Page last updated: 2024-10-29

isoniazid and Gaucher Disease

isoniazid has been researched along with Gaucher Disease in 2 studies

Hydra: A genus of freshwater polyps in the family Hydridae, order Hydroida, class HYDROZOA. They are of special interest because of their complex organization and because their adult organization corresponds roughly to the gastrula of higher animals.
hydrazide : Compounds derived from oxoacids RkE(=O)l(OH)m (l =/= 0) by replacing -OH by -NRNR2 (R groups are commonly H). (IUPAC).

Gaucher Disease: An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dulgar, O1
Eskazan, AE1
Ersen, E1
Demiroz, AS1
Turna, A1
Oz, B1
Tuzuner, N1
Ulbing, I1
Pelle, J1
Varga, T1

Other Studies

2 other studies available for isoniazid and Gaucher Disease

ArticleYear
Pleural tuberculosis in a patient with untreated type 1 Gaucher disease.
    Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2016, Volume: 22, Issue:1

    Topics: Adult; Antitubercular Agents; Drug Therapy, Combination; Ethambutol; Gaucher Disease; Humans; Isonia

2016
[Asymptomatic Gaucher's disease persisting for 5 years].
    Orvosi hetilap, 1968, Jan-07, Volume: 109, Issue:1

    Topics: Adult; Female; Gaucher Disease; Humans; Isoniazid

1968