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Boris Utsch

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American Journal of Medical Genetics. Part A|July 21, 2004
Dent disease-like phenotype and the chloride channel ClC-4 (CLCN4) geneMichael Ludwig, Boris Utsch
Deutsches Arzteblatt International|October 7, 2014
Urinalysis in children and adolescentsBoris Utsch, Günter Klaus
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 25, 2006
Recent advances in understanding the clinical and genetic heterogeneity of Dent's diseaseMichael Ludwig, Boris Utsch, Leo A H Monnens
Scandinavian Journal of Urology and Nephrology|December 17, 2003
Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadiasBoris Utsch, Ali Kaya, Atila Ozburun, et al.
Klinische Padiatrie|March 23, 2019
[Applicability of Neonatal Pain Scores depending on Level of Education and Work Experience in Child Care]Johanna Kaiser, Jan de Laffolie, Judith Kappesser, et al.
Human Genetics|June 20, 2002
A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?Boris Utsch, Karl Becker, Detlef Brock, et al.
Pediatric Nephrology (Berlin, Germany)|June 30, 2006
Hypercalciuria in patients with CLCN5 mutationsMichael Ludwig, Boris Utsch, Bernd Balluch, et al.
Kidney & Blood Pressure Research|July 30, 2003
Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variantMichael Ludwig, Siegfried Waldegger, Matti Nuutinen, et al.
Klinische Padiatrie|September 16, 2021
[Item Reduction to Improve Practicability of Neonatal Pain Assessment Tools - Comparison of NFCSshort and PIPP in Daily Clinical Practice]Max Tischler, Judith Kappesser, Boris Utsch, et al.
Human Genetics|May 17, 2005
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalizationMichael Ludwig, Jolanta Doroszewicz, Hannsjörg W Seyberth, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|July 21, 2004
Dent disease-like phenotype and the chloride channel ClC-4 (CLCN4) geneMichael Ludwig, Boris Utsch
Deutsches Arzteblatt International|October 7, 2014
Urinalysis in children and adolescentsBoris Utsch, Günter Klaus
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 25, 2006
Recent advances in understanding the clinical and genetic heterogeneity of Dent's diseaseMichael Ludwig, Boris Utsch, Leo A H Monnens
Scandinavian Journal of Urology and Nephrology|December 17, 2003
Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadiasBoris Utsch, Ali Kaya, Atila Ozburun, et al.
Klinische Padiatrie|March 23, 2019
[Applicability of Neonatal Pain Scores depending on Level of Education and Work Experience in Child Care]Johanna Kaiser, Jan de Laffolie, Judith Kappesser, et al.
Human Genetics|June 20, 2002
A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?Boris Utsch, Karl Becker, Detlef Brock, et al.
Pediatric Nephrology (Berlin, Germany)|June 30, 2006
Hypercalciuria in patients with CLCN5 mutationsMichael Ludwig, Boris Utsch, Bernd Balluch, et al.
Kidney & Blood Pressure Research|July 30, 2003
Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variantMichael Ludwig, Siegfried Waldegger, Matti Nuutinen, et al.
Klinische Padiatrie|September 16, 2021
[Item Reduction to Improve Practicability of Neonatal Pain Assessment Tools - Comparison of NFCSshort and PIPP in Daily Clinical Practice]Max Tischler, Judith Kappesser, Boris Utsch, et al.
Human Genetics|May 17, 2005
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalizationMichael Ludwig, Jolanta Doroszewicz, Hannsjörg W Seyberth, et al.
Pageof 4