Results 101 to 110 of about 2,216,391 (183)

Hungry bone syndrome following parathyroidectomy - a case report

open access: yes
One of the main causes of protracted, severe hypocalcemia after parathyroidectomy is hungry bone syndrome (HBS). We report the case of a 40-year-old man who was first admitted to the Endocrinology department of Zemun Clinical Hospital (ZCH) in order to ...
Sinik, Marija   +10 more
core   +1 more source

Hungry bone syndrome

open access: yesOTOLOGIA FUKUOKA, 2000
TAKAGI, Seiji   +5 more
openaire   +1 more source

Transient Bone Marrow Edema Syndrome (Case Report)

open access: yes, 2003
Transient bone marrow edema syndrome (BMES) is accepted as a possible cause of acute disabling hip pain. This syndrome is defined as local osteoporosis in hip in radiographies, BME in MRI which can be rarely seen and has a self-limiting course.
Leyla Kılıç Atakanlı   +8 more
core  

Peculiarity of Postoperative Period in Hemodialysis Patients after Parathyroidectomy

open access: yes, 2020
© 2016, Springer Science+Business Media New York.Signs of hypocalcemia of varying degrees of intensity are often shown in hemodialysis patients after parathyroidectomy for severe hyperparathyroidism on the background of the “hungry bone” syndrome ...
Belyaev A.   +5 more
core  

A Clinically Aligned Two-Stage Machine Learning Framework for Predicting Hungry Bone Syndrome After Parathyroidectomy. [PDF]

open access: yesEndocrinol Diabetes Metab
Yin SM   +10 more
europepmc   +1 more source

Vogt-Koyangi-Harada syndrome complcating allogeneic bone marrow transplantation

open access: yes, 1994
Vogt-Koyanagi-Harada (VKH) syndrome is an uncommon acute ophthalmological disorder, characterised by bilateral serous retinal detachment with diffuse choroiditis, in association with specific extra-ocular manifestations.
Neoh, C   +3 more
core  

A toddler with severe vitamin D-dependent rickets type 1 A (VDDR1A), hungry bone syndrome, and severe RSV infection: presentation and therapeutic challenges

open access: yes
Background: Vitamin D-dependent rickets type 1 A (VDDR1A) is an autosomal recessive disorder due to mutations in the CYP27B1 gene which result in inability to generate 1,25(OH)2D.
Paltoglou, George   +9 more
core  

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