Frank A Proudlock Selected Research

autosomal recessive Spastic paraplegia 15

10/2005

Kjellin syndrome: first case with retinal changes in carriers.

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Frank A Proudlock Research Topics

Disease

6	Albinism 11/2020 - 10/2013
4	Color Vision Defects (Color Blindness) 01/2016 - 05/2011
3	Amblyopia (Lazy Eye) 12/2016 - 04/2005
2	Glaucoma 01/2020 - 01/2019
2	Refractive Errors (Refractive Error) 12/2016 - 01/2016
2	Optic Nerve Diseases (Optic Neuropathy) 01/2016 - 02/2014
1	Ganglion Cysts (Ganglion) 07/2022
1	congenital fibrosis of the extraocular muscles 03/2021
1	Atrophy 01/2021
1	Cysts 01/2021
1	Cognitive Dysfunction 01/2021
1	Retinopathy of Prematurity (Retrolental Fibroplasia) 08/2020
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	X-Linked Infantile Nystagmus 02/2014
1	Diabetic Retinopathy (Retinopathy, Diabetic) 02/2014
1	Pathologic Nystagmus 03/2009
1	autosomal recessive Spastic paraplegia 15 10/2005

Drug/Important Bio-Agent (IBA)

17	Retinaldehyde (Retinal)IBA 07/2022 - 10/2005
1	poly(dG-dA)n.poly(dC-dT)n (((GA)n))IBA 08/2020
1	Biomarkers (Surrogate Marker)IBA 01/2018
1	Melanins (Melanin)IBA 01/2017
1	Memantine (Namenda)FDA Link 03/2009

Therapy/Procedure

2	Therapeutics 12/2016 - 04/2005
1	Telescopes 07/2010