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C Von Schnakenburg

Showing results (1-10 of 16) with videos related to

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Journal of Medical Genetics|June 1, 1997
Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the AGXT geneC von Schnakenburg, G Rumsby
Journal of Nephrology|May 30, 1998
Identification of new mutations in primary hyperoxaluria type 1 (PH1)C von Schnakenburg, G Rumsby
Annals of Human Genetics|July 1, 1997
Linkage of microsatellites to the AGXT gene on chromosome 2q37.3 and their role in prenatal diagnosis of primary hyperoxaluria type 1C von Schnakenburg, T Weir, G Rumsby
Pediatric Nephrology (Berlin, Germany)|April 27, 2001
A meta-analysis of cytotoxic treatment for frequently relapsing nephrotic syndrome in childrenK Latta, C von Schnakenburg, J H Ehrich
Journal of Inherited Metabolic Disease|November 5, 1997
Primary hyperoxaluria type 1: diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)A C Tarn, C von Schnakenburg, G Rumsby
Pediatric Transplantation|March 29, 2001
Post-transplant epididymitis and orchitis following Listeria monocytogenes septicaemiaC von Schnakenburg, B Hinrichs, J Fuchs, et al.
Klinische Padiatrie|October 3, 2001
[Pseudo-Acanthosis nigricans in a 12 year old boy after kidney transplantation]C von Schnakenburg, B Enke, K Jürgens, et al.
Klinische Padiatrie|January 11, 2005
[Sclerosing peritonitis without reduced ultrafiltration as complication of peritoneal dialysis]C von Schnakenburg, M Pohl, K Häffner, et al.
Archives of Disease in Childhood|June 24, 2009
Sonographic long-term study: paediatric growth charts for single kidneysE M Spira, C Jacobi, A Frankenschmidt, et al.
Klinische Padiatrie|July 13, 2006
[Left flank tumor of fluctuating size in a 5-week-old boy: perirenal urinoma caused by urethral valves]C von Schnakenburg, A Dorn, C Jacobi, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|June 1, 1997
Primary hyperoxaluria type 1: a cluster of new mutations in exon 7 of the AGXT geneC von Schnakenburg, G Rumsby
Journal of Nephrology|May 30, 1998
Identification of new mutations in primary hyperoxaluria type 1 (PH1)C von Schnakenburg, G Rumsby
Annals of Human Genetics|July 1, 1997
Linkage of microsatellites to the AGXT gene on chromosome 2q37.3 and their role in prenatal diagnosis of primary hyperoxaluria type 1C von Schnakenburg, T Weir, G Rumsby
Pediatric Nephrology (Berlin, Germany)|April 27, 2001
A meta-analysis of cytotoxic treatment for frequently relapsing nephrotic syndrome in childrenK Latta, C von Schnakenburg, J H Ehrich
Journal of Inherited Metabolic Disease|November 5, 1997
Primary hyperoxaluria type 1: diagnostic relevance of mutations and polymorphisms in the alanine:glyoxylate aminotransferase gene (AGXT)A C Tarn, C von Schnakenburg, G Rumsby
Pediatric Transplantation|March 29, 2001
Post-transplant epididymitis and orchitis following Listeria monocytogenes septicaemiaC von Schnakenburg, B Hinrichs, J Fuchs, et al.
Klinische Padiatrie|October 3, 2001
[Pseudo-Acanthosis nigricans in a 12 year old boy after kidney transplantation]C von Schnakenburg, B Enke, K Jürgens, et al.
Klinische Padiatrie|January 11, 2005
[Sclerosing peritonitis without reduced ultrafiltration as complication of peritoneal dialysis]C von Schnakenburg, M Pohl, K Häffner, et al.
Archives of Disease in Childhood|June 24, 2009
Sonographic long-term study: paediatric growth charts for single kidneysE M Spira, C Jacobi, A Frankenschmidt, et al.
Klinische Padiatrie|July 13, 2006
[Left flank tumor of fluctuating size in a 5-week-old boy: perirenal urinoma caused by urethral valves]C von Schnakenburg, A Dorn, C Jacobi, et al.
Pageof 2