Page last updated: 2024-08-23

1-deoxynojirimycin and Genetic Predisposition

1-deoxynojirimycin has been researched along with Genetic Predisposition in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (66.67)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Barth, JA; Castelli, JP; Hamazaki, T; Lagast, H; Narita, I; Ohashi, T; Sakai, N; Skuban, N	1
Hughes, DA; Mehta, A; Thomas, AS	1
Lo, SM; McNamara, J; Mistry, PK; Seashore, MR	1

Reviews

1 review(s) available for 1-deoxynojirimycin and Genetic Predisposition

Article	Year
Gaucher disease: haematological presentations and complications. British journal of haematology, 2014, Volume: 165, Issue:4 Topics: 1-Deoxynojirimycin; Anemia; Combined Modality Therapy; Disease Management; Enzyme Replacement Therapy; Gaucher Disease; Genetic Predisposition to Disease; Glucosylceramidase; Glycosphingolipids; Hemorrhagic Disorders; Humans; Inflammation; Lewy Body Disease; Lysosomes; Macrophage Activation; Multiple Myeloma; Parkinson Disease; Splenectomy; Splenomegaly; Thrombocytopenia; Unfolded Protein Response	2014

Article

Year

Gaucher disease: haematological presentations and complications.

British journal of haematology, 2014, Volume: 165, Issue:4

Topics: 1-Deoxynojirimycin; Anemia; Combined Modality Therapy; Disease Management; Enzyme Replacement Therapy; Gaucher Disease; Genetic Predisposition to Disease; Glucosylceramidase; Glycosphingolipids; Hemorrhagic Disorders; Humans; Inflammation; Lewy Body Disease; Lysosomes; Macrophage Activation; Multiple Myeloma; Parkinson Disease; Splenectomy; Splenomegaly; Thrombocytopenia; Unfolded Protein Response

2014

Trials

1 trial(s) available for 1-deoxynojirimycin and Genetic Predisposition

Article	Year
Efficacy and safety of migalastat in a Japanese population: a subgroup analysis of the ATTRACT study. Clinical and experimental nephrology, 2020, Volume: 24, Issue:2 Topics: 1-Deoxynojirimycin; Administration, Oral; Adult; alpha-Galactosidase; Fabry Disease; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Middle Aged; Mutation; Prospective Studies; Time Factors; Treatment Outcome	2020

Article

Year

Efficacy and safety of migalastat in a Japanese population: a subgroup analysis of the ATTRACT study.

Clinical and experimental nephrology, 2020, Volume: 24, Issue:2

Topics: 1-Deoxynojirimycin; Administration, Oral; Adult; alpha-Galactosidase; Fabry Disease; Female; Genetic Predisposition to Disease; Humans; Japan; Male; Middle Aged; Mutation; Prospective Studies; Time Factors; Treatment Outcome

2020

Other Studies

1 other study(ies) available for 1-deoxynojirimycin and Genetic Predisposition

Article	Year
Misdiagnosis of Niemann-Pick disease type C as Gaucher disease. Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3 Topics: 1-Deoxynojirimycin; Acid Phosphatase; Biomarkers; Carrier Proteins; Cells, Cultured; Cholesterol Esters; Diagnostic Errors; DNA Mutational Analysis; Enzyme Inhibitors; Enzyme Replacement Therapy; Esterification; Female; Gaucher Disease; Genetic Predisposition to Disease; Glucosylceramidase; Glucosyltransferases; Hepatomegaly; Heterozygote; Hexosaminidases; Humans; Infant; Intracellular Signaling Peptides and Proteins; Isoenzymes; Membrane Glycoproteins; Mutation; Niemann-Pick C1 Protein; Niemann-Pick Disease, Type C; Phenotype; Predictive Value of Tests; Splenomegaly; Tartrate-Resistant Acid Phosphatase; Unnecessary Procedures	2010

Article

Year

Misdiagnosis of Niemann-Pick disease type C as Gaucher disease.

Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3

Topics: 1-Deoxynojirimycin; Acid Phosphatase; Biomarkers; Carrier Proteins; Cells, Cultured; Cholesterol Esters; Diagnostic Errors; DNA Mutational Analysis; Enzyme Inhibitors; Enzyme Replacement Therapy; Esterification; Female; Gaucher Disease; Genetic Predisposition to Disease; Glucosylceramidase; Glucosyltransferases; Hepatomegaly; Heterozygote; Hexosaminidases; Humans; Infant; Intracellular Signaling Peptides and Proteins; Isoenzymes; Membrane Glycoproteins; Mutation; Niemann-Pick C1 Protein; Niemann-Pick Disease, Type C; Phenotype; Predictive Value of Tests; Splenomegaly; Tartrate-Resistant Acid Phosphatase; Unnecessary Procedures

2010