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Perception of genetic testing among patients with inherited retinal disease: Benefits and challenges in a Japanese population

Perception of genetic testing among patients with inherited retinal disease: Benefits and challenges in a Japanese population
Digital博士論文障害者向け資料あり
Inaba, Akira2022-05-23
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject Headinggenetic testing genetic counseling inherited retinal disease retinitis pigmentosa

網膜色素変性症モデルにおける視細胞アポト-シスの高濃度酸素療法による制御

網膜色素変性症モデルにおける視細胞アポト-シスの高濃度酸素療法による制御
Paper図書
仙崎, 英人, 関西医科大学2001-2002<Y151-H13671857>
National Diet Library
  • Subject HeadingRetinitis pigmentosa N-methyl-N-nitrosourea Apopto...

Branched chain amino acids attenuate major pathologies in mouse models of retinal degeneration and glaucoma

Branched chain amino acids attenuate major pathologies in mouse models of retinal degeneration and glaucoma
Digital博士論文障害者向け資料あり
Hasegawa, Tomoko2019-03-25
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject Headingbranched chain amino acids retinitis pigmentosa glaucoma neuronal cell degene...

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa
Digital博士論文障害者向け資料あり
立花, 信貴MDPI (Multidisciplinary Digital Publishing Institute)2022-02-16
National Diet Library
  • Subject Heading...ne RP1-related retinitis pigmentosa
  • Note (General)...th RP1-related retinitis pigmentosa. Although the clinical featur...

カスパーゼ阻害剤による網膜色素変性症モデルにおける視細胞アポトーシスの制御

カスパーゼ阻害剤による網膜色素変性症モデルにおける視細胞アポトーシスの制御
Paper図書
螺良, 愛郎, 関西医科大学2000-2001<Y151-H12671728>
National Diet Library
  • Subject HeadingRetinitis pigmentosa N-methyl-N-nitrosourea Apopto...

Comprehensive Molecular Diagnosis of a Large Cohort of Japanese Retinitis Pigmentosa and Usher Syndrome Patients by Next-Generation Sequencing

Comprehensive Molecular Diagnosis of a Large Cohort of Japanese Retinitis Pigmentosa and Usher Syndrome Patients by Next-Generation Sequencing
Digital博士論文障害者向け資料あり
Oishi, Maho2018-01-23
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject Headingretinitis pigmentosa Usher syndrome next generatio...

障がい者よ、街へ出よう : 「網膜色素変性症」で視覚をなくしても、現役プロデューサー

障がい者よ、街へ出よう : 「網膜色素変性症」で視覚をなくしても、現役プロデューサー
PaperRecording MediaDigital図書障害者向け資料あり
津久見圭 編プラチナボックス2012.2<E9-J511>
National Diet LibraryOther Libraries in Japan
  • Authority（Subject Heading/altLabel）Retinitis pigmentosa

Choroidal Vasculature in Bietti Crystalline Dystrophy With CYP4V2 Mutations and in Retinitis Pigmentosa With EYS Mutations

Choroidal Vasculature in Bietti Crystalline Dystrophy With CYP4V2 Mutations and in Retinitis Pigmentosa With EYS Mutations
Digital博士論文障害者向け資料あり
Hirashima, Takako2020-03-23
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject HeadingBietti Crystalline Dystrophy Retinitis Pigmentosa Choroidal Vasculature SS-OCT ...

Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations

Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations
Digital博士論文障害者向け資料あり
Ohashi(Arai), Yuuki2016-11-24
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject HeadingInherited retinal dystrophy Retinitis pigmentosa Genetic diagnosis EYS mutatio...

網膜色素変性症モデルにおける視細胞アポトーシスの分子機構の解析ならびにその制御

網膜色素変性症モデルにおける視細胞アポトーシスの分子機構の解析ならびにその制御
Paper図書
仙崎, 英人, 関西医科大学1999-2000<Y151-H11671763>
National Diet Library
  • Subject HeadingRetinitis pigmentosa N-methyl-N-nitrosourea Apopto...

Knockout of ccr2 alleviates photoreceptor cell death in a model of retinitis pigmentosa

Knockout of ccr2 alleviates photoreceptor cell death in a model of retinitis pigmentosa
Digital博士論文障害者向け資料あり
Guo, Congrong2015-01-23
Available onlineNational Diet LibraryOther Libraries in Japan
  • Subject Headingretinitis pigmentosa ccr2 mcp1 chemokine photorece...
  • Note (General)... in a model of retinitis pigmentosa, Experimental Eye Research, V...

Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa

Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa
Digital博士論文障害者向け資料あり
Zhao, Yang2013-09-20
National Diet Library
  • Subject HeadingRetinitis pigmentosa autosomal recessive USH2A gen...
  • Note (General)... non-syndromic retinitis pigmentosa (RP).Design: Case series. Par...

Retinitis pigmentosa : causes, diagnosis and treatment : softcover : alk. paper

Retinitis pigmentosa : causes, diagnosis and treatment : softcover : alk. paper
Paper図書
Michaël Baert and Cédric Peeters, editorsNova Biomedical Booksc2010
Other Libraries in Japan
  • Subject HeadingRetinitis pigmentosa Retinitis Pigmentosa -- etiology Retinitis Pigmentosa -- diagnosis Retinitis Pigmentosa -- therapy
  • Subject Heading (ID)Retinitis pigmentosa Retinitis Pigmentosa -- etiology Retinitis Pigmentosa -- diagnosis Retinitis Pigmentosa -- therapy

網膜色素変性症

網膜色素変性症
Paper図書
安達惠美子 編著医学書院1998.4<SC641-G53>
National Diet LibraryOther Libraries in Japan
  • Authority（Subject Heading/altLabel）Retinitis pigmentosa
  • Alternative TitleRetinitis pigmentosa
  • Alternative TitleRetinitis pigmentosa

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa

Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa
Digital博士論文
立花, 信貴MDPI (Multidisciplinary Digital Publishing Institute)2022-02-16Genes13 2p.359-
Available onlineOther Libraries in Japan
  • Summary, etc....th RP1-related retinitis pigmentosa. Although the clinical featur...
  • Subject Heading...ne RP1-related retinitis pigmentosa

Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa

Mutation analysis of the USH2A gene in Japanese patients with non-syndromic autosomal recessive retinitis pigmentosa
Digital博士論文
Zhao, Yang2013-09-20
Available onlineOther Libraries in Japan
  • Summary, etc.... non-syndromic retinitis pigmentosa (RP). Design: Case series. Pa...
  • Subject HeadingRetinitis pigmentosa autosomal recessive USH2A gen...

Retinitis pigmentosa : clinical implications of current research / edited by Maurice B. Landers, III ... [et al.]. (Advances in experimental medicine and biology ; v. 77)

Retinitis pigmentosa : clinical implications of current research / edited by Maurice B. Landers, III ... [et al.]. (Advances in experimental medicine and biology ; v. 77)
Paper図書
Plenum Pressc1977.<SC641-10>
National Diet Library
  • Subject HeadingRetinitis pigmentosa -- Congresses. Retinitis Pigmentosa -- congresses.

Genetic eye diseases : retinitis pigmentosa and other inherited eye disorders ; proceedings of the International Symposium on Genetics and Ophthalmology, held in Jerusalem, Israel, September 1981 / editors, Edward Cotlier, Irene H. Maumenee, Elaine R. Berman. (Birth defects original article series ; v. 18, no. 6, 1982)

Genetic eye diseases : retinitis pigmentosa and other inherited eye disorders ; proceedings of the International Symposium on Genetics and Ophthalmology, held in Jerusalem, Israel, September 1981 / editors, Edward Cotlier, Irene H. Maumenee, Elaine R. Berman. (Birth defects original article series ; v. 18, no. 6, 1982)
Paper図書
A.R. Lissc1982.<M15-A3953>
National Diet Library
  • Subject Heading...-- Congresses. Retinitis pigmentosa -- Genetic asp......-- Congresses. Retinitis pigmentosa -- Congresses.

網膜色素変性症と類縁疾患 (カラーアトラス網脈絡膜疾患シリーズ)

網膜色素変性症と類縁疾患 (カラーアトラス網脈絡膜疾患シリーズ)
PaperDigital図書
水野勝義 著ライフ・サイエンス出版1985.12<SC641-E62>
National Diet LibraryOther Libraries in Japan
  • Authority（Subject Heading/altLabel）網膜疾患 Retinitis pigmentosa

Retinitis pigmentosa

Retinitis pigmentosa
Paper図書
John R. Heckenlively ; with twelve contributorsLippincott1988
Other Libraries in Japan
  • Subject HeadingRetinitis pigmentosa Retinitis Pigmentosa
  • Subject Heading (ID)Retinitis pigmentosa Retinitis Pigmentosa
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