Results 71 to 80 of about 3,479 (203)

Pseudohypoparathyroidism and Growth

open access: yes, 2011
Pseudohypoparathyroidism (PHP) is a disorder characterized by hypocalcemia and hyperphosphatemia due to resistance to parathyroid hormone (PTH). There are two main subtypes of PHP, named as PHP types Ia and Ib and caused by genetic alterations within upstream of the GNAS locus. Heterozygous inactivating mutations within alpha subunit of the stimulatory
Duzcan, Füsun, Semiz, Serap
openaire   +4 more sources

Pseudohypoparathyroidism and G s α-cAMP-linked disorders : Current view and open issues

open access: yes, 2016
Pseudohypoparathyroidism exemplifies an unusual form of hormone resistance as the underlying molecular defect is a partial deficiency of the α subunit of the stimulatory G protein (G s α), a key regulator of the cAMP signalling pathway, rather than of ...
A. Spada   +5 more
core   +1 more source

Hyperphosphatemia in Celiac Disease: Hereditary or Acquired Pseudohypoparathyroidism

open access: yesEndocrinology Research and Practice, 2007
Calcium and vitamin D deficiencies caused by intestinal malabsorption in celiac disease lead to severe impairments of calcium and bone metabolisms. Indeed, malabsorption of calcium results in secondary hyperparathyroidism.
Ramazan Gen   +2 more
doaj   +2 more sources

Endocrinology and the arts at the feet of the dancing Lord: Parathyroid hormone resistance in an Indian icon

open access: yesIndian Journal of Endocrinology and Metabolism, 2014
The dance of Siva has a cosmic appeal. Nowhere has this dance been crystallised in its pristine form as in the Nataraja Bronzes from the Chola period. Mysticism surrounds the dancing form of the Nataraja. But does Nataraja dance upon an endocrine mystery.
Krishna G Seshadri
doaj   +1 more source

Single‐Stage Bilateral Repair of Simultaneous Distal Triceps Tendon Ruptures in Patients With Long‐Term Anabolic Steroid Use: A Two‐Case Report

open access: yesCase Reports in Orthopedics, Volume 2026, Issue 1, 2026.
Bilateral simultaneous distal triceps tendon ruptures are extremely rare, with only a few cases reported. This article presents two traumatic bilateral ruptures in middle‐aged men with a history of long‐term anabolic steroid use, a factor associated with tendon weakening.
Ewerton Lima   +9 more
wiley   +1 more source

Pseudohypoparathyroidism Type IB with Subclinical Hypothyroidism: a Pedigree Investigation and Literature Review [PDF]

open access: yes
Jie Liu, Lijuan Lu, Yu Wei, Yu Li, Qiong Wang, Lei Yu, Langen Zhuang, Guoxi Jin, Xiaoyan Pei Department of Endocrinology, the First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui Province, People’s Republic of ChinaCorrespondence: Guoxi ...
Lu L   +8 more
core  

Management of pseudohypoparathyroidism in pregnancy: a rare entity [PDF]

open access: yes, 2019
Pseudohypoparathyroidism is a very rare genetic disorder and during pregnancy poses multiple challenges related to its monitoring and management. Authors present the case of a  30year old primigravida who was a diagnosed case of pseudohypoparathyroidism ...
Ara, Anjum   +4 more
core   +1 more source

Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review

open access: yesFrontiers in Physiology, 2018
Background: Dental aberrations have been mentioned in relation to non-surgical hypoparathyroidism (Ns-HypoPT) and pseudohypoparathyroidism (PHP). However, a systematic review of dental characteristics have not been performed.
Jane Hejlesen   +8 more
doaj   +1 more source

Pseudohypoparathyroidism Ia with Evans syndrome.

open access: yes, 2008
Pseudohypoparathyroidism Ia (Albright hereditary osteodystrophy or Albright syndrome) is a rare disease, caused by the resistance to the action of the parathyroid hormone in target tissues, such as the bone, kidney, and intestine, with consequent ...
Pavone P   +3 more
core  

Pseudohypoparathyroidism : diagnosis and treatment

open access: yes, 2011
Context: The term pseudohypoparathyroidism (PHP) indicates a group of heterogeneous disorders whose common feature is represented by impaired signaling of various hormones (primarily PTH) that activate cAMP-dependent pathways via Gsα protein.
G. Mantovani, Giovanna Mantovani
core   +1 more source

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