Chihiro Terai - My portal - researchmap

Profile Information

Affiliation: Former Institution / Organization Tokyo Women's Medical University Institute of Rheumatology

Degree: (BLANK)

J-GLOBAL ID: 200901016677337372
researchmap Member ID: 1000080671

Research Interests

4

Research Areas

3

Committee Memberships

2

Misc.

39

Antiphospholipid syndrome with complete abdominal aorta occlusion and chondritis

Masakatsu Saji, Ayako Nakajima, Wako Sendo, Michi Tanaka, Yumi Koseki, Naomi Ichikawa, Masayoshi Harigai, Hideto Akama, Atsuo Taniguchi, Chihiro Terai …

Modern Rheumatology, 11(2) 159-161, 2001
Genotypes at ┣DBSAA1(/)-┫DB locus correlate with the clinical severity of AA-amyloidosis.

Amyloid, 8 115-120, 2001
Identification of a single nucleotide polymorphism in the 5' flanking region of SAA1 primarily associated with the risk of AA-amyloidosis in rheumatoid arthiritis patients.

Arth Rheum, 44 1266-2272, 2001
A prospective study on renal involvement in patients with early rheumatoid arthritis.

Ann Rheum Dis, 82 327-331, 2001
Renal function estimated from serum creatinine is overestimated in patients with rheumatoid arthritis because of their muscle atrophy

M. Moriguchi, C. Terai, Y. Koseki, M. Uesato, N. Kamatani

Modern Rheumatology, 10(4) 230-234, Jan 12, 2000
Rapidly progressive glomerulonephritis with D-penicillamine

Am J Med Sci, 320 398-402, 2000
Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis

M Moriguchi, C Terai, Y Koseki, M Uesato, A Nakajima, S Inada, M Nishinarita, S Uchida, A Nakajima, SY Kim …

HUMAN GENETICS, 105(4) 360-366, Oct, 1999
Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis

M Moriguchi, C Terai, Y Koseki, M Uesato, A Nakajima, S Inada, M Nishinarita, S Uchida, A Nakajima, SY Kim …

HUMAN GENETICS, 105(4) 360-366, Oct, 1999
A germline mutation abolishing the original stop codon of the human adenine phosphoribosyltransferase (APRT) gene leads to complete loss of the enzyme protein

A Taniguchi, M Hakoda, H Yamanaka, C Terai, K Hikiji, R Kawaguchi, N Konishi, S Kashiwazaki, N Kamatani

HUMAN GENETICS, 102(2) 197-202, Feb, 1998
Acute sympathetic hyperfunction in overlapping syndromes of systemic lupus erythematosus and polymyostis

J. Rheumatol., 25 1638, 1998
The origin of APRT^*J : The most common disease-related mutation of APRT gene among Japanese goes back to a prehistoric era

Adv. Exp. Med. Biol., 135, 1998
Optimal range of serum urate concentrations to minimize risk of gouty attacks during antihyperuricemic treatment

Adv. Exp. Med. Biol., 13, 1998
A case of eosinophilic fasciitis complicated with peripheral neuropathy

Masato MORIGUCHI, Chihiro TERAI, Soemu KUROKI, Eiichi TANAKA, Noriyuki SOMEYA, Yoshiho TSUNODA, Sadao KASHIWAZAKI

Internal Medicine, 37(4) 417-420, 1998
Sclerosing cholangitis associated with hypereosinophilic syndrome

N Ichikawa, A Taniguchi, H Akama, H Ishiguro, T Kurihara, C Terai, M Hara, S Kashiwazaki

INTERNAL MEDICINE, 36(8) 561-564, Aug, 1997
Intervention of somatic mutational events in vivo by a germline defect at the adenine phosphoribosyltransferase locus.

Hum. Genet., 99(2) 164-170, 1997
Generation and molecular characterisation of monoclonal IgG4 rheumatoid factor from a patient with rheumatoid arthritis

M Hakoda, N Kamatani, A Taniguchi, H Ueda, H Yamanaka, C Terai, S Kashiwazaki

ANNALS OF THE RHEUMATIC DISEASES, 56(1) 74-77, Jan, 1997
Differential binding avidities of human IgM for staphylococcal protein a derive from specific germ-line VH3 gene usage

M Hakoda, N Kamatani, S HayashimotoKurumada, GJ Silverman, H Yamanaka, C Terai, S Kashiwazaki

JOURNAL OF IMMUNOLOGY, 157(7) 2976-2981, Oct, 1996
Origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back to prehistoric era.

Hum. Genet., 98(5) 596-600, 1996
SELECTION AGAINST BLOOD-CELLS DEFICIENT IN HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) IN LESCH-NYHAN HETEROZYGOTES OCCURS AT THE LEVEL OF MULTIPOTENT STEM-CELLS

M HAKODA, Y HIRAI, M AKIYAMA, H YAMANAKA, C TERAI, N KAMATANI, S KASHIWAZAKI

HUMAN GENETICS, 96(6) 674-680, Dec, 1995
Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: Cellular and molecular confirmation

C Terai, M Hakoda, H Yamanaka, N Kamatani, M Okai, F Takahashi, S Kashiwazaki

CLINICAL GENETICS, 48(5) 246-250, Nov, 1995

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