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E Leumann

Showing results (41-50 of 47) with videos related to

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Schweizerische Medizinische Wochenschrift|July 12, 1994
[Cyclosporin in autoimmune diseases]F Follath, A Fontana, E Leumann, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severityB Hoppe, C J Danpure, G Rumsby, et al.
Contributions to Nephrology|January 1, 1985
Thyroid function in uremic children--studies at various stages of nephron loss and during treatment with hemodialysis and/or CAPDN G DeSanto, C Carella, R N Fine, et al.
Kidney International. Supplement|December 1, 1985
Thyroid function in uremic childrenN G De Santo, R N Fine, C Carella, et al.
Contributions to Nephrology|January 1, 1989
Therapy of renal anemia with recombinant human erythropoietin in children with end-stage renal diseaseP Scigalla, K E Bonzel, M Bulla, et al.
Journal of the American Society of Nephrology : JASN|February 1, 1997
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channelsS M Mulders, N V Knoers, A F Van Lieburg, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Schweizerische Medizinische Wochenschrift|July 12, 1994
[Cyclosporin in autoimmune diseases]F Follath, A Fontana, E Leumann, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1997
A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: lack of relationship between genotype, enzymic phenotype, and disease severityB Hoppe, C J Danpure, G Rumsby, et al.
Contributions to Nephrology|January 1, 1985
Thyroid function in uremic children--studies at various stages of nephron loss and during treatment with hemodialysis and/or CAPDN G DeSanto, C Carella, R N Fine, et al.
Kidney International. Supplement|December 1, 1985
Thyroid function in uremic childrenN G De Santo, R N Fine, C Carella, et al.
Contributions to Nephrology|January 1, 1989
Therapy of renal anemia with recombinant human erythropoietin in children with end-stage renal diseaseP Scigalla, K E Bonzel, M Bulla, et al.
Journal of the American Society of Nephrology : JASN|February 1, 1997
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channelsS M Mulders, N V Knoers, A F Van Lieburg, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
Pageof 5