المؤلفون: Leenders, J. M. P., Geurts, A. C. H., Steultjens, E. M. J., Packer, T. L., Cup, E. H. C.

المصدر: Disability & Rehabilitation; May2024, Vol. 46 Issue 10, p2138-2144, 7p

مصطلحات موضوعية: NEUROMUSCULAR diseases, STATISTICAL significance, RESEARCH funding, MUSCLE diseases, WORK-life balance, QUESTIONNAIRES, RESEARCH methodology evaluation, DISABILITY evaluation, RESEARCH evaluation, FACIOSCAPULOHUMERAL muscular dystrophy, MITOCHONDRIAL myopathy, DESCRIPTIVE statistics, OCCUPATIONAL therapy, STATISTICAL reliability, INTRACLASS correlation, CONFIDENCE intervals, DATA analysis software, ACTIVITIES of daily living, POSTURAL balance, EVALUATION

المؤلفون: Prayson, Richard A.^Aff3, Ahrendsen, Jared T.^Aff4

المساهمون: Prayson, Richard A.^Aff1, Ahrendsen, Jared T.^Aff2

المصدر: Neuropathology Review. :151-170

المؤلفون: Parith Wongkittichote, Cassandra Pantano, Miao He, Xinying Hong, Matthew M. Demczko

المصدر: JIMD Reports, Vol 65, Iss 2, Pp 102-109 (2024)

مصطلحات موضوعية: ferredoxin‐2, iron‐sulfur clusters, mitochondrial disorders, mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy, Diseases of the endocrine glands. Clinical endocrinology, RC648-665, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2192-8312

URL الوصول: https://doaj.org/article/58f5ede61b154c5a8b176c8c42ec6992

المؤلفون: Sprason, Charlotte, Tucker, Trudy, Clancy, David

المصدر: Frontiers in Aging Neuroscience; 2024, p1-13, 13p

مصطلحات موضوعية: MITOCHONDRIAL DNA analysis, DNA metabolism, MUSCLE diseases, GENETIC mutation, SEQUENCE analysis, MITOCHONDRIAL pathology, MITOCHONDRIAL myopathy, AGING, GENOMES, GENES, CELLS, POLYMERASE chain reaction

المؤلفون: Gao, Xinming, Feng, Binbin, Du, Chen, Hou, Congcong, Jin, Shan, Tang, Daojun, Zhu, Junquan

المصدر: Journal of Oceanology & Limnology; Jan2024, Vol. 42 Issue 1, p187-200, 14p

مصطلحات موضوعية: SPERMIOGENESIS in animals, MITOCHONDRIAL myopathy, PHASCOLOSOMA, PHASCOLOSOMATIDAE, LEBER'S hereditary optic atrophy

المؤلفون: Wu, Guiping, Han, Yijun, Zhao, Lifeng, Zhang, Hong, Fan, Xiuzhao, Li, Weiqin, Che, Xiaowen^{Aff3, IDs1287202303444z_cor7}, Zhou, Yun^{Aff4, IDs1287202303444z_cor8}

المصدر: BMC Cardiovascular Disorders. 23(1)

المؤلفون: Guiping Wu, Yijun Han, Lifeng Zhao, Hong Zhang, Xiuzhao Fan, Weiqin Li, Xiaowen Che, Yun Zhou

المصدر: BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-8 (2023)

مصطلحات موضوعية: Mitochondrial myopathy, Heart failure, Respiratory failure, Pulmonary artery hypertension, Left ventricular hypertrophy, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2261

URL الوصول: https://doaj.org/article/17cf07c3c4d8422fae3362f8c2fd97ee

المؤلفون: Moore, Margaret, Yeske, Philip, Parikh, Sumit

المصدر: Journal of Primary Care & Community Health; 8/30/2023, p1-7, 7p

مصطلحات موضوعية: MUSCLE diseases, GRIEF, DELAYED diagnosis, MEDICAL office management, PATIENT autonomy, PATIENT advocacy, SOCIAL stigma, MITOCHONDRIAL myopathy, EXPERIENCE, PATIENTS' attitudes, PRIMARY health care, SOCIAL isolation, HOLISTIC medicine, QUALITY of life, PSYCHOLOGY of caregivers, HEALTH care teams, ACCESS to information, SUPPORT groups, ECONOMIC aspects of diseases, RARE diseases

المؤلفون: Xiong Peng, Li-xiu Ma, Ce Xiao, Zhi-zhe Zhang, Min Zhu, Dao-jun Hong, Yi-an Zhan

المصدر: Heliyon, Vol 9, Iss 12, Pp e23300- (2023)

مصطلحات موضوعية: Mitochondrial myopathy, Severe pneumonia, Acute respiratory failure, Difficulty in weaning, A3243G mutation, Science (General), Q1-390, Social sciences (General), H1-99

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2405844023105081; https://doaj.org/toc/2405-8440

URL الوصول: https://doaj.org/article/8eb4498d311a405fb81190d3c0ac8444

المؤلفون: Martina Rimoldi, Francesca Magri, Sara Antognozzi, Michela Ripolone, Sabrina Salani, Daniela Piga, Letizia Bertolasi, Simona Zanotti, Patrizia Ciscato, Francesco Fortunato, Maurizio Moggio, Stefania Corti, Giacomo Pietro Comi, Dario Ronchi

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: mitochondrial myopathy, cytochrome c oxidase deficiency, COA8, mitochondrial encefalomyopathies, whole exome sequencing, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1278572/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/91ab41cbfebc447bbe1cb3ed47358bfb