Yahalom C - Search Results

1

Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease.

Yahalom C, Blumenfeld A, Hendler K, Wussuki-Lior O, Macarov M, Shohat M, Khateb S. Yahalom C, et al. Graefes Arch Clin Exp Ophthalmol. 2018 Nov;256(11):2157-2164. doi: 10.1007/s00417-018-4119-1. Epub 2018 Aug 30. Graefes Arch Clin Exp Ophthalmol. 2018. PMID: 30167917

2

Refractive profile in oculocutaneous albinism and its correlation with final visual outcome.

Yahalom C, Tzur V, Blumenfeld A, Greifner G, Eli D, Rosenmann A, Glanzer S, Anteby I. Yahalom C, et al. Br J Ophthalmol. 2012 Apr;96(4):537-9. doi: 10.1136/bjophthalmol-2011-300072. Epub 2011 Dec 1. Br J Ophthalmol. 2012. PMID: 22133989

3

Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family.

Yahalom C, Sharon D, Dalia E, Simhon SB, Shemesh E, Blumenfeld A. Yahalom C, et al. Ophthalmic Genet. 2015 Jun;36(2):175-9. doi: 10.3109/13816810.2015.1005318. Epub 2015 Feb 17. Ophthalmic Genet. 2015. PMID: 25687215

4

Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease.

Yahalom C, Macarov M, Lazer-Derbeko G, Altarescu G, Imbar T, Hyman JH, Eldar-Geva T, Blumenfeld A. Yahalom C, et al. Ophthalmic Genet. 2018 Aug;39(4):450-456. doi: 10.1080/13816810.2018.1474368. Epub 2018 May 21. Ophthalmic Genet. 2018. PMID: 29781739

5

Graded Anderson procedure for correcting abnormal head posture in infantile nystagmus.

Yahalom C, Hendler K, Galarza P, Dotan G. Yahalom C, et al. Eye (Lond). 2019 Aug;33(8):1248-1253. doi: 10.1038/s41433-019-0400-8. Epub 2019 Mar 25. Eye (Lond). 2019. PMID: 30911098 Free PMC article.

6

TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations.

AlTalbishi A, Zelinger L, Zeitz C, Hendler K, Namburi P, Audo I, Sheffer R, Yahalom C, Khateb S, Banin E, Sharon D. AlTalbishi A, et al. Among authors: yahalom c. Sci Rep. 2019 Aug 19;9(1):12047. doi: 10.1038/s41598-019-46811-7. Sci Rep. 2019. PMID: 31427709 Free PMC article.

7

An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers.

Kimchi A, Meiner V, Silverstein S, Macarov M, Mor-Shaked H, Blumenfeld A, Audo I, Zeitz C, Mechoulam H, Banin E, Sharon D, Yahalom C. Kimchi A, et al. Among authors: yahalom c. Ophthalmic Genet. 2019 Oct;40(5):443-448. doi: 10.1080/13816810.2019.1681008. Epub 2019 Oct 25. Ophthalmic Genet. 2019. PMID: 31651202

8

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children.

Levinger N, Hendler K, Banin E, Hanany M, Kimchi A, Mechoulam H, Meiner V, Parag Y, Sharon D, Macarov M, Yahalom C. Levinger N, et al. Among authors: yahalom c. Eur J Ophthalmol. 2021 Nov;31(6):3349-3354. doi: 10.1177/1120672120977343. Epub 2020 Nov 25. Eur J Ophthalmol. 2021. PMID: 33238767

9

SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis.

Yahalom C, Volovelsky O, Macarov M, Altalbishi A, Alsweiti Y, Schneider N, Hanany M, Khan MI, Cremers FPM, Anteby I, Banin E, Sharon D, Khateb S. Yahalom C, et al. Retina. 2021 Oct 1;41(10):2179-2187. doi: 10.1097/IAE.0000000000003138. Retina. 2021. PMID: 33512896

10

Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism.

Ehrenberg M, Bagdonite-Bejarano L, Fulton AB, Orenstein N, Yahalom C. Ehrenberg M, et al. Among authors: yahalom c. Ophthalmic Genet. 2021 Jun;42(3):243-251. doi: 10.1080/13816810.2021.1888128. Epub 2021 Feb 17. Ophthalmic Genet. 2021. PMID: 33594928

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