DATOS DE LOS ÚLTIMOS ENSAYOS CLÍNICOS DE LA ENFERMEDAD DE STARGARDT

TODOS ESTOS ARTÍCULOS Y ENSAYOS SON GRATUITOS Y ESTÁN A DISPOSICIÓN DE TODAS LAS PERSONAS QUE QUIERAN LEERLOS. ACTUALMENTE EXISTEN 20. NO HAY CURA PARA LA ENFERMEDAD DE STARGARDT. ENSAYOS CLÍNICOS Y OTROS ARTÍCULOS ESTÁN DESCRITOS AQUÍ: 

Optical Coherence Tomography Angiography Findings in Stargardt Disease.
Mastropasqua R, Toto L, Borrelli E, Di Antonio L, Mattei PA, Senatore A, Di Nicola M, Mariotti C.
PLoS One. 2017 Feb 2;12(2):e0170343. doi: 10.1371/journal.pone.0170343.
PMID: 28151966 Free Article

Select item 28149006
2.
Role of Lipids in Retinal Vascular and Macular Disorders.
Prakash G, Agrawal R, Natung T.
Indian J Clin Biochem. 2017 Mar;32(1):3-8. doi: 10.1007/s12291-016-0560-2. Review.
PMID: 28149006

Select item 28147405
3.
Prominent Optic Disc Featured in Inherited Retinopathy.
Todorova MG, Bojinova RI, Valmaggia C, Schorderet DF.
Klin Monbl Augenheilkd. 2017 Feb 1. doi: 10.1055/s-0042-121335. [Epub ahead of print]
PMID: 28147405

Select item 28127548
4.
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing.
Bernardis I, Chiesi L, Tenedini E, Artuso L, Percesepe A, Artusi V, Simone ML, Manfredini R, Camparini M, Rinaldi C, Ciardella A, Graziano C, Balducci N, Tranchina A, Cavallini GM, Pietrangelo A, Marigo V, Tagliafico E.
Biomed Res Int. 2016;2016:6341870. doi: 10.1155/2016/6341870.
PMID: 28127548 Free PMC Article

Select item 28121212
5.
Macular hole in Stargardt disease: Clinical and ultra-structural observation.
Rizzo S, Mucciolo DP, Bacherini D, Murro V, Vannozzi L, Virgili G, Bani D, Sodi A.
Ophthalmic Genet. 2017 Jan 25:1-4. doi: 10.1080/13816810.2016.1266666. [Epub ahead of print]
PMID: 28121212

Select item 28118664
6.
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Schulz HL, Grassmann F, Kellner U, Spital G, Rüther K, Jägle H, Hufendiek K, Rating P, Huchzermeyer C, Baier MJ, Weber BH, Stöhr H.
Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):394-403. doi: 10.1167/iovs.16-19936.
PMID: 28118664 Free PMC Article

Select item 28115520
7.
Cellular uptake and delivery of Myeloperoxidase to lysosomes promotes lipofuscin degradation and lysosomal stress in retinal cells.
Yogalingam G, Lee AR, Mackenzie DS, Maures TJ, Rafalko A, Prill H, Berguig G, Hague C, Christianson T, Bell SM, LeBowitz JH.
J Biol Chem. 2017 Jan 23. pii: jbc.M116.739441. doi: 10.1074/jbc.M116.739441. [Epub ahead of print]
PMID: 28115520 Free Article

Select item 28099317
8.
STARGARDT DISEASE: Beyond Flecks and Atrophy.
Light JG, Fard MA, Yaseri M, Aiyetan P, Handa JT, Ebrahimi KB.
Retina. 2017 Jan 17. doi: 10.1097/IAE.0000000000001484. [Epub ahead of print]
PMID: 28099317

Select item 28095140
9.
PROM1 gene variations in Brazilian patients with macular dystrophy.
Salles MV, Motta FL, Dias da Silva E, Varela Lima Teixeira P, Antunes Costa K, Filippelli-Silva R, Martin R, Pesquero JB, Ferraz Sallum JM.
Ophthalmic Genet. 2017 Jan-Feb;38(1):39-42. doi: 10.1080/13816810.2016.1275022.
PMID: 28095140

Select item 28050124
10.
Novel compound heterozygous mutations in <i>ABCA4</i> in a Chinese pedigree with Stargardt disease.
Zhang J, Qi A, Wang X, Pan H, Mo H, Huang J, Li H, Chen Z, Wei M, Wang B.
Mol Vis. 2016 Dec 30;22:1514-1521.
PMID: 28050124 Free PMC Article

Select item 28044389
11.
In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases.
Cornelis SS, Bax NM, Zernant J, Allikmets R, Fritsche LG, den Dunnen JT, Ajmal M, Hoyng CB, Cremers FP.
Hum Mutat. 2017 Jan 3. doi: 10.1002/humu.23165. [Epub ahead of print]
PMID: 28044389

Select item 28035529
12.
Hereditary Retinal Dystrophy.
Hohman TC.
Handb Exp Pharmacol. 2016 Dec 30. doi: 10.1007/164_2016_91. [Epub ahead of print]
PMID: 28035529

Select item 28005958
13.
Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing.
de Castro-Miró M, Tonda R, Escudero-Ferruz P, Andrés R, Mayor-Lorenzo A, Castro J, Ciccioli M, Hidalgo DA, Rodríguez-Ezcurra JJ, Farrando J, Pérez-Santonja JJ, Cormand B, Marfany G, Gonzàlez-Duarte R.
PLoS One. 2016 Dec 22;11(12):e0168966. doi: 10.1371/journal.pone.0168966.
PMID: 28005958 Free PMC Article

Select item 28002570
14.
Asymmetric Inter-Eye Progression in Stargardt Disease.
Lambertus S, Bax NM, Groenewoud JM, Cremers FP, van der Wilt GJ, Klevering BJ, Theelen T, Hoyng CB.
Invest Ophthalmol Vis Sci. 2016 Dec 1;57(15):6824-6830. doi: 10.1167/iovs.16-20963.
PMID: 28002570

Select item 27984836
15.
[Do We Still Need Electrophysiology in Ophthalmology?]
Tegetmeyer H.
Klin Monbl Augenheilkd. 2016 Dec;233(12):1339-1349. German.
PMID: 27984836

Select item 27941641
16.
Potential of Induced Pluripotent Stem Cells (iPSCs) for Treating Age-Related Macular Degeneration (AMD).
Fields M, Cai H, Gong J, Del Priore L.
Cells. 2016 Dec 8;5(4). pii: E44. Review.
PMID: 27941641 Free PMC Article

Select item 27939946
17.
Stargardt disease-associated mutation spectrum of a Russian Federation cohort.
Zolnikova IV, Strelnikov VV, Skvortsova NA, Tanas AS, Barh D, Rogatina EV, Egorova IV, Levina DV, Demenkova ON, Prikaziuk EG, Ivanova ME.
Eur J Med Genet. 2017 Feb;60(2):140-147. doi: 10.1016/j.ejmg.2016.12.002.
PMID: 27939946

Select item 27875314
18.
Receptor MER Tyrosine Kinase Proto-oncogene (MERTK) Is Not Required for Transfer of Bis-retinoids to the Retinal Pigmented Epithelium.
Palczewska G, Maeda A, Golczak M, Arai E, Dong Z, Perusek L, Kevany B, Palczewski K.
J Biol Chem. 2016 Dec 23;291(52):26937-26949. doi: 10.1074/jbc.M116.764563.
PMID: 27875314

Select item 27860478
19.
[Gene Therapy for Inherited RETINAL AND OPTIC NERVE Disorders: Current Knowledge].
Ďuďáková Ľ, Kousal B, Kolářová H, Hlavatá L, Lišková P.
Cesk Slov Oftalmol. 2016 Fall;72(4):128-136. Czech.
PMID: 27860478

Select item 27813578
20.
Analysis of ELOVL4 and PRPH2 genes in Turkish Stargardt disease patients.
Bardak H, Gunay M, Erçalık Y, Bardak Y, Ozbas H, Bagci O, Ayata A, Sönmez M, Alagöz C.
Genet Mol Res. 2016 Oct 24;15(4). doi: 10.4238/gmr15048774.
PMID: 27813578

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