Compounds > 2,2-bis(bromomethyl)-1,3-propanediol

Page last updated: 2024-08-22

2,2-bis(bromomethyl)-1,3-propanediol and Diarrhea

2,2-bis(bromomethyl)-1,3-propanediol has been researched along with Diarrhea in 8 studies

Research

Studies (8)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (62.50)	18.7374
1990's	1 (12.50)	18.2507
2000's	1 (12.50)	29.6817
2010's	1 (12.50)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Puntis, JW; Zamvar, V	1
Das, AM; Illsinger, S; Keiser, M; Lentze, MJ; Lücke, T; Naim, HY	1
AURICCHIO, S; MUERSET, G; PRADER, A	1
AURICCHIO, S; MUERSET, G; PRADER, A; WITT, G	1
DUGAS, M; GOURGON, R; GRENET, P; INIGUEZ, M; LESTRADET, H	1
GARTY, R; KARP, M; YONIS, JZ	1
JENSEN, PE	1
Olusanya, O; Olutiola, PO	1

Other Studies

8 other study(ies) available for 2,2-bis(bromomethyl)-1,3-propanediol and Diarrhea

Article	Year
Congenital sucrase-isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy. Archives of disease in childhood, 2015, Volume: 100, Issue:9 Topics: beta-Fructofuranosidase; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Diarrhea; Diarrhea, Infantile; Enzyme Replacement Therapy; Feces; Female; Follow-Up Studies; Humans; Infant; Male; Sucrase-Isomaltase Complex; Sucrose; Treatment Outcome	2015
Congenital and putatively acquired forms of sucrase-isomaltase deficiency in infancy: effects of sacrosidase therapy. Journal of pediatric gastroenterology and nutrition, 2009, Volume: 49, Issue:4 Topics: beta-Fructofuranosidase; Carbohydrate Metabolism, Inborn Errors; Chronic Disease; Diarrhea; Dietary Supplements; Female; Humans; Infant; Malabsorption Syndromes; Male; Sequence Analysis, DNA; Sucrase-Isomaltase Complex	2009
[Diarrhea due to hereditary deficiency of intestinal saccharase activity (saccharose intolerance)]. Schweizerische medizinische Wochenschrift, 1961, Apr-22, Volume: 91 Topics: beta-Fructofuranosidase; Child; Diarrhea; Glycoside Hydrolases; Infant; Intestines; Metabolic Diseases; Sucrose	1961
[Saccharose intolerance. Diarrhea due to herediatary lack of intestinal saccharase activity]. Helvetica paediatrica acta, 1961, Volume: 16 Topics: beta-Fructofuranosidase; Child; Diarrhea; Glycoside Hydrolases; Humans; Infant; Intestines; Malabsorption Syndromes; Sucrose	1961
[Absence of saccharase, a cause of chronic diarrhea in an infant]. Archives francaises de pediatrie, 1962, Volume: 19 Topics: beta-Fructofuranosidase; Diarrhea; Diarrhea, Infantile; Glycoside Hydrolases; Humans; Infant; Metabolic Diseases	1962
[Chronic diarrhea due to invertase deficiency]. Harefuah, 1962, Jun-01, Volume: 62 Topics: beta-Fructofuranosidase; Child; Diarrhea; Glycoside Hydrolases; Humans; Infant	1962
[Intestinal invertase deficiency as cause of chronic diarrhea. A case of cane sugar intolerance]. Ugeskrift for laeger, 1962, Mar-16, Volume: 124 Topics: beta-Fructofuranosidase; Canes; Carbohydrates; Diarrhea; Glycoside Hydrolases; Humans; Intestines; Malabsorption Syndromes	1962
The purification and characterization of intracellular invertase obtained from pathogenic Escherichia coli. African journal of medicine and medical sciences, 1994, Volume: 23, Issue:3 Topics: beta-Fructofuranosidase; Child, Preschool; Diarrhea; Escherichia coli; Escherichia coli Infections; Female; Glycoside Hydrolases; Humans; Hydrogen-Ion Concentration; Infant; Infant, Newborn; Intracellular Fluid; Male; Molecular Weight	1994