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S J Scheinman

Showing results (31-40 of 39) with videos related to

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The Journal of Urology|October 23, 1998
Medical reduction of stone risk in a network of treatment centers compared to a research clinicJ Lingeman, H Mardis, R Kahnoski, et al.
The Journal of Urology|March 19, 1999
Divergence between stone composition and urine supersaturation: clinical and laboratory implicationsJ Lingeman, R Kahnoski, H Mardis, et al.
Kidney International|November 13, 2001
Glomerular protein sieving and implications for renal failure in Fanconi syndromeA G Norden, M Lapsley, P J Lee, et al.
Journal of the American Society of Nephrology : JASN|January 1, 1995
Characterization of carrier females and affected males with X-linked recessive nephrolithiasisS C Reinhart, A G Norden, M Lapsley, et al.
Kidney International|March 7, 2008
A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunctionP Gailly, F Jouret, D Martin, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|September 12, 1998
CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasisR R Hoopes, P A Hueber, R J Reid, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
The Journal of Urology|October 23, 1998
Medical reduction of stone risk in a network of treatment centers compared to a research clinicJ Lingeman, H Mardis, R Kahnoski, et al.
The Journal of Urology|March 19, 1999
Divergence between stone composition and urine supersaturation: clinical and laboratory implicationsJ Lingeman, R Kahnoski, H Mardis, et al.
Kidney International|November 13, 2001
Glomerular protein sieving and implications for renal failure in Fanconi syndromeA G Norden, M Lapsley, P J Lee, et al.
Journal of the American Society of Nephrology : JASN|January 1, 1995
Characterization of carrier females and affected males with X-linked recessive nephrolithiasisS C Reinhart, A G Norden, M Lapsley, et al.
Kidney International|March 7, 2008
A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunctionP Gailly, F Jouret, D Martin, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|September 12, 1998
CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasisR R Hoopes, P A Hueber, R J Reid, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
Pageof 4