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Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma

PloS one, 2016-07, Vol.11 (7), p.e0159259-e0159259

2016

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A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma

PloS one, 2016-07, Vol.11 (7), p.e0160016-e0160016

2016

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Variants in the PRPF8 Gene are Associated with Glaucoma

Molecular neurobiology, 2018-05, Vol.55 (5), p.4504-4510

2018

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Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families

Genes, 2018-02, Vol.9 (2), p.112

2018

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Variable retinal presentations in nanophthalmos

Journal of the Pakistan Medical Association, 2009-11, Vol.59 (11), p.791-793

2009

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A case of systemic lupus erythematosus with aplastic anaemia

Journal of the Pakistan Medical Association, 2011-08, Vol.61 (8), p.817-819

2011

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Effects of Artisan aphakic intraocular lens on central corneal thickness and intra ocular pressure in pediatric eyes with crystalline subluxated lenses

Oman journal of ophthalmology, 2013, Vol.6 (1), p.44-47, Article 44

2013

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Ptosis associated with Monocular Elevation Deficiency

Journal of the Pakistan Medical Association, 2009-08, Vol.59 (8), p.522-524

2009

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Congenital Cataract, Nasolacrimal Duct Obstruction, and Methicillin-Resistant Staphylococcus aureus Conjunctivitis: When to Operate?

Journal of pediatric ophthalmology and strabismus, 2016-07, Vol.53 Online (6), p.e29

2016

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Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome

Cornea, 2019-06, Vol.38 (6), p.718-722

2019

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Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome

Neurogenetics, 2016-01, Vol.17 (1), p.17-23

2016

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Tumor Regression Patterns in Retinoblastoma

Journal of the College of Physicians and Surgeons--Pakistan, 2016-11, Vol.26 (11), p.896-899

2016

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Retinoblastoma presenting as total hyphema: Three year follow-up

Saudi journal of ophthalmology, 2017-10, Vol.31 (4), p.272-274

2017

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Ophthalmic manifestations of linear nevus sebaceous/organoid nevus syndrome

Journal of the College of Physicians and Surgeons--Pakistan, 2015-03, Vol.25 (3), p.220-222

2015

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Anisometropia and Ptosis in Patients with Monocular Elevation Deficiency

Journal of the College of Physicians and Surgeons--Pakistan, 2016-10, Vol.26 (10), p.835-838

2016

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Outcome of surgical treatment of monocular elevation deficiency

Journal of the Pakistan Medical Association, 2012-04, Vol.62 (4), p.355-357

2012

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Duane's syndrome: surgical outcome and non ophthalmologic associations

Journal of Ayub Medical College, Abbottabad, 2014-07, Vol.26 (3), p.328-330

2014

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Retinoblastoma in an adult

BMC research notes, 2013-08, Vol.6 (1), p.304-304, Article 304

2013

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Factors associated with breast arterial calcification on mammography

Journal of the College of Physicians and Surgeons--Pakistan, 2013-03, Vol.23 (3), p.178-181

2013

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Clinical course of retinoblastoma

Journal of the College of Physicians and Surgeons--Pakistan, 2013-08, Vol.23 (8), p.566-569

2013

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Retinal detachment in paediatric patients

Journal of the College of Physicians and Surgeons--Pakistan, 2013-04, Vol.23 (4), p.261-264

2013

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Monocular elevation deficiency with associated dextrocardia and situs inversus

Saudi journal of ophthalmology, 2013-04, Vol.27 (2), p.121-123

2013

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Detachment of Descemet's membrane following stromal hydration in phacoemulsification surgery

Journal of the College of Physicians and Surgeons--Pakistan, 2008-03, Vol.18 (3), p.179-180

2008

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Ocular manifestations of mucopolysaccharidosis

Journal of the College of Physicians and Surgeons--Pakistan, 2008-11, Vol.18 (11), p.730-731

2008

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Ocular manifestations of xeroderma pigmentosum

Journal of the College of Physicians and Surgeons--Pakistan, 2007-12, Vol.17 (12), p.751-753

2007

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Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma

A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma

Variants in the PRPF8 Gene are Associated with Glaucoma

Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families

Variable retinal presentations in nanophthalmos

A case of systemic lupus erythematosus with aplastic anaemia

Effects of Artisan aphakic intraocular lens on central corneal thickness and intra ocular pressure in pediatric eyes with crystalline subluxated lenses

Ptosis associated with Monocular Elevation Deficiency

Congenital Cataract, Nasolacrimal Duct Obstruction, and Methicillin-Resistant Staphylococcus aureus Conjunctivitis: When to Operate?

Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome

Tumor Regression Patterns in Retinoblastoma

Retinoblastoma presenting as total hyphema: Three year follow-up

Ophthalmic manifestations of linear nevus sebaceous/organoid nevus syndrome

Anisometropia and Ptosis in Patients with Monocular Elevation Deficiency

Outcome of surgical treatment of monocular elevation deficiency

Duane's syndrome: surgical outcome and non ophthalmologic associations

Retinoblastoma in an adult

Factors associated with breast arterial calcification on mammography

Clinical course of retinoblastoma

Retinal detachment in paediatric patients

Monocular elevation deficiency with associated dextrocardia and situs inversus

Detachment of Descemet's membrane following stromal hydration in phacoemulsification surgery

Ocular manifestations of mucopolysaccharidosis

Ocular manifestations of xeroderma pigmentosum

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