Hattori S - Search Results

1

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

Nakazato H, Yoshimuta J, Karashima S, Matsumoto S, Endo F, Matsuda I, Hattori S. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1999 Jan;55(1):63-70. doi: 10.1046/j.1523-1755.1999.00231.x. Kidney Int. 1999. PMID: 9893114 Free article.

2

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

Nakazato H, Hattori S, Furuse A, Kawano T, Karashima S, Tsuruta M, Yoshimuta J, Endo F, Matsuda I. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1997 Oct;52(4):895-900. doi: 10.1038/ki.1997.410. Kidney Int. 1997. PMID: 9328927 Free article.

3

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

Nakazato H, Hattori S, Ushijima T, Matsuura T, Karashima S, Uemura T, Endo F, Matsuda I. Nakazato H, et al. Among authors: hattori s. Am J Kidney Dis. 1995 Nov;26(5):732-9. doi: 10.1016/0272-6386(95)90436-0. Am J Kidney Dis. 1995. PMID: 7485125

4

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

Nakazato H, Hattori S, Ushijima T, Matsuura T, Koitabashi Y, Takada T, Yoshioka K, Endo F, Matsuda I. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1994 Nov;46(5):1307-14. doi: 10.1038/ki.1994.399. Kidney Int. 1994. PMID: 7853788 Free article.

5

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

Nakazato H, Hattori S, Matsuura T, Koitabashi Y, Endo F, Matsuda I. Nakazato H, et al. Among authors: hattori s. Kidney Int. 1993 Nov;44(5):1091-6. doi: 10.1038/ki.1993.353. Kidney Int. 1993. PMID: 8264140 Free article.

6

In situ evaluation of podocin in normal and glomerular diseases.

Horinouchi I, Nakazato H, Kawano T, Iyama K, Furuse A, Arizono K, Machida J, Sakamoto T, Endo F, Hattori S. Horinouchi I, et al. Among authors: hattori s. Kidney Int. 2003 Dec;64(6):2092-9. doi: 10.1046/j.1523-1755.2003.00303.x. Kidney Int. 2003. PMID: 14633131 Free article.

7

Membranoproliferative glomerulonephritis in congenital portosystemic shunt without liver cirrhosis.

Karashima S, Hattori S, Nakazato H, Awata H, Seguchi S, Ikeda S, Sera Y, Endo F. Karashima S, et al. Among authors: hattori s. Clin Nephrol. 2000 Mar;53(3):206-11. Clin Nephrol. 2000. PMID: 10749300

8

Asymptomatic low molecular weight proteinuria: studies in five patients.

Murakami T, Kawakami H, Matsuyama S, Terashima T, Karashima S, Hattori S. Murakami T, et al. Among authors: hattori s. Clin Nephrol. 1987 Aug;28(2):93-8. Clin Nephrol. 1987. PMID: 3308234

9

Familial progressive renal tubulopathy.

Furuse A, Futagoishi Y, Karashima S, Hattori S, Matsuda I. Furuse A, et al. Among authors: hattori s. Clin Nephrol. 1992 Apr;37(4):192-7. Clin Nephrol. 1992. PMID: 1582058

10

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.

Sun MS, Hattori S, Kubo S, Awata H, Matsuda I, Endo F. Sun MS, et al. Among authors: hattori s. J Am Soc Nephrol. 2000 Feb;11(2):291-300. doi: 10.1681/ASN.V112291. J Am Soc Nephrol. 2000. PMID: 10665936

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