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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 Tokgözoğlu, 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, 2015, Volume 36, Issue 17, pp. 1012 - 1022
no | Musclesymptoms | Mitochondrial | Lipids | Myalgia | Statin | Cholesterol | Consensus statement | Myopathy | Statin intolerance | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | 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 | Index Medicus | Review | Muscle symptoms
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2. 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
Life Sciences & Biomedicine | Rheumatology | Science & Technology | 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 | Index Medicus | Life Sciences | Immunology
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3. Full Text Aetiology and Pathogenesis of IUGR
by Sankaran, Srividhya, MRCOG and Kyle, Phillipa M., MD, FRCOG, FRANZCOG, CMFM
Best practice & research. Clinical obstetrics & gynaecology, ISSN 1521-6934, 2009, Volume 23, Issue 6, pp. 765 - 777
Obstetrics and Gynecology | IUGR | genes | uteroplacental insufficiency | intrauterine growth restriction | intrauterine programming | placenta | fetal growth | fetal circulation | Doppler | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Diseases, Inborn - embryology | Humans | Prenatal Exposure Delayed Effects - etiology | Gestational Age | Placenta Diseases - physiopathology | Pregnancy Complications, Infectious - physiopathology | Prenatal Nutritional Physiological Phenomena - physiology | Pregnancy | Kidney Diseases - embryology | Lung Diseases - embryology | Endocrine System Diseases - embryology | Brain Diseases - embryology | Muscular Diseases - embryology | Fetal Growth Retardation - etiology | Fetal Development - physiology | Female | Gastrointestinal Diseases - embryology | Cardiovascular Diseases - embryology | Placental Circulation - physiology | Index Medicus
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4. 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 for the DMD Care Considerations Working Group and DMD Care Considerations and DMD Care Considerations Working Group
Lancet neurology, ISSN 1474-4422, 2010, Volume 9, Issue 2, pp. 177 - 189
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | 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 | Index Medicus | Pain | Nutrition | Duchenne's muscular dystrophy | Gastroenterology | Longevity | Rehabilitation | Quality of life
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5. Medically unexplained illness
: gender and biopsychosocial implications
by Johnson, Susan K
2008, 1st ed., ISBN 9780979212581, x, 271
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6. Full Text GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges
by Carrillo, Nuria and Malicdan, May C and Huizing, Marjan
Neurotherapeutics, ISSN 1933-7213, 10/2018, Volume 15, Issue 4, pp. 900 - 914
rare diseases | Neurology | Neurosciences | Biomedicine | GNE myopathy | genetics | sialic acid | Neurobiology | gene therapy | ManNAc | Neurosurgery | Pharmacology & Pharmacy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Muscular Diseases - diagnosis | Magnetic Resonance Imaging | Animals | Humans | Multienzyme Complexes - genetics | Muscular Diseases - genetics | Mutation - genetics | Muscular Diseases - therapy | Muscular Diseases - etiology | Atrophy | Polysaccharides | Etiology | Quadriceps muscle | Diagnosis | Mutation |