Results 81 to 90 of about 9,429,824 (263)
Association of Pathways to Success Launch With Quality inBeneficiaries With Traditional Medicare
Health Services Research, EarlyView.ABSTRACT Objective To evaluate the association between implementation of “Pathways to Success” and quality among beneficiaries cared for in Shared Savings Program accountable care organizations (ACOs). Study Setting and Design Medicare initiated “Pathways to Success” in 2019 that required upside‐risk only ACOs in Shared Savings Program to transition to
Meiling Ying +5 more
wiley +1 more source
Autoimmune oophoritis: A rarely encountered ovarian lesion
Indian Journal of Pathology and Microbiology, 2015 Autoimmune oophoritis is a rare disorder causing ovarian failure clinically characterized by amenorrhea and infertility. It often occurs in a setting of autoimmune polyendocrine syndromes.
Sunitha Jacob, Murat Koc
doaj +1 more source
Cutaneous signs of endocrinopathies [PDF]
, 2006 peer reviewedSome cutaneous lesions accompany or reveal endocrine disorders. Identifying the endocrinopathy is very important because it sometimes allows corrective rather than symptomatic treatment.
Beckers, Albert +6 more
core
Clinical Endocrinology, EarlyView.ABSTRACT Context Screening morning serum cortisol is used to select patients for ACTH stimulation testing to diagnose adrenal insufficiency (AI) but may be affected by pre‐analytical factors. Careful consideration to discontinue confounding medications beforehand may preclude the need for subsequent stimulation testing.
Christopher J. Symonds +2 more
wiley +1 more source
Combined atypical primary hypoadrenocorticism and primary hypothyroidism in a dog [PDF]
, 2016 A dog with combined atypical primary hypoadrenocorticism and primary hypothyroidism is described. The dog presented with waxing and waning, vague complaints since more than a year and had been treated with several drugs without complete resolution of ...
Binst, Dominique +5 more
core
The Genetic Landscape of Hereditary Spastic Paraplegia in Greece
Clinical Genetics, EarlyView.We investigated 112 Greek index‐cases with hereditary spastic paraplegia collected over > 25 years using NGS and MLPA. We identified a causative variant in 68 patients (60.7%), including 7 novel causative variants. This study presents a comprehensive overview of the phenotypic and genotypic spectrum of HSP in the Greek population.
Georgios Koutsis +19 more
wiley +1 more source
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases
Frontiers in Neurology, 2019 X-linked adrenoleukodystrophy (x-ALD) is a rare genetic disorder caused by a mutation in the ABCD1 gene, which encodes for a peroxisomal very long chain fatty acid transporter.
Matteo Foschi +12 more
doaj +1 more source
European Journal of Dental Education, EarlyView.ABSTRACT Aim To compare the item difficulty and discriminative index of multiple‐choice questions (MCQs) generated by ChatGPT with those created by dental educators, based on the performance of dental students in a real exam setting. Materials and Methods A total of 40 MCQs—20 generated by ChatGPT 4.0 and 20 by dental educators—were developed based on ...
Nezaket Ezgi Özer +4 more
wiley +1 more source
International Journal of Preventive Medicine, 2014 Coexistence of Addison′s disease and systemic lupus erythematosus (SLE) is a rare occurrence with only few reported cases in the literature. We describe a 29-year-old woman who presented to us with clinical features of acute Addisonian crisis and SLE ...
Okwuonu Chimezie Godswill +1 more
doaj
Continued DDT Persistence in Mississippi River Delta Streams: A Case Study [PDF]
, 1986 Fish samples representative of several trophic levels were taken from the Wolf and Loosahatchie Rivers of western Tennessee during the early 1980s. Results indicate that DDT, with metabolites DDD and DDE, remains common in fish tissues in these areas and
Knight, Luther A., Jr. +1 more
core +2 more sources