Pronađeno: 1-10 / 12 radova

Autori: Hedrich Katja

>> Filter: Samo Article i Review

>> Sve godine

  • 1
  • 2
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
  • 1
  • 2
>> Sve godine

Ispis zapisa u formatu:TXT | BibTeX