glycine has been researched along with ARSA Deficiency in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Schlotawa, L | 2 |
| Preiskorn, J | 1 |
| Ahrens-Nicklas, R | 1 |
| Schiller, S | 1 |
| Adang, LA | 2 |
| Gärtner, J | 2 |
| Friede, T | 1 |
| Groeschel, S | 1 |
| Kehrer, C | 1 |
| Harzer, K | 1 |
| Staretz-Chacham, O | 1 |
| Silva, TO | 1 |
| Schwartz, IVD | 1 |
| De Castro, M | 1 |
| Costin, C | 1 |
| Montgomery, EF | 1 |
| Dierks, T | 1 |
| Radhakrishnan, K | 1 |
| Ahrens-Nicklas, RC | 1 |
| Takakusaki, Y | 1 |
| Hisayasu, S | 2 |
| Hirai, Y | 2 |
| Shimada, T | 2 |
| Kurai, T | 1 |
| Kitagawa, R | 1 |
| Migita, M | 1 |
| Suzuki, H | 1 |
| Honke, K | 1 |
| Kobayashi, T | 1 |
| Fujii, T | 1 |
| Gasa, S | 1 |
| Xu, M | 1 |
| Takamaru, Y | 1 |
| Kondo, R | 1 |
| Tsuji, S | 1 |
| Makita, A | 1 |
| Kreysing, J | 1 |
| Bohne, W | 1 |
| Bösenberg, C | 1 |
| Marchesini, S | 1 |
| Turpin, JC | 1 |
| Baumann, N | 1 |
| von Figura, K | 1 |
| Gieselmann, V | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| The Myelin Disorders Biorepository Project and Global Leukodystrophy Initiative Clinical Trials Network[NCT03047369] | 12,000 participants (Anticipated) | Observational [Patient Registry] | 2016-12-08 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 review available for glycine and ARSA Deficiency
| Article | Year |
|---|---|
A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency.
Topics: Glycine; Humans; Leukodystrophy, Metachromatic; Mucopolysaccharidoses; Multiple Sulfatase Deficiency | 2020 |
5 other studies available for glycine and ARSA Deficiency
| Article | Year |
|---|---|
Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease.
Topics: Adolescent; Child; Child, Preschool; Female; Genotype; Glycine; Humans; Infant; Internationality; Le | 2020 |
Coexpression of formylglycine-generating enzyme is essential for synthesis and secretion of functional arylsulfatase A in a mouse model of metachromatic leukodystrophy.
Topics: Alanine; Animals; Blood-Brain Barrier; Cerebroside-Sulfatase; Chlorocebus aethiops; COS Cells; Gene | 2005 |
AAV1 mediated co-expression of formylglycine-generating enzyme and arylsulfatase a efficiently corrects sulfatide storage in a mouse model of metachromatic leukodystrophy.
Topics: Animals; Arylsulfatases; Dependovirus; Disease Models, Animal; Gene Expression Regulation, Enzymolog | 2007 |
An adult-type metachromatic leukodystrophy caused by substitution of serine for glycine-122 in arylsulfatase A.
Topics: Adult; Animals; Base Sequence; Cell Line; Cerebroside-Sulfatase; Chlorocebus aethiops; DNA Mutationa | 1993 |
High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophy.
Topics: Alleles; Animals; Base Sequence; Cells, Cultured; Cerebroside-Sulfatase; Cricetinae; DNA Mutational | 1993 |