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hydrogen and Genetic Diseases, Inborn

hydrogen has been researched along with Genetic Diseases, Inborn in 1 studies

Hydrogen: The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas.
dihydrogen : An elemental molecule consisting of two hydrogens joined by a single bond.

Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.

Research Excerpts

ExcerptRelevanceReference
"Metabolic alkalosis is a unique acid-base disorder because it can be induced and sustained by functional alterations in renal ion transport."2.47Pathophysiology of metabolic alkalosis: a new classification based on the centrality of stimulated collecting duct ion transport. ( Gennari, FJ, 2011)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gennari, FJ1

Reviews

1 review available for hydrogen and Genetic Diseases, Inborn

ArticleYear
Pathophysiology of metabolic alkalosis: a new classification based on the centrality of stimulated collecting duct ion transport.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2011, Volume: 58, Issue:4

    Topics: Aldosterone; Alkalosis; Chlorides; Diuretics; Epithelial Sodium Channels; Genetic Diseases, Inborn;

2011