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Sickle cell nephropathy

Journal of the American Society of Nephrology, 1999, Vol.10 (1), p.187-192

1999

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Transplantation for primary hyperoxaluria in the United States

Kidney international, 1999-09, Vol.56 (3), p.1094-1100

1999

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Primary hyperoxaluria in infants: Medical, ethical, and economic issues

The Journal of pediatrics, 1999-12, Vol.135 (6), p.746-750

1999

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Tools to detect and modify sickle cell nephropathy

Kidney international, 2006-06, Vol.69 (11), p.1927-1930

Scheinman, J.I.

2006

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Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

American journal of human genetics, 1993-08, Vol.53 (2), p.417-432

1993

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Transplantation for primary hyperoxaluria in the USA

Nephrology, dialysis, transplantation, 1995, Vol.10 (supp8), p.42-46

1995

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Primary hyperoxaluria: Therapeutic strategies for the 90's

Kidney international, 1991-09, Vol.40 (3), p.389-399

Scheinman, Jon I.

1991

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Renal disease in type I glycogen storage disease

The New England journal of medicine, 1988-01, Vol.318 (1), p.7-11

1988

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Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1

Nephrology, dialysis, transplantation, 1995, Vol.10 (supp8), p.53-57

1995

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Neoantigen of the polymerized ninth component of complement: characterization of a monoclonal antibody and immunohistochemical localization in renal disease

The Journal of clinical investigation, 1983-08, Vol.72 (2), p.560-573

1983

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Monoclonal antibody to type IV collagen with selective basement membrane localization

Laboratory investigation, 1984-01, Vol.50 (1), p.101

1984

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Antibodies to laminin in Chagas' disease

The Journal of experimental medicine, 1982-04, Vol.155 (4), p.1161-1171

1982

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Polyantigenic expansion of basement membrane constituents in diabetic nephropathy

Diabetes (New York, N.Y.), 1983-06, Vol.32 Suppl 2 (Supplement_2), p.34-39

1983

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Amelioration of Proximal Renal Tubular Dysfunction in Type I Glycogen Storage Disease with Dietary Therapy

The New England journal of medicine, 1990-08, Vol.323 (9), p.590-593

1990

Volltextzugriff (PDF)

Sickle cell disease and the kidney

Nature clinical practice. Nephrology, 2009-02, Vol.5 (2), p.78-88

Scheinman, Jon I

2009

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Chronic renal failure: an overview from a pediatric perspective

Nephron (2015), 1998-10, Vol.80 (2), p.134-148

1998

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The Kidney in Acid-Base Balance

The Pediatric clinics of North America, 1995-12, Vol.42 (6), p.1365-1395

1995

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Hemofiltration in children

International journal of artificial organs, 1998-07, Vol.21 (7), p.371-377

1998

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Successful strategies for renal transplantation in primary oxalosis

Kidney international, 1984-05, Vol.25 (5), p.804-811

1984

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Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity

Kidney international, 1992-12, Vol.42 (6), p.1408-1411

1992

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Capillary gas chromatography measurement of oxalate in plasma and urine

Kidney international, 1985-07, Vol.28 (1), p.82-84

1985

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Hyperglycaemia associated with lactic acidaemia in a renal allograft recipient with type I glycogen storage disease

Journal of inherited metabolic disease, 1991-01, Vol.14 (1), p.80-86

1991

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Radiological aspects of primary hyperoxaluria

American journal of roentgenology (1976), 1986-02, Vol.146 (2), p.395-401

1986

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Recent data on results of isolated kidney or combined kidney/liver transplantation in the U.S.A. for primary hyperoxaluria

Journal of nephrology, 1998-03, Vol.11 Suppl 1, p.42-45

Scheinman, J I

1998

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Optimal management of renal failure in primary hyperoxaluria in infancy, and the use of combined kidney/liver transplantation

Pediatric transplantation, 1997-08, Vol.1 (1), p.4-7

1997

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Sickle cell nephropathy

Transplantation for primary hyperoxaluria in the United States

Primary hyperoxaluria in infants: Medical, ethical, and economic issues

Tools to detect and modify sickle cell nephropathy

Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation

Transplantation for primary hyperoxaluria in the USA

Primary hyperoxaluria: Therapeutic strategies for the 90's

Renal disease in type I glycogen storage disease

Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1

Neoantigen of the polymerized ninth component of complement: characterization of a monoclonal antibody and immunohistochemical localization in renal disease

Monoclonal antibody to type IV collagen with selective basement membrane localization

Antibodies to laminin in Chagas' disease

Polyantigenic expansion of basement membrane constituents in diabetic nephropathy

Amelioration of Proximal Renal Tubular Dysfunction in Type I Glycogen Storage Disease with Dietary Therapy

Sickle cell disease and the kidney

Chronic renal failure: an overview from a pediatric perspective

The Kidney in Acid-Base Balance

Hemofiltration in children

Successful strategies for renal transplantation in primary oxalosis

Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity

Capillary gas chromatography measurement of oxalate in plasma and urine

Hyperglycaemia associated with lactic acidaemia in a renal allograft recipient with type I glycogen storage disease

Radiological aspects of primary hyperoxaluria

Recent data on results of isolated kidney or combined kidney/liver transplantation in the U.S.A. for primary hyperoxaluria

Optimal management of renal failure in primary hyperoxaluria in infancy, and the use of combined kidney/liver transplantation

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