MRI-negative cerebellar syndrome caused by medication-induced magnesium deficiency: a case report. [PDF]
BMC NeurolJüchtern M.
europepmc +1 more source
Are the Clinical Presentations (Phenotypes) of Gitelman's and Bartter's Syndromes Gene Mutations Driven by Their Effects on Intracellular pH, Their "pH" Enotype? [PDF]
Int J Mol Sci, 2020 Calò LA, Davis PA.
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Renal Potassium Handling and Associated Inherited Tubulopathies Leading to Hypokalemia [PDF]
, 2012 Jelena Stojanovic, John Sayer
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Profound Hypomagnesemia Due to Proton Pump Inhibitor Use-Associated Wernicke's Encephalopathy: A Case Report on Excitotoxicity. [PDF]
CureusDelforge B +3 more
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Inwardly rectifying K+ channels 4.1 and 5.1 (Kir4.1/Kir5.1) in the renal distal nephron.
Am J Physiol Cell Physiol, 2022 Wang WH, Lin DH.
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Genetic variants of accessory proteins and G proteins in human genetic disease. [PDF]
Crit Rev Clin Lab SciThompson MD +4 more
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Thirty years of the NaCl cotransporter: from cloning to physiology and structure.
Am J Physiol Renal Physiol, 2023 Gamba G.
europepmc +1 more source
Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variation. [PDF]
J Transl MedBirch CL +10 more
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A novel homozygous mutation in the solute carrier family 12 member 3 gene in a Chinese family with Gitelman syndrome [PDF]
, 2016 Cruz DN +23 more
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Gitelman syndrome patient managed with amiloride during pregnancy and lactation. [PDF]
BMC NephrolIbrahim A +3 more
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