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Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2008, Volume 3, Issue 1, pp. 12 - 12
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 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 of Hepatology, ISSN 0168-8278, 2011, Volume 56, Issue 1, pp. 184 - 191
Background & Aims Mosaic G-protein alpha-subunit ( GNAS )-activating mutations are responsible for the McCune–Albright (MCA) syndrome. This oncogene that... 
Gastroenterology and Hepatology | CRP | interleukine 6 signal transducer | GTP | C-reactive protein | jun N-terminal kinase | serum amyloid A | JNK | macroregenerative nodule | complementary deoxyribonucleic acid | MRN | mitogen activated proteins kinase | cAMP | glycoprotein 130 | neuroendocrine secretory protein 55 | hepatocyte nuclear factor 1A | G-protein alpha stimulatory subunit | cDNA | gp130 | protein kinase A | hepatocellular carcinoma | β catenin | IHCA | McCune-Albright syndrome | HCA | PKA | HCC | MAP kinase | MCA | HNF1A | inflammatory hepatocellular adenoma | SAA | cyclic adenosine monophosphate | hepatocellular adenoma | GNAS | CTNNB1 | NESP55 | guanosine-5′-triphosphate | IL6ST | INACTIVATION | PATHWAY | HEPATOCELLULAR ADENOMA | GS-ALPHA | GROWTH | CLASSIFICATION | HUMAN CANCERS | MCCUNE-ALBRIGHT-SYNDROME | GASTROENTEROLOGY & HEPATOLOGY | G-PROTEIN | BINDING | Liver Neoplasms - classification | Humans | Middle Aged | Adenoma, Liver Cell - pathology | Male | Fibrous Dysplasia, Polyostotic - genetics | GTP-Binding Protein alpha Subunits, Gs - genetics | Chromogranins | DNA Mutational Analysis | Base Sequence | Carcinoma, Hepatocellular - genetics | Adult | Female | Liver Neoplasms - pathology | Adenoma, Liver Cell - genetics | STAT3 Transcription Factor - metabolism | Liver Neoplasms - genetics | Signal Transduction | Adenoma, Liver Cell - metabolism | Models, Biological | Carcinoma, Hepatocellular - pathology | Liver Neoplasms - metabolism | Aged | DNA, Neoplasm - genetics | Mutation | Carcinoma, Hepatocellular - metabolism | Liver cancer | Genetic aspects | Nucleic acids | Adenylic acid | Mitogens | Protein kinases | Index Medicus | GTP-Binding Protein alpha Subunits, Gs | Fibrous Dysplasia, Polyostotic | Liver Neoplasms | Life Sciences | Adenoma, Liver Cell | DNA, Neoplasm | STAT3 Transcription Factor | Carcinoma, Hepatocellular | Cancer
Journal Article