These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
142 related articles for article (PubMed ID: 37180414)
1. End-stage crystalline maculopathy with retinal atrophy in Sjögren-Larsson syndrome: a case report and review of the literature. Lambert LH; Shaikh N; Marx JL; Ramsey DJ Ther Adv Rare Dis; 2022; 3():26330040221122496. PubMed ID: 37180414 [TBL] [Abstract][Full Text] [Related]
6. Retinal Morphology in Sjögren-Larsson Syndrome on OCT: From Metabolic Crystalline Maculopathy to Early-Onset Macular Degeneration. Staps P; Cruysberg JRM; Roeleveld N; Willemsen MAAP; Theelen T Ophthalmol Retina; 2019 Jun; 3(6):500-509. PubMed ID: 31174672 [TBL] [Abstract][Full Text] [Related]
7. Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome. Haug S; Braun-Falco M Gene Ther; 2006 Jul; 13(13):1021-6. PubMed ID: 16525484 [TBL] [Abstract][Full Text] [Related]
8. Genotype and phenotype variability in Sjögren-Larsson syndrome. Weustenfeld M; Eidelpes R; Schmuth M; Rizzo WB; Zschocke J; Keller MA Hum Mutat; 2019 Feb; 40(2):177-186. PubMed ID: 30372562 [TBL] [Abstract][Full Text] [Related]
9. Retinal Capillary Abnormalities in Sjögren-Larsson Syndrome Maculopathy. Staps P; de Breuk A; Cruysberg JRM; Willemsen M; Theelen T Case Rep Ophthalmol; 2022; 13(2):341-349. PubMed ID: 35702653 [TBL] [Abstract][Full Text] [Related]
10. A rare case of Sjogren-Larsson syndrome with recurrent pneumonia and asthma. Tavasoli A; Sayyahfar S; Behnam B Korean J Pediatr; 2016 Jun; 59(6):276-9. PubMed ID: 27462357 [TBL] [Abstract][Full Text] [Related]
11. Genetic assessment of ten Egyptian patients with Sjögren-Larsson syndrome: expanding the clinical spectrum and reporting a novel ALDH3A2 mutation. Amr K; El-Bassyouni HT; Ismail S; Youness E; El-Daly SM; Ebrahim AY; El-Kamah G Arch Dermatol Res; 2019 Nov; 311(9):721-730. PubMed ID: 31388754 [TBL] [Abstract][Full Text] [Related]
12. Clinical, biochemical, and genetic aspects of Sjögren-Larsson syndrome. Cho KH; Shim SH; Kim M Clin Genet; 2018 Apr; 93(4):721-730. PubMed ID: 28543186 [TBL] [Abstract][Full Text] [Related]
13. Compound heterozygous mutations in the Liu YD; Lin HJ; Li CY; Sun GF; Hu XB; Ma MY; Sun Y; Feng BZ; Li QB; Kong QX Int J Neurosci; 2020 Nov; 130(11):1156-1160. PubMed ID: 31944864 [No Abstract] [Full Text] [Related]