Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 236

1.

Genotype and phenotype correlations in congenital glaucoma.

Hollander DA, Sarfarazi M, Stoilov I, Wood IS, Fredrick DR, Alvarado JA.

Trans Am Ophthalmol Soc. 2006;104:183-95.

2.

Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics.

Hollander DA, Sarfarazi M, Stoilov I, Wood IS, Fredrick DR, Alvarado JA.

Am J Ophthalmol. 2006 Dec;142(6):993-1004.

PMID:
17157584
3.

Sturge-Weber syndrome with congenital glaucoma and cytochrome P450 (CYP1B1) gene mutations.

Tanwar M, Sihota R, Dada T, Gupta V, Das TK, Yadav U, Dada R.

J Glaucoma. 2010 Aug;19(6):398-404. doi: 10.1097/IJG.0b013e3181c4ae74.

PMID:
20051892
4.

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.

de Melo MB, Mandal AK, Tavares IM, Ali MH, Kabra M, de Vasconcellos JP, Senthil S, Sallum JM, Kaur I, Betinjane AJ, Moura CR, Paula JS, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE, Costa VP, Belfort R Jr, Chakrabarti S.

PLoS One. 2015 May 15;10(5):e0127147. doi: 10.1371/journal.pone.0127147.

5.

Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.

Abu-Amero KK, Osman EA, Mousa A, Wheeler J, Whigham B, Allingham RR, Hauser MA, Al-Obeidan SA.

Mol Vis. 2011;17:2911-9.

6.

CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.

Kelberman D, Islam L, Jacques TS, Russell-Eggitt I, Bitner-Glindzicz M, Khaw PT, Nischal KK, Sowden JC.

Ophthalmology. 2011 Sep;118(9):1865-73. doi: 10.1016/j.ophtha.2011.01.044.

PMID:
21600657
7.

Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients.

Tanwar M, Dada T, Sihota R, Das TK, Yadav U, Dada R.

Mol Vis. 2009 Jun 13;15:1200-9.

8.

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.

Hilal L, Boutayeb S, Serrou A, Refass-Buret L, Shisseh H, Bencherifa F, El Mzibri M, Benazzouz B, Berraho A.

Mol Vis. 2010 Jul 2;16:1215-26.

9.

Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma.

Suri F, Yazdani S, Narooie-Nejhad M, Zargar SJ, Paylakhi SH, Zeinali S, Pakravan M, Elahi E.

Ophthalmology. 2009 Nov;116(11):2101-9. doi: 10.1016/j.ophtha.2009.04.045.

PMID:
19744731
10.

CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability.

Campos-Mollo E, López-Garrido MP, Blanco-Marchite C, Garcia-Feijoo J, Peralta J, Belmonte-Martínez J, Ayuso C, Escribano J.

Mol Vis. 2009;15:417-31.

11.

Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.

Al-Haddad C, Abdulaal M, Badra R, Barikian A, Noureddine B, Farra C.

Ophthalmic Genet. 2016;37(1):31-6. doi: 10.3109/13816810.2014.924015.

PMID:
24940937
12.

Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma.

Panicker SG, Mandal AK, Reddy AB, Gothwal VK, Hasnain SE.

Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1149-56.

PMID:
15037581
13.

CYP1B1 gene analysis in primary congenital glaucoma Brazilian patients: novel mutations and association with poor prognosis.

Della Paolera M, de Vasconcellos JP, Umbelino CC, Kasahara N, Rocha MN, Richeti F, Costa VP, Tavares A, de Melo MB.

J Glaucoma. 2010 Mar;19(3):176-82. doi: 10.1097/IJG.0b013e3181a98bae.

PMID:
19528825
14.

Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.

Millá E, Mañé B, Duch S, Hernan I, Borràs E, Planas E, Dias Mde S, Carballo M, Gamundi MJ; Spanish Multicenter Glaucoma Group-Estudio Multicéntrico Español de Investigación Genética del Glaucoma, EMEIGG..

Mol Vis. 2013 Aug 4;19:1707-22.

15.

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

Chitsazian F, Tusi BK, Elahi E, Saroei HA, Sanati MH, Yazdani S, Pakravan M, Nilforooshan N, Eslami Y, Mehrjerdi MA, Zareei R, Jabbarvand M, Abdolahi A, Lasheyee AR, Etemadi A, Bayat B, Sadeghi M, Banoei MM, Ghafarzadeh B, Rohani MR, Rismanchian A, Thorstenson Y, Sarfarazi M.

J Mol Diagn. 2007 Jul;9(3):382-93.

16.

Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.

Sheikh SA, Waryah AM, Narsani AK, Shaikh H, Gilal IA, Shah K, Qasim M, Memon AI, Kewalramani P, Shaikh N.

Mol Vis. 2014 Jul 7;20:991-1001.

17.

Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.

Cella W, de Vasconcellos JP, de Melo MB, Kneipp B, Costa FF, Longui CA, Costa VP.

Invest Ophthalmol Vis Sci. 2006 May;47(5):1803-9.

PMID:
16638984
18.

[Development of the iridocorneal angle and congenital glaucoma].

Tamm ER.

Ophthalmologe. 2011 Jul;108(7):610-4, 616-7. doi: 10.1007/s00347-010-2294-5. Review. German.

PMID:
21796509
19.

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

El-Ashry MF, Abd El-Aziz MM, Bhattacharya SS.

J Glaucoma. 2007 Jan;16(1):104-11.

PMID:
17224759
20.

Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population.

Geyer O, Wolf A, Levinger E, Harari-Shacham A, Walton DS, Shochat C, Korem S, Bercovich D.

Am J Ophthalmol. 2011 Feb;151(2):263-71.e1. doi: 10.1016/j.ajo.2010.08.038.

PMID:
21168818
Items per page

Supplemental Content

Support Center