S. Hattori

发表

Quantitative and qualitative changes of apolipoprotein AI-containing lipoproteins in patients on continuous ambulatory peritoneal dialysis.

T. Ohta, A. Higashi, S. Nishiyama, 1989, Metabolism: clinical and experimental.

Studies on the lipid and apolipoprotein compositions of two species of apoA-I-containing lipoproteins in normolipidemic males and females.

T. Ohta, S. Nishiyama, I. Matsuda, 1988, Journal of lipid research.

Clinicopathological correlation of IgA nephropathy in children.

I. Matsuda, S. Hattori, S. Karashima, 1985, American journal of nephrology.

T. Ohta, S. Nishiyama, I. Matsuda, 1989, Arteriosclerosis.

Remodeling of HDL containing apoA-I but not apoA-II (LpA-I) by lipoprotein-deficient plasma and hepatic lipase: its effect on the structure and cellular cholesterol-reducing capacity of LpA-I.

Y. Ikeda, T. Ohta, I. Matsuda, 1996, Biochimica et biophysica acta.

Isolation of apolipoprotein A-I-containing lipoproteins by immunoaffinity chromatography using a formylated derivative of cellulose gel.

S. Horiuchi, T. Ohta, S. Nishiyama, 1989, Clinica chimica acta; international journal of clinical chemistry.

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

F. Endo, I. Matsuda, H. Nakazato, 1999, Kidney international.

A case of congenital nephrotic syndrome associated with partial deficiency of lecithin cholesterol acyltransferase (LCAT) and hypothyroidism.

I. Matsuda, H. Maeda, S. Hattori, 1984, The International journal of pediatric nephrology.

HLA antigens in mucocutaneous lymph node syndrome.

I. Matsuda, S. Hattori, N. Nagata, 1977, American journal of diseases of children.

Insulin receptor of erythrocytes and glucose metabolism in uremic children.

I. Matsuda, S. Hattori, C. Nakahara, 1983, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Follow up study on children with dyslipidaemia detected by mass screening at 18 months of age: effect of 12 months dietary treatment

Y. Ikeda, T. Ohta, I. Matsuda, 1993, European Journal of Pediatrics.

Dosage schedule of gentamicin for chronic renal insufficiency in children.

H. Yoshioka, I. Matsuda, S. Hattori, 1978, Archives of disease in childhood.

Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency.

S. Horiuchi, J. Frohlich, Y. Ikeda, 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.

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

F. Endo, I. Matsuda, Y. Koitabashi, 1994, Kidney international.

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

F. Endo, I. Matsuda, Y. Koitabashi, 1993, Kidney international.

Circulating immune complex in glomerulonephropathy associated with hepatitis B virus infection.

I. Matsuda, S. Hattori, S. Karashima, 1982, Nephron.

Methylmalonic acidemia

I. Akaboshi, I. Matsuda, S. Hattori, 2004, European Journal of Pediatrics.

Membranoproliferative glomerulonephritis in congenital portosystemic shunt without liver cirrhosis.

F. Endo, S. Ikeda, Y. Sera, 2000, Clinical nephrology.

[Effect of albumin pH on ionized calcium (Ca++) determination. 2].

I. Matsuda, S. Nishiyama, S. Hattori, 1983, Horumon to rinsho. Clinical endocrinology.

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

F. Endo, I. Matsuda, H. Nakazato, 1997, Kidney international.

Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblasts.

F. Endo, I. Matsuda, H. Nakazato, 1995, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Another autosomal recessive form of focal glomerulosclerosis with neurological findings

F. Endo, H. Nakazato, S. Hattori, 2002, Pediatric Nephrology.

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.

A new variant of Lowe oculocerebrorenal syndrome.

I. Matsuda, K. Shimazoe, S. Hattori, 1980, The Tohoku journal of experimental medicine.

Glomerular IgA1 and IgA2 deposits in IgA nephropathies.

I. Matsuda, K. Kobayashi, S. Hattori, 1983, Nephron.

[Clinicopathological survey of persistent hypocomplementemic glomerulonephritis in children; correlation of DPGN and MPGN type I].

I. Matsuda, S. Takebayashi, S. Hattori, 1992, Nihon Jinzo Gakkai shi.

Dramatic response to corticosteroid therapy of nephrotic syndrome associated with IgA nephropathy.

I. Matsuda, N. Adachi, S. Hattori, 1985, The International journal of pediatric nephrology.

MEMBRANOUS GLOMERULONEPHRITIS AND HB-e ANTIGEN

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

Familial progressive renal tubulopathy.

I. Matsuda, S. Hattori, S. Karashima, 1992, Clinical nephrology.