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1. Full Text Statin-associated muscle symptoms: impact on statin therapy - European Atherosclerosis Society Consensus Panel Statement on Assessment, Aetiology and Management
by Stroes, Erik S and Thompson, Paul D and Corsini, Alberto and Vladutiu, Georgirene D and Raal, Frederick J and Ray, Kausik K and Roden, Michael and Stein, Evan and Tokgözoʇlu, Lale and Nordestgaard, Børge G and Bruckert, Eric and De Backer, Guy and Krauss, Ronald M and Laufs, Ulrich and Santos, Raul D and Hegele, Robert A and Hovingh, G. Kees and Leiter, Lawrence A and Mach, Francois and März, Winfried and Newman, Connie B and Wiklund, Olov and Jacobson, Terry A and Catapano, Alberico L and Chapman, M. John and Ginsberg, Henry N and European Atherosclerosis Society and European Atherosclerosis Society Consensus Panel
European Heart Journal, ISSN 0195-668X, 05/2015, Volume 36, Issue 17, pp. 1012 - 1022
Statin-associated muscle symptoms (SAMS) are one of the principal reasons for statin non-adherence and/or discontinuation, contributing to adverse... 
Musclesymptoms | Mitochondrial | Lipids | Myalgia | Statin | Cholesterol | Consensus statement | Myopathy | Statin intolerance | HYPERLIPIDEMIC PATIENTS | CARDIAC & CARDIOVASCULAR SYSTEMS | SAFETY | RANDOMIZED-TRIAL | MONOCLONAL-ANTIBODY | INDUCED MYOPATHY | MITOCHONDRIAL-DNA | LDL CHOLESTEROL | SKELETAL-MUSCLE | DENSITY-LIPOPROTEIN CHOLESTEROL | GENETIC RISK | Cholesterol Ester Transfer Proteins - antagonists & inhibitors | Proprotein Convertases - antagonists & inhibitors | Mitochondria, Muscle | Humans | Risk Factors | Consensus | Muscular Diseases - diagnosis | Genetic Predisposition to Disease - etiology | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacokinetics | Mitochondrial Diseases - complications | Complementary Therapies | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Diet | Creatine Kinase - metabolism | Hypolipidemic Agents - therapeutic use | Muscular Diseases - chemically induced | Serine Endopeptidases | Muscular Diseases - therapy | Proprotein Convertase 9 | Review | Muscle symptoms
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2. Full Text Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care
by Bushby, Katharine, MD and Finkel, Richard, MD and Birnkrant, David J, MD and Case, Laura E, DPT and Clemens, Paula R, MD and Cripe, Linda, MD and Kaul, Ajay, MD and Kinnett, Kathi, MSN and McDonald, Craig, MD and Pandya, Shree, PT and Poysky, James, PhD and Shapiro, Frederic, MD and Tomezsko, Jean, PhD and Constantin, Carolyn, PhD and DMD Care Considerations and DMD Care Considerations Working Group
Lancet Neurology, The, ISSN 1474-4422, 2010, Volume 9, Issue 2, pp. 177 - 189
Summary Optimum management of Duchenne muscular dystrophy (DMD) requires a multidisciplinary approach that focuses on anticipatory and preventive measures as... 
Neurology | VENTRICULAR SYSTOLIC DYSFUNCTION | PEAK COUGH FLOW | VERTEBRAL COMPRESSION | ANKLE-FOOT ORTHOSES | SPINAL-FUSION | MECHANICAL INSUFFLATION-EXSUFFLATION | PHYSICAL-ACTIVITY | DILATED CARDIOMYOPATHY | REHABILITATION MANAGEMENT | NONINVASIVE VENTILATION | CLINICAL NEUROLOGY | Nutritional Requirements | Bone Diseases - therapy | Respiration Disorders - etiology | Physical Therapy Specialty - methods | Humans | Pain Management | Gastrointestinal Diseases - etiology | Patient Care Team | Gastrointestinal Diseases - therapy | Treatment Outcome | Language Disorders - therapy | Muscular Dystrophy, Duchenne - complications | Muscular Dystrophy, Duchenne - psychology | Respiration Disorders - therapy | Ambulatory Care | Exercise Therapy | Bone Diseases - etiology | Language Disorders - etiology | Heart Diseases - etiology | Heart Diseases - therapy | Pain - etiology | Quality of Life | Muscular Dystrophy, Duchenne - therapy | Muscular Dystrophy, Duchenne - diagnosis | Care and treatment | Molecular genetics | Duchenne muscular dystrophy | Therapeutics, Physiological | Strategic planning (Business) | Respiratory agents | Diagnosis | Natural history | Physical therapy | Pain | Nutrition | Duchenne's muscular dystrophy | Gastroenterology | Longevity | Rehabilitation | Quality of life
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3. Full Text Treatment of primary Sjögren syndrome
by Saraux, Alain and Pers, Jacques-Olivier and Devauchelle-Pensec, Valérie
Nature Reviews Rheumatology, ISSN 1759-4790, 08/2016, Volume 12, Issue 8, pp. 456 - 471
Primary Sjogren syndrome (pSS) is a progressive autoimmune disease characterized by sicca and systemic manifestations. In this Review, we summarize the... 
DRY EYE SYMPTOMS | CUTANEOUS LUPUS-ERYTHEMATOSUS | MESSENGER-RNA EXPRESSION | REGULATORY B-CELLS | SMALL FIBER NEUROPATHY | DOUBLE-BLIND | GLAND EPITHELIAL-CELLS | OPEN-LABEL | RANDOMIZED CONTROLLED-TRIAL | RHEUMATOLOGY | SALIVARY-GLANDS | Arthralgia - etiology | Xerostomia - drug therapy | Humans | Fatigue - etiology | Lung Diseases - drug therapy | Molecular Targeted Therapy | Lung Diseases - etiology | Muscular Diseases - etiology | Muscular Diseases - drug therapy | Arthritis - etiology | Nephritis, Interstitial - drug therapy | Severity of Illness Index | Biological Therapy | Dry Eye Syndromes - drug therapy | Sjogren's Syndrome - drug therapy | Cryoglobulinemia - drug therapy | Nervous System Diseases - drug therapy | Skin Diseases - drug therapy | Cryoglobulinemia - etiology | Skin Diseases - etiology | Arthritis - drug therapy | Nephritis, Interstitial - etiology | Nervous System Diseases - etiology | Xerostomia - etiology | Sjogren's Syndrome - complications | Dry Eye Syndromes - etiology | Arthralgia - drug therapy | Complications and side effects | Sjogren's syndrome | Care and treatment | Research | Health aspects | Immunosuppressive agents | Life Sciences | Immunology
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4. Manipulative therapy
: musculoskeletal medicine
by Lewit, Karel
2010, 1st English ed., ISBN 9780702030567, xiii, 436
"Manipulative Therapy" provides a systematic overview of chain reactions which are the basis of a rational holistic approach. These reactions are closely... 
Musculoskeletal Manipulations | Muscular Diseases | methods | therapy | etiology | Manipulation (Therapeutics) | Nursing & Ancillary Services | Muscles
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5. Full Text Iron deficiency and heart failure: Diagnostic dilemmas and therapeutic perspectives
by Jankowska, Ewa A and Von Haehling, Stephan and Anker, Stefan D and MacDougall, Iain C and Ponikowski, Piotr
European Heart Journal, ISSN 0195-668X, 03/2013, Volume 34, Issue 11, pp. 816 - 826
Iron is a micronutrient essential for cellular energy and metabolism, necessary for maintaining body homoeostasis. Iron deficiency is an important co-morbidity... 
Heart failure | Prognosis | Soluble transferrin receptor | Exercise capacity | Iron deficiency | Hepcidin | ETIOLOGY | HOMEOSTASIS | CARDIAC & CARDIOVASCULAR SYSTEMS | DISEASE | ANEMIA | Diagnosis, Differential | Humans | Iron, Dietary - administration & dosage | Cardiomyopathies - etiology | Muscular Diseases - etiology | Depression - etiology | Heart Failure - therapy | Iron - physiology | Iron - therapeutic use | Exercise Tolerance - physiology | Iron - deficiency | Dietary Supplements | Heart Failure - etiology | Review
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6. 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 Int Conf SMA Stand C 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
Spinal muscular atrophy is a neurodegenerative disease that requires multidisciplinary medical care. Recent progress in the understanding of molecular... 
Standard of care | Consensus statement | Spinal muscular atrophy | COMMUNITY-ACQUIRED PNEUMONIA | LEAN BODY-MASS | HIP DISLOCATION | NEUROMUSCULAR DISORDERS | standard of care | RESPIRATORY-DISTRESS | FUNCTIONAL MOTOR SCALE | WERDNIG-HOFFMANN DISEASE | NATURAL-HISTORY | CLINICAL NEUROLOGY | consensus statement | OUTCOME MEASURES | PEDIATRICS | spinal muscular atrophy | NONINVASIVE VENTILATION | 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
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7. Full Text Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
by Mendell, Jerry R and Al-Zaidy, Samiah and Shell, Richard and Arnold, W. Dave and Rodino-Klapac, Louise R and Prior, Thomas W and Lowes, Linda and Alfano, Lindsay and Berry, Katherine and Church, Kathleen and Kissel, John T and Nagendran, Sukumar and L’Italien, James and Sproule, Douglas M and Wells, Courtney and Cardenas, Jessica A and Heitzer, Marjet D and Kaspar, Allan and Kaspar, Brian K and Corcoran, Sarah and Braun, Lyndsey and Likhite, Shibi and Miranda, Carlos and Meyer, Kathrin and Foust, K.D and Burghes, Arthur H.M
The New England Journal of Medicine, ISSN 0028-4793, 11/2017, Volume 377, Issue 18, pp. 1713 - 1722
Fifteen children with spinal muscular atrophy type 1 received gene-replacement therapy with a single dose of adeno-associated virus containing SMN. In marked... 
SURVIVAL | MEDICINE, GENERAL & INTERNAL | MOUSE MODEL | DISEASE | PHENOTYPE | SMN2 | MOTOR-NEURON | DELIVERY | Spinal Muscular Atrophies of Childhood - genetics | Humans | Infant | Male | Dependovirus | Respiration, Artificial | Spinal Muscular Atrophies of Childhood - therapy | Disease-Free Survival | Liver Diseases - etiology | Survival of Motor Neuron 1 Protein - genetics | Female | Spinal Muscular Atrophies of Childhood - physiopathology | Historically Controlled Study | Infusions, Intravenous | Genetic Vectors | Nutritional Support | Motor Skills | Infant, Newborn | Cohort Studies | Genetic Therapy - adverse effects | Neuromuscular diseases | Intravenous administration | Cell survival | Gene transfer | Neurons | SMN protein | Nervous system | Patients | Children & youth | Spinal muscular atrophy | Proteins | Motor neuron diseases | Children | Gene therapy | Neuromuscular system | Prednisolone | Age | Deoxyribonucleic acid--DNA
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