166 related articles for article (PubMed ID: 27157923)
21. Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation.
Nasser F; Mulahasanovic L; Alkhateeb M; Biskup S; Stingl K; Zrenner E
Doc Ophthalmol; 2019 Apr; 138(2):153-160. PubMed ID: 30710256
[TBL] [Abstract][Full Text] [Related]
22. Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy.
Halford S; Holt R; Németh AH; Downes SM
Arch Ophthalmol; 2012 Nov; 130(11):1490-2. PubMed ID: 23143461
[No Abstract] [Full Text] [Related]
23. Hypotrichosis with juvenile macular dystrophy: clinical and electrophysiological assessment of visual function.
Leibu R; Jermans A; Hatim G; Miller B; Sprecher E; Perlman I
Ophthalmology; 2006 May; 113(5):841-7.e3. PubMed ID: 16650681
[TBL] [Abstract][Full Text] [Related]
24. Phenotypic diversity and mutation spectrum in hypotrichosis with juvenile macular dystrophy.
Indelman M; Hamel CP; Bergman R; Nischal KK; Thompson D; Surget MO; Ramon M; Ganthos H; Miller B; Richard G; Lurie R; Leibu R; Russell-Eggitt I; Sprecher E
J Invest Dermatol; 2003 Nov; 121(5):1217-20. PubMed ID: 14708629
[TBL] [Abstract][Full Text] [Related]
25. Novel homozygous sequence variants in the CDH3 gene encoding P-cadherin underlying hypotrichosis with juvenile macular dystrophy in consanguineous families.
Ahmad F; Ali RH; Muhammad D; Nasir A; Umair M; Wakil SM; Ramzan K; Basit S; Ahmad W
Eur J Dermatol; 2016 Dec; 26(6):610-612. PubMed ID: 27456782
[No Abstract] [Full Text] [Related]
26.
Karti O; Abali S; Ayhan Z; Gokmeydan E; Nalcaci S; Yaman A; Saatci AO
Am J Ophthalmol Case Rep; 2017 Sep; 7():129-133. PubMed ID: 29260097
[TBL] [Abstract][Full Text] [Related]
27. Retinal cadherins and the retinal cadherinopathies: Current concepts and future directions.
Yusuf IH; Garrett AM; MacLaren RE; Charbel Issa P
Prog Retin Eye Res; 2022 Sep; 90():101038. PubMed ID: 35066146
[TBL] [Abstract][Full Text] [Related]
28. Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report.
Carnovale-Scalzo G; Carnevali A; Piccoli G; Ceravolo D; Bruzzichessi D; Iuliano R; Tallerico R; Gatti V; Giannaccare G; Scorcia V
BMC Ophthalmol; 2021 Jul; 21(1):284. PubMed ID: 34301208
[TBL] [Abstract][Full Text] [Related]
29. Multimodal imaging and multifocal electroretinography demonstrate autosomal recessive Stargardt disease may present like occult macular dystrophy.
Sisk RA; Leng T
Retina; 2014 Aug; 34(8):1567-75. PubMed ID: 24743636
[TBL] [Abstract][Full Text] [Related]
30. Sparse scalp hair and vision loss: think hypotrichosis with juvenile macular dystrophy.
Narayan A; Moosajee M
BMJ Case Rep; 2019 Oct; 12(10):. PubMed ID: 31645385
[TBL] [Abstract][Full Text] [Related]
31. A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy.
Avitan-Hersh E; Indelman M; Khamaysi Z; Leibu R; Bergman R
Int J Dermatol; 2012 Mar; 51(3):325-7. PubMed ID: 22348569
[No Abstract] [Full Text] [Related]
32. Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).
Kjaer KW; Hansen L; Schwabe GC; Marques-de-Faria AP; Eiberg H; Mundlos S; Tommerup N; Rosenberg T
J Med Genet; 2005 Apr; 42(4):292-8. PubMed ID: 15805154
[TBL] [Abstract][Full Text] [Related]
33. INSIGHTS INTO AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY THROUGH MULTIMODALITY DIAGNOSTIC IMAGING.
Palejwala NV; Gale MJ; Clark RF; Schlechter C; Weleber RG; Pennesi ME
Retina; 2016 Jan; 36(1):119-30. PubMed ID: 26110599
[TBL] [Abstract][Full Text] [Related]
34. A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesia.
Fan KC; Patel NA; Yannuzzi NA; Prakhunhungsit S; Negron CI; Basora E; Colin AA; Tekin M; Berrocal AM
Am J Ophthalmol Case Rep; 2019 Sep; 15():100486. PubMed ID: 31431935
[TBL] [Abstract][Full Text] [Related]
35. Complement modulation in the retinal pigment epithelium rescues photoreceptor degeneration in a mouse model of Stargardt disease.
Lenis TL; Sarfare S; Jiang Z; Lloyd MB; Bok D; Radu RA
Proc Natl Acad Sci U S A; 2017 Apr; 114(15):3987-3992. PubMed ID: 28348233
[TBL] [Abstract][Full Text] [Related]
36. Hypotrichosis with juvenile macular dystrophy.
Oliveira-Ferreira C; Leuzinger-Dias M; Tavares-Ferreira J; Silva SE; Brandão E; Falcão-Reis F; Rocha-Sousa A
Ophthalmic Genet; 2019 Dec; 40(6):574-577. PubMed ID: 31718366
[No Abstract] [Full Text] [Related]
37. Hypotrichosis with juvenile macular dystrophy with novel mutations in CDH3 gene.
Liu Y; Xu Z; Sun Y; Zhang B; Wang X; Ma L
Australas J Dermatol; 2024 Feb; 65(1):91-94. PubMed ID: 37850495
[No Abstract] [Full Text] [Related]
38. Clinical, genetic, and electron microscopy of hair findings in a patient with CDH3 -related hypotrichosis with juvenile macular dystrophy.
Leal-Rodríguez R; Barragán-Arévalo T; Pérez-Torres A; Giraldo-Gómez DM; Zenteno JC
Clin Dysmorphol; 2023 Apr; 32(2):62-64. PubMed ID: 36779776
[No Abstract] [Full Text] [Related]
39. An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease.
Mäkeläinen S; Gòdia M; Hellsand M; Viluma A; Hahn D; Makdoumi K; Zeiss CJ; Mellersh C; Ricketts SL; Narfström K; Hallböök F; Ekesten B; Andersson G; Bergström TF
PLoS Genet; 2019 Mar; 15(3):e1007873. PubMed ID: 30889179
[TBL] [Abstract][Full Text] [Related]
40. Novel therapeutics for Stargardt disease.
Lu LJ; Liu J; Adelman RA
Graefes Arch Clin Exp Ophthalmol; 2017 Jun; 255(6):1057-1062. PubMed ID: 28285324
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]