Page last updated: 2024-08-23

transferrin and Deep Vein Thrombosis

transferrin has been researched along with Deep Vein Thrombosis in 2 studies

Research

Studies (2)

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	1 (50.00)	24.3611
2020's	1 (50.00)	2.80

Authors

Authors	Studies
Bauchard, E; Borgel, D; Bruneel, A; Damaj, L; De Lonlay, P; Debray, D; Dobbelaere, D; Douillard, C; Dupré, T; Fabre, M; Girard, M; Kuster, A; Lacaille, F; McLin, V; Mention, K; Schiff, M; Seta, N; Torre, S; Vuillaumier-Barrot, S	1
Holzgreve, H	1

Other Studies

2 other study(ies) available for transferrin and Deep Vein Thrombosis

Article	Year
Long term outcome of MPI-CDG patients on D-mannose therapy. Journal of inherited metabolic disease, 2020, Volume: 43, Issue:6 Topics: Administration, Oral; Child; Child, Preschool; Congenital Disorders of Glycosylation; Female; Humans; Hypertension; Infant; Liver Cirrhosis; Male; Mannose; Mannose-6-Phosphate Isomerase; Medication Adherence; Retrospective Studies; Transferrin; Treatment Outcome; Venous Thrombosis	2020
[Hereditary hyperferritinemia cataract syndrome]. Deutsche medizinische Wochenschrift (1946), 2011, Volume: 136, Issue:38 Topics: Adult; Cataract; Cataract Extraction; Chromosome Aberrations; DNA Mutational Analysis; Ferritins; Genes, Dominant; Genetic Carrier Screening; Genetic Testing; Humans; Hypertension, Renal; Iron; Iron Metabolism Disorders; Iron-Regulatory Proteins; Kidney; Male; Phenotype; Postthrombotic Syndrome; Transferrin; Vena Cava, Inferior; Venous Thrombosis	2011

Article

Year

Long term outcome of MPI-CDG patients on D-mannose therapy.

Journal of inherited metabolic disease, 2020, Volume: 43, Issue:6

Topics: Administration, Oral; Child; Child, Preschool; Congenital Disorders of Glycosylation; Female; Humans; Hypertension; Infant; Liver Cirrhosis; Male; Mannose; Mannose-6-Phosphate Isomerase; Medication Adherence; Retrospective Studies; Transferrin; Treatment Outcome; Venous Thrombosis

2020

[Hereditary hyperferritinemia cataract syndrome].

Deutsche medizinische Wochenschrift (1946), 2011, Volume: 136, Issue:38

Topics: Adult; Cataract; Cataract Extraction; Chromosome Aberrations; DNA Mutational Analysis; Ferritins; Genes, Dominant; Genetic Carrier Screening; Genetic Testing; Humans; Hypertension, Renal; Iron; Iron Metabolism Disorders; Iron-Regulatory Proteins; Kidney; Male; Phenotype; Postthrombotic Syndrome; Transferrin; Vena Cava, Inferior; Venous Thrombosis

2011