Creatine

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Nume		Creatine

Vezi şi

Boli A-Z		Aceruloplasminemia Acquired Immunodeficiency Syndrome Acute Kidney Failure Acute Myocardial Infarction Adult Dermatomyositis Aging Amino Acid Metabolic Disorder Aminoacidopathies Amyloidosis Amyloidosis Aa Amyotrophic Lateral Sclerosis 1 Aneurysm Angelman Syndrome Angina Pectoris Anoxia Anxiety Arteries, Anomalies of Arteriosclerosis Arthritis Arthropathy Asperger Syndrome Atrial Fibrillation Atrophic Muscular Disease Attention Deficit-Hyperactivity Disorder Autism Autism X-Linked 2 Autoimmune Disease Basal Ganglia Disease B-Cell Growth Factor Bipolar Disorder Bipolar I Disorder Blood Coagulation Disease Bone Fracture Breast Cancer Brucellosis Cardiac Arrest Cardiac Arrhythmia Cardiomyopathy, Dilated, 3b Central Nervous System Disease Central Serous Chorioretinopathy Cerebral Creatine Deficiency Syndrome 1 Cerebral Creatine Deficiency Syndrome 2 Cerebral Creatine Deficiency Syndrome 3 Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Hereditary Neuropathy Childhood Type Dermatomyositis Chromosomal Disease Chronic Fatigue Syndrome Chronic Kidney Failure Colitis Collagen Disease Colonic Disease Congestive Heart Failure Connective Tissue Disease Constipation Coronary Artery Anomaly Coronary Heart Disease 1 Cranial Nerve Disease Creatine Deficiency Syndromes Dementia Demyelinating Disease Dermatomyositis Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diabetic Neuropathy Diabetic Polyneuropathy Diarrhea Drug Dependence Dysphagia Ectopic Pregnancy Encephalopathy End Stage Renal Failure Enthesopathy Epidermoid Cysts Epilepsy Exanthem Facioscapulohumeral Muscular Dystrophy 1 Facioscapulohumeral Muscular Dystrophy 2 Fainting Food Allergy Gastroenteritis Gastrointestinal System Disease Gilles De La Tourette Syndrome Glucose Metabolism Disease Head Injury Heart Disease Heart Valve Disease Hemophilia a Heparin-Induced Thrombocytopenia Hereditary Motor and Sensory Neuropathy V Hereditary Neuropathy with Liability to Pressure Palsy Hereditary Spastic Paraplegia Heritable Pulmonary Arterial Hypertension Huntington Disease Hypertonia Hypogonadism Hypogonadotropism Hypoxia Idiopathic Inflammatory Myopathy Immune Suppression Immune System Disease Inborn Amino Acid Metabolism Disorder Infantile-Onset Ascending Hereditary Spastic Paralysis Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Intermediate Coronary Syndrome Intermittent Claudication Intestinal Disease Ischemia Ischemic Heart Disease Joint Disorders Kidney Disease L-Arginine:glycine Amidinotransferase Deficiency Lateral Sclerosis Lipid Metabolism Disorder Lung Disease Lupus Erythematosus Major Depressive Disorder Mental Depression Microcephaly Mitochondrial Disorders Mitral Valve Insufficiency Mood Disorder Motor Neuron Disease Motor Neuro-Ophthalmic Disorders Motor Peripheral Neuropathy Movement Disease Mucositis Multiple Sclerosis Muscle Disorders Muscle Hypertrophy Muscle Tissue Disease Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Myocardial Infarction Myofascial Pain Syndrome Myopathy Myopia Myositis Myotonia Congenita, Autosomal Recessive Nerve Compression Syndrome Nervous System Disease Neuritis Neuroleptic Malignant Syndrome Neuromuscular Disease Neuropathy Neuropathy, Hereditary, with Liability to Pressure Palsies Obsessive-Compulsive Disorder Ocular Motility Disease Oculocerebral Syndrome with Hypopigmentation Osteoarthritis Osteoporosis Osteoporotic Fracture Paine Syndrome Paraplegia Paresthesia Parkinson Disease, Late-Onset Peripheral Artery Disease Peripheral Nervous System Disease Phototoxic Dermatitis Pituitary Gland Disease Placenta Accreta Placenta Disease Placenta Praevia Polymyositis Polyneuropathy Primary Progressive Multiple Sclerosis Psychotic Disorder Pulmonary Embolism Pulmonary Hypertension Pulmonary Hypertension, Primary, 1 Respiratory System Disease Retinal Disease Rett Syndrome Rheumatic Disease Rheumatoid Arthritis Roussy-Levy Hereditary Areflexic Dystasia Schizophrenia Secondary Progressive Multiple Sclerosis Seizure Disorder Spastic Diplegia Spasticity Spastic Paralysis, Infantile-Onset Ascending Spastic Paraparesis Speech and Communication Disorders Spinal Cord Disease Spinal Cord Injury Stereotypic Movement Disorder Substance Abuse Supranuclear Palsy, Progressive, 1 Swallowing Disorders Syncope Systemic Lupus Erythematosus Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombophilia Due to Thrombin Defect Thrombosis Tic Disorder Toxic Encephalopathy Tremor Trichohepatoenteric Syndrome 2 Ulcerative Colitis Urinary System Disease Vascular Disease Viral Infectious Disease