Browse by ["viewname_eprint_publisher" not defined]

A

Apaolaza, P. S. and del Pozo-Rodriguez, A. and Torrecilla, J. and Rodriguez-Gascon, A. and Rodriguez, J. M. and Friedrich, U. and Weber, B. H. F. and Solinis, M. A. (2015) Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model. JOURNAL OF CONTROLLED RELEASE, 217. pp. 273-283. ISSN 0168-3659, 1873-4995

C

Czeschik, Johanna Christina and Hehr, Ute and Hartmann, Britta and Luedecke, Hermann-Josef and Rosenbaum, Thorsten and Schweiger, Bernd and Wieczorek, Dagmar (2013) 160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndrome. EUROPEAN JOURNAL OF MEDICAL GENETICS, 56 (12). pp. 689-694. ISSN 1769-7212, 1878-0849

F

Fogarasi, Marton and Janssen, Andreas and Weber, Bernhard H. F. and Stoehr, Heidi (2008) Molecular dissection of TIMP3 mutation S156C associated with Sorsby fundus dystrophy. MATRIX BIOLOGY, 27 (5). pp. 381-392. ISSN 0945-053X

G

Grassmann, Felix and Fauser, Sascha and Weber, Bernhard H. F. (2015) The genetics of age-related macular degeneration (AMD) - Novel targets for designing treatment options? EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 95. pp. 194-202. ISSN 0939-6411, 1873-3441

H

Herbst, Saskia M. and Proepper, Christiane R. and Geis, Tobias and Borggraefe, Ingo and Hahn, Andreas and Debus, Otfried and Haeussler, Martin and von Gersdorff, Gero and Kurlemann, Gerhard and Ensslen, Matthias and Beaud, Nathalie and Budde, Joerg and Gilbert, Michael and Heiming, Ralf and Morgner, Rita and Philippi, Heike and Ross, Sophia and Strobl-Wildemann, Gertrud and Muelleder, Kerstin and Vosschulte, Paul and Morris-Rosendahl, Deborah J. and Schuierer, Gerhard and Hehr, Ute (2016) LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs. BRAIN & DEVELOPMENT, 38 (4). pp. 399-406. ISSN 0387-7604, 1872-7131

K

Keilhauer, Claudia N. and Fritsche, Lars G. and Guthoff, Rainer and Haubitz, Imme and Weber, Bernhard H. (2013) Age-related macular degeneration and coronary heart disease: Evaluation of genetic and environmental associations. EUROPEAN JOURNAL OF MEDICAL GENETICS, 56 (2). pp. 72-79. ISSN 1769-7212

Kraus, Dominik and Karlstetter, Marcus and Walczak, Yana and Hilfinger, Daniela and Langmann, Thomas and Weber, Bernhard H. F. (2011) Retinal expression of the X-linked juvenile retinoschisis (RS1) gene is controlled by an upstream CpG island and two opposing CRX-bound regions. BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 1809 (4-6). pp. 245-254. ISSN 1874-9399

S

Sell, Katharina and Storch, Katja and Hahn, Gabriele and Lee-Kirsch, Min Ae and Ramantani, Georgia and Jackson, Sandra and Neilson, Derek and von der Hagen, Maja and Hehr, Ute and Smitka, Martin (2016) Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation. BRAIN & DEVELOPMENT, 38 (8). pp. 777-780. ISSN 0387-7604, 1872-7131

Shamsara, Jamal and Behravan, Javad and Falsoleiman, Homa and Mohammadpour, Amir Hooshang and Rendeirs, Joerg and Ramezani, Mohammad (2011) Pentoxifylline administration changes protein expression profile of coronary artery disease patients. GENE, 487 (1). pp. 107-111. ISSN 0378-1119, 1879-0038

W

Winner, Beate and Gross, Claudia and Uyanik, Goekhan and Schulte-Mattler, Wilhelm and Luerding, Ralf and Marienhagen, Joerg and Bogdahn, Ulrich and Windpassinger, Christian and Hehr, Ute and Winkler, Juergen (2006) Thin corpus callosum and amyotrophy in spastic paraplegia - Case report and review of literature. CLINICAL NEUROLOGY AND NEUROSURGERY, 108 (7). pp. 692-698. ISSN 0303-8467