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The Journal of biological chemistry, ISSN 0021-9258, 02/2014, Volume 289, Issue 7, pp. 4273 - 4285
Journal Article
The New England journal of medicine, ISSN 1533-4406, 2018, Volume 378, Issue 17, pp. 1604 - 1610
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2012, Volume 7, Issue Suppl 1, pp. S4 - S4
Fibrous dysplasia (FD) is sometimes accompanied by extraskeletal manifestations that can include any combination of cafe-au-lait macules, hyperfunctioning... 
G-ALPHA-S | MEDICINE, RESEARCH & EXPERIMENTAL | PRIMARY HYPERPARATHYROIDISM | SOMATOSTATIN ANALOG | GROWTH-HORMONE EXCESS | ADENYLYL-CYCLASE | GENETICS & HEREDITY | TERM-FOLLOW-UP | OSTEOSARCOMA | PATIENT | STIMULATORY G-PROTEIN | BONE | Aromatase Inhibitors - pharmacology | Fibrous Dysplasia, Polyostotic - drug therapy | Hyperthyroidism - diagnosis | Humans | Cushing Syndrome - diagnosis | Fibrous Dysplasia of Bone - drug therapy | Cafe-au-Lait Spots - diagnosis | Puberty, Precocious - drug therapy | Cafe-au-Lait Spots - complications | Hypophosphatemia - complications | Fibrous Dysplasia, Polyostotic - genetics | GTP-Binding Protein alpha Subunits, Gs - genetics | Acromegaly - complications | Chromogranins | Fibrous Dysplasia, Polyostotic - complications | Acromegaly - genetics | Cushing Syndrome - drug therapy | Fibrous Dysplasia of Bone - genetics | Fibrous Dysplasia, Polyostotic - diagnosis | Cafe-au-Lait Spots - genetics | Hypophosphatemia - diagnosis | Cushing Syndrome - genetics | Hyperthyroidism - drug therapy | Acromegaly - diagnosis | Fibrous Dysplasia of Bone - diagnosis | Acromegaly - drug therapy | Cafe-au-Lait Spots - drug therapy | Puberty, Precocious - diagnosis | Hyperthyroidism - genetics | Hyperthyroidism - complications | Physical Examination | Fibrous Dysplasia of Bone - complications | Puberty, Precocious - complications | Hypophosphatemia - drug therapy | Mutation | Cohort Studies | Studies | Disease | Meetings | Thyroid diseases | Clinical trials | Growth hormones | Clinical medicine | Manuscripts | Bars
Journal Article
Journal Article
Journal Article
Circulation (New York, N.Y.), ISSN 0009-7322, 11/2017, Volume 136, Issue 21, pp. 2068 - 2082
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by ventricular arrhythmias and an increased risk of sudden... 
death, sudden, cardiac | risk assessment | Defibrillators | Cardiac | Death | arrhythmogenic right ventricular dysplasia | syncope | Sudden | Implantable | defibrillators, implantable | CARDIAC & CARDIOVASCULAR SYSTEMS | FAMILY-MEMBERS | CARDIOVERTER-DEFIBRILLATOR THERAPY | NORTH-AMERICAN MULTIDISCIPLINARY | DESMOSOMAL MUTATION CARRIERS | CLINICAL PRESENTATION | SUDDEN CARDIAC DEATH | CATHETER ABLATION | TERM-FOLLOW-UP | PERIPHERAL VASCULAR DISEASE | IMPLANTABLE DEFIBRILLATOR | DYSPLASIA/CARDIOMYOPATHY | Arrhythmias, Cardiac - mortality | Humans | Middle Aged | Child, Preschool | Infant | Male | Arrhythmias, Cardiac - physiopathology | Arrhythmogenic Right Ventricular Dysplasia - physiopathology | Patient Selection | Young Adult | Defibrillators, Implantable | Aged, 80 and over | Adult | Female | Child | Infant, Newborn | Death, Sudden - etiology | Arrhythmias, Cardiac - therapy | Risk Assessment | Risk Factors | Treatment Outcome | Arrhythmias, Cardiac - etiology | Arrhythmogenic Right Ventricular Dysplasia - therapy | Arrhythmogenic Right Ventricular Dysplasia - mortality | Arrhythmogenic Right Ventricular Dysplasia - complications | Electric Countershock - instrumentation | Adolescent | Aged | Death, Sudden - prevention & control | implantable cardioverter defibrillator | risk stratification | sudden cardiac death | Arrhythmogenic right ventricular cardiomyopathy
Journal Article
Nature (London), ISSN 1476-4687, 2013, Volume 494, Issue 7435, pp. 105 - 110
Journal Article