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Autori: Ludwig Michael

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Naslov Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association (Article)
Autori Saisawat Pawaree Kohl Stefan Hilger Alina C Hwang Daw-Yang Gee Heon Yung Dworschak Gabriel C Tasic Velibor Pennimpede Tracie Natarajan Sivakumar Sperry Ethan Matassa Danilo S Stajic Natasa Bogdanovic Radovan M de Blaauw Ivo Marcelis Carlo LM Wijers Charlotte HW Bartels Enrika Schmiedeke Eberhard Schmidt Dominik Maerzheuser Stefanie Grasshoff-Derr Sabine Holland-Cunz Stefan Ludwig Michael Noethen Markus M Draaken Markus Brosens Erwin Heij Hugo Tibboel Dick Herrmann Bernhard G Solomon Benjamin D de Klein Annelies van Rooij Iris ALM Esposito Franca Reutter Heiko M Hildebrandt Friedhelm 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1310-1317
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]; March of Dimes Foundation [6FY11-241]; Division of Intramural Research; National Human Genome Research Institute (NHGRI); National Institutes of Health and Human services; Bundesministerium fur B
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Liddle syndrome in a Serbian family and literature review of underlying mutations (Review)
Autori Bogdanovic Radovan M Kuburovic Vladimir Stajic Natasa Mughal S Hilger A Ninic Sanja S Prijic Sergej M  Ludwig Michael 
Info EUROPEAN JOURNAL OF PEDIATRICS, (2012), vol. 171 br. 3, str. 471-478
Projekat Ministry of Science of the Republic of Serbia[145046]; Ministry of Education and Science[OI175079]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Liddle syndrome: the first family with proven mutation (PRO618SER) in the southeastern Europe (Meeting Abstract)
Autori Bogdanovic Radovan M Kuburovic Vladimir Stajic Natasa Mughal S Hilger A Kosutic Jovan Lj Ninic Sanja S Prijic Sergej M  Vukomanovic Vladislav A Ludwig Michael 
Info PEDIATRIC NEPHROLOGY, (2011), vol. 26 br. 9, str. 1717-1717
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency (Article)
Autori Bogdanovic Radovan M Draaken Markus Toromanovic Alma Djordjevic Maja S Stajic Natasa Ludwig Michael 
Info PEDIATRIC NEPHROLOGY, (2010), vol. 25 br. 11, str. 2363-2368
Projekat Ministry of Science, Republic of Serbia [145046D]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Dent Disease (Article)
Autori Pavicevic Snezana Bogdanovic Radovan M Ludwig Michael Samardzic Mira P 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2008), vol. 136 br. , Suppl. Suppl. 4, str. 312-315
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Dent disease - from clinical features to gene analysis (Meeting Abstract)
Autori Pavicevic Snezana Bogdanovic Radovan M Ludwig Michael 
Info PEDIATRIC NEPHROLOGY, (2007), vol. 22 br. 9, str. 1498-1498
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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