biotin has been researched along with Failure to Thrive in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hauth, I; van der Crabben, SN; van Karnebeek, CDM; Wanders, RJA; Waterham, HR | 1 |
| Aytac, S; Coskun, T; Kalkanoglu, S; Kratz, C; Niemeyer, C; Ortmann, C; Yetgin, S | 1 |
| Berry, SA; Nyhan, WL; Thuy, LP; Tuchman, M | 1 |
| Bartlett, K; Low, LC; Seakins, JW; Shaikh, SA; Stephenson, JB | 1 |
4 other study(ies) available for biotin and Failure to Thrive
| Article | Year |
|---|---|
A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classification.
Topics: Biotin; Child; Failure to Thrive; Humans; Pantothenic Acid; Sodium; Symporters | 2022 |
Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents.
Topics: Biotin; Biotinidase Deficiency; Bone Marrow; Consanguinity; Failure to Thrive; Female; Genes, ras; Hepatomegaly; Humans; Infant; Leukemia, Myelomonocytic, Chronic; Splenomegaly | 2007 |
Partial methylcrotonyl-coenzyme A carboxylase deficiency in an infant with failure to thrive, gastrointestinal dysfunction, and hypertonia.
Topics: Biotin; Carbon-Carbon Ligases; Failure to Thrive; Gastrointestinal Diseases; Glycine; Humans; Infant; Ligases; Male; Metabolism, Inborn Errors; Muscle Hypertonia; Valerates | 1993 |
Biotin-reversible neurodegenerative disease in infancy.
Topics: Acidosis; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Failure to Thrive; Female; Humans; Infant; Ligases; Methylmalonyl-CoA Decarboxylase; Muscular Diseases; Myoclonus; Pyruvate Carboxylase Deficiency Disease | 1986 |