furosemide has been researched along with Familial Hypokalemia-Hypomagnesemia in 4 studies
Furosemide: A benzoic-sulfonamide-furan. It is a diuretic with fast onset and short duration that is used for EDEMA and chronic RENAL INSUFFICIENCY.
furosemide : A chlorobenzoic acid that is 4-chlorobenzoic acid substituted by a (furan-2-ylmethyl)amino and a sulfamoyl group at position 2 and 5 respectively. It is a diuretic used in the treatment of congestive heart failure.
Excerpt | Relevance | Reference |
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"However, the terminology of Bartter syndrome and Gitelman syndrome does not always accurately reflect their pathophysiological basis or clinical presentation, and some patients are difficult to diagnose from their clinical presentations." | 1.36 | The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies. ( Hashimura, Y; Igarashi, T; Iijima, K; Kaito, H; Kamei, K; Kanda, K; Komatsu, H; Kugo, M; Mabe, H; Matsuo, M; Miyashita, R; Nakanishi, K; Ninchoji, T; Nozu, K; Ohashi, H; Otsubo, A; Satomura, K; Yamazaki, H; Yoshikawa, N, 2010) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Conticini, E | 1 |
Negro, A | 1 |
Magnani, L | 1 |
Ugolini, R | 1 |
Atienza-Mateo, B | 1 |
Frediani, B | 1 |
Salvarani, C | 1 |
Nozu, K | 1 |
Iijima, K | 1 |
Kanda, K | 1 |
Nakanishi, K | 1 |
Yoshikawa, N | 1 |
Satomura, K | 1 |
Kaito, H | 1 |
Hashimura, Y | 1 |
Ninchoji, T | 1 |
Komatsu, H | 1 |
Kamei, K | 1 |
Miyashita, R | 1 |
Kugo, M | 1 |
Ohashi, H | 1 |
Yamazaki, H | 1 |
Mabe, H | 1 |
Otsubo, A | 1 |
Igarashi, T | 1 |
Matsuo, M | 1 |
Yang, SS | 1 |
Lo, YF | 1 |
Wu, CC | 1 |
Lin, SW | 1 |
Yeh, CJ | 1 |
Chu, P | 1 |
Sytwu, HK | 1 |
Uchida, S | 1 |
Sasaki, S | 1 |
Lin, SH | 1 |
Favre, GA | 1 |
Nau, V | 1 |
Kolb, I | 1 |
Vargas-Poussou, R | 1 |
Hannedouche, T | 1 |
Moulin, B | 1 |
4 other studies available for furosemide and Familial Hypokalemia-Hypomagnesemia
Article | Year |
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Gitelman syndrome associated with chondrocalcinosis and severe neuropathy: a novel heterozygous mutation in SLC12A3 gene.
Topics: Aged; Chondrocalcinosis; Electromyography; Furosemide; Gitelman Syndrome; Glycyrrhiza; Humans; Hyper | 2020 |
The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.
Topics: Adolescent; Adult; Bartter Syndrome; Child; Diuretics; DNA Mutational Analysis; Exons; Female; Frame | 2010 |
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction.
Topics: Animals; Aorta; Blood Pressure; Disease Models, Animal; Diuretics; Female; Furosemide; Gitelman Synd | 2010 |
Localization of tubular adaptation to renal sodium loss in Gitelman syndrome.
Topics: Adaptation, Physiological; Adult; Case-Control Studies; Diuretics; Female; France; Furosemide; Genet | 2012 |