Hypoparathyroidism

Hypoparathyroidism

Hypoparathyroidism is a disease characterized by inadequately low circulating concentrations of parathyroid hormone (PTH) resulting in low calcium levels and increased phosphate levels in the blood. Symptoms of the disease result from increased neuromuscular irritability caused by hypocalcaemia and...

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Príomhchruthaitheoirí:	Mannstadt, M, Bilezikian, JP, Thakker, RV, Hannan, FM, Clarke, BL, Rejnmark, L, Mitchell, DM, Vokes, TJ, Winer, KK, Shoback, DM
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	Springer Nature 2017

Míreanna comhchosúla

Hypoparathyroidism
de réir: Bilezikian, J, et al.
Foilsithe / Cruthaithe: (1997)

The PARADIGHM (physicians advancing disease knowledge in hypoparathyroidism) registry for patients with chronic hypoparathyroidism: study protocol and interim baseline patient characteristics
de réir: Neil Gittoes, et al.
Foilsithe / Cruthaithe: (2021-11-01)

Hypoparathyroidism: genetics and diagnosis
de réir: Mannstadt, M, et al.
Foilsithe / Cruthaithe: (2022)

Spectrum of germline AIRE mutations causing APS-1 and familial hypoparathyroidism
de réir: Cranston, T, et al.
Foilsithe / Cruthaithe: (2022)

Treatment of Hypoparathyroidism by Re-Establishing the Effects of Parathyroid Hormone
de réir: Lars Rejnmark
Foilsithe / Cruthaithe: (2024-04-01)

Gain-of-Function Mutations in G alpha 11 Cause a Novel Form of Autosomal-Dominant Hypoparathyroidism
de réir: Mannstadt, M, et al.
Foilsithe / Cruthaithe: (2013)

Therapy of Hypoparathyroidism by Replacement with Parathyroid Hormone
de réir: Lars Rejnmark, et al.
Foilsithe / Cruthaithe: (2014-01-01)

Hypoparathyroidism: Replacement Therapy with Parathyroid Hormone
de réir: Lars Rejnmark, et al.
Foilsithe / Cruthaithe: (2015-12-01)

Genetic developments in hypoparathyroidism.
de réir: Thakker, R
Foilsithe / Cruthaithe: (2001)

Molecular genetics of hypoparathyroidism
de réir: Thakker, R
Foilsithe / Cruthaithe: (2003)

Management of endocrine disease: Postsurgical hypoparathyroidism: current treatments and future prospects for parathyroid allotransplantation
de réir: Mihai, R, et al.
Foilsithe / Cruthaithe: (2021)

AUTOSOMAL DOMINANT HYPOCALCEMIA (HYPOPARATHYROIDISM) TYPES 1 AND 2
de réir: Kelly Lauter Roszko, et al.
Foilsithe / Cruthaithe: (2016-10-01)

Total thyroidectomy: reduction in postoperative hypoparathyroidism
de réir: Rasmus Reinke, et al.
Foilsithe / Cruthaithe: (2023-08-01)

A Phase I Randomized Trial of Once‐Daily Versus Twice‐Daily Recombinant Human Parathyroid Hormone (1‐84) for Hypoparathyroidism
de réir: Steven W. Ing, et al.
Foilsithe / Cruthaithe: (2023-07-01)

Hypoparathyroidism - A Review of the Molecular Genetic Testing Service in Oxford
de réir: Cranston, T, et al.
Foilsithe / Cruthaithe: (2008)

Changes in treatment needs for chronic postoperative hypoparathyroidism during initiation of conventional treatment compared to stable phase of treatment
de réir: Pernille Storm, et al.
Foilsithe / Cruthaithe: (2021-07-01)

Challenges in the management of chronic hypoparathyroidism
de réir: Guido Zavatta, et al.
Foilsithe / Cruthaithe: (2020-10-01)

Calcimimetic and calcilytic therapies for inherited disorders of the calcium-sensing receptor signalling pathway
de réir: Hannan, FM, et al.
Foilsithe / Cruthaithe: (2017)

Transcription factors in parathyroid development: lessons from hypoparathyroid disorders.
de réir: Grigorieva, I, et al.
Foilsithe / Cruthaithe: (2011)

Molecular diagnosis of hypoparathyroidism: 2 illustrative cases
de réir: Hampson, G, et al.
Foilsithe / Cruthaithe: (2003)

Hypoparathyroidism
de réir: N S Kuznetsov, et al.
Foilsithe / Cruthaithe: (2012-09-01)

ILLEGITIMATE TRANSCRIPTION OF THE PARATHYROID-HORMONE GENE IN LYMPHOCYTES FROM NORMAL AND HYPOPARATHYROID INDIVIDUALS
de réir: Parkinson, D, et al.
Foilsithe / Cruthaithe: (1992)

Design and topline results of TransCon PTH, a long-acting PTH, phase 2 trial in patients with hypoparathyroidism
de réir: David B. Karpf, et al.
Foilsithe / Cruthaithe: (2020-10-01)

Hypercalcemic disorders in children
de réir: Stokes, VJ, et al.
Foilsithe / Cruthaithe: (2017)

Week 26 results from the PaTH Forward Open-Label Extension Trial Support TransCon PTH as a potential hormone replacement therapy for patients with hypoparathyroidism
de réir: Lars Rejnmark, et al.
Foilsithe / Cruthaithe: (2021-04-01)

Genetics of monogenic disorders of calcium and bone metabolism
de réir: Newey, PJ, et al.
Foilsithe / Cruthaithe: (2021)

Genetics of skeletal disorders
de réir: Hannan, FM, et al.
Foilsithe / Cruthaithe: (2020)

New candidate genes for X-linked recessive hypoparathyroidism.
de réir: Mumm, S, et al.
Foilsithe / Cruthaithe: (1999)

Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review
de réir: Jane Hejlesen, et al.
Foilsithe / Cruthaithe: (2018-06-01)

Hypoparathyroidism: update of guidelines from the 2022 International Task Force
de réir: Bart L. Clarke
Foilsithe / Cruthaithe: (2022-12-01)

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism.
de réir: Parkinson, D, et al.
Foilsithe / Cruthaithe: (1992)

A family with hypoparathyroidism, deafness and renal anomaly syndrome - Clinical and molecular studies
de réir: Dobbie, A, et al.
Foilsithe / Cruthaithe: (2001)

Dystonia and Hypoparathyroidism
de réir: J Gordon Millichap
Foilsithe / Cruthaithe: (1988-10-01)

Hypoparathyroidism in pregnancy
de réir: A Sendhil Coumary, et al.
Foilsithe / Cruthaithe: (2021-01-01)

Studies of mice deleted for Sox3 and uc482: Relevance to X-linked hypoparathyroidism
de réir: Gaynor, KU, et al.
Foilsithe / Cruthaithe: (2020)

Postoperative hypoparathyroidism after thyroid operation and exploration of permanent hypoparathyroidism evaluation
de réir: Xi Wang, et al.
Foilsithe / Cruthaithe: (2023-05-01)

Canine hypoparathyroidism: case report
de réir: M.J.L. Cardoso, et al.
Foilsithe / Cruthaithe: (2015-04-01)

Management of hypoparathyroidism in pregnancy and lactation — A report of 10 cases
de réir: B.L. Hatswell, et al.
Foilsithe / Cruthaithe: (2015-12-01)

P255: Gain-of-function CASR variants, a common genetic cause of non-surgical hypoparathyroidism: Findings from a sponsored genetic testing program
de réir: Arun Mathew, et al.
Foilsithe / Cruthaithe: (2024-01-01)

Characteristics of hearing loss in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome.
de réir: Looij, v, et al.
Foilsithe / Cruthaithe: (2006)