Lista de obras - Adriano Magli - Dominio Público Uruguay

A Case of Parinaud’s Syndrome in a Boy with Delayed Puberty

Adalimumab for juvenile idiopathic arthritis-associated uveitis

artículo científico publicado en 2013

Augmented vertical rectus transpositions: Intraoperative measurement of torsion following sequential muscle detachment

artículo científico publicado en 2020

Bilateral methicillin-resistant Staphylococcus aureus keratitis following hyperopic photorefractive surgery

artículo científico publicado en 2012

CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX

artículo científico publicado en 2002

Cataract management in juvenile idiopathic arthritis: simultaneous versus secondary intraocular lens implantation

artículo científico publicado en 2013

Coloboma of the lens associated with coloboma of the alar nasal cartilages in a pair of female monozygotic twins: A new syndrome?

Developmental visual deprivation: long term effects on human cone driven retinal function.

artículo científico publicado en 2017

Epithelium-Off Corneal Collagen Cross-linking Versus Transepithelial Cross-linking for Pediatric Keratoconus

Essential infantile esotropia: postoperative motor outcomes and inferential analysis of strabismus surgery

artículo científico publicado en 2014

Evaluation of retinal nerve fiber layer and ganglion cell complex thickness after ocular blunt trauma

artículo científico publicado en 2013

Familial juvenile nephronophthisis and associated ocular anomalies (Senior's syndrome). A study of three families

Functional changes after treatment of optic pathway paediatric low-grade gliomas

artículo científico publicado en 2013

Genetic and ultrasound study of abnormalities of the optic nerve head

artículo científico publicado en 1985

Genetic and ultrasound study of hereditary pure microphthalmos

Hereditary colobomatous anomalies of the optic nerve head*

artículo científico publicado en 1986

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

artículo científico publicado en 2003

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

artículo científico publicado en 2010

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).

artículo científico publicado en 2004

Long-Term Follow-Up after Surgery for Congenital and Developmental Cataracts

artículo científico publicado en 2014

Long-Term Outcomes of Primary Intraocular Lens Implantation for Unilateral Congenital Cataract

artículo científico publicado en 2015

Long-term development of refractive error in refractive, nonrefractive and partially accommodative esotropia

scientific article published in PLoS ONE

Long-term outcome of primary versus secondary intraocular lens implantation after simultaneous removal of bilateral congenital cataract

article published in 2012

Lower Eyelid Surgery for Lagophthalmos in Möbius and Poland-Möbius Syndromes

article

Measuring contrast sensitivity in aretinopathic patients with insulin dependent diabetes mellitus

artículo científico publicado en 1996

Molecular and clinical characterization of albinism in a large cohort of Italian patients

artículo científico publicado en 2011

Ocular coloboma with congenital heart disease in the absence of chromosomal abnormalities.

artículo científico publicado en 1980

Ocular complications of eyebrow piercing

artículo científico publicado en 2008

Optical coherence tomography angiography for the measurement of optic disc: Macular relationship

artículo científico publicado en 2020

Refractive surgery for accommodative esotropia: 5-year follow-up

artículo científico publicado en 2014

Reoperation in esotropic Duane retraction syndrome: Long-term motor outcome of superior rectus transposition

scientific article published on 30 December 2019

Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly.

artículo científico publicado en 2008

Spontaneous Resolution of Congenital Bilateral Brown’s Syndrome

The Annette von Droste-Hulshoff syndrome: Pseudostrabismus due to macular ectopia in retinopathy of prematurity

artículo científico publicado en 1988

Treatment of infantile capillary hemangioma of the eyelid with systemic propranolol

artículo científico publicado en 2012

Unilateral Inferior Altitudinal Hemianopsia, Argyll Robertson Pupil and Dendritic Keratitis in a Young Patient with Herpes Zoster

Visual dysfunction in patients with mitochondrial myopathies

artículo científico publicado en 1995

Lista de obras de Adriano Magli

A Case of Parinaud’s Syndrome in a Boy with Delayed Puberty

Adalimumab for juvenile idiopathic arthritis-associated uveitis

Augmented vertical rectus transpositions: Intraoperative measurement of torsion following sequential muscle detachment

Bilateral methicillin-resistant Staphylococcus aureus keratitis following hyperopic photorefractive surgery

CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX

Cataract management in juvenile idiopathic arthritis: simultaneous versus secondary intraocular lens implantation

Coloboma of the lens associated with coloboma of the alar nasal cartilages in a pair of female monozygotic twins: A new syndrome?

Developmental visual deprivation: long term effects on human cone driven retinal function.

Epithelium-Off Corneal Collagen Cross-linking Versus Transepithelial Cross-linking for Pediatric Keratoconus

Essential infantile esotropia: postoperative motor outcomes and inferential analysis of strabismus surgery

Evaluation of retinal nerve fiber layer and ganglion cell complex thickness after ocular blunt trauma

Familial juvenile nephronophthisis and associated ocular anomalies (Senior's syndrome). A study of three families

Functional changes after treatment of optic pathway paediatric low-grade gliomas

Genetic and ultrasound study of abnormalities of the optic nerve head

Genetic and ultrasound study of hereditary pure microphthalmos

Hereditary colobomatous anomalies of the optic nerve head*

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).

Long-Term Follow-Up after Surgery for Congenital and Developmental Cataracts

Long-Term Outcomes of Primary Intraocular Lens Implantation for Unilateral Congenital Cataract

Long-term development of refractive error in refractive, nonrefractive and partially accommodative esotropia

Long-term outcome of primary versus secondary intraocular lens implantation after simultaneous removal of bilateral congenital cataract

Lower Eyelid Surgery for Lagophthalmos in Möbius and Poland-Möbius Syndromes

Measuring contrast sensitivity in aretinopathic patients with insulin dependent diabetes mellitus

Molecular and clinical characterization of albinism in a large cohort of Italian patients

Ocular coloboma with congenital heart disease in the absence of chromosomal abnormalities.

Ocular complications of eyebrow piercing

Optical coherence tomography angiography for the measurement of optic disc: Macular relationship

Refractive surgery for accommodative esotropia: 5-year follow-up

Reoperation in esotropic Duane retraction syndrome: Long-term motor outcome of superior rectus transposition

Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly.

Spontaneous Resolution of Congenital Bilateral Brown’s Syndrome

The Annette von Droste-Hulshoff syndrome: Pseudostrabismus due to macular ectopia in retinopathy of prematurity

Treatment of infantile capillary hemangioma of the eyelid with systemic propranolol

Unilateral Inferior Altitudinal Hemianopsia, Argyll Robertson Pupil and Dendritic Keratitis in a Young Patient with Herpes Zoster

Visual dysfunction in patients with mitochondrial myopathies