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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.
61

筋萎縮性側索硬化症2型原因遺伝子のショウジョウバエホモログの生体内機能

高山, 雄太 23 May 2014 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(生命科学) / 甲第18483号 / 生博第312号 / 新制||生||41(附属図書館) / 31361 / 京都大学大学院生命科学研究科統合生命科学専攻 / (主査)教授 上村 匡, 教授 垣塚 彰, 教授 藤田 尚志 / 学位規則第4条第1項該当 / Doctor of Philosophy in Life Sciences / Kyoto University / DFAM
62

Amyotrophic lateral sclerosis models derived from human embryonic stem cells with different superoxide dismutase 1 mutations exhibit differential drug responses / ヒト胚性幹細胞由来筋萎縮性側索硬化症モデル細胞はSOD1変異の違いにより異なる薬剤反応性を示す

Isobe, Takehisa 23 March 2016 (has links)
Final publication is available at http://www.sciencedirect.com/science/article/pii/S1873506115001191 / 京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第19579号 / 医博第4086号 / 新制||医||1013(附属図書館) / 32615 / 京都大学大学院医学研究科医学専攻 / (主査)教授 井上 治久, 教授 髙橋 良輔, 教授 岩田 想 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
63

The prevalence and perceptions of hearing loss in individuals diagnosed with adult onset motor neuron disease (MND).

Philippou, Elena 18 February 2013 (has links)
Although it is well-known that motor neuron disease (MND) primarily affects motor neurons, the involvement of sensory pathways in the disease is currently receiving more attention. There is a dearth of information regarding the atypical effects of MND, resulting in limited understanding of the vulnerability of for example the auditory system. The presence of hearing loss negatively impacts on participation across all communicative contexts, stripping individuals of autonomy and self-worth, ultimately resulting in withdrawal and isolation. These factors form the foundation for individual desire to pursue life-prolonging measures. Hearing loss, combined with dysarthria and the use of augmentative and alternative communicative strategies, implies that individuals with MND require additional support to meet their daily communicative needs. This descriptive, exploratory study aimed to identify the prevalence of hearing loss in eight individuals with adult onset MND. In addition, perceptions relating to the implications of auditory impairment and value of auditory diagnosis were explored. An evaluation of auditory function was performed on eight individuals with a neurologist confirmed diagnosis of MND. Auditory function was assessed using a comprehensive audiological test battery including both objective and subjective measures. Perceptions related to auditory impairment were determined using the Hearing Handicap Inventory for Adults (HHIA) and the Hearing Experience Questionnaire. Both individuals with MND and their primary caregivers completed the Hearing Experience Questionnaire. The results of the study indicate that a high frequency sensorineural hearing loss was identified in six participants. Auditory handicap, as measured by the Hearing Handicap Inventory for Adults, was reported in four participants, with social handicaps reported more than emotional handicaps. Individuals with MND and their caregivers identified communication as the most important functional skill. Interestingly, the caregivers related more to the threats auditory impairment than individuals with MND. The nature of hearing loss identified in this study mimics the pattern of a presbycustic (age-related) hearing loss. It is postulated that hearing loss may arise during disease course. Participants‘ limited understanding of the devastating consequences of hearing loss on quality of life highlights the need for inclusion of an audiologist as part of the multidisciplinary management team in MND. Audiological assessment, management, counseling and education will serve to guide the process of sensory regulation and limit psychosocial threats posed by MND. This will in turn promote enhanced quality of life and maintenance of individual autonomy.
64

Genetic analysis of amyotrophic lateral sclerosis and other motor neuron disorders

Valdmanis, Paul Nils. January 2009 (has links)
No description available.
65

Elucidating the Mechanism of Disease Pathogenesis in SMA by Studying SMN Missense Mutant Function

Blatnik, Anton J., III January 2020 (has links)
No description available.
66

Characterization of Mutant SMN and Development of Mutant SMN Transgenic Mice

Workman, Eileen 26 June 2009 (has links)
No description available.
67

Transcriptional Programming of Spinal Motor Neurons from Stem Cells

Murtha, Matthew J., III 15 January 2010 (has links)
No description available.
68

Investigating the pre-mRNA splicing of the Survival Motor Neuron genes to model the Spinal Muscular Atrophy disease phenotype

Gladman, Jordan Tanin 12 October 2010 (has links)
No description available.
69

Temporally inducible SMN expression and splicing modulation of the SMN2 gene in SMA mouse models

Bebee, Thomas Wayne 19 June 2012 (has links)
No description available.
70

Generation and Analysis of Motor Neuron Disease Models in Zebrafish

Lyon, Alison Nicole 22 June 2012 (has links)
No description available.

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