ammonium hydroxide has been researched along with Biotinidase Deficiency in 1 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Biotinidase Deficiency: The late onset form of MULTIPLE CARBOXYLASE DEFICIENCY (deficiency of the activities of biotin-dependent enzymes propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to a defect or deficiency in biotinidase which is essential for recycling BIOTIN.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Biotinidase deficiency is a treatable cause of infantile epilepsy and the presentation can be nonspecific." | 1.40 | Abnormal cerebrospinal fluid biochemistry in biotinidase deficiency causing diagnostic conundrum. ( Brown, R; Calvin, J; Hogg, S; Krishnakumar, D; Maw, A; Parker, AP, 2014) |
| 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 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Krishnakumar, D | 1 |
| Maw, A | 1 |
| Brown, R | 1 |
| Hogg, S | 1 |
| Calvin, J | 1 |
| Parker, AP | 1 |
1 other study available for ammonium hydroxide and Biotinidase Deficiency
| Article | Year |
|---|---|
Abnormal cerebrospinal fluid biochemistry in biotinidase deficiency causing diagnostic conundrum.
Topics: Ammonia; Biotinidase Deficiency; Electroencephalography; Epilepsy; Female; Humans; Infant; Lactic Ac | 2014 |