tyrosine and Concomitant Strabismus

tyrosine has been researched along with Concomitant Strabismus in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Cadilla, CL; García-Rodríguez, O; Izquierdo, NJ; Jardón, J; Renta, JY	1
O'Halloran, MT; Yu, JS	1

Other Studies

2 other study(ies) available for tyrosine and Concomitant Strabismus

Article	Year
Ocular Findings in Patients with the Hermansky-Pudlak Syndrome (Types 1 and 3). Ophthalmic genetics, 2016, Volume: 37, Issue:1 Topics: Adolescent; Adult; Aged; Carrier Proteins; Child; DNA Mutational Analysis; Exons; Eye Color; Female; Hermanski-Pudlak Syndrome; Humans; Intracellular Signaling Peptides and Proteins; Iris Diseases; Male; Membrane Proteins; Membrane Transport Proteins; Middle Aged; Mutation; Polymerase Chain Reaction; Retinal Diseases; Retrospective Studies; Strabismus; Tyrosine; Vision Disorders; Visual Acuity; Young Adult	2016
Children of mothers with phenylketonuria. Lancet (London, England), 1970, Jan-31, Volume: 1, Issue:7640 Topics: Adolescent; Adult; Child; Child, Preschool; Diet Therapy; Family Planning Services; Female; Growth Disorders; Heart Defects, Congenital; Heterozygote; Homozygote; Humans; Intellectual Disability; Male; Microcephaly; Middle Aged; Phenylalanine; Phenylketonurias; Seizures; Strabismus; Tyrosine	1970

Article

Year

Ocular Findings in Patients with the Hermansky-Pudlak Syndrome (Types 1 and 3).

Ophthalmic genetics, 2016, Volume: 37, Issue:1

Topics: Adolescent; Adult; Aged; Carrier Proteins; Child; DNA Mutational Analysis; Exons; Eye Color; Female; Hermanski-Pudlak Syndrome; Humans; Intracellular Signaling Peptides and Proteins; Iris Diseases; Male; Membrane Proteins; Membrane Transport Proteins; Middle Aged; Mutation; Polymerase Chain Reaction; Retinal Diseases; Retrospective Studies; Strabismus; Tyrosine; Vision Disorders; Visual Acuity; Young Adult

2016

Children of mothers with phenylketonuria.

Lancet (London, England), 1970, Jan-31, Volume: 1, Issue:7640

Topics: Adolescent; Adult; Child; Child, Preschool; Diet Therapy; Family Planning Services; Female; Growth Disorders; Heart Defects, Congenital; Heterozygote; Homozygote; Humans; Intellectual Disability; Male; Microcephaly; Middle Aged; Phenylalanine; Phenylketonurias; Seizures; Strabismus; Tyrosine

1970