Irene Gottlob Selected Research

Color Vision Defects (Color Blindness)

1/2022	Normal and abnormal foveal development.
1/2021	Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia.
1/2016	Pediatric Optical Coherence Tomography in Clinical Practice-Recent Progress.
10/2015	Retinal Development in Infants and Young Children with Achromatopsia.
9/2014	Re: Sundaram et al.: retinal structure and function in achromatopsia: implications for gene therapy (Ophthalmology 2014;121:234-45).
9/2012	Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia.
8/2011	Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
5/2011	High-resolution in vivo imaging in achromatopsia.

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Irene Gottlob Research Topics

Disease

11	Albinism 11/2020 - 08/2011
8	Color Vision Defects (Color Blindness) 01/2022 - 05/2011
5	Amblyopia (Lazy Eye) 06/2019 - 04/2005
3	X-Linked Infantile Nystagmus 02/2014 - 01/2010
2	congenital fibrosis of the extraocular muscles 03/2021 - 12/2003
2	Glaucoma 01/2020 - 01/2019
2	Esotropia (Esophoria) 01/2020 - 01/2018
2	Refractive Errors (Refractive Error) 12/2016 - 01/2016
2	Optic Nerve Diseases (Optic Neuropathy) 01/2016 - 02/2014
2	Pathologic Nystagmus 03/2009 - 11/2002
2	Strabismus (Squint) 10/2006 - 12/2003
1	Ganglion Cysts (Ganglion) 07/2022
1	Atrophy 01/2021
1	Blindness (Hysterical Blindness) 01/2021
1	Cysts 01/2021
1	Cognitive Dysfunction 01/2021
1	Retinopathy of Prematurity (Retrolental Fibroplasia) 08/2020
1	Microcephaly 01/2018
1	Schizophrenia (Dementia Praecox) 01/2018
1	Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders) 01/2017
1	Optic Nerve Hypoplasia 03/2014
1	Papilledema 02/2014
1	Diabetic Retinopathy (Retinopathy, Diabetic) 02/2014
1	Neuroblastoma 01/2010
1	Nervous System Diseases (Neurological Disorders) 01/2010
1	Weight Gain 02/2008
1	Trochlear Nerve Diseases (Fourth Nerve Palsy) 02/2008
1	Amyloidosis 07/2007
1	Congenital Nystagmus 02/2007
1	autosomal recessive Spastic paraplegia 15 10/2005
1	3B Congenital Fibrosis of Extraocular Muscles 12/2003
1	Disease Progression 12/2002
1	Multiple Sclerosis 11/2002

Drug/Important Bio-Agent (IBA)

26	Retinaldehyde (Retinal)IBA 07/2022 - 10/2005
5	Proteins (Proteins, Gene)FDA Link 01/2020 - 12/2003
3	Memantine (Namenda)FDA Link 03/2009 - 02/2007
3	Gabapentin (Neurontin)FDA LinkGeneric 02/2008 - 11/2002
1	poly(dG-dA)n.poly(dC-dT)n (((GA)n))IBA 08/2020
1	Long Noncoding RNAIBA 01/2020
1	MicroRNAs (MicroRNA)IBA 01/2020
1	Atropine FDA LinkGeneric 06/2019
1	Tryptophan (L-Tryptophan)FDA Link 01/2018
1	Biomarkers (Surrogate Marker)IBA 01/2018
1	Melanins (Melanin)IBA 01/2017
1	Protein Isoforms (Isoforms)IBA 04/2016
1	Cholinergic ReceptorsIBA 04/2016
1	Myosin Heavy Chains (Myosin Heavy Chain)IBA 04/2016
1	Brain-Derived Neurotrophic Factor (BDNF)IBA 04/2016
1	Tretinoin (Retinoic Acid)FDA LinkGeneric 01/2010
1	TubulinIBA 01/2010
1	Amyloid (Amyloid Fibrils)IBA 07/2007
1	Pharmaceutical PreparationsIBA 02/2007
1	Mydriatics (Cycloplegics)IBA 10/2006
1	KinesinsIBA 12/2003
1	Anti-Bacterial Agents (Antibiotics)IBA 12/2002

Therapy/Procedure

3	Therapeutics 06/2019 - 04/2005
3	Telescopes 06/2019 - 12/2003
1	Aftercare (After-Treatment) 10/2006