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Naslov Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy (Article)
Autori Atkinson Derek Nikodinovic-Glumac Jelena Asselbergh Bob Ermanoska Biljana Blocquel David Steiner Regula Estrada-Cuzcano Alejandro Peeters Kristien Ooms Tinne De Vriendt Els Yang Xiang-Lei Hornemann Thorsten Milic-Rasic Vedrana M Jordanova Albena 
Info NEUROLOGY, (2017), vol. 88 br. 6, str. 533-542
Projekat University of Antwerp [TOP BOF 29069]; Fund for Scientific Research-Flanders (FWO) [G.0543.13, G0D7713N]; Belgian Association against Neuromuscular Disorders (ABMM); NIH [NS 085092]; Fund for Scientific Research-Flanders
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family (Meeting Abstract)
Autori Atkinson Derek Asselbergs B De Vriendt Els Ooms T Estrada-Cuzcano A Nikodinovic Jelena Milic-Rasic Vedrana M Jordanova Albena 
Info JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, (2016), vol. 21 br. 3, str. 233-233
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 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 MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2 (Article)
Autori Verhoeven K Claeys Kristl G Zuchner S Schroder JM Weis J Ceuterick C Jordanova Albena Nelis Eva De Vriendt Els Van Hul M Seeman Pavel Mazanec Radim Saifi GM Szigeti K Mancias P Butler IJ Kochanski Andrzej Ryniewicz B De Bleecker Jan L Van den Bergh Peter 
Info BRAIN, (2006), vol. 129 br. , str. 2093-2102
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe (Article)
Autori Dork T Macek M Mekus F Tummler B Tzountzouris J Casals T Krebsova A Koudova M Sakmaryova I Macek M Vavrova V Zemkova D Ginter E Petrova NV Ivaschenko T Baranov V Witt M Pogorzelski A Bal J Zekanowsky C Wagner K Stuhrmann M Bauer I Seydewitz HH Neumann T Jakubiczka S Kraus C Thamm B Nechiporenko M Livshits LA Mosse N Tsukerman G Kadasi Ludevit Ravnik-Glavac M Glavac D Komel R Vouk K Kucinskas V Krumina A Teder M Kocheva S Efremov GD Onay T Kirdar B Malone G Schwarz M Zhou ZQ Friedman KJ Carles S Claustres M Bozon D Verlingue C Ferec C Tzetis M Kanavakis E Cuppens H Bombieri C Pignatti PF Sangiuolo F Jordanova Albena Kusic Jelena S  Radojkovic Dragica P Sertic Jadranka Richter D Rukavina-Stavljenic Ana Bjorck E Strandvik B Cardoso H Montgomery M Nakielna B Hughes D Estivill X Aznarez I Tullis E Tsui LC Zielenski J 
Info HUMAN GENETICS, (2000), vol. 106 br. 3, str. 259-268
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