Results 81 to 90 of about 27,268 (276)

Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort [PDF]

open access: yes, 2018
Objective: Fibrous dysplasia (FD) presents as skeletal lesions in which normal bone is replaced by abnormal fibrous tissue due to mosaic GNAS mutation.
Bjornsdottir, Sigridur   +4 more
core   +1 more source

Wernicke's Encephalopathy Following 40 Days of Water‐Only Fasting: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Wernicke's encephalopathy (WE) is an acute neurological disorder that develops due to thiamine (vitamin B1) deficiency. While it is common in chronic alcoholism, WE can also manifest due to other conditions, including extreme fasting. This report presents a unique case of WE occurring after a 40‐day water‐only fast, emphasizing the importance ...
Ruba Adel Aweer   +3 more
wiley   +1 more source

Genetic evidence of serum phosphate-independent functions of FGF-23 on bone [PDF]

open access: yes, 2011
Maintenance of physiologic phosphate balance is of crucial biological importance, as it is fundamental to cellular function, energy metabolism, and skeletal mineralization.
Bergwitz, Clemens   +7 more
core   +1 more source

Hypercalcemia Secondary to Hyperparathyroidism Mimicking Eclampsia During Postpartum Period in a Young Hypertensive Woman: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT We report a rare case of hyperparathyroidism due to parathyroid adenoma causing hypercalcemia, presenting as a generalized prolonged seizure on the seventh postpartum day mimicking eclampsia. Eclampsia developing on the seventh postpartum day in a woman without features of impending eclampsia is rare.
Wanni Arachchige Dhanushka Prasad Wanniarachchi   +2 more
wiley   +1 more source

Unveiling the heightened susceptibility: Exploring early hypophosphatemia in critically ill trauma patients

open access: yesJournal of the Formosan Medical Association
Background: Phosphorus is a vital mineral crucial for various physiological functions. Critically ill trauma patients frequently experience hypophosphatemia during the immediate post-traumatic phase, potentially impacting outcomes.
Chi-Ju Yang   +5 more
doaj   +1 more source

Iatrogenic Persistent Hypophosphatemia In A Simultaneous Liver-Kidney Transplant Recipient

open access: yesKidney Research and Clinical Practice, 2012
Hypophosphatemia from renal phosphate wasting during the immediate postoperative kidney transplant period is common and improves with supplementation.
Ekamol Tantisattamo   +1 more
doaj   +1 more source

Effect of Increased Activity on Metabolic Markers in Captive Black Rhinos: A Pilot Study [PDF]

open access: yes, 2009
Ex situ (captive) black rhinoceros populations exhibit higher rates of disease than free-ranging counterparts. Preliminary data from an ongoing study supports the association between excessive adipose tissue, iron overload, insulin resistance and ...
Bryk, Josephine M.
core  

Особенности обмена микроэлементов у детей в критических состояниях [PDF]

open access: yes, 2019
МИКРОЭЛЕМЕНТЫМИКРОЭЛЕМЕНТЫКРИТИЧЕСКИЕ СОСТОЯНИЯИНТЕНСИВНАЯ ТЕРАПИЯПИТАНИЕ ПАРЕНТЕРАЛЬНОЕПАРЕНТЕРАЛЬНОЕ ПИТАНИЕПИТАНИЕ ЭНТЕРАЛЬНОЕЭНТЕРАЛЬНОЕ ПИТАНИЕДЕТИЦель.
Кизименко, А. Н.   +1 more
core   +1 more source

Osmotic Demyelination Syndrome Complicating Moderate Hyponatremia Correction in the Emergency Department: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Osmotic demyelination syndrome (ODS) is a rare neurological complication that can be associated with rapid correction of hyponatremia. This report describes a middle‐aged male patient with a chronic alcoholism history who developed ODS following moderate hyponatremia correction with 1.5 L of isotonic saline in the emergency department ...
Khaled Alsa'ed   +4 more
wiley   +1 more source

Consideration of a family case of X-linked hypophosphatemia through the prism of modern diagnostic and treatment methods

open access: yesPočki
Background. X-linked hypophosphatemia is the most common form of hereditary vitamin D-resistant rickets. Today, there is a late diagnosis, later treatment start and a significant deterioration in the quality of life of patients with X-linked ...
L.I. Vakulenko
doaj   +1 more source

Home - About - Disclaimer - Privacy