tyrosine and Eye Abnormalities

tyrosine has been researched along with Eye Abnormalities 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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Eccles, MR; Walker, RJ; Wilson, JC; Yoon, HS	1
Liu, J; Wang, J; Zhang, Q	1

Other Studies

2 other study(ies) available for tyrosine and Eye Abnormalities

Article	Year
A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2007, Volume: 22, Issue:5 Topics: Adult; Aged; Biopsy; Collagen Type IV; Cysteine; Eye Abnormalities; Female; Genetic Linkage; Glomerular Basement Membrane; Hearing Loss; Humans; Kidney; Male; Middle Aged; Mutation; Nephritis, Hereditary; New Zealand; Pedigree; Renal Insufficiency; Tyrosine	2007
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome. Molecular vision, 2007, Jan-26, Volume: 13 Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Forkhead Box Protein L2; Forkhead Transcription Factors; Guanine; Heterozygote; Histidine; Humans; Mutation; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Serine; Syndrome; Thymine; Tyrosine	2007

Article

Year

A novel Cys1638Tyr NC1 domain substitution in alpha5(IV) collagen causes Alport syndrome with late onset renal failure without hearing loss or eye abnormalities.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2007, Volume: 22, Issue:5

Topics: Adult; Aged; Biopsy; Collagen Type IV; Cysteine; Eye Abnormalities; Female; Genetic Linkage; Glomerular Basement Membrane; Hearing Loss; Humans; Kidney; Male; Middle Aged; Mutation; Nephritis, Hereditary; New Zealand; Pedigree; Renal Insufficiency; Tyrosine

2007

FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.

Molecular vision, 2007, Jan-26, Volume: 13

Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Forkhead Box Protein L2; Forkhead Transcription Factors; Guanine; Heterozygote; Histidine; Humans; Mutation; Mutation, Missense; Polymorphism, Single-Stranded Conformational; Serine; Syndrome; Thymine; Tyrosine

2007