Results 91 to 100 of about 1,253,968 (181)

Patient Perceptions of Medicare Annual Wellness Visits: Findings From a Pilot Survey

Journal of the American Geriatrics Society, Volume 74, Issue 10, Page 3105-3107, October 2026.
Amy Cunningham, Lauren Hersh, Brooke Salzman, Kristine Swartz, Michael Danielewicz, Rebecca Berger, Elizabeth Clark, Payton McCready, Tushar Kumar, Stephanie Michael, Susan Mockus Parks   +10 more
wiley   +1 more source

Barakat syndrome presenting as isolated sensorineural hearing loss

Otolaryngology Case Reports
Barakat syndrome is a rare autosomal dominant disease caused by haplo-insufficiency of transcription factor GATA3 on chromosome 10p14. It is characterized by a triad of hypoparathyroidism, sensorineural hearing loss, and renal disease with high ...
Angela S. Zhu, Danielle Reny Larrow, Michael S. Cohen   +2 more
doaj   +1 more source

Barakat syndrome: clinical case

Лечащий Врач
Background. Barakat syndrome (HDR syndrome, Hypoparathyroidism, Deafness, Renal dysplasia syndrome, OMIM 146255) is a hereditary disease characterized by hypoparathyroidism, hearing loss and renal disease. The syndrome was first described by the American
L. S. Sozaeva, A. A. Dzhamaludinova, I, V. Kopylova, A. L. Kalinin, I. S. Chugunov   +4 more
doaj   +1 more source

10p12.1 deletion: HDR phenotype without DGS2 features.

, 2009
GATA3 gene encodes a transcription factor expressed during thymus, liver, kidney, adrenal gland, central and peripheral nervous systems, placenta and T lymphocytes embryonic development. Mutations of GATA3 cause Hypoparathyroidism, sensorineural Deafness
ANDREETTA, BARBARA, Bordugo A, Benetti E, Murer L, Artifoni L.   +4 more
core   +1 more source

Identification of a novel de novo GATA3 mutation in a patient with HDR syndrome

Journal of International Medical Research, 2015
We describe the case of a 21-year-old male with hypocalcaemia, hyperphosphataemia, recurrent limb twitch, deafness, proteinuria, increased serum creatinine and urea nitrogen levels, and shrinkage of both kidneys. Brain computed tomography showed intracranial calcifications.
Liu, Chen, Bing, Chen, Wuilin, Leng, Xiaotian, Lui, Qinan, Wu, Xinshou, Ouyang, Ziwen, Liang   +6 more
openaire   +2 more sources

Tucannon River Temperature Study, Prepared for : Watershed Resource Inventory Area (WRIA) 35.

, 2006
This report presents the results of a temperature analysis of the Tucannon River completed for the WRIA 35 Planning Unit. The Tucannon River is located in southeastern Washington and flows approximately 100 kilometers (km) (62 miles) from the Blue ...
Engineering., HDR
core   +1 more source

Tone rendering vs tone mapping : the history and practice of HDR imaging

, 2013
An invited critical survey about the history and the practice of HDR ...
A. Rizzi
core   +2 more sources

An Unusual Presentation of Barakat Syndrome: Gene Deletion at Chromosome 10p15

Case Reports in Nephrology
Barakat syndrome, also known as HDR syndrome (HDRS), is an autosomal dominant genetic disease classically characterized by hypoparathyroidism (H), deafness (D), and renal disease (R).
Matthew Satariano, Shaarav Ghose, Sergul Erzurum, Erdal Sarac   +3 more
doaj   +1 more source

A framework for HDR stereo matching using multi-exposed images

, 2013
Real world scenes that contain high dynamic range illumination present a special challenge for stereo matching algorithms due to a lack of texture in over- or under-exposed image regions. In this paper, we discuss possibilities for combining state-of-the-
Yoo, Hyunjin, Akhavan, Tara, Gelautz, Margrit   +2 more
core   +2 more sources

High-fidelity colour reproduction for high-dynamic-range imaging [PDF]

, 2010
The aim of this thesis is to develop a colour reproduction system for high-dynamic-range (HDR) imaging. Classical colour reproduction systems fail to reproduce HDR images because current characterisation methods and colour appearance models fail to ...
Kim, M.H.
core