V E Torres|P C Harris - JoVE Visualize

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Archives of Pathology & Laboratory Medicine|February 1, 1990

The liver in autosomal dominant polycystic kidney disease. Implications for pathogenesisA Ramos, V E Torres, K E Holley, et al.

Kidney International|June 1, 1994

Renal ammonia in autosomal dominant polycystic kidney diseaseV E Torres, D S Keith, K P Offord, et al.

Blood|November 15, 1990

Molecular and hematologic characterization of Scottish-Irish type (epsilon gamma delta beta)zero thalassemiaR J Trent, B G Williams, A Kearney, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1992

Cyst fluid from human autosomal dominant polycystic kidneys promotes cyst formation and expansion by renal epithelial cells in vitroM Ye, M Grant, M Sharma, et al.

Mayo Clinic Proceedings|March 1, 1984

Meclofenamate treatment of recurrent idiopathic nephrotic syndrome with focal segmental glomerulosclerosis after renal transplantationV E Torres, J A Velosa, K E Holley, et al.

Nature|August 30, 1990

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.

Genomics|June 1, 1996

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy geneP G Olsson, C Löhning, S Horsley, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomereM A Vickers, P Vyas, P C Harris, et al.

British Heart Journal|October 1, 1993

Pathogenesis of oedema in chronic severe anaemia: studies of body water and sodium, renal function, haemodynamic variables, and plasma hormonesI S Anand, Y Chandrashekhar, R Ferrari, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 1, 1990

Long-term outcome of renal transplantation in autosomal dominant polycystic kidney diseaseP M Fitzpatrick, V E Torres, J W Charboneau, et al.

Pageof 16

Showing results (71-80 of 157) with videos related to

Sort By:

Pageof 16

Archives of Pathology & Laboratory Medicine|February 1, 1990

The liver in autosomal dominant polycystic kidney disease. Implications for pathogenesisA Ramos, V E Torres, K E Holley, et al.

Kidney International|June 1, 1994

Renal ammonia in autosomal dominant polycystic kidney diseaseV E Torres, D S Keith, K P Offord, et al.

Blood|November 15, 1990

Molecular and hematologic characterization of Scottish-Irish type (epsilon gamma delta beta)zero thalassemiaR J Trent, B G Williams, A Kearney, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1992

Cyst fluid from human autosomal dominant polycystic kidneys promotes cyst formation and expansion by renal epithelial cells in vitroM Ye, M Grant, M Sharma, et al.

Mayo Clinic Proceedings|March 1, 1984

Meclofenamate treatment of recurrent idiopathic nephrotic syndrome with focal segmental glomerulosclerosis after renal transplantationV E Torres, J A Velosa, K E Holley, et al.

Nature|August 30, 1990

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.

Genomics|June 1, 1996

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy geneP G Olsson, C Löhning, S Horsley, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomereM A Vickers, P Vyas, P C Harris, et al.

British Heart Journal|October 1, 1993

Pathogenesis of oedema in chronic severe anaemia: studies of body water and sodium, renal function, haemodynamic variables, and plasma hormonesI S Anand, Y Chandrashekhar, R Ferrari, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 1, 1990

Long-term outcome of renal transplantation in autosomal dominant polycystic kidney diseaseP M Fitzpatrick, V E Torres, J W Charboneau, et al.

Pageof 16