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Frontiers of Hormone Research, ISSN 0301-3073, 2018, Volume 51, p. VII
Journal Article
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
2015, ISBN 9788847053755
Hypoparathyroidism, a condition in which insufficient parathyroid hormone (PTH) is produced to maintain normocalcemia is associated with a variety of acute and... 
Medicine | Human physiology | Internal medicine | Surgery | Endocrinology
Web Resource
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 01/2018, Volume 15, Issue 1, p. 7
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 10/2017, Volume 14, Issue 3, p. 279
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
Nature reviews. Endocrinology, ISSN 1759-5029, 12/2018, Volume 15, Issue 1, pp. 33 - 51
The Ca 2+ -sensing receptor (CaSR) is a dimeric family C G-protein-coupled receptor that is expressed in calcitropic tissues such as the parathyroid glands and... 
Journal Article
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
Frontiers of hormone research, 2019, Volume 51, p. 139
Parathyroid hormone (PTH) is one of the major hormones that regulates serum calcium. Hypoparathyroidism occurs when PTH secretion is insufficient. The main... 
Journal Article
Frontiers of hormone research, 2019, Volume 51, p. 160
The treatment of hypoparathyroidism depends on the severity of hypocalcemia, how rapidly the hypocalcemia developed, and the symptomatology. Chronic... 
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 2017, Volume 14, Issue 1, p. 11
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 2017, Volume 14, Issue 2, pp. 119 - 119
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 2017, Volume 14, Issue 1, pp. 11 - 11
Journal Article
Frontiers of hormone research, 2019, Volume 51, p. 52
Familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT) are genetically determined variants of primary hyperparathyroidism.... 
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 05/2016, Volume 13, Issue 2, p. 79
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 05/2018, Volume 15, Issue 2, pp. 235 - 241
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 2016, Volume 13, Issue 3, pp. 169 - 169
Journal Article
Clinical Cases in Mineral and Bone Metabolism, ISSN 1724-8914, 2016, Volume 13, Issue 3, p. 169
Journal Article
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