1-anilino-8-naphthalenesulfonate has been researched along with Cardiomyopathy, Congestive in 3 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Distal myopathy is a group of heterogeneous disorders affecting predominantly distal muscles usually appearing from young to late adulthood with very rare cardiac complications." | 1.35 | Distal lipid storage myopathy due to PNPLA2 mutation. ( Hayashi, YK; Malicdan, MC; Nishino, I; Noguchi, S; Nomura, K; Nonaka, I; Ohji, S; Ohkuma, A; Sugie, H, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Higashi, M | 1 |
| Hirano, K | 1 |
| Kobayashi, K | 2 |
| Ikeda, Y | 1 |
| Issiki, A | 1 |
| Otsuka, T | 1 |
| Suzuki, A | 1 |
| Yamaguchi, S | 1 |
| Zaima, N | 1 |
| Hamada, S | 1 |
| Hanada, H | 1 |
| Suzuki, C | 1 |
| Nakamura, H | 1 |
| Nagasaka, H | 1 |
| Miyata, T | 1 |
| Miyamoto, Y | 1 |
| Naito, H | 1 |
| Toda, T | 1 |
| Muggenthaler, M | 1 |
| Petropoulou, E | 1 |
| Omer, S | 1 |
| Simpson, MA | 1 |
| Sahak, H | 1 |
| Rice, A | 1 |
| Raju, H | 1 |
| Conti, FJ | 1 |
| Bridges, LR | 1 |
| Anderson, LJ | 1 |
| Sharma, S | 1 |
| Behr, ER | 1 |
| Jamshidi, Y | 1 |
| Ohkuma, A | 1 |
| Nonaka, I | 1 |
| Malicdan, MC | 1 |
| Noguchi, S | 1 |
| Ohji, S | 1 |
| Nomura, K | 1 |
| Sugie, H | 1 |
| Hayashi, YK | 1 |
| Nishino, I | 1 |
3 other studies available for 1-anilino-8-naphthalenesulfonate and Cardiomyopathy, Congestive
| Article | Year |
|---|---|
Distinct cardiac phenotype between two homozygotes born in a village with accumulation of a genetic deficiency of adipose triglyceride lipase.
Topics: Cardiomyopathy, Dilated; Female; Heart Failure; Homozygote; Humans; Japan; Lipase; Male; Mutation; P | 2015 |
Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease.
Topics: Cardiomyopathy, Dilated; Exome; Humans; Lipase; Lipid Metabolism, Inborn Errors; Male; Muscular Dise | 2016 |
Distal lipid storage myopathy due to PNPLA2 mutation.
Topics: Adult; Atrophy; Cardiomyopathy, Dilated; Distal Myopathies; Hand; Humans; Leg; Lipase; Lipid Metabol | 2008 |