Results 31 to 40 of about 1,023,457 (221)

Malingering and factitious disorder (Münchausen-syndrome) can be mitochondrial

Indian Journal of Psychological Medicine, 2016
Malingering and factitious disorder (Münchausen-syndrome) has not been reported as a manifestation of a mitochondrial-disorder (MID). Here, we report a 46 years-old female with a MID due to a combined complex I-IV defect, manifesting in the cerebrum ...
Josef Finsterer, Lässer Stefan
doaj   +1 more source

Analysis of clinical and histopathology characteristics of asymptomatic and pauci ⁃ symptomatic hyperCKemia

Chinese Journal of Contemporary Neurology and Neurosurgery, 2023
Objective To evaluate the diagnostic value of skeletal muscle biopsy in asymptomatic and pauci‑symptomatic hyperCKemia. Methods and Results A total of 146 patients with asymptomatic or pauci ‑ symptomatic hyperCKemia diagnosed in Peking University First ...
YUAN Yu‑jing, LIU Chang, XIE Zhi‑ying, ZHAO Ya‑wen, MENG Ling‑chao, LÜ He, WANG Zhao‑xia, YUAN Yun, ZHANG Wei   +8 more
doaj   +1 more source

Cardiac Myopathy and Metabolic Disorders among Elderly Patients in Saudi Arabia: A Systematic Review [PDF]

, 2023
Cardiac myopathy and metabolic disorders are increasingly common health issues among the elderly population in Saudi Arabia. These conditions can have significant impacts on the health and well-being of older individuals, and it is important to ...
Abdulrahman Sameer Basabrain, Waleed omar bawazeer, Yara Salah Menshawi, Sahar Abdulhaq Albloshi, Hisham Ghaith Alsharief, Rahaf Fouad Wajdi   +5 more
core  

Electron microscopy in the diagnosis of skeletal muscle disorders: Its utility and limitations

Indian Journal of Pathology and Microbiology, 2022
Electron microscopy (EM) has a substantial role in the diagnosis of skeletal muscle disorders. The ultrastructural changes can be observed in muscle fibers and other components of the muscle tissue. EM serves as a confirmatory tool where the diagnosis is
Rashmi Santhoshkumar, Gayathri Narayanappa   +1 more
doaj   +1 more source

Myopathy in acute hypothyroidism [PDF]

, 1987
Hypothyroid myopathy has so far been reported in long standing cases of hypothyroidism. We describe two adult patients with myopathy associated with acute transient hypothyroidism. Both presented with severe muscle aches and cramps, stiffness and spasms.
Ma, JTC, Kung, AWC, Yu, YL
core   +1 more source

Woody breast myopathy broiler show age-dependent adaptive differential gene expression in Pectoralis major and altered in-vivo triglyceride kinetics in adipogenic tissues

Poultry Science, 2021
: A study was conducted to understand the differentially expressed genes in Pectoralis (P) major under woody breast (WB) myopathy condition in a high yielding broiler strain using RNA-sequencing at the growing (d 21) and finishing (d 42 and d 56) grow ...
Pramir Maharjan, Antonio Beitia, Jordan Weil, Nawin Suesuttajit, Katie Hilton, Justina Caldas, Cole Umberson, Diego Martinez, Byungwhi Kong, Casey M. Owens, Craig Coon   +10 more
doaj   +1 more source

Cardiopulmonary Exercise Testing (CPET) Guided Sub-Anaerobic Threshold Rehabilitation in MELAS Syndrome: A Case Report. [PDF]

Kaohsiung J Med Sci
The Kaohsiung Journal of Medical Sciences, EarlyView.
Tsai YL, Cheng KY, Lu YS, Lin KL.
europepmc   +2 more sources

AASLD practice guidance on drug, herbal, and dietary supplement–induced liver injury

, 2022
Hepatology, EarlyView.
Robert J. Fontana, Iris Liou, Adrian Reuben, Ayako Suzuki, M. Isabel Fiel, William Lee, Victor Navarro   +6 more
wiley   +1 more source

Critical Illness Myopathy. [PDF]

, 2020
Critical illness myopathy (CIM) is a primary myopathy associated with increased mortality and morbidity, which frequently develops in severely ill patients.
Hatice Tankisi, Werner J. Z'Graggen, Tankisi, Hatice, Z'Graggen, Werner J., Tankisi H, ZʼGraggen WJ   +5 more
core   +1 more source

Digital Cognitive Testing in Mitochondrial Disease: Validity and Challenges for Clinical Trial Use

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Primary mitochondrial disease is a group of genetic disorders caused by pathogenic variants in nuclear or mitochondrial DNA, often resulting in progressive neurodegeneration and cognitive decline. Current management is primarily supportive, though recent research offers hope for disease‐modifying treatments in the future.
Oksana Pogoryelova, Jan Smeitink, Herma Renkema, Rosabeth White, Frankie Barton, Rachel Lyon, Jane Newman, Aye Moe, Yi Shiau Ng, Grainne Siobhan Gorman   +9 more
wiley   +1 more source