Charbel Issa P - Search Results

1

Neurologic and ocular phenotype in Pitt-Hopkins syndrome and a zebrafish model.

Brockschmidt A, Filippi A, Charbel Issa P, Nelles M, Urbach H, Eter N, Driever W, Weber RG. Brockschmidt A, et al. Among authors: charbel issa p. Hum Genet. 2011 Nov;130(5):645-55. doi: 10.1007/s00439-011-0999-4. Epub 2011 May 5. Hum Genet. 2011. PMID: 21544580

2

Clinical evaluation of simultaneous confocal scanning laser ophthalmoscopy imaging combined with high-resolution, spectral-domain optical coherence tomography.

Helb HM, Charbel Issa P, Fleckenstein M, Schmitz-Valckenberg S, Scholl HP, Meyer CH, Eter N, Holz FG. Helb HM, et al. Among authors: charbel issa p. Acta Ophthalmol. 2010 Dec;88(8):842-9. doi: 10.1111/j.1755-3768.2009.01602.x. Acta Ophthalmol. 2010. PMID: 19706019 Free article.

3

Tracking progression with spectral-domain optical coherence tomography in geographic atrophy caused by age-related macular degeneration.

Fleckenstein M, Schmitz-Valckenberg S, Adrion C, Krämer I, Eter N, Helb HM, Brinkmann CK, Charbel Issa P, Mansmann U, Holz FG. Fleckenstein M, et al. Among authors: charbel issa p. Invest Ophthalmol Vis Sci. 2010 Aug;51(8):3846-52. doi: 10.1167/iovs.09-4533. Epub 2010 Mar 31. Invest Ophthalmol Vis Sci. 2010. PMID: 20357194 Clinical Trial.

4

High-resolution optical coherence tomography of subpigment epithelial structures in patients with pigment epithelium detachment secondary to age-related macular degeneration.

Clemens CR, Krohne TU, Charbel Issa P, Helb HM, Kosanetzky N, Lommatzsch A, Holz FG, Eter N. Clemens CR, et al. Among authors: charbel issa p. Br J Ophthalmol. 2012 Aug;96(8):1088-91. doi: 10.1136/bjophthalmol-2011-301415. Epub 2012 Jun 13. Br J Ophthalmol. 2012. PMID: 22694959

5

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.

Ebermann I, Scholl HP, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, Millán JM, Aller E, Mitter D, Bolz H. Ebermann I, et al. Among authors: charbel issa p. Hum Genet. 2007 Apr;121(2):203-11. doi: 10.1007/s00439-006-0304-0. Epub 2006 Dec 15. Hum Genet. 2007. PMID: 17171570

6

An update on the ocular phenotype in patients with pseudoxanthoma elasticum.

Gliem M, Zaeytijd JD, Finger RP, Holz FG, Leroy BP, Charbel Issa P. Gliem M, et al. Among authors: charbel issa p. Front Genet. 2013 Apr 4;4:14. doi: 10.3389/fgene.2013.00014. eCollection 2013. Front Genet. 2013. PMID: 23577018 Free PMC article.

7

Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction.

Ebermann I, Walger M, Scholl HP, Charbel Issa P, Lüke C, Nürnberg G, Lang-Roth R, Becker C, Nürnberg P, Bolz HJ. Ebermann I, et al. Among authors: charbel issa p. Hum Mutat. 2007 Jun;28(6):571-7. doi: 10.1002/humu.20478. Hum Mutat. 2007. PMID: 17301963

8

Structure-function correlation of the human central retina.

Charbel Issa P, Troeger E, Finger R, Holz FG, Wilke R, Scholl HP. Charbel Issa P, et al. PLoS One. 2010 Sep 22;5(9):e12864. doi: 10.1371/journal.pone.0012864. PLoS One. 2010. PMID: 20877651 Free PMC article. Clinical Trial.

9

X-linked juvenile retinoschisis in a consanguineous family: phenotypic variability and report of a homozygous female patient.

Gliem M, Holz FG, Stöhr H, Weber BH, Charbel Issa P. Gliem M, et al. Among authors: charbel issa p. Retina. 2014 Dec;34(12):2472-8. doi: 10.1097/IAE.0000000000000243. Retina. 2014. PMID: 25054456

10

High-resolution spectral domain-OCT imaging in geographic atrophy associated with age-related macular degeneration.

Fleckenstein M, Charbel Issa P, Helb HM, Schmitz-Valckenberg S, Finger RP, Scholl HP, Loeffler KU, Holz FG. Fleckenstein M, et al. Among authors: charbel issa p. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):4137-44. doi: 10.1167/iovs.08-1967. Epub 2008 May 16. Invest Ophthalmol Vis Sci. 2008. PMID: 18487363

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