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A D Paterson

Showing results (61-70 of 85) with videos related to

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BMJ (Clinical Research Ed.)|February 22, 1992
Cost benefits of low dose subcutaneous erythropoietin in patients with anaemia of end stage renal diseaseM E Stevens, G P Summerfield, A A Hall, et al.
Kidney International|May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) geneY Pei, K Wang, M Kasenda, et al.
Clinical Genetics|February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Nephron|January 1, 1986
A comparison of fine needle aspiration cytology and tru-cut tissue biopsy in the diagnosis of acute renal allograft rejectionR S Reeve, G Cooksey, P W Wenham, et al.
Placenta|February 20, 2004
Umbilical vein and placental vessels from newborns with hereditary haemorrhagic telangiectasia type 1 genotype are normal despite reduced expression of endoglinN L M Chan, A Bourdeau, S Vera, et al.
American Journal of Human Genetics|February 17, 2001
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22E Héon, A D Paterson, M Fraser, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 24, 1999
Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophreniaV S Basile, M Masellis, F Badri, et al.
British Journal of Cancer|May 1, 1985
Treatment of malignant hypercalcaemia with clodronateR C Percival, A D Paterson, A J Yates, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
BMJ (Clinical Research Ed.)|February 22, 1992
Cost benefits of low dose subcutaneous erythropoietin in patients with anaemia of end stage renal diseaseM E Stevens, G P Summerfield, A A Hall, et al.
Kidney International|May 9, 1998
A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) geneY Pei, K Wang, M Kasenda, et al.
Clinical Genetics|February 1, 2005
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13S H E Zaidi, V Peltekova, S Meyer, et al.
Nephron|January 1, 1986
A comparison of fine needle aspiration cytology and tru-cut tissue biopsy in the diagnosis of acute renal allograft rejectionR S Reeve, G Cooksey, P W Wenham, et al.
Placenta|February 20, 2004
Umbilical vein and placental vessels from newborns with hereditary haemorrhagic telangiectasia type 1 genotype are normal despite reduced expression of endoglinN L M Chan, A Bourdeau, S Vera, et al.
American Journal of Human Genetics|February 17, 2001
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22E Héon, A D Paterson, M Fraser, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 24, 1999
Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophreniaV S Basile, M Masellis, F Badri, et al.
British Journal of Cancer|May 1, 1985
Treatment of malignant hypercalcaemia with clodronateR C Percival, A D Paterson, A J Yates, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Pageof 9