H. Nakamura

发表

ACE gene polymorphism in childhood IgA nephropathy: association with clinicopathologic findings.

N. Yoshikawa, K. Iijima, R. Tanaka, 1998, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Repeat renal biopsy in children with IgA nephropathy.

N. Yoshikawa, K. Iijima, H. Nakamura, 1990, Clinical nephrology.

Prognostic indicators in childhood IgA nephropathy.

N. Yoshikawa, H. Nakamura, H. Ito, 1992, Nephron.

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.

Role of platelet-activating factor acetylhydrolase gene mutation in Japanese childhood IgA nephropathy.

N. Yoshikawa, M. Miwa, K. Iijima, 1999, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Successful treatment of a young infant who developed high‐titer inhibitors against VWF‐cleaving protease (ADAMTS‐13): Important discrimination from Upshaw‐Schulman syndrome

M. Matsumoto, Y. Fujimura, H. Tamai, 2002, American journal of hematology.

A quantitative analysis of the mesangium in children with IgA nephropathy: Sequential study

N. Yoshikawa, H. Nakamura, J. Suzuki, 1990, The Journal of pathology.

Haemophilus parainfluenzae antigen and antibody in children with IgA nephropathy and Henoch-Schönlein nephritis.

N. Yoshikawa, K. Iijima, S. Suzuki, 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Glomerular anionic sites in minimal change nephrotic syndrome and focal segmental glomerulosclerosis.

N. Yoshikawa, H. Nakamura, Y. Kitano, 1993, Clinical nephrology.

Polymorphism of immunoglobulin heavy chain switch region gene in children with severe IgA nephropathy.

N. Yoshikawa, K. Iijima, M. Miyazaki, 1995, Clinical nephrology.

Asymptomatic constant isolated proteinuria in children.

N. Yoshikawa, R. Tanaka, H. Nakamura, 1991, The Journal of pediatrics.

IgA nephropathy in children from Japan. Clinical and pathological features.

N. Yoshikawa, H. Nakamura, H. Ito, 1988, Child nephrology and urology.

Activated mesangial cells produce vascular permeability factor in early-stage mesangial proliferative glomerulonephritis.

Y. Hayashi, K. Iijima, H. Nakamura, 1998, Journal of the American Society of Nephrology : JASN.

Platelet-activating factor acetylhydrolase gene mutation in Japanese children with Escherichia coli O157-associated hemolytic uremic syndrome.

N. Yoshikawa, M. Miwa, K. Iijima, 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Novel nonsense mutation in the Na+/HCO3- cotransporter gene (SLC4A4) in a patient with permanent isolated proximal renal tubular acidosis and bilateral glaucoma.

Y. Takeshima, G. Seki, H. Endou, 2001, Journal of the American Society of Nephrology : JASN.

Mutation in alpha 5(IV) collagen chain gene in nonfamilial hematuria.

H. Nishio, K. Nakanishi, K. Sano, 1995, Journal of the American Society of Nephrology : JASN.

Platelet-activating factor acetylhydrolase gene mutation in Japanese nephrotic children.

N. Yoshikawa, M. Miwa, K. Iijima, 1998, Kidney international.

Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.

K. Nakanishi, N. Yoshikawa, Y. Sado, 1998, Journal of the American Society of Nephrology : JASN.

Human mesangial cells and peripheral blood mononuclear cells produce vascular permeability factor.

D. Connolly, N. Yoshikawa, K. Iijima, 1993, Kidney international.

Activation-induced expression of vascular permeability factor by human peripheral T cells: a non-radioisotopic semiquantitative reverse transcription-polymerase chain reaction assay.

K. Iijima, H. Nakamura, N. Yoshikawa, 1996, Journal of immunological methods.

Detection of mutations in the COL4A5 gene in over 90% of male patients with X-linked Alport's syndrome by RT-PCR and direct sequencing.

H. Nishio, K. Nakanishi, N. Yoshikawa, 1999, American journal of kidney diseases : the official journal of the National Kidney Foundation.

The Up-Regulation of CXCL12-CXCR4 Axis By Radiotherapy Could Accelerate Glioma Progression

N. Nonoguchi, S. Miyatake, D. Okuzaki, 2021 .

[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.

Lymphocyte subpopulations and function in childhood IgA nephropathy.

H. Nakamura, A. Kameda, S. Shiozawa, 1991, Nephron.

[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.

Infusion of peripheral blood mononuclear cell products from nephrotic children increases albuminuria in rats.

R. Tanaka, H. Nakamura, H. Ito, 1992, Nephron.

Long-term cyclosporin in steroid-dependent nephrotic syndrome.

N. Yoshikawa, R. Tanaka, H. Nakamura, 1995, Contributions to nephrology.

IgG-associated primary glomerulonephritis in children.

N. Yoshikawa, K. Iijima, H. Nakamura, 1994, Clinical nephrology.

Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis.

K. Nakanishi, N. Yoshikawa, Y. Sado, 1994, Kidney international.

Immunohistochemical analysis of renin activity in chronic cyclosporine nephropathy in childhood nephrotic syndrome.

N. Yoshikawa, K. Iijima, N. Yoshikawa, 2000, Journal of the American Society of Nephrology : JASN.

Expression of type IV collagen alpha 3 and alpha 4 chain mRNA in X-linked Alport syndrome.

K. Nakanishi, K. Iijima, H. Nakamura, 1996, Journal of the American Society of Nephrology : JASN.

PAX2 gene mutation in a family with isolated renal hypoplasia.

N. Yoshikawa, K. Iijima, K. Satomura, 2001, Journal of the American Society of Nephrology : JASN.