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Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome

Ophthalmology (Rochester, Minn.), 2014-07, Vol.121 (7), p.1461-1468

2014

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HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1−/− Mice

American journal of human genetics, 2012-07, Vol.91 (1), p.171-179

2012

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The clinical spectrum of homozygous HOXA1 mutations

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1235-1240

2008

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Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2

Ophthalmic genetics, 2016-06, Vol.37 (2), p.130-136

2016

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The genetics of nonsyndromic bilateral Duane retraction syndrome

Journal of AAPOS, 2016-10, Vol.20 (5), p.396-400.e2

2016

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Ophthalmic Features of Joubert Syndrome

Ophthalmology (Rochester, Minn.), 2008-12, Vol.115 (12), p.2286-2289

2008

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Visual Loss in Orbitofacial Neurofibromatosis Type 1

Ophthalmology (Rochester, Minn.), 2012-10, Vol.119 (10), p.2168-2173

2012

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Bilateral Synergistic Convergence Associated with Homozygous ROB03 Mutation (p.Pro771Leu)

Ophthalmology (Rochester, Minn.), 2008-12, Vol.115 (12), p.2262-2265

2008

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Long-term Results of an Intraoperative Adjustable Superior Oblique Tendon Suture Spacer Using Nonabsorbable Suture for Brown Syndrome

Ophthalmology (Rochester, Minn.), 2008-10, Vol.115 (10), p.1800-1804

2008

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Ophthalmoplegia and Congenital Cranial Dysinnervation Disorders

Journal of binocular vision and ocular motility, 2018-01, Vol.68 (1), p.31-33

Oystreck, Darren T.

2018

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Ocular motility abnormalities in orbitofacial neurofibromatosis type 1

Journal of AAPOS, 2014-08, Vol.18 (4), p.338-343

2014

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A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

Brain (London, England : 1878), 2013-02, Vol.136 (Pt 2), p.522-535

2013

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Congenital cranial dysinnervation disorders: a concept in evolution

Current opinion in ophthalmology, 2013-09, Vol.24 (5), p.398-406

2013

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Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

BMC medical genetics, 2011-02, Vol.12 (1), p.31-31, Article 31

2011

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Ophthalmic features of ataxia telangiectasia–like disorder

Journal of AAPOS, 2008-04, Vol.12 (2), p.186-189

2008

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Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

Nature genetics, 2005-10, Vol.37 (10), p.1035-1037

2005

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When straight eyes won't move: phenotypic overlap of genetically distinct ocular motility disturbances

Canadian journal of ophthalmology, 2011-12, Vol.46 (6), p.477-480

2011

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Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders

Journal of neuro-ophthalmology, 2011-03, Vol.31 (1), p.69-77

2011

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The neurology of carbonic anhydrase type II deficiency syndrome

Brain (London, England : 1878), 2011-12, Vol.134 (12), p.3499-3512

2011

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Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A

Brain (London, England : 1878), 2006-09, Vol.129 (9), p.2363-2374

2006

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Duane Retraction Syndrome Associated with a Small X Chromosome Deletion

Canadian journal of neurological sciences, 2016-05, Vol.43 (3), p.445-447

2016

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NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS-SAYRE SYNDROME

Retinal cases & brief reports, 2018, Vol.12 (4), p.349-358

2018

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CCDD Phenotype Associated with a Small Chromosome 2 Deletion

Seminars in ophthalmology, 2015-11, Vol.30 (5-6), p.435-442

2015

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Variable Ptosis after Botulinum Toxin Type A Injection with Positive Ice Test Mimicking Ocular Myasthenia Gravis

Journal of neuro-ophthalmology, 2013-06, Vol.33 (2), p.169-171

2013

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Synergistic Divergence: A Distinct Ocular Motility Dysinnervation Pattern

Investigative ophthalmology & visual science, 2009-11, Vol.50 (11), p.5213-5216

2009

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Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1−/− Mice

The clinical spectrum of homozygous HOXA1 mutations

Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2

The genetics of nonsyndromic bilateral Duane retraction syndrome

Ophthalmic Features of Joubert Syndrome

Visual Loss in Orbitofacial Neurofibromatosis Type 1

Bilateral Synergistic Convergence Associated with Homozygous ROB03 Mutation (p.Pro771Leu)

Long-term Results of an Intraoperative Adjustable Superior Oblique Tendon Suture Spacer Using Nonabsorbable Suture for Brown Syndrome

Ophthalmoplegia and Congenital Cranial Dysinnervation Disorders

Ocular motility abnormalities in orbitofacial neurofibromatosis type 1

A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3

Congenital cranial dysinnervation disorders: a concept in evolution

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

Ophthalmic features of ataxia telangiectasia–like disorder

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

When straight eyes won't move: phenotypic overlap of genetically distinct ocular motility disturbances

Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders

The neurology of carbonic anhydrase type II deficiency syndrome

Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A

Duane Retraction Syndrome Associated with a Small X Chromosome Deletion

NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS-SAYRE SYNDROME

CCDD Phenotype Associated with a Small Chromosome 2 Deletion

Variable Ptosis after Botulinum Toxin Type A Injection with Positive Ice Test Mimicking Ocular Myasthenia Gravis

Synergistic Divergence: A Distinct Ocular Motility Dysinnervation Pattern

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