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Results: 1-10 |
Results: 10
A NOVEL MUTATION OF COPROPORPHYRINOGEN OXIDASE (CPO) GENE IN A JAPANESE FAMILY
Authors: SUSA S DAIMON M YAMAMORI I KONDO M YAMATANI K SASAKI H KATO T
Citation: S. Susa et al., A NOVEL MUTATION OF COPROPORPHYRINOGEN OXIDASE (CPO) GENE IN A JAPANESE FAMILY, JOURNAL OF HUMAN GENETICS, 43(3), 1998, pp. 182-184
THE CALCIFICATION OF THE TMJ DISCS IN JAPANESE CADAVER
Authors: YAMAMORI I SHIBATA T
Citation: I. Yamamori et T. Shibata, THE CALCIFICATION OF THE TMJ DISCS IN JAPANESE CADAVER, Journal of dental research, 77(5), 1998, pp. 1296-1296
THE MODIFIED DIRECT ASPIRATION TECHNIQUE FOR TMJ SYNOVIAL-FLUID ANALYSIS
Authors: SHIBATA T MURAKAMI K KUBOTA E YAMAMORI I YOSHIZAWA N
Citation: T. Shibata et al., THE MODIFIED DIRECT ASPIRATION TECHNIQUE FOR TMJ SYNOVIAL-FLUID ANALYSIS, Journal of dental research, 77, 1998, pp. 265-265
INTRACELLULAR PARTICLE-SIZE OF BREAKDOWN SILICONE TMJ INTERPOSITIONALIMPLANTS
Authors: YAMAMORI I SHIBATA T YOSHIZAWA N
Citation: I. Yamamori et al., INTRACELLULAR PARTICLE-SIZE OF BREAKDOWN SILICONE TMJ INTERPOSITIONALIMPLANTS, Journal of dental research, 77, 1998, pp. 1849-1849
COLLECTIVE TESTS OF SYNOVIAL-FLUID WITH A LAVAGE ASPIRATION TECHNIQUE
Authors: SHIBATA T KUBOTA E MURAKAMI K MIZOGUCHI M YAMAMORI I YOSHIZAWA N
Citation: T. Shibata et al., COLLECTIVE TESTS OF SYNOVIAL-FLUID WITH A LAVAGE ASPIRATION TECHNIQUE, Journal of dental research, 76, 1997, pp. 3468-3468
2 DIFFERENT CALCIFIED MECHANISM OF THE HUMAN TMJ DISCS
Authors: YAMAMORI I SHIBATA T MIZOGUCHI M YOSHIZAWA N
Citation: I. Yamamori et al., 2 DIFFERENT CALCIFIED MECHANISM OF THE HUMAN TMJ DISCS, Journal of dental research, 76, 1997, pp. 3470-3470
A TRUNCATED THYROXINE-BINDING GLOBULIN DUE TO A FRAMESHIFT MUTATION IS RETAINED WITHIN THE ROUGH ENDOPLASMIC-RETICULUM - A POSSIBLE MECHANISM OF COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY IN JAPANESE
Authors: MIURA Y KAMBE F YAMAMORI I MORI Y TANI Y MURATA Y OISO Y SEO H
Citation: Y. Miura et al., A TRUNCATED THYROXINE-BINDING GLOBULIN DUE TO A FRAMESHIFT MUTATION IS RETAINED WITHIN THE ROUGH ENDOPLASMIC-RETICULUM - A POSSIBLE MECHANISM OF COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY IN JAPANESE, The Journal of clinical endocrinology and metabolism, 78(2), 1994, pp. 283-287
GENE SCREENING OF 23 JAPANESE FAMILIES WITH COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY - IDENTIFICATION OF A NUCLEOTIDE DELETION AT CODON-352 AS A COMMON-CAUSE
Authors: YAMAMORI I MORI Y MIURA Y TANI Y IMAMURA S OISO Y SEO H
Citation: I. Yamamori et al., GENE SCREENING OF 23 JAPANESE FAMILIES WITH COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY - IDENTIFICATION OF A NUCLEOTIDE DELETION AT CODON-352 AS A COMMON-CAUSE, Endocrine journal, 40(5), 1993, pp. 563-569
SEQUENCE OF A VARIANT THYROXINE-BINDING GLOBULIN (TBG) IN A FAMILY WITH PARTIAL TBG DEFICIENCY IN JAPANESE (TBG-PDJ)
Authors: MIURA Y MORI Y YAMAMORI I TANI Y MURATA Y YOSHIMOTO M KINOSHITA E MATSUMOTO T OISO Y SEO H
Citation: Y. Miura et al., SEQUENCE OF A VARIANT THYROXINE-BINDING GLOBULIN (TBG) IN A FAMILY WITH PARTIAL TBG DEFICIENCY IN JAPANESE (TBG-PDJ), Endocrine journal, 40(1), 1993, pp. 127-132
HEREDITARY COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY - IDENTIFICATION BY T(3) RESIN UPTAKE TEST AND DNA ANALYSIS
Authors: NOGUCHI T YAMAMORI I TAKAMATSU J NAKAJIMA T MORI Y KUMAHARA Y
Citation: T. Noguchi et al., HEREDITARY COMPLETE THYROXINE-BINDING GLOBULIN DEFICIENCY - IDENTIFICATION BY T(3) RESIN UPTAKE TEST AND DNA ANALYSIS, Japanese journal of medicine, 32(1), 1993, pp. 6-9
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