S. Hattori

发表

Steroid treatment for severe childhood IgA nephropathy: a randomized, controlled trial.

K. Nakanishi, N. Yoshikawa, K. Iijima, 2006, Clinical journal of the American Society of Nephrology : CJASN.

Urinary excretion of soluble tumour necrosis factor receptor 1 as a marker of increased risk of progressive kidney function deterioration in patients with primary chronic glomerulonephritis

K. Nakanishi, N. Yoshikawa, K. Iijima, 2010 .

A controlled trial of combined therapy for newly diagnosed severe childhood IgA nephropathy. The Japanese Pediatric IgA Nephropathy Treatment Study Group.

N. Yoshikawa, Y. Seino, M. Awazu, 1999, Journal of the American Society of Nephrology : JASN.

A prospective controlled study of Sairei-to in childhood IgA nephropathy with focal/minimal mesangial proliferation

N. Yoshikawa, Y. Seino, Hajime Nakamura, 1997 .

Rapidly progressive crescentic IgA glomerulonephritis with glomerular peripheral capillary granular IgA deposits in 6-year old boy

I. Matsuda, T. Taguchi, S. Hattori, 1995 .

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

Yuriko Tanaka, N. Yoshikawa, T. Ando, 2010, Pediatric Nephrology.

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

K. Okumura, F. Endo, M. Shinohara, 2007, Cloning and stem cells.

The 1998 report of the Japanese National Registry data on pediatric end-stage renal disease patients

M. Honda, Hiroshi Ito, O. B. O. T. A. F. P. Nephrology, 2002, Pediatric Nephrology.

Tubulointerstitial Nephritis Antigen: Primary Structure, Expression and Role in Health and Disease

K. Yoshioka, T. Takemura, S. Hattori, 2001, Nephron.

The Nature and Molecular Weight of the Circulating Immune Complex in Glomerulonephropathy Associated With Hepatitis B Virus Infection

I. Matsuda, S. Hattori, S. Karashima, 1986 .

Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart.

Tetsurou Yamamoto, R. Harvey, H. Kurihara, 2007, Molecular genetics and metabolism.

Mitochondrial cytopathy with lactic acidosis, carnitine deficiency and DeToni-Fanconi-Debré syndrome

A. Kitano, T. Miike, I. Matsuda, 1986, Brain and Development.

Hepatitis B e antigen-mediated membranous glomerulonephritis. Correlation of ultrastructural changes with HBeAg in the serum and glomeruli.

Y. Miyakawa, M. Mayumi, H. Yoshizawa, 1981, Laboratory investigation; a journal of technical methods and pathology.

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

K. Nakanishi, N. Yoshikawa, K. Iijima, 2009, Pediatric Nephrology.

In situ evaluation of podocin in normal and glomerular diseases.

K. Iyama, K. Arizono, J. Machida, 2003, Kidney international.

GENETIC RENAL DISEASE / ORIGINAL AR T ICLE

H. Nakazato, S. Hattori, S. Karashima, 2002 .

Complete Rescue of Lethal Albino c 14CoS Mice by Null Mutation of 4-Hydroxyphenylpyruvate Dioxygenase and Induction of Apoptosis of Hepatocytes in These Mice by in VivoRetrieval of the Tyrosine Catabolic Pathway*

J. Miyazaki, Tetsurou Yamamoto, I. Matsuda, 1997, The Journal of Biological Chemistry.

[A prospective controlled study of sairei-to in childhood IgA nephropathy with focal/minimal mesangial proliferation. Japanese Pediatric IgA Nephropathy Treatment Study Group].

Y. Seino, M. Awazu, M. Honda, 1997, Nihon Jinzo Gakkai shi.

Developmental changes in carbonic anhydrase II in the rat kidney

I. Matsuda, H. Nakazato, S. Hattori, 1998, Pediatric Nephrology.

Effective and safe treatment with cyclosporine in nephrotic children: a prospective, randomized multicenter trial.

K. Nakanishi, N. Yoshikawa, K. Iijima, 2008, Kidney international.

[Standard versus long-term prednisolone with sairei-to for initial therapy in childhood steroid-responsive nephrotic syndrome: a prospective controlled study].

I. Matsuda, Y. Seino, K. Iijima, 1998, Nihon Jinzo Gakkai shi.

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

S. Hisano, F. Yamashita, S. Hattori, 1994, Pediatric nephrology (Berlin, West).

Epidemiologic Survey of Children with End‐Stage Renal Disease

M. Uchiyama, N. Kuriya, T. Yanase, 1990, Acta paediatrica Japonica : Overseas edition.

Treatment with microemulsified cyclosporine in children with frequently relapsing nephrotic syndrome.

K. Nakanishi, N. Yoshikawa, K. Iijima, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

THE ROLE OF HBe ANTIGEN IN THE PATHOGENESIS OF HB ASSOCIATED MEMBRANOUS GLOMERULONEPHRITIS

I. Matsuda, M. Mayumi, S. Hattori, 1980, Pediatric Research.

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

Tetsurou Yamamoto, F. Endo, Kazunori Koiwai, 1998, Hepatology.

Analysis in the CLCN5 gene in patients with familial idiopathic low-molecular-weight proteinuria.

I. Matsuda, H. Nakazato, S. Hattori, 1998 .

Unusual case of diffuse connective tissue disease with nodule formations in muscle, lung, kidney and brain

Y. Nobukuni, T. Miike, I. Matsuda, 1986, Brain and Development.

Childhood‐type myositis and linear scleroderma

T. Miike, T. Kageshita, T. Ono, 1983, Neurology.

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.

F. Endo, I. Matsuda, S. Kubo, 2000, Journal of the American Society of Nephrology : JASN.

Chronic nephritis, sensorineural deafness, growth and developmental retardation, hyperkinesis, and cleft soft palate in a 5-year-old boy. A new combination?

T. Taguchi, T. Kajii, S. Hattori, 1990, Nephron.