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Investigation of hypercalcemia.
Endres DB. Endres DB. Clin Biochem. 2012 Aug;45(12):954-63. doi: 10.1016/j.clinbiochem.2012.04.025. Epub 2012 May 5. Clin Biochem. 2012. PMID: 22569596 Review.
Less common causes of hypercalcemia include vitamin D-related (granulomatous diseases, lymphoma, vitamin D intoxication), other endocrine (thyrotoxicosis), medications (milk-alkali, thiazides, lithium) and other causes (immobilization, familial hypocalciuric hype
Less common causes of hypercalcemia include vitamin D-related (granulomatous diseases, lymphoma, vitamin D intoxication), other endocrine (t …
Calcium homeostasis and hyperparathyroidism: Nephrologic and endocrinologic points of view.
Lemoine S, Figueres L, Bacchetta J, Frey S, Dubourg L. Lemoine S, et al. Ann Endocrinol (Paris). 2022 Aug;83(4):237-243. doi: 10.1016/j.ando.2022.05.003. Epub 2022 May 19. Ann Endocrinol (Paris). 2022. PMID: 35598638 Review.
PTH promotes calcium release from the bone, renal calcium reabsorption and phosphate excretion, and conversion of 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D-3. Hyperparathyroidism consists in PTH elevation, which may be adapted (secondary hyperparathyroidism) or non-ad …
PTH promotes calcium release from the bone, renal calcium reabsorption and phosphate excretion, and conversion of 25-hydroxyvitamin D to 1,2 …
Persistent hypercalcemia with similar familial Hypocalciuric hypercalcemia features: a case report and literature review.
Zahedi M, Hizomi Arani R, Rafati M, Amouzegar A, Hadaegh F. Zahedi M, et al. BMC Endocr Disord. 2021 Nov 4;21(1):220. doi: 10.1186/s12902-021-00881-9. BMC Endocr Disord. 2021. PMID: 34736428 Free PMC article. Review.
BACKGROUND: Primary hyperparathyroidism (PHPT) and familial hypocalciuric hypercalcemia (FHH) are the most important differential diagnosis of parathyroid hormone (PTH)-dependent hypercalcemia. ...Biochemical features showed normal values of serum creatinine, …
BACKGROUND: Primary hyperparathyroidism (PHPT) and familial hypocalciuric hypercalcemia (FHH) are the most important di …
Cinacalcet therapy in a child with novel homozygous CASR p.Glu353Lys mutation causing familial hypocalciuric hypercalcemia type 1: case report and review of the literature.
Koca SB. Koca SB. Turk J Pediatr. 2023;65(5):853-861. doi: 10.24953/turkjped.2022.1040. Turk J Pediatr. 2023. PMID: 37853976 Free article. Review.
BACKGROUND: Familial hypocalciuric hypercalcemia (FHH) is one of the conditions that should be considered in the differential diagnosis of hypercalcemia and normo-hypophosphatemia in childhood. ...CASE: A 26-month-old boy was examined for a recurrent rash. Du …
BACKGROUND: Familial hypocalciuric hypercalcemia (FHH) is one of the conditions that should be considered in the differ …
Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical Perspective.
Marx SJ, Goltzman D. Marx SJ, et al. J Bone Miner Res. 2019 Jan;34(1):22-37. doi: 10.1002/jbmr.3650. Epub 2018 Dec 10. J Bone Miner Res. 2019. PMID: 30536424 Free PMC article. Review.
We review advancing and overlapping stages for our understanding of the expressions of six hyperparathyroid (HPT) syndromes: multiple endocrine neoplasia type 1 (MEN1) or type 4, multiple endocrine neoplasia type 2A (MEN2A), hyperparathyroidism-jaw tumor syndrome, familial
We review advancing and overlapping stages for our understanding of the expressions of six hyperparathyroid (HPT) syndromes: multiple endocr …
Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
Marx SJ, Lourenço DM Jr. Marx SJ, et al. Horm Metab Res. 2017 Nov;49(11):805-815. doi: 10.1055/s-0043-120670. Epub 2017 Nov 14. Horm Metab Res. 2017. PMID: 29136674 Review.
Six syndromes of familial hyperparathyroidism are compared: 1) Familial hypocalciuric hypercalcemia (FHH) expresses primary hyperparathyroidism (PHPT) beginning at birth with lifelong hypercalcemia. ...Five of the PHPT syndromes reflect overgrowth of parathyr …
Six syndromes of familial hyperparathyroidism are compared: 1) Familial hypocalciuric hypercalcemia (FHH) expresses pri …
Genetics of hereditary forms of primary hyperparathyroidism.
English KA, Lines KE, Thakker RV. English KA, et al. Hormones (Athens). 2024 Mar;23(1):3-14. doi: 10.1007/s42000-023-00508-9. Epub 2023 Dec 1. Hormones (Athens). 2024. PMID: 38038882 Free PMC article. Review.
The associated syndromic disorders include multiple endocrine neoplasia types 1-5 (MEN1-5) and hyperparathyroidism with jaw tumor (HPT-JT) syndromes, and the non-syndromic forms include familial hypocalciuric hypercalcemia types 1-3 (FHH1-3), fa …
The associated syndromic disorders include multiple endocrine neoplasia types 1-5 (MEN1-5) and hyperparathyroidism with jaw tumor (HPT-JT) s …
Primary hyperparathyroidism and familial hypocalciuric hypercalcemia: relationships and clinical implications.
Eldeiry LS, Ruan DT, Brown EM, Gaglia JL, Garber JR. Eldeiry LS, et al. Endocr Pract. 2012 May-Jun;18(3):412-7. doi: 10.4158/EP11272.RA. Endocr Pract. 2012. PMID: 22232026 Review.
OBJECTIVE: To discuss the unusual occurrence of both familial hypocalciuric hypercalcemia (FHH) and primary hyperparathyroidism in the same patient and to explore potential mechanisms of association and issues related to clinical management. ...
OBJECTIVE: To discuss the unusual occurrence of both familial hypocalciuric hypercalcemia (FHH) and primary hyperparath …
[Asymptomatic primary hyperparathyroidism : Operation or observation?].
Gollisch K, Siggelkow H. Gollisch K, et al. Internist (Berl). 2021 May;62(5):496-504. doi: 10.1007/s00108-021-00996-0. Epub 2021 Mar 12. Internist (Berl). 2021. PMID: 33710361 Review. German.
Borderline laboratory findings occur especially in asymptomatic PHPT and the differential diagnosis of familial hypocalciuric hypercalcemia must be considered. Once the diagnosis is made sonography, radiography or computed tomography (CT) is used to search fo …
Borderline laboratory findings occur especially in asymptomatic PHPT and the differential diagnosis of familial hypocalciuric
32 results