Results 121 to 130 of about 6,714 (210)

Calcium Unresponsive Hypocalcemic Tetany: Gitelman Syndrome with Hypocalcemia

open access: yesCase Reports in Medicine, 2013
Introduction. Gitelman’s syndrome (GS) is autosomal recessive renal tubular disorder characterized by hypokalemia, hypomagnesemia, hypocalciuria, metabolic alkalosis, and hyperreninemic hyperaldosteronism.
Madhav Desai   +2 more
doaj   +1 more source

Bartter Syndrome. A New Therapeutic Approach [PDF]

open access: yes, 2011
A Síndrome de Bartter é uma tubulopatia hereditária perdedora de sal, rara (cerca de 1,2 novos casos por 100 000 nados vivos por ano1), caracterizada por alcalose metabólica, hipocaliémia, hiperreninémia e hiperaldosterolémia de gravidade variável.
Castro, I, Mendonça, M, Pinheiro, A
core  

Is traumatic and non-traumatic neck pain associated with brain alterations? : a systematic review [PDF]

open access: yes, 2017
Background: Chronic neck pain affects 50% - 85% of people who have experienced an acute episode. This transition and the persistence of chronic complaints are believed to be mediated by brain alterations among different central mechanisms.
Caeyenberghs, Karen   +5 more
core  

Prevention of cardiac arrhythmias in pediatric patients with normotensive-hypokalemic tubulopathy: Current attitude among European pediatricians [PDF]

open access: yes, 2018
Potassium deficiency predisposes to cardiac arrhythmias culminating in syncope or sudden death. Because of the uncertainty related to the possible occurrence of such cardiac arrhythmias in the context of normotensive-hypokalemic tubulopathies, 19 ...
Bettinelli, Alberto   +3 more
core  

Inherited renal tubular defects with hypokalemia

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2009
Bartter′s and Gitelman′s syndrome are two ends of a spectrum of inherited renal tubular disorders that present with hypokalemic metabolic alkalosis of varying severity.
Muthukrishnan J   +3 more
doaj  

Research Analysis of SLC12A3 Gene Mutation and Molecular Mechanism in Gitelman Syndrome

open access: yes罕见病研究
ObjectiveThis study aimed at conducting retrospective analysis of the clinical symptoms and genetic mutations in 20 children with Gitelman syndrome treated at the Affiliated Children′s Hospital of Nanjing Medical University from August 2015 to November ...
WANG Chunli   +6 more
doaj   +1 more source

Chondrocalcinosis and osteoporosis in a patient with renal tubular disorder [PDF]

open access: yes, 2003
We report the case of a 50-year old male patient presenting with a combination of chondrocalcinosis and osteoporosis related to a renal tubular disorder.
Ambühl, Patrice M.   +3 more
core  

Outlook Magazine, Autumn 2011 [PDF]

open access: yes, 2011
https://digitalcommons.wustl.edu/outlook/1184/thumbnail ...

core   +1 more source

Partial motor status epilepticus as a clinical manifestation of carotid stenosis [PDF]

open access: yes, 2011
Limb shaking (LS) is often confused with focal motor seizures. Distinguishing between both is crucial, because LS may represent an indicator of severe carotid occlusive disease and patients are at high risk of stroke. We report the case of a patient with
Calleja, Sergio   +4 more
core  

Does conservative treatment change the brain in patients with chronic musculoskeletal pain? : a systematic review [PDF]

open access: yes, 2017
Background: Chronic musculoskeletal pain is characterized by maladaptive central neuroplastic changes. Many observational studies have demonstrated that chronic pain states are associated with brain alterations regarding structure and/or function ...
Cagnie, Barbara   +7 more
core   +1 more source

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