9 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 35102031 | Clinical and genetic studies of thiamine metabolism dysfunction syndrome-4: case series and review of the literature. | 2022 Jul 1 | 1 |
2 | 33544541 | SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature. | 2021 Feb 23 | 2 |
3 | 34587972 | Identification and functional analysis of novel SLC25A19 variants causing thiamine metabolism dysfunction syndrome 4. | 2021 Sep 29 | 3 |
4 | 31095747 | Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies. | 2019 Jul | 2 |
5 | 31295743 | Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation: Treatable Thiamine Metabolic Disorder-A Report of Two Indian Cases. | 2019 Oct | 2 |
6 | 31506564 | Functional analysis of the third identified SLC25A19 mutation causative for the thiamine metabolism dysfunction syndrome 4. | 2019 Nov | 2 |
7 | 27191787 | Treatment of genetic defects of thiamine transport and metabolism. | 2016 Jul | 1 |
8 | 24607307 | Analysis of thiamine transporter genes in sporadic beriberi. | 2014 Apr | 2 |
9 | 19798730 | SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis. | 2009 Sep | 1 |