Results 31 to 40 of about 4,398 (180)

McArdle’s disease: A case of exercise intolerance and myopathy

Journal of Dr. NTR University of Health Sciences
McArdle disease is a hereditary glycogen storage disorder caused by a deficiency in the enzyme myophosphorylase, leading to impaired glycogen breakdown in skeletal muscles.
Prince Saha, Adil Mohammed Siddiqui, Nirupam Nadella   +2 more
doaj   +1 more source

Oclacitinib for Controlling Pruritus and Associated Skin Lesions in 16 Horses With Allergic Dermatitis

Veterinary Dermatology, Volume 37, Issue 5, Page 672-680, October 2026.
Background: Oclacitinib is a Janus kinase inhibitor approved for the treatment of pruritus associated with allergic dermatitis in dogs and may be effective in horses. Objectives: To evaluate the efficacy of oclacitinib in reducing pruritus and skin lesions in horses with allergic dermatitis.
Maturawan Tunhikorn, Photchanun Maneephan, Natcha Tovanakasame, Chalidaporn Kampang, Pusprapa Jandee, Panpanga Sangsuriya, Nuttawut Nuchprayoon   +6 more
wiley   +1 more source

Multiple Organ‐Dysfunction Secondary to Multiple Bee Sting: A Case Report From Tanzania

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT An 8‐year‐old boy sustained over 200 bee stings, developing airway‐threatening facial oedema requiring intubation and ICU admission, with severe anemia (Hb 3.2 g/dL), rhabdomyolysis, intravascular haemolysis and marked hepatic injury (AST 2505 U/L), yet preserved renal function.
Kelvin M. Musa, Auson Albert, Jane G. Zakaria, Ronald G. Mbwasi, Anorld David, Elton Meleki   +5 more
wiley   +1 more source

Seronegative Granulomatous Myositis With Bulbar Weakness and Reversible Cardiomyopathy: A Case Report

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT A 64‐year‐old woman presented with seronegative idiopathic granulomatous myositis, featuring severe bulbar weakness, reversible cardiomyopathy (ejection fraction 20%–25%), hepatic injury, and acute kidney injury. Muscle biopsy confirmed granulomatous inflammation.
Balachandran R. Vaidyanathan, Muhamed Abubacker, John Ponugupati   +2 more
wiley   +1 more source

Hypophosphatemia-induced Rhabdomyolysis: A Case Report on Uncommon Complication of Diabetic Ketoacidosis - A Case Report

Apollo Medicine, 2023
Background: Diabetic ketoacidosis (DKA) is an acute complication of diabetes mellitus, which is diagnosed by the triad of hyperglycemia, metabolic acidosis, and ketosis.
Rutvi Chahal, Anish Garg, Gautam Jesrani, Monica Gupta   +3 more
doaj   +1 more source

Exploring the Content Validity of Patient‐Reported Outcome Measures to Capture the Patient Experience of Becker Muscular Dystrophy

Muscle &Nerve, Volume 74, Issue 3, Page 559-569, September 2026.
ABSTRACT Introduction/Aims The patient experience of Becker muscular dystrophy (BMD) is not well understood, making it difficult to evaluate the conceptual relevance of proposed patient‐reported outcome (PRO) measures. This study aimed to conceptualize the patient experience of BMD and evaluate content validity and perceptions of meaningful changes of ...
Abby Bronson, Katie Mellor, Nicole Kilburn, Ryan Fischer, Natalie Aldhouse, Chris Marshall, Tamara Al‐zubeidi   +6 more
wiley   +1 more source

Dermatomyositis presenting with rhabdomyolysis and acute renal failure; an uncommon manifestation

Annals of Indian Academy of Neurology, 2009
Rhabdomyolysis and myoglobinuria are a rare complication of dermatomyositis. Such patient can land up in acute renal failure. Recognition of this fact has important therapeutic implications as patients require immunotherapy in addition to the symptomatic
Joshi Deepika, Kumar Niraj, Rai Anand
doaj  

Clinical Case and Follow‐Up of Babesia banethi Infection in a Red Fox

Veterinary Medicine and Science, Volume 12, Issue 5, September 2026.
A naturally occurring Babesia banethi infection in a sick red fox was followed up for more than one year through cytology, haematobiochemical profiles and molecular analyses. Imidocarb treatment resulted in temporary clinical improvement and later relapse, whereas atovaquone/proguanil combined with azithromycin led to clinical recovery and parasite ...
Mariaelisa Carbonara, Michela Prioletti, Antonio Camarda, Stefano Castellana, Giuseppe Menga, Giovanna Girardi, Gad Baneth, Domenico Otranto   +7 more
wiley   +1 more source

The Molecular Diagnosis of Myopathies: Integrating Genomic, Proteomic, and Pathological Insights Toward Precision Medicine

Clinical Genetics, Volume 110, Issue 1, Page 15-28, July 2026.
Advances in genomic, proteomic, and transcriptomic technologies are transforming the diagnosis of genetic myopathies. When integrated with traditional muscle pathology, multi‐omics approaches improve diagnostic yield, clarify disease mechanisms, and support more precise, mechanism‐based therapeutic strategies for patients with neuromuscular disorders ...
Ludmila Alem, Denise de Abreu Pereira, Katia Carneiro   +2 more
wiley   +1 more source

Lipin proteins and metabolic homeostasis

Journal of Lipid Research, 2009
The lipin protein family, consisting of three members, was first identified early this century. In the last few years, the lipin proteins have been shown to have important roles in glycerolipid biosynthesis and gene regulation, and mutations in the ...
Karen Reue, Jennifer R. Dwyer
doaj   +1 more source