ornithine and Cyst

ornithine has been researched along with Cyst 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
Abdel-Kader, AA; Elnahry, AG; Hassan, FK	1
Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S	1

Other Studies

2 other study(ies) available for ornithine and Cyst

Article	Year
Bevacizumab for the treatment of intraretinal cystic spaces in a patient with gyrate atrophy of the choroid and retina. Ophthalmic genetics, 2018, Volume: 39, Issue:6 Topics: Adolescent; Angiogenesis Inhibitors; Bevacizumab; Cysts; Female; Fluorescein Angiography; Gyrate Atrophy; Humans; Intravitreal Injections; Ornithine; Retinal Diseases; Tomography, Optical Coherence; Vascular Endothelial Growth Factor A; Visual Acuity; Visual Fields	2018
A novel mutation, P126R, in a Japanese patient with HHH syndrome. Pediatric neurology, 2002, Volume: 26, Issue:1 Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gene Expression; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Methionine; Mitochondrial Diseases; Molecular Sequence Data; Ornithine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Septum Pellucidum; Syndrome; Tomography, X-Ray Computed	2002

Article

Year

Bevacizumab for the treatment of intraretinal cystic spaces in a patient with gyrate atrophy of the choroid and retina.

Ophthalmic genetics, 2018, Volume: 39, Issue:6

Topics: Adolescent; Angiogenesis Inhibitors; Bevacizumab; Cysts; Female; Fluorescein Angiography; Gyrate Atrophy; Humans; Intravitreal Injections; Ornithine; Retinal Diseases; Tomography, Optical Coherence; Vascular Endothelial Growth Factor A; Visual Acuity; Visual Fields

2018

A novel mutation, P126R, in a Japanese patient with HHH syndrome.

Pediatric neurology, 2002, Volume: 26, Issue:1

Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gene Expression; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Methionine; Mitochondrial Diseases; Molecular Sequence Data; Ornithine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Septum Pellucidum; Syndrome; Tomography, X-Ray Computed

2002