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Autori: Hedrich Katja

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Naslov Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification (Article)
Autori Djarmati Ana  Guzvic Miodrag  Gruenewald Anne  Lang Anthony E  Pramstaller Peter P  Simon David K  Kaindl Angela M  Vieregge Peter  Nygren Anders OH  Beetz Christian  Hedrich Katja  Klein Christine 
Info MOVEMENT DISORDERS, (2007), vol. 22 br. 12 , Suppl. , str. 1708 -1714
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease? (Article)
Autori Djarmati Ana  Hedrich Katja  Svetel Marina V  Lohnau T  Schwinger E  Romac Stanka P  Pramstaller Peter P  Kostic Vladimir S  Klein Christine 
Info MOVEMENT DISORDERS, (2006), vol. 21 br. 9, str. 1526-1530
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease (Article)
Autori Hedrich Katja  Winkler Susan  Hagenah Johann M  Kabakci Kemal  Kasten Meike  Schwinger E  Volkmann Jens  Pramstaller Peter P  Kostic Vladimir S  Vieregge Peter  Klein Christine 
Info MOVEMENT DISORDERS, (2006), vol. 21 br. 9, str. 1506-1510
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease Role of a single hit? (Article)
Autori Hedrich Katja  Hagenah Johann M  Djarmati Ana  Hiller A  Lohnau T  Lasek K  Grunewald RA  Hilker R  Steinlechner S  Boston H  Kock Norman  Schneider-Gold C  Kress W  Siebner Hartwig R  Binkofski Ferdinand  Lencer R  Munchau A  Klein Christine 
Info ARCHIVES OF NEUROLOGY, (2006), vol. 63 br. 6, str. 833-838
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease? (Article)
Autori Hedrich Katja  Pramstaller Peter P  Stubke K  Hiller A  Kabakci Kemal  Purmann S  Kasten Meike  Scaglione C  Schwinger E  Volkmann J  Kostic Vladimir S  Vieregge Peter  Martinelli P  Abbruzzese G  Klein Christine  Zuhlke C 
Info MOVEMENT DISORDERS, (2005), vol. 20 br. 8, str. 1060-1062
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism (Article)
Autori Klein Christine  Djarmati Ana  Hedrich Katja  Schafer N  Scaglione C  Marchese R  Kock Norman  Schule B  Hiller A  Lohnau T  Winkler Susan  Wiegers K  Hering R  Bauer P  Riess O  Abbruzzese G  Martinelli P  Pramstaller Peter P 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2005), vol. 13 br. 9, str. 1086-1093
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genetic heterogeneity in ten families with myoclonus-dystonia (Article)
Autori Schule B  Kock Norman  Svetel Marina V  Dragasevic Natasa T  Hedrich Katja  Aguiar PD  Liu L  Kabakci Kemal  Garrels J  Meyer EM  Berisavac Ivana I  Schwinger E  Kramer PL  Ozelius LJ  Klein Christine  Kostic Vladimir S 
Info JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, (2004), vol. 75 br. 8, str. 1181-1185
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Mutations in DYT1 - Extension of the phenotypic and mutational spectrum (Article)
Autori Kabakci Kemal  Hedrich Katja  Leung JC  Mitterer M  Vieregge Peter  Lencer R  Hagenah Johann M  Garrels J  Witt K  Klostermann F  Svetel Marina V  Friedman J  Kostic Vladimir S  Bressman SB  Breakefield XO  Ozelius LJ  Pramstaller Peter P  Klein Christine 
Info NEUROLOGY, (2004), vol. 62 br. 3, str. 395-400
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease (Article)
Autori Hedrich Katja  Djarmati Ana  Schafer N  Hering R  Wellenbrock C  Weiss PH  Hilker R  Vieregge Peter  Ozelius LJ  Heutink P  Bonifati V  Schwinger E  Lang Anthony E  Noth J  Bressman SB  Pramstaller Peter P  Riess O  Klein Christine 
Info NEUROLOGY, (2004), vol. 62 br. 3, str. 389-394
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov The R98Q variation in DJ-1 represents a rare polymorphism (Letter)
Autori Hedrich Katja  Schafer N  Hering R  Hagenah Johann M  Lanthaler AJ  Schwinger E  Kramer PL  Ozelius LJ  Bressman SB  Abbruzzese G  Martinelli P  Kostic Vladimir S  Pramstaller Peter P  Vieregge Peter  Riess O  Klein Christine 
Info ANNALS OF NEUROLOGY, (2004), vol. 55 br. 1, str. 145-145
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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