Page last updated: 2024-10-16

carbon monoxide and Genetic Diseases, Inborn

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

Carbon Monoxide: Carbon monoxide (CO). A poisonous colorless, odorless, tasteless gas. It combines with hemoglobin to form carboxyhemoglobin, which has no oxygen carrying capacity. The resultant oxygen deprivation causes headache, dizziness, decreased pulse and respiratory rates, unconsciousness, and death. (From Merck Index, 11th ed)
carbon monoxide : A one-carbon compound in which the carbon is joined only to a single oxygen. It is a colourless, odourless, tasteless, toxic gas.

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

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Featherstone, RM1
Settle, W1

Reviews

1 review available for carbon monoxide and Genetic Diseases, Inborn

ArticleYear
[The pharmacology of the rare gases (helium, neon, argon, krypton, xenon)].
    Actualites pharmacologiques, 1974, Volume: 27

    Topics: Anesthesia; Animals; Argon; Carbon Monoxide; Dogs; Genetic Diseases, Inborn; Helium; Hemoglobins; Hu

1974