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Friedrich Asmus

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Christoph Kamm; Christine Klein; Friedrich Asmus; Reiner Benecke; Thomas Gasser; Johann Hagenah; Alexander Münchau; Jens Pahnke; Christoph Schrader; Nils Uflacker; Jens Volkmann; Matthias Wittstock; Alexander Wolters; Katja Lohmann
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia.
Jörn K Pomper; H Wilhelm; S K Tayebati; Friedrich Asmus; Rebecca Schüle; K-D Sievert; C-A Haensch; Arthur Melms; Thomas Haarmeier
A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor.
Matthis Synofzik; Rebecca Schüle; Claudia Schulte; Rejko Krüger; Tobias Lindig; Ludger Schöls; Friedrich Asmus
Complex hyperkinetic movement disorders associated with POLG mutations.

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All Publications

2011: Christoph Kamm; Christine Klein; Friedrich Asmus; Reiner Benecke; Thomas Gasser; Johann Hagenah; Alexander Münchau; Jens Pahnke; Christoph Schrader; Nils Uflacker; Jens Volkmann; Matthias Wittstock; Alexander Wolters; Katja Lohmann
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia.
Movement disorders : official journal of the Movement Disorder Society 2011;26(11):2136-7.
2011: Jörn K Pomper; H Wilhelm; S K Tayebati; Friedrich Asmus; Rebecca Schüle; K-D Sievert; C-A Haensch; Arthur Melms; Thomas Haarmeier
A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor.
Neurology 2011;76(5):451-5.
2010: Matthis Synofzik; Rebecca Schüle; Claudia Schulte; Rejko Krüger; Tobias Lindig; Ludger Schöls; Friedrich Asmus
Complex hyperkinetic movement disorders associated with POLG mutations.
Movement disorders : official journal of the Movement Disorder Society 2010;25(14):2472-5.
2010: Daniel Weiss; Tobias Wächter; Sorin Breit; Simon N Jacob; Jörn K Pomper; Friedrich Asmus; Josep Valls-Solé; Christian Plewnia; Thomas Gasser; Alireza Gharabaghi; Rejko Krüger
Involuntary eyelid closure after STN-DBS: evidence for different pathophysiological entities.
Journal of neurology, neurosurgery, and psychiatry 2010;81(9):1002-7.
2010: Friedrich Asmus; Thomas Gasser
Dystonia-plus syndromes.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2010;17 Suppl 1():37-45.
2010: Matthis Synofzik; Friedrich Asmus; Matthias Reimold; Ludger Schöls; Daniela Berg
Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2010;25(2):243-5.
2009: Friedrich Asmus; Annette Langseth; Elaine Doherty; Therese Nestor; Marita Munz; Thomas Gasser; Tim Lynch; Mary D King
"Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
Movement disorders : official journal of the Movement Disorder Society 2009;24(5):702-9.
2008: Friedrich Asmus; Heiko Huber; Thomas Gasser; Ludger Schöls
Kick and rush: paradoxical kinesia in Parkinson disease.
Neurology 2008;71(9):695.
2008: Rainer Von Coelln; Armin Raible; Thomas Gasser; Friedrich Asmus
Ultrasound-guided injection of the iliopsoas muscle with botulinum toxin in camptocormia.
Movement disorders : official journal of the Movement Disorder Society 2008;23(6):889-92.
2007: Friedrich Asmus; Anita Devlin; Marita Munz; Alexander Zimprich; Thomas Gasser; Patrick F Chinnery
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
Movement disorders : official journal of the Movement Disorder Society 2007;22(14):2104-9.
2007: Friedrich Asmus; Lena Elisabeth Hjermind; Erik Dupont; Janine Wagenstaller; Edda Haberlandt; Marita Munz; Tim M Strom; Thomas Gasser
Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype.
Brain : a journal of neurology 2007;130(Pt 10):2736-45.
2006: Christoph Kamm; Friedrich Asmus; Jörg Müller; Petra Mayer; Manu Sharma; U J Muller; Stefan Beckert; R Ehling; T Illig; H E Wichmann; Werner Poewe; Jakob C Mueller; Thomas Gasser
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.
Neurology 2006;67(10):1857-9.
2006: Elisabeth Stogmann; Peter Lichtner; Christoph Baumgartner; M Schmied; Christoph Hotzy; Friedrich Asmus; Fritz Leutmezer; Silvia Beatrice Bonelli; Eva Assem-Hilger; Karl Vass; K Hatala; Tim M Strom; Thomas Meitinger; Fritz Zimprich; Alexander Zimprich
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.
Neurogenetics 2006;7(4):265-8.
2006: Angela Deutschländer; Friedrich Asmus; Elena Marelli; Thomas Klopstock; Thomas Gasser; Kai Bötzel
Excellent response to apomorphine in Parkinsonism with optic atrophy unresponsive to oral antiparkinsonian medication.
Movement disorders : official journal of the Movement Disorder Society 2006;21(9):1523-5.
2006: Nils Peters; Christoph Kamm; Friedrich Asmus; Elke Holinski-Feder; Eduardo Kraft; Martin Dichgans; Roland Brüning; Thomas Gasser; Kai Bötzel
Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
Movement disorders : official journal of the Movement Disorder Society 2006;21(1):98-102.
2005: Friedrich Asmus; Farid Salih; Lena Elisabeth Hjermind; Karen Ostergaard; Marita Munz; Andrea A Kühn; Erik Dupont; Andreas Kupsch; Thomas Gasser
Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene.
Annals of neurology 2005;58(5):792-7.
2005: Anne Hofer; Daniela Berg; Friedrich Asmus; M Niwar; Gerhard Ransmayr; M Riemenschneider; Silvia Beatrice Bonelli; Michaela Steffelbauer; A Ceballos-Baumann; Peter Haussermann; Stefanie Behnke; Rejko Krüger; Jürgen Prestel; Manu Sharma; Alexander Zimprich; Olaf Riess; Thomas Gasser
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies.
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(9):1249-54.
2005: Friedrich Asmus; V Horber; J Pohlenz; D Schwabe; Alexander Zimprich; Marita Munz; M Schöning; Thomas Gasser
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa.
Neurology 2005;64(11):1952-4.
2005: Friedrich Asmus; Sarah Schoenian; Peter Lichtner; Marita Munz; Petra Mayer; Bertram Muller-Myhsok; Alexander Zimprich; Helmut Remschmidt; Johannes Hebebrand; Oliver Bandmann; Thomas Gasser
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome.
Neurogenetics 2005;6(1):55-6.
2005: Jürgen Prestel; Manu Sharma; Petra Leitner; Alexander Zimprich; Jenny R Vaughan; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; Hasmet Hanagasi; Matthew J Farrer; Anne Hofer; Friedrich Asmus; Giampiero Volpe; Giuseppe Meco; Alexis Brice; Nicholas W Wood; Bertram Müller-Myhsok; Thomas Gasser
PARK11 is not linked with Parkinson's disease in European families.
European journal of human genetics : EJHG 2005;13(2):193-7.
2005: Angela Deutschländer; Friedrich Asmus; Thomas Gasser; Ulrich Steude; Kai Bötzel
Sporadic rapid-onset dystonia-parkinsonism syndrome: failure of bilateral pallidal stimulation.
Movement disorders : official journal of the Movement Disorder Society 2005;20(2):254-7.
2005: Bernd Sporer; Klaus Seelos; Friedrich Asmus; K Boetzel; Hans-Walter Pfister
Posterior fossa tremor induced by HIV-associated progressive multifocal leukoencephalopathy.
European neurology 2005;53(2):96-7.
2004: Alexander Zimprich; Saskia Biskup; Petra Leitner; Peter Lichtner; Matthew J Farrer; Sarah J Lincoln; Jennifer Kachergus; Mary Hulihan; Ryan Uitti; Donald B Calne; A Jon Stoessl; Ronald F Pfeiffer; Nadja Patenge; Iria Carballo Carbajal; Peter Vieregge; Friedrich Asmus; Bertram Müller-Myhsok; dennis dickson; Thomas Meitinger; Tim M Strom; Zbigniew K Wszolek; Thomas Gasser
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Neuron 2004;44(4):601-7.
2004: Alexander Zimprich; Bertram Müller-Myhsok; Matthew J Farrer; Petra Leitner; Manu Sharma; Mary Hulihan; Paul Lockhart; Audrey Strongosky; Jennifer Kachergus; Donald B Calne; Jon Stoessl; Ryan Uitti; Ronald F Pfeiffer; Claudia Trenkwalder; Nikolaus Homann; Erwin Ott; Karoline Wenzel; Friedrich Asmus; John Hardy; Zbigniew K Wszolek; Thomas Gasser
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
American journal of human genetics 2004;74(1):11-9.
2003: Dirk Sibbing; Friedrich Asmus; Inke R König; Sophie Tezenas du Montcel; Marie Vidailhet; S Sangla; Wolfgang H Oertel; Alexis Brice; Andreas Ziegler; Thomas Gasser; Oliver Bandmann
Candidate gene studies in focal dystonia.
Neurology 2003;61(8):1097-101.
2003: Alexander Zimprich; Friedrich Asmus; Petra Leitner; Mirna Castro; Benjamin Bereznai; Nikolaus Homann; Erwin Ott; A Wijnand F Rutgers; Gyri Wieditz; Claudia Trenkwalder; Thomas Gasser
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease.
Neurogenetics 2003;4(4):219-20.
2003: Monika Grabowski; Alexander Zimprich; Bettina Lorenz-Depiereux; Vera Kalscheuer; Friedrich Asmus; Thomas Gasser; Thomas Meitinger; Tim M Strom
The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted.
European journal of human genetics : EJHG 2003;11(2):138-44.
2002: Friedrich Asmus; Alexander Zimprich; Sophie Tezenas du Montcel; Christian Kabus; Günther Deuschl; Andreas Kupsch; Ulf Ziemann; Mirna Castro; Andrea A Kühn; Tim M Strom; Marie Vidailhet; Kailash P Bhatia; Alexandra Dürr; Nicholas W Wood; Alexis Brice; Thomas Gasser
Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.
Annals of neurology 2002;52(4):489-92.
2002: Oliver Bandmann; Friedrich Asmus; Dirk Sibbing; M Grundmann; Sibylle G Schwab; Jörg Müller; Dieter B Wildenauer; Werner Poewe; Thomas Gasser; Wolfgang H Oertel
Copper genes are not implicated in the pathogenesis of focal dystonia.
Neurology 2002;59(5):782-3.
2001: Alexander Zimprich; Monika Grabowski; Friedrich Asmus; M Naumann; Daniela Berg; M Bertram; K Scheidtmann; P Kern; Juliane Winkelmann; Bertram Müller-Myhsok; L Riedel; M Bauer; Thomas Müller; Mirna Castro; Thomas Meitinger; Tim M Strom; Thomas Gasser
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.
Nature genetics 2001;29(1):66-9.
2001: Friedrich Asmus; Alexander Zimprich; M Naumann; Daniela Berg; M Bertram; Andres O Ceballos-Baumann; R Pruszak-Seel; Christian Kabus; Martin Dichgans; S Fuchs; Bertram Müller-Myhsok; Thomas Gasser
Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.
Annals of neurology 2001;49(1):121-4.
1999: Roger Hullin; Friedrich Asmus; Andreas Ludwig; J Hersel; Peter Boekstegers
Subunit expression of the cardiac L-type calcium channel is differentially regulated in diastolic heart failure of the cardiac allograft.
Circulation 1999;100(2):155-63.
1997: Roger Hullin; Friedrich Asmus; G Steinbeck
Competitive RT-PCR for studying gene expression in micro biopsies.
Molecular and cellular biochemistry 1997;172(1-2):89-95.