Results 61 to 70 of about 28,678 (267)

Mucocutaneous manifestations of acquired hypoparathyroidism: An observational study

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
Hypoparathyroidism is a disorder of calcium and phosphorus metabolism due to decreased secretion of parathyroid hormone. Hypoparathyroidism can be hereditary and acquired. Acquired hypoparathyroidism usually occurs following neck surgery (thyroid surgery
Somenath Sarkar   +3 more
doaj   +1 more source

Parathyroid Hormone Sampling From the Anterior Jugular Vein Versus Peripheral Vein After Total Thyroidectomy

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Background To determine if anterior jugular vein sampling (AJVS) is non‐inferior to peripheral venous sampling (PVS) for measuring intraoperative parathyroid hormone (PTH) levels following total thyroidectomy. Methods This was a prospective non‐inferiority trial conducted at a tertiary academic medical center.
Noel M. Phan   +4 more
wiley   +1 more source

Robotic‐Assisted Transaxillary Parathyroidectomy: A Safe and Cosmetically Alternative for Primary Hyperparathyroidism

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Purpose This study aimed to describe the initial experience with robot‐assisted transaxillary parathyroidectomy (RATP) and to investigate its safety and efficacy as a surgical approach for the treatment of primary hyperparathyroidism (PHPT).
Xi‐Jun Lin   +7 more
wiley   +1 more source

Predictive factors for permanent hypoparathyroidism following total thyroidectomy: A retrospective cohort study of 5,671 cases [PDF]

open access: yesArchives of Endocrinology and Metabolism
Objective: To evaluate the rates of permanent hypoparathyroidism based on demographic variables, patient comorbidities, clinical staging of the disease, surgery performed, and severity of transient hypoparathyroidism.
Daniela Tamega Joaquim   +4 more
doaj   +1 more source

Surgical Management of Substernal Goiters: A Systematic Review and Meta‐Analysis

open access: yesThe Laryngoscope, Volume 136, Issue 2, Page 575-585, February 2026.
This systematic review and meta‐analysis of 15,706 patients with substernal goiter highlights that while surgery is often prompted by symptoms or imaging evidence of compression, over a quarter of patients were asymptomatic. The majority of cases (88.7%) were successfully managed through a cervical approach, with only a minority requiring thoracic ...
Matthew H. Cheung   +4 more
wiley   +1 more source

Hypoparathyroidism diagnosed by neurological signs and widespread intracerebral calcifications [PDF]

open access: yesRomanian Journal of Neurology, 2010
Neurological signs associated with intracerebral calcifications require a complex management of calcium, phosphate and parathormone levels and search of a series of general and cerebral disease too.
Monica Sabau   +3 more
doaj   +1 more source

A novel homozygous mutation of the AIRE gene in an APECED patient from Pakistan: case report and review of the literature [PDF]

open access: yes, 2018
Autoimmune-poly-endocrinopathy-candidiasis-ectodermal-dystrophy syndrome (APECED) is a rare monogenic recessive disorder caused by mutations in the autoimmune regulator (AIRE) gene.
Bellacchio, Emanuele   +5 more
core   +2 more sources

Acute collapse in a dog with multiple autoimmune syndromes and polymyositis complicated by suspected organophosphate/carbamate toxicity

open access: yesVeterinary Record Case Reports, Volume 14, Issue 1, February 2026.
Abstract A 6.5‐year‐old, spayed, female dog presented in acute respiratory distress. On admission, the dog exhibited dyspnoea, bradycardia, cyanosis and gastrointestinal signs, requiring immediate intubation and mechanical ventilation. Diagnostic evaluation revealed reduced butyrylcholinesterase activity, non‐cardiogenic pulmonary oedema, elevated ...
Sarah Hefer   +6 more
wiley   +1 more source

Sanjad-Sakati Syndrome Dental Management: A Case Report [PDF]

open access: yes, 2013
Sanjad-Sakati syndrome (SSS) is a rare genetic disorder with autosomal recessive pattern of inheritance characterized by hypoparathyroidism, sever growth failure, mental retardation, susceptibility to chest infection, and dentofacial anomalies.
Hisham Y. El Batawi
core   +1 more source

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