Búsqueda | Biblioteca Virtual en Salud

1.

Identification of ADAMTS18 as a gene mutated in Knobloch syndrome.

Aldahmesh, Mohammed A; Khan, Arif O; Mohamed, Jawahir Y; Alkuraya, Hisham; Ahmed, Hala; Bobis, Steve; Al-Mesfer, Saleh; Alkuraya, Fowzan S.

J Med Genet ; 48(9): 597-601, 2011 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-21862674

2.

Trends in antibiotic resistance in ocular samples in a tertiary eye centre in Saudi Arabia in 2003-2019.

Alsarhani, Waleed K; AlOtaibi, Humoud; AlEraij, Sheikah; Bukhari, Thamer; Ahmad, Syed Khabir; Al-Mesfer, Saleh; Martinez-Osorio, Hernan.

Can J Ophthalmol ; 2022 Sep 17.

Artículo en Inglés | MEDLINE | ID: mdl-36126695

3.

Adult presentation of retinoblastoma in Saudi patient.

Al Rashaed, Saba; Elkhamary, Sahar M; Al Sheikh, Osama; Al Mesfer, Saleh; Al-Dhibi, Hassan; Al Maktabi, Azza.

Saudi J Ophthalmol ; 34(2): 136-138, 2020.

Artículo en Inglés | MEDLINE | ID: mdl-33575539

4.

Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi families.

Khan, Arif O; Aldahmesh, Mohammed A; Ghadhfan, Faisal E; Al-Mesfer, Saleh; Alkuraya, Fowzan S.

Mol Vis ; 15: 1407-11, 2009 Jul 24.

Artículo en Inglés | MEDLINE | ID: mdl-19633732

5.

ACVR1C/SMAD2 signaling promotes invasion and growth in retinoblastoma.

Asnaghi, Laura; White, David T; Key, Nolan; Choi, Joshua; Mahale, Alka; Alkatan, Hind; Edward, Deepak P; Elkhamary, Sahar M; Al-Mesfer, Saleh; Maktabi, Azza; Hurtado, Christopher G; Lee, Grace Y; Carcaboso, Angel M; Mumm, Jeff S; Safieh, Leen Abu; Eberhart, Charles G.

Oncogene ; 38(12): 2056-2075, 2019 03.

Artículo en Inglés | MEDLINE | ID: mdl-30401983

6.

Ophthalmic features of hypoparathyroidism-retardation-dysmorphism.

Khan, Arif O; Al-Assiri, Abdullah; Al-Mesfer, Saleh.

J AAPOS ; 11(3): 288-90, 2007 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-17257873

7.

Lack of efficacy of dilated screening for retinoblastoma.

Khan, Arif O; Al-Mesfer, Saleh.

J Pediatr Ophthalmol Strabismus ; 42(4): 205-10; quiz 233-4, 2005.

Artículo en Inglés | MEDLINE | ID: mdl-16121549

8.

Recessive COL25A1 mutations cause isolated congenital ptosis or exotropic Duane syndrome with synergistic divergence.

Khan, Arif O; Al-Mesfer, Saleh.

J AAPOS ; 19(5): 463-5, 2015 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-26486031

9.

MicroRNA profiling in intraocular medulloepitheliomas.

Edward, Deepak P; Alkatan, Hind; Rafiq, Qundeel; Eberhart, Charles; Al Mesfer, Saleh; Ghazi, Nicola; Al Safieh, Leen; Kondkar, Altaf A; Abu Amero, Khaled K.

PLoS One ; 10(3): e0121706, 2015.

Artículo en Inglés | MEDLINE | ID: mdl-25807141

10.

Results of surgery for bilateral cataract associated with sensory nystagmus in children.

Rabiah, Peter K; Smith, Scott D; Awad, Abdulaziz H; Al-garni, Abdullah; Al-mesfer, Saleh A; Al-turkmani, Shahira.

Am J Ophthalmol ; 134(4): 586-91, 2002 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-12383816

11.

Retinoblastoma in older children.

Karcioglu, Zeynel A; Abboud, Emad B; Al-Mesfer, Saleh A; Al-Rashed, Waleed; Pilapil, Delia H.

J AAPOS ; 6(1): 26-32, 2002 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-11907476

12.

Cerulean ("blue-dot") cataract.

Ghadfan, Faisal E; Al-Mesfer, Saleh; Khan, Arif O.

J Pediatr Ophthalmol Strabismus ; 46(3): 190, 2009.

Artículo en Inglés | MEDLINE | ID: mdl-19496508

13.

Genetic analysis of strictly defined Leber congenital amaurosis with (and without) neurodevelopmental delay.

Khan, Arif O; Al-Mesfer, Saleh; Al-Turkmani, Shahira; Bergmann, Carsten; Bolz, Hanno J.

Br J Ophthalmol ; 98(12): 1724-8, 2014 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-24997176

14.

Ocular malignant tumors. Review of the Tumor Registry at a tertiary eye hospital in central Saudi Arabia.

Khandekar, Rajiv B; Al-Towerki, Abdulelah A; Al-Katan, Hind; Al-Mesfer, Saleh S; Abboud, Emad B; Al-Hussain, Hailah M; Sheikh, Osama H; Chaudhry, Imtiaz A; Ahmed, Wafa A; Zaman, Babar M; Asghar, Nasira; Edward, Deepak P.

Saudi Med J ; 35(4): 377-84, 2014 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-24749135

15.

The distinct ophthalmic phenotype of Knobloch syndrome in children.

Khan, Arif O; Aldahmesh, Mohammed A; Mohamed, Jawahir Y; Al-Mesfer, Saleh; Alkuraya, Fowzan S.

Br J Ophthalmol ; 96(6): 890-5, 2012 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-22399687

16.

Medulloepithelioma of the ciliary body: the delay in diagnosis and frequent initial mismanagement.

Alkatan, Hind; Al-Amry, Mohammad; Al-Hussain, Hailah; Al-Dhibi, Hassan; Al-Mesfer, Saleh.

Can J Ophthalmol ; 46(5): 431-8, 2011 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-21995988

17.

Histopathologic findings of eyes enucleated after treatment with chemosurgery for retinoblastoma.

Graeber, Carolyn P; Gobin, Y Pierre; Marr, Brian P; Dunkel, Ira J; Brodie, Scott E; Bornfeld, Norbert; Char, Devron H; Folberg, Robert; Imhof, Saskia M; Lin, Amy Y; Berry, Jesse L; Al Mesfer, Saleh; Moll, Annette C; Abramson, David H.

Open Ophthalmol J ; 5: 1-5, 2011 Jan 18.

Artículo en Inglés | MEDLINE | ID: mdl-21399766

18.

Opacification of IOLs.

Khan, Arif O; Al-Mesfer, Saleh.

Ophthalmology ; 112(8): 1482; author reply 1482-3, 2005 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-16061107

19.

Pediatric ophthalmology and strabismus in the Kingdom of Saudi Arabia.

Khan, Arif O; Al-Mesfer, Saleh.

J AAPOS ; 8(6): 513-4, 2004 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-15616496

20.

Intraocular metastatic Wilms' tumour in a child.

Al-Mesfer, Saleh; Alkatan, Hind.

Can J Ophthalmol ; 45(6): 646-7, 2010 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-20648066

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Identification of ADAMTS18 as a gene mutated in Knobloch syndrome.

Trends in antibiotic resistance in ocular samples in a tertiary eye centre in Saudi Arabia in 2003-2019.

Adult presentation of retinoblastoma in Saudi patient.

Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi families.

ACVR1C/SMAD2 signaling promotes invasion and growth in retinoblastoma.

Ophthalmic features of hypoparathyroidism-retardation-dysmorphism.

Lack of efficacy of dilated screening for retinoblastoma.

Recessive COL25A1 mutations cause isolated congenital ptosis or exotropic Duane syndrome with synergistic divergence.

MicroRNA profiling in intraocular medulloepitheliomas.

Results of surgery for bilateral cataract associated with sensory nystagmus in children.

Retinoblastoma in older children.

Cerulean ("blue-dot") cataract.

Genetic analysis of strictly defined Leber congenital amaurosis with (and without) neurodevelopmental delay.

Ocular malignant tumors. Review of the Tumor Registry at a tertiary eye hospital in central Saudi Arabia.

The distinct ophthalmic phenotype of Knobloch syndrome in children.

Medulloepithelioma of the ciliary body: the delay in diagnosis and frequent initial mismanagement.

Histopathologic findings of eyes enucleated after treatment with chemosurgery for retinoblastoma.

Opacification of IOLs.

Pediatric ophthalmology and strabismus in the Kingdom of Saudi Arabia.

Intraocular metastatic Wilms' tumour in a child.