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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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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