glutamic acid and Eye Diseases, Hereditary

glutamic acid has been researched along with Eye Diseases, Hereditary in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Andrews, C; Balasubramanian, R; Chan, WM; Chew, S; Engle, EC; Kang, PB; MacKinnon, SE	1
Fawzi, A; He, S; Lim, JI; O'Hearn, TM; Rao, NA	1

Other Studies

2 other study(ies) available for glutamic acid and Eye Diseases, Hereditary

Article	Year
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome. The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3 Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Developmental Disabilities; Endocrine System Diseases; Eye Diseases, Hereditary; Female; Fibrosis; Glutamic Acid; Humans; Kallmann Syndrome; Lysine; Male; Ophthalmoplegia; Pedigree; Phenotype; Syndrome; Tubulin	2015
Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF. The British journal of ophthalmology, 2007, Volume: 91, Issue:12 Topics: Adult; Age of Onset; Amyloid Neuropathies, Familial; Asian People; Eye Diseases, Hereditary; Fluorescein Angiography; Fundus Oculi; Glutamic Acid; Glycine; Humans; Male; Mutation; Prealbumin; Vascular Endothelial Growth Factor A; Vitrectomy; Vitreous Body	2007

Article

Year

Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndrome.

The Journal of clinical endocrinology and metabolism, 2015, Volume: 100, Issue:3

Topics: Adult; Aged; Amino Acid Substitution; Child; Child, Preschool; Developmental Disabilities; Endocrine System Diseases; Eye Diseases, Hereditary; Female; Fibrosis; Glutamic Acid; Humans; Kallmann Syndrome; Lysine; Male; Ophthalmoplegia; Pedigree; Phenotype; Syndrome; Tubulin

2015

Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.

The British journal of ophthalmology, 2007, Volume: 91, Issue:12

Topics: Adult; Age of Onset; Amyloid Neuropathies, Familial; Asian People; Eye Diseases, Hereditary; Fluorescein Angiography; Fundus Oculi; Glutamic Acid; Glycine; Humans; Male; Mutation; Prealbumin; Vascular Endothelial Growth Factor A; Vitrectomy; Vitreous Body

2007