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Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart

Molecular genetics and metabolism, 2007-07, Vol.91 (3), p.285-293

2007

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Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome

Pediatric nephrology (Berlin, West), 2009-11, Vol.24 (11), p.2177-2185

2009

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Treatment with microemulsified cyclosporine in children with frequently relapsing nephrotic syndrome

Nephrology, dialysis, transplantation, 2010-12, Vol.25 (12), p.3956-3962

2010

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Tubulointerstitial nephritis antigen: primary structure, expression and role in health and disease

Nephron (2015), 2002-01, Vol.90 (1), p.1-7

2002

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Combination therapy with steroids and mizoribine in juvenile SLE: a randomized controlled trial

Pediatric nephrology (Berlin, West), 2010-05, Vol.25 (5), p.877-882

2010

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Isolation, tissue localization, and cellular characterization of progenitors derived from adult human salivary glands

Cloning and stem cells, 2007, Vol.9 (2), p.191-205

2007

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The 1998 report of the Japanese national registry data on pediatric end-stage renal disease patients

Pediatric nephrology (Berlin, West), 2002-06, Vol.17 (6), p.456-461

2002

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Erratum to: Combination therapy with steroids and mizoribine in juvenile SLE: a randomized controlled trial

Pediatric nephrology (Berlin, West), 2010-05, Vol.25 (5), p.995-995

2010

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Identification of a single base insertion in the COL4A5 gene in Alport syndrome

Kidney international, 1993-11, Vol.44 (5), p.1091-1096

1993

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Intracellular distribution of the Wilson's disease gene product (atpase7b) afterin vitro andin vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease

Hepatology (Baltimore, Md.), 1998-03, Vol.27 (3), p.799-807

1998

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In situ evaluation of podocin in normal and glomerular diseases

Kidney international, 2003-12, Vol.64 (6), p.2092-2099

2003

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Mutations in the COL4A5 gene in Alport syndrome: A possible mutation in primordial germ cells

Kidney international, 1994-11, Vol.46 (5), p.1307-1314

1994

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A mouse model of renal tubular injury of tyrosinemia type 1 : Development of de Toni Fanconi syndrome and apoptosis of renal tubular cells in Fah/Hpd double mutant mice

Journal of the American Society of Nephrology, 2000-02, Vol.11 (2), p.291-300

2000

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Comparison of asymptomatic and symptomatic childhood glomerulonephritis progressing to renal failure : a report of Kyushu Pediatric Nephrology Study Group

Pediatric nephrology (Berlin, West), 1994-08, Vol.8 (4), p.423-426

1994

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Intracellular distribution of the Wilson's disease gene product (atpase7b) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease

Hepatology (Baltimore, Md.), 1998-03, Vol.27 (3), p.799-807

1998

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Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria

Kidney international, 1997-10, Vol.52 (4), p.895-900

1997

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A case of minimal change nephrotic syndrome associated with acute renal failure after excessive exercise

The Japanese Journal of Nephrology, 1993/04/25, Vol.35(4), pp.387-391

1993

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The Standard Manual for School Urinary Screening in Kyushu: A Project for Standardization of Urinary Screening system

Japanese journal of pediatric nephrology, 2008/11/15, Vol.21(2), pp.146-156

2008

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Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria

Kidney international, 1999-01, Vol.55 (1), p.63-70

1999

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The 2003 Report of the Japanese National Registry Data on Pediatric End-Stage Renal Disease Patients

Japanese journal of pediatric nephrology, 2004, Vol.17(2), pp.121-130

2004

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Developmental changes in carbonic anhydrase II in the rat kidney

Pediatric nephrology (Berlin, West), 1998-05, Vol.12 (4), p.263-268

1998

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Childhood-type myositis and linear scleroderma

Neurology, 1983-07, Vol.33 (7), p.928-928

1983

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Another autosomal recessive form of focal glomerulosclerosis with neurological findings

Pediatric nephrology (Berlin, West), 2002, Vol.17 (1), p.16-19

2002

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Effect of superoxide dismutase on serum sickness nephritis

The Japanese Journal of Nephrology, 1990, Vol.32(9), pp.967-972

1990

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The influence of exercise loading for a long period on the renal function of the children with mesangial proliferative glomerulonephritis

The Japanese Journal of Nephrology, 1991, Vol.33(11), pp.1081-1087

1991

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Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart

Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome

Treatment with microemulsified cyclosporine in children with frequently relapsing nephrotic syndrome

Tubulointerstitial nephritis antigen: primary structure, expression and role in health and disease

Combination therapy with steroids and mizoribine in juvenile SLE: a randomized controlled trial

Isolation, tissue localization, and cellular characterization of progenitors derived from adult human salivary glands

The 1998 report of the Japanese national registry data on pediatric end-stage renal disease patients

Erratum to: Combination therapy with steroids and mizoribine in juvenile SLE: a randomized controlled trial

Identification of a single base insertion in the COL4A5 gene in Alport syndrome

Intracellular distribution of the Wilson's disease gene product (atpase7b) afterin vitro andin vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease

In situ evaluation of podocin in normal and glomerular diseases

Mutations in the COL4A5 gene in Alport syndrome: A possible mutation in primordial germ cells

A mouse model of renal tubular injury of tyrosinemia type 1 : Development of de Toni Fanconi syndrome and apoptosis of renal tubular cells in Fah/Hpd double mutant mice

Comparison of asymptomatic and symptomatic childhood glomerulonephritis progressing to renal failure : a report of Kyushu Pediatric Nephrology Study Group

Intracellular distribution of the Wilson's disease gene product (atpase7b) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease

Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria

A case of minimal change nephrotic syndrome associated with acute renal failure after excessive exercise

The Standard Manual for School Urinary Screening in Kyushu: A Project for Standardization of Urinary Screening system

Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria

The 2003 Report of the Japanese National Registry Data on Pediatric End-Stage Renal Disease Patients

Developmental changes in carbonic anhydrase II in the rat kidney

Childhood-type myositis and linear scleroderma

Another autosomal recessive form of focal glomerulosclerosis with neurological findings

Effect of superoxide dismutase on serum sickness nephritis

The influence of exercise loading for a long period on the renal function of the children with mesangial proliferative glomerulonephritis

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