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1. Full Text The role and regulation of MAFbx/atrogin-1 and MuRF1 in skeletal muscle atrophy
by Foletta, Victoria C and White, Lloyd J and Larsen, Amy E and Léger, Bertrand and Russell, Aaron P
Pflügers Archiv, ISSN 0031-6768, 3/2011, Volume 461, Issue 3, pp. 325 - 335
Regeneration | Myosin heavy chain | Myogenic response | Biomedicine | Human Physiology | Muscle damage | Skeletal muscle | Life Sciences & Biomedicine | Physiology | Science & Technology | Muscular Atrophy - metabolism | Fasting - physiology | Humans | SKP Cullin F-Box Protein Ligases - physiology | Immobilization - adverse effects | Pulmonary Disease, Chronic Obstructive - physiopathology | Sepsis - physiopathology | Ubiquitin-Protein Ligases - physiology | Tripartite Motif Proteins | Acquired Immunodeficiency Syndrome - physiopathology | Animals | Renal Insufficiency - physiopathology | Aging - physiology | Diabetes Mellitus - physiopathology | Spinal Cord Injuries - physiopathology | Muscle Proteins - physiology | Cachexia - physiopathology | Denervation | Ubiquitin | Chronic diseases | Messenger RNA | Muscle proteins | Ligases | Myosin | Index Medicus
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2. Full Text Disease-Induced Skeletal Muscle Atrophy and Fatigue
by Powers, Scott K and Lynch, Gordon S and Murphy, Kate T and Reid, Michael B and Zijdewind, Inge
Medicine and science in sports and exercise, ISSN 0195-9131, 11/2016, Volume 48, Issue 11, pp. 2307 - 2319
OXIDATIVE STRESS | CRITICAL ILLNESS | MUSCLE ATROPHY | MECHANICAL VENTILATION | NEUROLOGICAL DISORDERS | NECROSIS-FACTOR-ALPHA | INDUCED DIAPHRAGM DYSFUNCTION | CANCER | CANCER-RELATED FATIGUE | TUMOR-BEARING MICE | MULTIPLE-SCLEROSIS | INTENSIVE-CARE-UNIT | DIRECTED MYOSTATIN INHIBITION | RENIN-ANGIOTENSIN SYSTEM | INFLAMMATION | Muscular Atrophy - physiopathology | Humans | Critical Illness | Nervous System Diseases - physiopathology | Neoplasms - physiopathology | Muscle Fatigue - physiology | Chronic Disease | Cachexia - physiopathology | Inflammation - physiopathology | Muscles | Fatigue | Research | Index Medicus | cancer | muscle atrophy | inflammation | critical illness | neurological disorders
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3. Full Text Consensus Statement for Standard of Care in Spinal Muscular Atrophy
by Wang, Ching H and Finkel, Richard S and Bertini, Enrico S and Schroth, Mary and Simonds, Anita and Wong, Brenda and Aloysius, Annie and Morrison, Leslie and Main, Marion and Crawford, Thomas O and Trela, Anthony and Participants of the International Conference on SMA Standard of Care
Journal of child neurology, ISSN 0883-0738, 08/2007, Volume 22, Issue 8, pp. 1027 - 1049
Standard of care | Consensus statement | Spinal muscular atrophy | Muscular Atrophy, Spinal - diagnosis | Postoperative Complications - etiology | Gastrointestinal Diseases - physiopathology | Humans | Gastrointestinal Diseases - etiology | Postoperative Complications - prevention & control | Respiratory Insufficiency - etiology | Respiratory Paralysis - therapy | Respiratory Paralysis - physiopathology | Deglutition Disorders - therapy | Child Nutrition Disorders - etiology | Respiratory Paralysis - etiology | Child Nutrition Disorders - physiopathology | Gait Disorders, Neurologic - physiopathology | Child Nutrition Disorders - prevention & control | Deglutition Disorders - etiology | Child | Deglutition Disorders - physiopathology | Respiratory Insufficiency - physiopathology | Diagnosis, Differential | Gastrointestinal Diseases - therapy | Respiratory Insufficiency - therapy | Consensus | Gait Disorders, Neurologic - therapy | Muscular Atrophy, Spinal - therapy | Muscular Atrophy, Spinal - complications | Gait Disorders, Neurologic - etiology | Index Medicus
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4. Full Text Signaling in Muscle Atrophy and Hypertrophy
by Marco Sandri
Physiology, ISSN 1548-9213, 06/2008, Volume 23, Issue 3, pp. 160 - 170
Life Sciences & Biomedicine | Physiology | Science & Technology | Animals | Muscular Atrophy - physiopathology | Humans | Muscle Contraction - physiology | Muscle, Skeletal - physiopathology | Muscle, Skeletal - metabolism | Signal Transduction - physiology | Muscle, Skeletal - pathology | Contractile Proteins - metabolism | Hypertrophy - physiopathology | Index Medicus
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5. Full Text Irisin prevents and restores bone loss and muscle atrophy in hind-limb suspended mice
by Colaianni, Graziana and Mongelli, Teresa and Cuscito, Concetta and Pignataro, Paolo and Lippo, Luciana and Spiro, Giovanna and Notarnicola, Angela and Severi, Ilenia and Passeri, Giovanni and Mori, Giorgio and Brunetti, Giacomina and Moretti, Biagio and Tarantino, Umberto and Colucci, Silvia C and Reseland, Janne E and Vettor, Roberto and Cinti, Saverio and Grano, Maria
Scientific reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 2811 - 16
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fibronectins - administration & dosage | Humans | Femur - drug effects | Muscular Atrophy - genetics | Recombinant Proteins - genetics | Femur - physiopathology | Muscular Atrophy - drug therapy | Hindlimb Suspension - physiology | Recombinant Proteins - administration & dosage | Bone Diseases, Metabolic - drug therapy | Bone Density - drug effects | Animals | Muscular Atrophy - physiopathology | Muscle, Skeletal - drug effects | Muscle, Skeletal - physiopathology | Lower Extremity - physiopathology | Fibronectins - genetics | Mice | Bone Diseases, Metabolic - genetics | Bone Diseases, Metabolic - physiopathology | Physical Conditioning, Animal | Atrophy | Osteoporosis | Bone mass | Computed tomography | Myosin | Bone mineral density | Bone loss | Bone (cortical) | Bone (trabecular) | Microgravity | Skeletal muscle | Geriatrics | Index Medicus
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6. Full Text Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4
by Wadman, R. I and Wijngaarde, C. A and Stam, M and Bartels, B and Otto, L. A. M and Lemmink, H. H and Schoenmakers, M. A. G. C and Cuppen, I and van den Berg, L. H and van der Pol, W. L
European journal of neurology, ISSN 1351-5101, 03/2018, Volume 25, Issue 3, pp. 512 - 518
muscle strength | NUSINERSEN | SMA | DISEASE | spinal muscular atrophy | milestones | NATURAL-HISTORY | natural history | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cross-Sectional Studies | Motor Skills - physiology | Humans | Middle Aged | Child, Preschool | Infant | Male | Disease Progression | Young Adult | Muscle, Skeletal - physiopathology | Adolescent | Adult | Female | Aged | Spinal Muscular Atrophies of Childhood - physiopathology | Muscle Weakness - physiopathology | Child | Muscular Atrophy, Spinal - physiopathology | Muscle Strength - physiology | Medical research | Analysis | Medicine, Experimental | Explosives | Children | Spinal muscular atrophy | Diseases | Cluster analysis | Cell survival | Human motion | Motor ability | Muscles | Motor skill | Infants | Patients | Atrophy | Skills | Quadriceps muscle | Muscular strength | Age | Index Medicus
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7. Full Text Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
by Finkel, Richard S and Mercuri, Eugenio and Darras, Basil T and Connolly, Anne M and Kuntz, Nancy L and Kirschner, Janbernd and Chiriboga, Claudia A and Saito, Kayoko and Servais, Laurent and Tizzano, Eduardo and Topaloglu, Haluk and Tulinius, Már and Montes, Jacqueline and Glanzman, Allan M and Bishop, Kathie and Zhong, Z. John and Gheuens, Sarah and Bennett, C. Frank and Schneider, Eugene and Farwell, Wildon and De Vivo, Darryl C and ENDEAR Study Grp and ENDEAR Study Group and Sahlgrenska akademin and Institute of Clinical Sciences, Department of Pediatrics and Göteborgs universitet and Gothenburg University and Institutionen för kliniska vetenskaper, Avdelningen för pediatrik and Sahlgrenska Academy
The New England journal of medicine, ISSN 0028-4793, 11/2017, Volume 377, Issue 18, pp. 1723 - 1732
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Injections, Spinal | Spinal Muscular Atrophies of Childhood - genetics | Double-Blind Method | Oligonucleotides - therapeutic use | Humans | Spinal Muscular Atrophies of Childhood - drug therapy | Infant | Male | Oligonucleotides - adverse effects | Oligonucleotides, Antisense - adverse effects | RNA, Messenger - metabolism | Survival of Motor Neuron 2 Protein - metabolism | Respiration, Artificial | Disease-Free Survival | Oligonucleotides, Antisense - therapeutic use | Survival of Motor Neuron 2 Protein - genetics | Age of Onset | Survival Analysis | Female | Spinal Muscular Atrophies of Childhood - mortality | Spinal Muscular Atrophies of Childhood - physiopathology | Motor Skills | RNA, Messenger - drug effects | Care and treatment | Usage | Surgery | Patient outcomes | Motor ability | Analysis | Spinal muscular atrophy | Pediatrics | Neuromuscular diseases | Cell survival | Splicing | Neurons | SMN protein | Antisense oligonucleotides | mRNA | Infants | Motor task performance | Hereditary diseases | Children & youth | Babies | Proteins | Neurology | Ventilation | Death | Mutation | Drug therapy | Drug dosages | Age | Index Medicus | Abridged Index Medicus | trials | Pediatrik
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