Results 121 to 130 of about 1,023,457 (221)
Wildlife Biology, EarlyView.Many clinical signs of chronic wasting disease (CWD) in white‐tailed deer Odocoileus virginianus are consistent with those of chronic stress including hyperexcitability, head tremors, teeth grinding, pacing, excessive salivation, drinking, and urination. Deer with CWD‐positive (CWD+) status are more likely to exhibit poor body condition and to die, and
Cameron G. Mitchell +6 more
wiley +1 more source
Myopathy or Neuropathy in Thyrotoxicosis
, 1973 To the Editor: Thyrotoxicosis is very often associated with weakness and wasting of muscles, and 80 to 90 per cent of the patients show abnormal electromyographic features1, 2 characteristic of a myopathy.
Scarpalezos, S., Panayiotopoulos, C.P.
core +1 more source
Radial outer retina reflectivity (RORR) sign in LAMP2‐associated retinopathy
Acta Ophthalmologica, EarlyView.Abstract Purpose To describe the radial outer retina reflectivity (RORR) sign in patients carrying pathogenic variants in the X‐linked lysosome‐associated membrane protein‐2 (LAMP2) gene and to review the histologic characteristics of LAMP2 expression in the human retina.
Rachael C. Heath Jeffery +17 more
wiley +1 more source
Capture myopathy in red deer and wild goat
Archives of Razi Institute, 2011 This syndrome is a shock-like hyper metabolic myopathy triggered in susceptible animals by stress. Capture myopathy (C.M.) is a commonly occurring condition in mammals following trapping and ransportation. In this case 12 to 24 hours after transportation
Mirian, J., Alhami, A., Hamidieh, H.
doaj
A myopathy with unusual features caused by PNPLA2 gene mutations
, 2015 Introduction: The PNPLA2 gene encodes the enzyme adipose triglyceride lipase (ATGL), which catalyzes the first step of triglyceride hydrolysis. Mutations in this gene are associated with an autosomal recessive lipid-storage myopathy, neutral lipid ...
Tavian, Daniela, Missaglia, Sara
core +1 more source
Poultry Science: Wooden breast (WB) myopathy is a common myopathy found in commercial broiler chickens worldwide. Although extensive research on WB has been conducted using transcriptomics, effectively screening and analyzing key target information remains a challenge.
Xinrui Zhang +4 more
doaj +1 more source
Genetic analysis of limb girdle muscular dystrophy and Miyoshi myopathy [PDF]
, 2003 The autosomal recessive muscular dystrophies encompass limb girdle muscular dystrophy (LGMD) and Miyoshi myopathy (MM), which can show clinical and genetic overlap.
Summerill, Gillian
core
A novel myopathy with autophagic vacuoles associated with biallelic variants in CLN8
Brain Pathology, EarlyView.We describe a novel adult‐onset myopathy with autophagic vacuoles and characteristic features of ceroid lipofuscinosis associated with biallelic CLN8 variants, seizures, and muscle weakness. Autophagosomal/lysosomal deposition of curvilinear, autofluorescent material containing the mitochondrial adenosine triphosphate (ATP) synthase membrane subunit c ...
Ulrika Lindgren +5 more
wiley +1 more source
Brain Pathology, EarlyView.The study highlights differences in the regulatory processes of skeletal muscle, such as sarcomeric contractility, lysosomal and autophagic function, metabolic activity and immune regulation, at transcriptomic and proteomic levels in infantile and adult Pompe disease.
Alexander Schaiter +16 more
wiley +1 more source
British Journal of Pharmacology, EarlyView.Immune checkpoint inhibitor (ICI)‐associated myocarditis has emerged as a severe and clinically complex immune‐related toxicity that poses significant challenges for therapeutic decision‐making in routine cardio‐oncological care. High‐dose corticosteroids remain the first‐line therapy, yet their timing, dosage and tapering require careful clinical ...
Raluca I. Mincu +10 more
wiley +1 more source