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Myotendinous Junction

Perlecan at a Myotendinous Junction

Pathology
Myopathy: Inflammatory & Immune   Brachio-Cervical   Chondroitin sulfate C, Deficient   Complement deposition   Decorin (BJ) antibody   Dermatomyositis     Childhood pattern     Variant adult pattern   Fasciitis   Focal myositis   Granulomas   Hemophagocytic lymphohistiocytosis   IMPP   Inclusion Body Myositis   Inflammation: Muscle   Inflammation: Cell patterns   Jo-1 Myositis   MHC-1   Macrophages, abundant (IMAM)   Macrophagic myofasciitis   Mitochondrial dysfunction   Necrosis: Muscle fibers   Neonatal perifascicular   Nodular myositis   Paraneoplastic necrotic   Perimysial pathology   Pipestem capillaries   Scleromyxedema   Signal recognition particle   Trichinosis: Acute; Chronic   Vasculitis: Small & Large vessel Myopathy: Other   Atrophy: Type I; Type 2   CADASIL: Vessels   Calciphylaxis   Colchicine   Cytoplasmic bodies   Hemosiderin   Internal architecture: NADH   Lymphoma, Intravascular   Mitochondrial     Cytochrome oxidase deficiency     Megaconial     MELAS     Ultrastructure   Myosin-loss myopathy   Posterior neck   Ring fibers   Tubular aggregates Muscle   Exercise changes   Unknowns	Muscle: Storage   Amyloid     Pathology; Birefringence   CADASIL   Carbohydrate     Acid Maltase Deficiency       Child & Adult     Phosphorylase deficiency     Also see: Pathways   Lipid   Lipofuscin   Myofibrillar (Desmin-storage) Myopathy: Congenital   Cap   Central core   Centronuclear (Myotubular)   Congenital muscular dystrophy   Fiber type size disproportion     Fiber type disorders     Type I small     Type II small   Fukuyama   Marinesco-Sjögren   Multicore   Nemaline rod myopathy   Reducing body   Ullrich CMD Myopathy: Hereditary   Autophagy   Becker MD   Danon disease   Distal myopathy: Vacuolar   Duchenne MD   Dystrophin & related proteins   Emery-Dreifuss MD   FKRP   FSH Dystrophy   Hereditary IBM 2   IBM, Paget's & Dementia   LGMD 1A   LGMD 2A   LGMD 2B   LGMD 2C   LGMD 2D   Myotonic: DM1; DM2   Oculopharyngeal   Periodic paralysis, Hypokalemic Myelin   CIDP     Childhood   Demyelination: Chronic   Dysmyelination   Proteins	Neuromuscular junction   Anti-AChR antibody actions   Distal motor axons   Normal   Myasthenia Gravis   Terminal axons   Presynaptic   Postsynaptic Neuropathy & Neuronopathy   Amyloid   Angiotropic Lymphoma   Antibody-related     MAG     TS-HDS   Axonal loss     Bungner bands     Large fiber   Axonal swellings     Giant axonal neuropathy     Polygucosan bodies   Botulism   Demyelination     Active     Chronic     Tomaculae   Denervation of muscle     ALS     Chronic denervation       Inactive: Fiber type grouping       Partial: Large grouped atrophy       Partial: Ongoing     Spinal muscular atrophy         Bulbospinal         SMA 5q     Target fibers   Differential fascicular loss   Dysmyelination   Minifascicles   Nerve: Normal     Neurofilament stain   Perineuritis   Regeneration   Subperineurial edema   Tabes dorsalis   Terminal sprouting   Vasculitis   Vasculopathy     Vessel: Thick wall   Wallerian degeneration