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11/2018, Frontiers of hormone research, ISBN 9783318064087, Volume 51, 188
This work is devoted exclusively to hyper- and hypoparathyroidism with a focus on clinical practice guidelines explained by experts in the field. The clinical,... 
Parathyroid glands
eBook
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 11/2018, Volume 13, Issue 1, pp. 205 - 205
BackgroundMultiple endocrine neoplasia (MEN1) is a rare inherited multi-tumour syndrome, affecting specific neuroendocrine organs and non-endocrine tissues... 
Gastro-entero-pancreatic neuroendocrine tumours (GEP-NETs) | Multiple endocrine neoplasia type 1 (MEN1) | Genetic test | MEN1 gene | Patients' database | Pituitary adenomas | Primary hyperparathyroidism (PHPT) | MEDICINE, RESEARCH & EXPERIMENTAL | PRIMARY HYPERPARATHYROIDISM | PITUITARY-TUMORS | DES TUMEURS ENDOCRINES | GENE | MEN1 PATIENTS | GENETICS & HEREDITY | GTE | COHORT | MUTATIONS | DMSG | Humans | Middle Aged | Lipoma - genetics | Child, Preschool | Infant | Male | Stomach Neoplasms - pathology | Hyperparathyroidism, Primary - genetics | Lipoma - pathology | Multiple Endocrine Neoplasia Type 1 - genetics | Young Adult | Adult | Female | Child | Intestinal Neoplasms - genetics | Neuroendocrine Tumors - pathology | Stomach Neoplasms - genetics | Introns - genetics | Pituitary Neoplasms - genetics | Pancreatic Neoplasms - pathology | Exons - genetics | Pancreatic Neoplasms - genetics | Mutation - genetics | Intestinal Neoplasms - pathology | Neuroendocrine Tumors - genetics | Adolescent | Multiple Endocrine Neoplasia Type 1 - pathology | Aged | Adenomatosis, Familial endocrine | Gene mutations | Research | Phenotypes | Prognosis | Statistical analysis | Disease | Data processing | Hormones | Metastasis | Patients | Epidemiology | Data bases | Genetic screening | Studies | Genotype & phenotype | Databases | Multiple endocrine neoplasia | Medical prognosis | Surgery | Genetic analysis | Mutation | Pancreas | Genotypes | Tumors | Neuroendocrine tumors | Index Medicus
Journal Article
L'Endocrinologo, ISSN 1590-170X, 4/2019, Volume 20, Issue 2, pp. 78 - 83
La biomineralizzazione è un processo caratterizzato dalla deposizione di minerali fuori o dentro le cellule di molti organismi. La fosfatasi alcalina (FA) è... 
Medicine & Public Health | Ipofosfatasia | Metabolic Diseases | Gene ALPL | Internal Medicine | Medicine/Public Health, general | Fosfatasi alcalina | Terapia enzimatica sostitutiva | Endocrinology | Alkaline phosphatase
Journal Article
ENDOCRINE JOURNAL, ISSN 0918-8959, 2019, Volume 66, Issue 4, pp. 319 - 327
Abstract. Hyperparathyrodism-jaw tumor (HPT-JT) syndrome is an autosomal dominant disorder. Loss of function of the cell division cycle protein 73 homolog... 
Journal Article
Expert Review of Endocrinology and Metabolism, ISSN 1744-6651, 11/2012, Volume 7, Issue 6, pp. 587 - 588
Journal Article
Endocrine Practice, ISSN 1530-891X, 2011, Volume 17, Issue 4, pp. 655 - 655
During the past decade, there has been tremendous progress in our understanding of the pathogenesis of hereditary endocrine tumors. The networks involved in... 
ENDOCRINOLOGY & METABOLISM
Journal Article
Expert Review of Endocrinology and Metabolism, ISSN 1744-6651, 05/2012, Volume 7, Issue 3, pp. 255 - 257
Journal Article
Frontiers of Hormone Research, ISSN 0301-3073, 2018, Volume 51, p. VII
Journal Article
Seminars in Arthritis and Rheumatism, ISSN 0049-0172, 2015, Volume 45, Issue 4, pp. S3 - S11
Journal Article
by Estrada Gil, Karol and Styrkarsdottir, Unnur and Evangelou, Evangelos and Hsu, Yi-Hsiang and Duncan, Emma and Ntzani, Evangelia and Oei, Ling and Albagha, Omar M and Amin, Najaf and Kemp, John and Koller, Daniel and Li, Guo and Liu, Ching-Ti and Minster, Ryan and Moayyeri, Alireza and Vandenput, Liesbeth and Willner, Dana and Xiao, Su-Mei and Yerges-Armstrong, Laura and Zheng, Hou-Feng and Alonso, Nerea and Eriksson, Joel and Kammerer, Candace and Kaptoge, Stephen and Leo, Paul and Thorleifsson, Gudmar and Wilson, Scott and Wilson, James and Aalto, Ville and Alen, Theo and Aragaki, Aaron and Aspelund, Thor and Center, Jacqueline and Dailiana, Zoe and Duggan, C and Garcia, Melissa and Garcia-Giralt, Natàlia and Giroux, Sylvie and Hallmans, Göran and Hocking, Lynne and Husted, Lise Bjerre and Jameson, Karen and Khusainova, Rita and Kim, Ghi Su and Kooperberg, Charles and Koromila, Theodora and Kruk, Marcin and Laaksonen, Marika and LaCroix, Anea and Lee, Seung and Leung, Ping and Lewis, Joshua and Masi, Laura and Mencej-Beac, Simona and Nguyen, Tuan and Nogues, Xavier and Patel, Millan and Prezelj, Janez and Rose, Lynda and Scollen, Serena and Siggeirsdottir, Kristin and Smith, G.D and Svensson, Olle and Trompet, Stella and Trummer, Olivia and Schoor, Natasja and Woo, Margaret M and Zhu, Kun and Balcells, Susana and Brandi, M.L and Buckley, Brendan M and Cheng, Sulin and Christiansen, C and Cooper, Charles and Dedoussis, George and Ford, Ian and Frost, Morten and Goltzman, David and González-Macías, Jesús and Kähönen, Mika and Karlsson, Magnus and Khusnutdinova, Elza and Koh, Jung-Min and Kollia, Panagoula and Langdahl, Bente and Leslie, William and Lips, Paul and Ljunggren, Östen and Lorenc, Roman and Marc, Janja and Mellström, Dan and Obermayer-Pietsch, Barbara and Olmos, David and Pettersson-Kymmer, Ulrika and Reid, David and Riancho, José and Ridker, Paul and Rousseau, Francois and Lagboom, P Eline and Tang, Nelson L and ... and Medicinska fakulteten and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk farmakologi and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap
Nature Genetics, ISSN 1061-4036, 05/2012, Volume 44, Issue 5, pp. 491 - 501
textabstractBone mineral density (BMD) is the most widely used predictor of fracture risk. We performed the largest meta-analysis to date on lumbar spine and... 
WOMEN | POPULATION | IMPUTATION | VARIANTS | DISEASE | GENETICS & HEREDITY | OSTEOPOROTIC FRACTURES | GENE-EXPRESSION | LRP5 | PATTERNS | IMPUTED DATA | Glycoproteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Low Density Lipoprotein Receptor-Related Protein-5 - genetics | Extracellular Matrix Proteins - genetics | Humans | Risk Factors | Computational Biology | Intercellular Signaling Peptides and Proteins - genetics | European Continental Ancestry Group | Genotype | Male | Bone Density - genetics | Gene Expression Profiling | Phosphoproteins - genetics | Fractures, Bone - genetics | Mitochondrial Membrane Transport Proteins - genetics | Polymorphism, Single Nucleotide - genetics | Female | Femur Neck - physiopathology | Osteoporosis - genetics | Spectrin - genetics | Quantitative Trait Loci | Lumbar Vertebrae - physiopathology | Quantitative trait loci | Measurement | Fractures | Bones | Genetic aspects | Identification and classification | Density | Risk factors | Medical research | Osteoporosis | Genomics | Bone density | Gene loci | Index Medicus | Vèrtebres lumbars | Gens | Femur | Genes | Bone densitometry | Densitometria òssia | Fèmur | Lumbar vertebrae | Basic Medicine | Medical Genetics | Medicinsk genetik | ortopedi | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | genetik | Genetics | Orthopaedics
Journal Article