SHIIHARA Takashi 椎原隆

… Alternative Names

椎原隆シイハラタカシ

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Researcher Number	90372333
Affiliation (Current)	2025: 群馬県衛生環境研究所, 研究企画係, 研究員
Affiliation (based on the past Project Information) *help	2006: 山形大, 医学部, 助手 2004 – 2005: 山形大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics Except Principal Investigator Pediatrics
Keywords	Principal Investigator EMX2遺伝子 / 裂脳症 / 多少脳回 Except Principal Investigator HSP27 / MFN2 / distal hereditary motor neuropathy / PRX / sodium channel / Charcot-Marie-Tooth disease / hereditary neuropathy … More / Hsp27 / Hsp22 / CMT / distal heredistary motor nuerophathy / 遺伝子ニューロパチー / denaturing high performance liquid chromatography / Charcot-Marie-Tooth病 / 遺伝性ニューロパチー Less

多小脳回と裂脳症の原因遺伝子同定Principal Investigator
- Principal Investigator
  
  椎原隆
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University
Molecular Basis of Hereditary Neuropathy
- Principal Investigator
  
  HAYASAKA Kiyoshi
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yamagata University

All 2005 2004

All Journal Article

[Journal Article] Costello syndrome showing moyamoya-like vasculopathy.2005
- Author(s)
  Shiihara T, et al.
- Journal Title
  
  Pediatr Neurol 32(5)
  
  Pages: 361-363
- Data Source
  KAKENHI-PROJECT-17790688
[Journal Article] Phenotypic consequences of genetic variation at hemizygous alleles : Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency.2005
- Author(s)
  Kurotaki N, Shiihara T, et al.
- Journal Title
  
  Genet Med 7(7)
  
  Pages: 479-483
- Data Source
  KAKENHI-PROJECT-17790688
[Journal Article] No abstract Clinically mild encephalitis/encephalopathy with a reversible splenial lesion.2005
- Author(s)
  Shiihara T, et al.
- Journal Title
  
  Neurology 64(8)
  
  Pages: 1487-1487
- Data Source
  KAKENHI-PROJECT-17790688
[Journal Article] Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP2004
- Author(s)
  Shiihara T 他
- Journal Title
  
  J Neurol Sci 225巻
  
  Pages: 125-127
- Data Source
  KAKENHI-PROJECT-16591008

1. HAYASAKA Kiyoshi (20142961)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
2. 白幡恵美 (60400553)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

SHIIHARA Takashi 椎原隆

椎原隆シイハラタカシ

Research Projects

Research Products

Co-Researchers

多小脳回と裂脳症の原因遺伝子同定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular Basis of Hereditary Neuropathy

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Costello syndrome showing moyamoya-like vasculopathy.2005

Author(s)

Journal Title

Data Source

[Journal Article] Phenotypic consequences of genetic variation at hemizygous alleles : Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency.2005

Author(s)

Journal Title

Data Source

[Journal Article] No abstract Clinically mild encephalitis/encephalopathy with a reversible splenial lesion.2005

Author(s)

Journal Title

Data Source

[Journal Article] Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP2004

Author(s)

Journal Title

Data Source

SHIIHARA Takashi 椎原 隆

椎原 隆 シイハラ タカシ

Research Projects

Research Products

Co-Researchers

多小脳回と裂脳症の原因遺伝子同定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular Basis of Hereditary Neuropathy

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Costello syndrome showing moyamoya-like vasculopathy.2005

Author(s)

Journal Title

Data Source

[Journal Article] Phenotypic consequences of genetic variation at hemizygous alleles : Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency.2005

Author(s)

Journal Title

Data Source

[Journal Article] No abstract Clinically mild encephalitis/encephalopathy with a reversible splenial lesion.2005

Author(s)

Journal Title

Data Source

[Journal Article] Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP2004

Author(s)

Journal Title

Data Source

SHIIHARA Takashi 椎原隆

椎原隆シイハラタカシ