Compounds > 2,2-bis(bromomethyl)-1,3-propanediol
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2,2-bis(bromomethyl)-1,3-propanediol and Carbohydrate Metabolism, Inborn Error

2,2-bis(bromomethyl)-1,3-propanediol has been researched along with Carbohydrate Metabolism, Inborn Error in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boney, A; Elser, HE; Silver, HJ1
Puntis, JW; Zamvar, V1
Baker, SS; Navarrete, M; Nichols, BL; Opekun, AR; Quezada-Calvillo, R; Robayo-Torres, CC; Smith, EO; Villa, X1
Das, AM; Illsinger, S; Keiser, M; Lentze, MJ; Lücke, T; Naim, HY1
Treem, WR1

Other Studies

6 other study(ies) available for 2,2-bis(bromomethyl)-1,3-propanediol and Carbohydrate Metabolism, Inborn Error

ArticleYear
Relationships among Dietary Intakes and Persistent Gastrointestinal Symptoms in Patients Receiving Enzyme Treatment for Genetic Sucrase-Isomaltase Deficiency.
    Journal of the Academy of Nutrition and Dietetics, 2018, Volume: 118, Issue:3

    Topics: Adolescent; Adult; beta-Fructofuranosidase; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Defecation; Diet; Diet Surveys; Dietary Carbohydrates; Dietary Fats; Dietary Fiber; Eating; Female; Gastrointestinal Diseases; Humans; Infant; Lactose; Male; Maltose; Nutrients; Prospective Studies; Statistics, Nonparametric; Sucrase-Isomaltase Complex; Young Adult

2018
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
13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.
    Journal of pediatric gastroenterology and nutrition, 2009, Volume: 48, Issue:4

    Topics: Adolescent; beta-Fructofuranosidase; Biopsy; Breath Tests; Carbohydrate Metabolism, Inborn Errors; Carbon Dioxide; Carbon Isotopes; Child; Child, Preschool; Dietary Supplements; Female; Glucose; Humans; Infant; Male; Sucrase; Sucrase-Isomaltase Complex; Sucrose

2009
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
Clinical heterogeneity in congenital sucrase-isomaltase deficiency.
    The Journal of pediatrics, 1996, Volume: 128, Issue:6

    Topics: beta-Fructofuranosidase; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Glycoside Hydrolases; Humans; Infant; Infant Food; Phenotype; Saccharomyces cerevisiae; Sucrase-Isomaltase Complex

1996
Sacrosidase.
    American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2001, Dec-15, Volume: 58, Issue:24

    Topics: beta-Fructofuranosidase; Carbohydrate Metabolism, Inborn Errors; Contraindications; Glycoside Hydrolases; Humans; Oligo-1,6-Glucosidase; Sucrase

2001