122 related articles for article (PubMed ID: 35996915)
21. 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]
22. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report.
Blanco-Kelly F; Rodrigues-Jacy da Silva L; Sanchez-Navarro I; Riveiro-Alvarez R; Lopez-Martinez MA; Corton M; Ayuso C
BMC Med Genet; 2017 Jan; 18(1):1. PubMed ID: 28061825
[TBL] [Abstract][Full Text] [Related]
23. A novel splice-acceptor site mutation in CDH3 gene in a consanguineous family exhibiting hypotrichosis with juvenile macular dystrophy.
Kamran-ul-Hassan Naqvi S; Azeem Z; Ali G; Ahmad W
Arch Dermatol Res; 2010 Nov; 302(9):701-3. PubMed ID: 20140736
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy.
Indelman M; Eason J; Hummel M; Loza O; Suri M; Leys MJ; Bayne M; Schwartz FL; Sprecher E
Clin Exp Dermatol; 2007 Mar; 32(2):191-6. PubMed ID: 17342797
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.
Souied E; Amalric P; Chauvet ML; Chevallier C; Le Hoang P; Munnich A; Kaplan J
Ophthalmic Genet; 1995 Mar; 16(1):11-5. PubMed ID: 7648037
[TBL] [Abstract][Full Text] [Related]
30. A novel splice-site mutation in the CDH3 gene in hypotrichosis with juvenile macular dystrophy.
Jelani M; Salman Chishti M; Ahmad W
Clin Exp Dermatol; 2009 Jan; 34(1):68-73. PubMed ID: 19076794
[TBL] [Abstract][Full Text] [Related]
31. [Multimodal Approaches for the Analysis of Retinal Functional Disorders―Focusing on Retinal Detachment].
Terasaki H
Nippon Ganka Gakkai Zasshi; 2017 Mar; 121(3):185-231. PubMed ID: 30088405
[TBL] [Abstract][Full Text] [Related]
32. Histopathology of hypotrichosis with juvenile macular dystrophy.
Bergman R; Sapir M; Sprecher E
Am J Dermatopathol; 2004 Jun; 26(3):205-9. PubMed ID: 15166507
[TBL] [Abstract][Full Text] [Related]
33. Lifecycles of Individual Subretinal Drusenoid Deposits and Evolution of Outer Retinal Atrophy in Age-Related Macular Degeneration.
Zhang Y; Wang X; Sadda SR; Clark ME; Witherspoon CD; Spaide RF; Owsley C; Curcio CA
Ophthalmol Retina; 2020 Mar; 4(3):274-283. PubMed ID: 31924545
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. A novel ocular phenotype associated with pathogenic variants in
Beckman M; Clevenger L; DeBenedictis MJ; Yuan A; Sharma S
Ophthalmic Genet; 2023 Dec; 44(6):606-609. PubMed ID: 36861499
[TBL] [Abstract][Full Text] [Related]
37. Histologic and Optical Coherence Tomographic Correlates in Drusenoid Pigment Epithelium Detachment in Age-Related Macular Degeneration.
Balaratnasingam C; Messinger JD; Sloan KR; Yannuzzi LA; Freund KB; Curcio CA
Ophthalmology; 2017 May; 124(5):644-656. PubMed ID: 28153442
[TBL] [Abstract][Full Text] [Related]
38. Case report: the first case of unilateral retinal pigment epithelium dysgenesis in China.
Ding Y; Yao B; Xie K; Ye H; Yu Y
BMC Ophthalmol; 2020 Aug; 20(1):340. PubMed ID: 32819322
[TBL] [Abstract][Full Text] [Related]
39. Near-infrared fundus autofluorescence in subclinical best vitelliform macular dystrophy.
Parodi MB; Iacono P; Del Turco C; Bandello F
Am J Ophthalmol; 2014 Dec; 158(6):1247-1252.e2. PubMed ID: 25174897
[TBL] [Abstract][Full Text] [Related]
40. Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.
Qian CX; Charran D; Strong CR; Steffens TJ; Jayasundera T; Heckenlively JR
Ophthalmology; 2017 Apr; 124(4):456-463. PubMed ID: 28187978
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
