Bartter syndrome and related renal tubulopathies comprise a group of rare, inherited disorders primarily affecting the reabsorption processes in the thick ascending limb of the loop of Henle and ...
Bartter syndrome refers to a set of rare genetic disorders characterized by distinct kidney function abnormalities. These flaws impede the kidney's ability to reabsorb salt, resulting in electrolyte ...
This page lists all known medications that could potentially lead to 'Pseudo-Bartter syndrome' as a side effect. It's important to note that mild side effects are quite common with medications. The ...
Bartter syndrome type 3 is the result of several structural variants in the genome. By using long-read sequencing, Janine Altmüller and her team from the Max Delbrück Center, the BIH and University ...
The Market Research Survey by “Fact.MR, A Market Research and Competitive Intelligence Provider” highlights the key reasons behind increasing demand of Bartter Syndrome Treatment. Bartter Syndrome ...
Freiburg - Wissenschafter der Universitäts-Kinderklinik Freiburg haben ein Gen identifiziert, das eine Nierenerkrankung mit Taubheit bedingt. Die Erkrankung, Bartter-Syndrom mit Taubheit (BSND) ...
Ein bereits im auswärtigen Haus durchgeführter Schweißtest, als die Patientin zwölf Monate alt war, ergab einen erhöhten Chloridgehalt von 74 mmol/l. Auch als der Schweißtest bei uns bei einem Alter ...
Jetzt wissen Forscher, warum Patienten mit einer bestimmten Form des seltenen Erbleidens Bartter-Syndrom auch taub sind. Dr. Gesa Rickheit und Prof. Thomas Jentsch vom Max-Delbrück-Centrum für ...
Since the description in 1962 of a syndrome of "hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis" 1 a number of reports of the same and of similar syndromes ...
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