan 19; 6(1):e15125.

Linthorst GE, Germain DP, Hollak CE, Hughes D, Rolfs A, Wanner C, Mehta A; European Medicines Agency.
Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT).
Mol Genet Metab. (2011) Jan; 102(1):99-102. Epub 2010 Nov 30.