Anja Harder neé Klose

Papers authored by Anja Harder neé Klose

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2011 Mateusz Kolanczyk, Victor Mautner, Nadine Kossler, Rosa Nguyen, Jirko Kühnisch, Tomasz Zemojtel, Aleksander Jamsheer, Eike Wegener, Boris Thurisch, Sigrid Tinschert, Nikola Holtkamp, Su-Jin Park, Patricia Birch, David Kendler, Anja Harder

and 2 other authors

MIA is a potential biomarker for tumour load in neurofibromatosis type 1

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2010 Anja Harder

, Sabrina Titze, Lena Herbst, Thomas Harder, Katrin Guse, Sigrid Tinschert, Dieter Kaufmann, Thorsten Rosenbaum, Victor Felix Mautner, Elke Windt, Ute Wahlländer-Danek, Katharina Wimmer, Stefan Mundlos, Hartmut Peters

Monozygotic Twins With Neurofibromatosis Type 1 (NF1) Display Differences in Methylation ofNF1Gene Promoter Elements, 5' Untranslated region, Exon and Intron 1

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Thomas Harder, Andreas Plagemann, Anja Harder

Birth weight and risk of neuroblastoma: A meta-analysis

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Andreas Plagemann, Katharina Roepke, Thomas Harder, Matthias Brunn, Anja Harder

, Manon Wittrock-Staar, Thomas Ziska, Karen Schellong, Elke Rodekamp, Kerstin Melchior, Joachim W. Dudenhausen

Epigenetic malprogramming of the insulin receptor promoter due to developmental overfeeding

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2009 Andreas Plagemann, Thomas Harder, Matthias Brunn, Anja Harder

, Katharina Roepke, Manon Wittrock-Staar, Thomas Ziska, Karen Schellong, Elke Rodekamp, Kerstin Melchior, Joachim W. Dudenhausen

Hypothalamic proopiomelanocortin promoter methylation becomes altered by early overfeeding: an epigenetic model of obesity and the metabolic syndrome

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Sabrina Titze, Hartmut Peters, Sandra Währisch, Thomas Harder, Katrin Guse, Annegret Buske, Sigrid Tinschert, Anja Harder

Differential MSH2 promoter methylation in blood cells of Neurofibromatosis type 1 (NF1) patients

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2008 Thomas Harder, Andreas Plagemann, Anja Harder

Birth Weight and Subsequent Risk of Childhood Primary Brain Tumors: A Meta-Analysis

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2006 A. Harder

, V‐F-F. Mautner, R. E. Friedrich, T. Harder, A. Plagemann, A. von Deimling

Transcription factor AP-2 is expressed in human Schwann cell-derived tumours

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T. Picht, J. Jansons, A. van Baalen, A. Harder

, T. A. Pietilae

Infant with Unusually Large Choroid Plexus Papilloma Undergoing Emergency Surgery

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2004 A. Harder

, M. Rosche, D. E. Reuß, N. Holtkamp, K. Uhlmann, R. Friedrich, V. F. Mautner, A. von Deimling

Methylation analysis of the neurofibromatosis type 1 (NF1) promoter in peripheral nerve sheath tumours

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2003 Nikola Holtkamp, Victor-F. Mautner, Reinhard E. Friedrich, Anja Harder

, Christian Hartmann, Agota Theallier-Janko, Karl T. Hoffmann, Andreas von Deimling

Differentially expressed genes in neurofibromatosis 1-associated neurofibromas and malignant peripheral nerve sheath tumors

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A. Harder

, C. Dudel, I. Anagnostopoulos, M. Hummel, W. Brück

Molecular genetic diagnosis of a primary central nervous system T cell lymphoma

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2002 Jens P. Dreier, Oliver W. Sakowitz, Anja Harder

, Claus Zimmer, Ulrich Dirnagl

, Jos� M Valdueza, Andreas W. Unterberg

Focal laminar cortical MR signal abnormalities after subarachnoid hemorrhage

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Ursula Felderhoff-Mueser, Katja Grohmann, Anja Harder

, Christine Stadelmann, Klaus Zerres, Christoph Buhrer, Michael Obladen

Severe Spinal Muscular Atrophy Variant Associated With Congenital Bone Fractures

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Randolf Klingebiel, Cyrus Djamchidi, Anja Harder

, Rüdiger Lehmann, Volker Jahnke

Neurofibroma in the Mastoid Segment of the Facial Canal

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1999 Anja Harder

, Klaus Jendroska, Friedmar Kreuz, Torsten Wirth, Constanze Schafranka, Nadja Karnatz, Aguta Th�allier-Janko, Jens Dreier, Karsten Lohan, Dirk Emmerich, Jorge Cerv�s-Navarro, Otto Windl, Hans A. Kretzschmar, Peter N�rnberg, Regine Witkowski

Novel twelve-generation kindred of fatal familial insomnia from Germany representing the entire spectrum of disease expression

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Anja Klose

, Hartmut Peters, Sven Hoffmeyer, Annegret Buske, Andrea Lüder, Andrea L�der, Detlef Heß, Detlef He�, R�diger Lehmann, Peter Nürnberg, Peter N�rnberg, Sigrid Tinschert

Two independent mutations in a family with neurofibromatosis type 1 (NF1)

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

H. Peters, A. Lüder, A. Harder

, M. Schuelke, S. Tinschert

Mutation screening of neurofibromatosis type 1 (NF1) exons 28 and 29 with single strand conformation polymorphism (SSCP): five novel mutations, one recurrent transition and two polymorphisms in a panel of 118 unrelated NF1 patients. Mutations in brief no. 229. Online.

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1998 A. Klose

Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1

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Anja Klose

, Peter Nicholas Robinson

, Andreas Gewies, Lan Kluwe, Dieter Kaufmann, Annegret Buske, Sigrid Tinschert, H. Peters

Two novel mutations in exons 19a and 20 and a BsaI polymorphism in a newly characterized intron of the neurofibromatosis type 1 gene

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Papers authored by Anja Harder neé Klose