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Autori: Hildebrandt Friedhelm

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Naslov Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract (Article)
Autori Kohl Stefan  Hwang Daw-Yang  Dworschak Gabriel C  Hilger Alina C  Saisawat Pawaree  Vivante Asaf  Stajic Natasa  Bogdanovic Radovan M  Reutter Heiko M  Kehinde Elijah O  Tasic Velibor  Hildebrandt Friedhelm 
Info JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2014), vol. 25 br. 9, str. 1917-1922
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract (Article)
Autori Hwang Daw-Yang  Dworschak Gabriel C  Kohl Stefan  Saisawat Pawaree  Vivante Asaf  Hilger Alina C  Reutter Heiko M  Soliman Neveen A  Bogdanovic Radovan M  Kehinde Elijah O  Tasic Velibor  Hildebrandt Friedhelm 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1429-1433
Projekat National Institutes of Health [R01-DK088767]; March of Dimes Foundation [6FY11-241]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations (Letter)
Autori Hoskins Bethan E  Cramer Carl HII  Tasic Velibor  Kehinde Elijah O  Ashraf Shazia  Bogdanovic Radovan M  Hoefele Julia  Pohl Martin  Hildebrandt Friedhelm 
Info NEPHROLOGY DIALYSIS TRANSPLANTATION, (2008), vol. 23 br. 2 , Suppl. , str. 777 -779
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9 (Article)
Autori Mucha B  Ozaltin F  Hinkes BG  Hasselbacher K  Ruf RG  Schultheiss M  Hangan D  Hoskins Bethan E  Everding AS  Bogdanovic Radovan M  Seeman T  Hoppe B  Hildebrandt Friedhelm 
Info PEDIATRIC RESEARCH, (2006), vol. 59 br. 2, str. 325-331
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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