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Muscle NMJ Nerve Spinal Ataxia Antibody & Biopsy Patient Information

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Myotendinous Junction

Perlecan at a Myotendinous Junction

Pathology
Myopathy: Inflammatory & Immune   Absent chondroitin sulfate C   Anti-Decorin (BJ) antibody   Brachio-Cervical   Complement deposition   Decorin   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   Mitochondrial     Cytochrome oxidase deficiency     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   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 partial denervation     Fiber type grouping     Large grouped atrophy     Ongoing     Spinal muscular atrophy         Bulbospinal         SMA 5q     Target fibers   Differential fascicular loss   Dysmyelination   Minifascicles   Nerve: Normal   Perineuritis   Regeneration   Subperineurial edema   Tabes dorsalis   Terminal sprouting   Vasculitis   Vasculopathy     Vessel: Thick wall   Wallerian degeneration