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Autori: De Jonghe Peter

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Naslov Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response (Article)
Autori Beijer Danique Agnew Thomas Rack Johannes Gregor Matthias Prokhorova Evgeniia Deconinck Tine Ceulemans Berten Peric Stojan Z  Milic-Rasic Vedrana M De Jonghe Peter Ahel Ivan Baets Jonathan 
Info LIFE SCIENCE ALLIANCE, (2021), vol. 4 br. 11, str. -
Projekat Association Belge contre les Maladies Neuromusculaire (ABMM) -Aide a la Recherche ASBL [2017-2018/05]; EU FP7/2007-2013 [2012-305121]; EU Horizon 2020 program [779257]; Wellcome TrustEuropean Commission [101794, 210634]; Biotechnology and Bi
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Mutations in SACS cause atypical and late-onset forms of ARSACS (Article)
Autori Baets Jonathan Deconinck Tine Smets K Goossens D Van den Bergh Peter Dahan K Schmedding E Santens P Milic-Rasic Vedrana M Van Damme P Robberecht Wim De Meirleir L Michielsens B Del-Favero J Jordanova Albena De Jonghe Peter 
Info NEUROLOGY, (2010), vol. 75 br. 13, str. 1181-1188
Projekat University of Antwerp ; Fund for Scientific Research (FWO-Flanders) ; Medical Foundation Queen Elisabeth (GSKE) ; "Association Belge contre les Maladies Neuromusculaires" (ABMM) ; Belgian Federal Science Policy Office (BELSPO) ; Flemish Government ; E. vo
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome (Article)
Autori Rakocevic-Stojanovic Vidosava M Milic-Rasic Vedrana M Peric Stojan Z  Baets Jonathan Timmerman Vincent Dierick Ines Pavlovic Sanja De Jonghe Peter 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2010), vol. 296 br. 1-2, str. 107-109
Projekat FWO-Flanders
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Naslov Heterozygous missense mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy or silver syndrome (Meeting Abstract)
Autori Rakocevic-Stojanovic Vidosava M Milic-Rasic Vedrana M Van Broeckhoven C De Jonghe Peter Nelis Eva Nikolic Ana V Tasic Z Marjanovic Ivan V Lavrnic Dragana V 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2009), vol. 285 br. , Suppl. Suppl. 1, str. S333-S333
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study (Article)
Autori Dierick Ines Baets Jonathan Irobi Joy Jacobs An De Vriendt Els Deconinck Tine Merlini Luciano Van den Bergh Peter Milic-Rasic Vedrana M Robberecht Wim Fischer Dirk Morales Raul Juntas Mitrovic Zoran Seeman Pavel Mazanec Radim Kochanski Andrzej Jordanova Albena Auer-Grumbach Michaela Helderman-van den Enden ATJM Wokke John HJ Nelis Eva De Jonghe Peter Timmerman Vincent 
Info BRAIN, (2008), vol. 131 br. , str. 1217-1227
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Genotype-phenotype analysis in patients with giant axonal neuropathy (GAN) (Article)
Autori Koop Olga Schirmacher Anja Nelis Eva Timmerman Vincent De Jonghe Peter Ringelstein Bernd Milic-Rasic Vedrana M Evrard Philippe Gdrtner Jutta Claeys Kristl G Appenzeller Silke Rautenstrauss Bernd Hiffine Kathrin Ramos-Arroyo Maria A Wrle Helmut Moilanen Jukka S HammanS Simon Kuhlenbdumer Gregor 
Info NEUROMUSCULAR DISORDERS, (2007), vol. 17 br. 8 , Suppl. , str. 624 -630
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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