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Brain Pathology, ISSN 1015-6305, 11/2017, Volume 27, Issue 6, pp. 781 - 794
Alpha‐motoneurons and muscle fibres are structurally and functionally interdependent. Both cell types particularly rely on endoplasmic reticulum (ER/SR)... 
ER chaperones | Neurogenic muscular atrophy (NMA) | VAPB | Neuromuscular junction (NMJ) | ALS | Motor neuron disease (MND) | Sigma Receptor 1 (SigR1) | MOTONEURON SURVIVAL | MARIE-TOOTH-DISEASE | MYOSIN ISOFORMS | MATRIN 3 | REGULAR EXERCISE | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | TUBULAR-AGGREGATE MYOPATHY | DISTAL MYOPATHY | TRANSGENIC MOUSE MODEL | BULBAR MUSCULAR-ATROPHY | Immunohistochemistry | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Muscle Denervation | Mice, Transgenic | Motor Neuron Disease - pathology | Vesicular Transport Proteins - physiology | Motor Neurons - metabolism | Endoplasmic Reticulum - pathology | Animals | Autopsy | Membrane Proteins - physiology | Spinal Cord - pathology | Neuromuscular Junction | Superoxide Dismutase-1 - metabolism | Membrane Proteins - metabolism | Mice | Muscle, Skeletal - pathology | Superoxide Dismutase - metabolism | Disease Models, Animal | Proteins | Neurons | Analysis | Muscles | Heat shock proteins | Amyotrophic lateral sclerosis | Web sites | Animal models | Disintegration | Motor neuron disease | Immunoblotting | Superoxide dismutase | Chaperones | Autophagy | Sclerosis | Fibers | Atrophy | Protein folding | Rodents | Localization | Dynamic response | Motor neurons | Autopsies | Markers | Patients | Skeletal muscle | Pathology | Biopsy | Hsp27 protein | Mutation | Position (location) | Endoplasmic reticulum | Phagocytosis | Denervation | Index Medicus
Journal Article
Book
08/2013, ISBN 9781118635469, 986
Edited by Hans H. Goebel, MD, Professor of Neuropathology, Charité – Universitätsmedizin Berlin, Berlin, Germany -- Department of Neuropathology, Johannes... 
Muscles | Genetics | Diseases
eBook
1983, ISBN 0398046905, xv, 487 p., [14] p. of plates
Book
Circulation, ISSN 0009-7322, 08/2017, Volume 136, Issue 13, pp. e200 - e231
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of morbidity and mortality. The management of cardiac disease in NMDs is made... 
Neuromuscular disease | Pediatrics | Cardiomyopathy | Muscular dystrophy | AHA Scientific Statements | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | MECHANICAL CIRCULATORY SUPPORT | neuromuscular disease | CONVERTING ENZYME-INHIBITORS | LUNG TRANSPLANTATION GUIDELINES | LEFT-VENTRICULAR NONCOMPACTION | muscular dystrophy | pediatrics | CHEYNE-STOKES RESPIRATION | LAMIN A/C GENE | PERIPHERAL VASCULAR DISEASE | DUCHENNE MUSCULAR-DYSTROPHY | MYOCARDIAL DELAYED ENHANCEMENT | cardiomyopathy | CARDIOSELECTIVE BETA-BLOCKERS | Myotonic Dystrophy - metabolism | Barth Syndrome - metabolism | Friedreich Ataxia - pathology | Myotonic Dystrophy - diagnosis | United States | Humans | Myopathies, Structural, Congenital - genetics | Neuromuscular Diseases - pathology | Barth Syndrome - pathology | Myotonic Dystrophy - pathology | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Cardiomyopathies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Friedreich Ataxia - metabolism | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Diseases - metabolism | Risk Factors | Friedreich Ataxia - diagnosis | Muscular Dystrophy, Emery-Dreifuss - pathology | Cardiomyopathies - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Diseases - pathology | Barth Syndrome - diagnosis | American Heart Association | Muscular Diseases - diagnosis | Muscular Dystrophy, Emery-Dreifuss - metabolism | Muscular Dystrophies, Limb-Girdle - metabolism | Barth Syndrome - genetics | Neuromuscular Diseases - complications | Myopathies, Structural, Congenital - pathology | Cardiomyopathies - complications | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - metabolism | Myopathies, Structural, Congenital - metabolism | Muscular Dystrophy, Duchenne - diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
1985, Current histopathology, ISBN 9780852003251, Volume 9, 168
Book
British Journal of Dermatology, ISSN 0007-0963, 12/2015, Volume 173, Issue 6, pp. 1505 - 1513
Journal Article
1994, ISBN 9780723420163, vi, 202
Book
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2015, Volume 96, Issue 2, pp. 266 - 274
Singleton-Merten syndrome (SMS) is an autosomal-dominant multi-system disorder characterized by dental dysplasia, aortic calcification, skeletal abnormalities,... 
OPEN-ANGLE GLAUCOMA | ACTIVATION | RNA | GENE | GENETICS & HEREDITY | CALCIFICATION | SENSOR | SPECTRUM | IDENTIFICATION | GAIN | MDA5 | Odontodysplasia - pathology | Humans | Vascular Calcification - genetics | Child, Preschool | Molecular Sequence Data | Male | Metacarpus - abnormalities | Mutation, Missense - genetics | Base Sequence | Adult | Female | Osteoporosis - genetics | Odontodysplasia - diagnostic imaging | DEAD-box RNA Helicases - chemistry | Aortic Diseases - pathology | DEAD Box Protein 58 | Musculoskeletal Abnormalities - diagnostic imaging | Cells, Cultured | Models, Molecular | Muscular Diseases - pathology | Vascular Calcification - pathology | Sequence Analysis, DNA | Radiography | DEAD-box RNA Helicases - genetics | Aortic Diseases - genetics | Exome - genetics | Osteoporosis - pathology | Pedigree | Musculoskeletal Abnormalities - genetics | Metacarpus - pathology | Polymorphism, Single Nucleotide - genetics | Odontodysplasia - genetics | Muscular Diseases - genetics | Dental Enamel Hypoplasia - pathology | Glaucoma - genetics | Dental Enamel Hypoplasia - genetics | Genes, Dominant - genetics | Physiological aspects | Genetic research | Genetic disorders | Research | Gene mutations | Glaucoma | Psoriasis | RNA-protein interactions | ABC transporters | Mutation | Gene expression | Index Medicus | Report
Journal Article