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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Genetic and clinical heterogeneity of Moyamoya disease

Farrugia, Luca 12 July 2017 (has links)
BACKGROUND: Moyamoya disease (MMD) is a chronic, occlusive cerebrovascular disease characterized by progressive stenosis of intracranial arteries, specifically the internal carotid arteries, and the compensatory formation of an abnormal vascular network at the base of the brain. The exact cause of MMD is still not well understood. Many factors including genetic, environmental, and immunologic have been associated with the disease. RNF213 is considered the main susceptibility gene, especially in Eastern Asian patients. The founder mutation, p.R4810K, has been associated strongly with MMD, especially in Japan and Korea but has been shown to have low penetrance and has never been described in non-Eastern Asian MMD cases. RNF213 encodes for an E3 ubiquitin-protein ligase with ATPase activity. It has described to regulate angiogenesis giving rise to the possibility that variants in RNF213 may play a role in cerebrovascular diseases other than MMD. OBJECTIVES: The aims of this study were to determine if variation in the RNF213 gene contributes to MMD in a cohort of 15 unrelated patients with MMD of predominantly European descent, to investigate other potential genes implicated in MMD in these 15 patients, and to investigate if RNF213 also influences more common vascular phenotypes. METHODS: Patient history, detailed family history and a blood sample were collected from 15 patients with well-characterized MMD. DNA was extracted from a peripheral venous blood sample, assessed for quality, and DNA concentration quantified by PicoGreen®. The extracted DNA was sent for whole exome sequencing. Genome_GPS_2.0 was used to carry out secondary analysis of sequencing data and all data were stored in Oracle TRC. The files were aligned using Novoalign, variants analyzed using GATK, visualized using IGV and annotated using BioR-Web. Variants of interest were determined using Ingenuity® Variant Analysis™. To determine if RNF213 also influences more common vascular phenotypes, previously collected and whole exome sequenced samples from the Mayo Clinic Florida Familial Cerebrovascular Diseases Registry were analyzed. Variants in RNF213 were determined using the same approach as for MMD. RESULTS: Likely pathogenic variants in RNF213 were found in 13% (2/15) of patients. The p.R4810K variant has been previously published as the founder mutation for MMD in Eastern Asian populations. The affected patient was also of Eastern Asian origin. The other variant, p.R4019C, was found in a European descent case and has been described as a candidate pathogenic variant. Eight variants in five other genes previously associated with MMD were found. Of these, one previously reported variant, p.D455H in RPTN, was found in two patients. The other seven have not previously been described in MMD. In the analysis of the potential role for RNF213 in other cerebrovascular diseases, 54% (22/41) of African American patients had a non-synonymous, exonic variant in RNF213 with a MAF of less than 3%. A novel RNF213 variant was also found in a Caucasian patient who had a subarachnoid hemorrhage. CONCLUSION: The p.R4810K variant in RNF213 was confirmed to only be associated with MMD in Eastern Asians and not found in other ethnicities. However, a variant in RNF213 was found in a Caucasian patient suggesting RNF213 may indeed be disease causing in patients of diverse origin. RNF213 may also be implicated in other cerebrovascular diseases suggesting a common pathogenesis while other genes also appear to be involved in the pathogenesis of MMD.
2

Cerebral Hemorrhage and Cerebral Infarction in 30 Cases of Adult Moyamoya Disease: Comparison between Conservative Therapy and Superficial Temporal Artery-Middle Cerebral Artery Anastomosis

WADA, KENTARO, NODA, TOMOYUKI, HATTORI, KENICHI, MAKI, HIDEKI, KITO, AKIRA, OYAMA, HIROFUMI 02 1900 (has links)
No description available.
3

Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner / もやもや病感受性遺伝子産物RNF213のRINGドメイン内もやもや病患者変異はユビキチンリガーゼ活性を低下させ、NFκB活性化およびアポトーシスをAAA+ドメイン依存的に促進する

Takeda, Midori 23 September 2020 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(社会健康医学) / 甲第22749号 / 社医博第110号 / 新制||社医||11(附属図書館) / 京都大学大学院医学研究科社会健康医学系専攻 / (主査)教授 髙橋 良輔, 教授 髙折 晃史, 教授 中山 健夫 / 学位規則第4条第1項該当 / Doctor of Public Health / Kyoto University / DFAM
4

Impact of posterior cerebral artery involvement on long-term clinical and social outcome of pediatric moyamoya disease / 小児もやもや病の成人後の臨床・社会的予後に対する後大脳動脈病変の影響

Funaki, Takeshi 23 January 2015 (has links)
京都大学 / 0048 / 新制・論文博士 / 博士(医学) / 乙第12888号 / 論医博第2088号 / 新制||医||1007(附属図書館) / 31642 / (主査)教授 小泉 昭夫, 教授 平家 俊男, 教授 福山 秀直 / 学位規則第4条第2項該当 / Doctor of Medical Science / Kyoto University / DFAM
5

Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease / もやもや病感受性多型であるRNF213 p.R4810Kは冠動脈疾患と有意に関連する

Morimoto, Takaaki 25 March 2019 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第21666号 / 医博第4472号 / 新制||医||1035(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 松田 文彦, 教授 佐藤 俊哉, 教授 Shohab YOUSSEFIAN / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
6

Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease / もやもや病と血管症関連ウイルスの抗体陽性率との関連解析

Nakamura, Yasuhisa 23 May 2023 (has links)
京都大学 / 新制・課程博士 / 博士(社会健康医学) / 甲第24806号 / 社医博第130号 / 新制||社医||12(附属図書館) / 京都大学大学院医学研究科社会健康医学系専攻 / (主査)教授 松田 文彦, 教授 YOUSSEFIAN Shohab, 教授 永井 洋士 / 学位規則第4条第1項該当 / Doctor of Public Health / Kyoto University / DFAM
7

Cortical Distribution of Fragile Periventricular Anastomotic Collateral Vessels in Moyamoya Disease: An Exploratory Cross-Sectional Study of Japanese Patients with Moyamoya Disease / もやもや病における脆弱な脳室周囲吻合の皮質分布-日本人もやもや病患者を対象とした探索的横断研究

Miyakoshi, Akinori 24 September 2021 (has links)
京都大学 / 新制・論文博士 / 博士(医学) / 乙第13436号 / 論医博第2235号 / 新制||医||1054(附属図書館) / (主査)教授 花川 隆, 教授 YOUSSEFIAN Shohab, 教授 髙橋 良輔 / 学位規則第4条第2項該当 / Doctor of Medical Science / Kyoto University / DFAM
8

Magnetic resonance angiography with compressed sensing: an evaluation of moyamoya disease / 圧縮センシングを用いたMRアンギオグラフィによるもやもや病の検討

Yamamoto, Takayuki 26 March 2018 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第21001号 / 医博第4347号 / 新制||医||1027(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 溝脇 尚志, 教授 辻川 明孝, 教授 小泉 昭夫 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
9

Plasticity of the Bony Carotid Canal and Its Clinical Use for Assessing Negative Remodeling of the Internal Carotid Artery / 頚動脈管の経時的狭小化と内頚動脈陰性リモデリング評価への応用

Oichi, Yuki 23 March 2022 (has links)
京都大学 / 新制・課程博士 / 博士(医学) / 甲第23807号 / 医博第4853号 / 新制||医||1058(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 湊谷 謙司, 教授 YOUSSEFIAN Shohab, 教授 石見 拓 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
10

Cognitive Improvement After Microsurgical Revascularization for the Treatment of Moyamoya Disease

Varzoni, Thais Coutinho 01 January 2014 (has links)
Moyamoya disease is a rare entity characterized by progressive narrowing of intracranial blood vessels. In most cases, Moyamoya does not respond well to medical therapy and often leads to surgical revascularization. The physiological benefits of the revascularization surgery for Moyamoya patients have been well documented, yet the effects of surgery on cognitive skills and abilities are far less studied. Participants in the current study were 33 patients, 24 to 85 years of age, who underwent revascularization surgery at the Mayo Clinic in Jacksonville, Florida. All patients underwent a physical and cognitive preoperative evaluation, where speech, memory, and intellectual processes were measured. After surgery, patients returned for three follow-up assessments over a period of six months. All patients experienced stabilization or improvement of physiological symptoms. Regarding cognitive functions, speech, memory, and intellectual processes improved significantly after surgery. Results showed not only a reduction of physiological symptoms, but also a significant cognitive improvement postsurgery. This study adds to the research of this disease and to the benefits of treatment. More research can only strengthen these findings and educate healthcare professionals; helping them reaffirm Moyamoya patients have a better quality of life, by reinforcing the benefits of revascularization surgery.

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