Results 151 to 160 of about 50,140 (235)

The myositis autoantibody phenotypes of the juvenile idiopathic inflammatory myopathies.

, 2013
The juvenile idiopathic inflammatory myopathies (JIIM) are systemic autoimmune diseases characterized by skeletal muscle weakness, characteristic rashes, and other systemic features.
Rider, Lisa G, LG;Shah, Mona, M;Mamyrova, Gulnara, G;Huber, Adam M, AM;Rice, Madeline Murguia, MM;Targoff, Ira N, IN;Miller, Frederick W, FW;Childhood Myositis Heterogeneity Collaborative Study Group
core  

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2289-2308, October 2026.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu, Rosan Kenana, Rana Chakrabarti, Sarah D. P. Wilhelm, Joseph Andrews, Susan J. Leat, Christina Parker, Michael Miller, Leslie A. Nangle, Wendy McCaul, Ashfia Chowdhury, Natalie Hutchings, Ryan A. Adams, Lauren Guy, Mandy Rhody, Verena Juncal, Marisa I. Mendes, Desiree E. C. Smith, Gajja S. Salomons, Angelica A. Moresco, Daphne L. McCulloch, D. Holmes Morton, Ilka U. Heinemann, C. Anthony Rupar   +23 more
wiley   +1 more source

Orbital Myositis

, 1997
Orbital myositis is a subgroup of the nonspecific inflammatory syndrome or orbital pseudotumor and is characterized by a primary inflammation of extraocular muscles.
Morganho, A, Jacinto, V, Dias, M, Passão, V, Pedrosa, R, Aguiar, T   +5 more
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Distribution of Big Tau Isoforms in the Human Central and Peripheral Nervous System

Annals of Neurology, Volume 100, Issue 4, Page 709-736, October 2026.
Objective Tau is widely studied in neurodegeneration, yet most work has focused on canonical brain tau isoforms. A longer isoform, “big tau,” produced by inclusion of exon 4a, is expressed in the peripheral nervous system (PNS) and central nervous system (CNS) regions.
Rama Krishna Koppisetti, Nicolas R. Barthélemy, Kanta Horie, Cindy V. Ly, Kaleigh F. Roberts, Srinivas Koutarapu, Richard J. Perrin, Erin E. Franklin, Chiara Pedicone, Joshua Orrick, Justin Melendez, Timothy M. Miller, Chihiro Sato, Nupur Ghoshal, Alison M. Goate, Celeste M. Karch, Randall J. Bateman, Soumya Mukherjee   +17 more
wiley   +1 more source

Assessment of Pain Characteristics, Attribution, and Nociplasticity in Patients With Inflammatory Myopathies: An International Survey Study. [PDF]

ACR Open Rheumatol
Radaideh M, Schmukler J, Best A, Fair J, Lubinus M, Lee YC, Saygin D.   +6 more
europepmc   +1 more source

Mitochondrial DNA variants in inclusion body myositis

, 2000
Mitochondrial DNA variants have been shown to be associated with many diseases. Mutations at mitochondrial DNA nucleotide positions 3192, 3196, 3397 and 4336 have been described in association with late-onset Alzheimer's disease.
Kok, C.C., Kiers, L., Martins, R., Gaudieri, S., Garleep, M., Mastaglia, F., Boyt, A., Askanas, V., Dalakas, M.   +8 more
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Efficacy and Safety of First‐Line Treatment Options for Oncogene Wild‐Type Lung Adenocarcinoma With Liver Metastases

Cancer Medicine, Volume 15, Issue 10, October 2026.
ABSTRACT Objective Liver metastasis represents one of the frequent drivers for cancer‐related mortality in lung adenocarcinoma. For advanced lung adenocarcinoma harboring wild‐type oncogene drivers, chemotherapies in combination with immune checkpoint inhibitors (ICIs) and/or bevacizumab (named IC, BC, and IBC, respectively) are alternative first‐line ...
Jie Li, Yihui Ge, Qiaohong Liu, Xiaojuan Wei, Jian Wang, Xiufen Wang, Dahai Wang, Jiannan Liu, Yuping Sun, Aiqin Gao   +9 more
wiley   +1 more source

Inclusion Body Myositis

, 2010
Keywords: inclusion body myositis; sporadic inclusion body myositis (sIBM) - common myopathy in Caucasians over 50 years of age; epidemiology and genetic susceptibility; genetic susceptibility, linked to HLA-DR3 and 8.1 MHC ancestral haplotype (AH)
Mastaglia, F.L., Needham, M.
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Melorheostosis Involving the Carpal and Metacarpal Bones: Diagnostic Insights From Multimodal Imaging

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Multimodal imaging enables non‐invasive diagnosis of carpal melorheostosis, avoiding biopsy. Two‐year follow‐up confirms stability.
Zhiwei Zhang, Zhi Deng, Wen Yang, Aiguo Zou, Pengyuan Leng, Yuewen Peng   +5 more
wiley   +1 more source

Nailfold capillary phenotypes distinguish juvenile myositis subtypes and associate with disease activity. [PDF]

Clin Transl Med
McClellan N, Chen L, Matossian S, Rynda A, Grant K, Janssen E, Kahlenberg JM, Turnier JL.   +7 more
europepmc   +1 more source