choline has been researched along with Optic Atrophy in 5 studies
Optic Atrophy: Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.
Excerpt | Relevance | Reference |
---|---|---|
"Choline treatments could restore the membrane lipids, repair cellular organelles and protect mutant cells from acute iron overload." | 1.56 | Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. ( Agarwal, P; Bakovic, M; Brady, L; Distelmaier, F; Dolinsky, VW; Fagerberg, CR; Gade, E; Hejbøl, EK; Jamra, RA; Kibæk, M; Klee, D; Larsen, MJ; Markovic, L; Nagy, P; Rouse, N; Schrøder, HD; Seibt, A; Tarnopolsky, M; Taylor, A; Wieczorek, D, 2020) |
"Neuromyelitis optica is a rare, severe idiopathic disease that predominantly involves optic nerves and spinal cord." | 1.39 | Unusual manifestations of pediatric neuromyelitis optica. ( Kiresi, D; Yavuz, H, 2013) |
"PEHO syndrome is a rare symptom complex of severe progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy." | 1.33 | Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome. ( Boltshauser, E; Huisman, TA; Klein, A; Straube, T; Werner, B, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (60.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Fagerberg, CR | 1 |
Taylor, A | 1 |
Distelmaier, F | 1 |
Schrøder, HD | 1 |
Kibæk, M | 1 |
Wieczorek, D | 1 |
Tarnopolsky, M | 1 |
Brady, L | 1 |
Larsen, MJ | 1 |
Jamra, RA | 1 |
Seibt, A | 1 |
Hejbøl, EK | 1 |
Gade, E | 1 |
Markovic, L | 1 |
Klee, D | 1 |
Nagy, P | 1 |
Rouse, N | 1 |
Agarwal, P | 1 |
Dolinsky, VW | 1 |
Bakovic, M | 1 |
Yavuz, H | 1 |
Kiresi, D | 1 |
Marszał, E | 1 |
Jamroz, E | 1 |
Paprocka, J | 1 |
Kluczewska, E | 1 |
Sokół, M | 1 |
Jurkiewicz, E | 1 |
Mierzewska, H | 1 |
Bekiesińska-Figatowska, M | 1 |
Pakua-Kościesza, I | 1 |
Kmieć, T | 1 |
Scheper, G | 1 |
van der Knaap, MS | 1 |
Pronicka, E | 1 |
Huisman, TA | 1 |
Klein, A | 1 |
Werner, B | 1 |
Straube, T | 1 |
Boltshauser, E | 1 |
5 other studies available for choline and Optic Atrophy
Article | Year |
---|---|
Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration.
Topics: Adolescent; Antigens, CD; Ataxia; Atrophy; Cerebellum; Choline; Cognitive Dysfunction; Cytoplasmic V | 2020 |
Unusual manifestations of pediatric neuromyelitis optica.
Topics: Adolescent; Anti-Inflammatory Agents; Azathioprine; Brain; Choline; Diagnosis, Differential; Disease | 2013 |
Leukoencephalopathy with macrocephaly and mild clinical course.
Topics: Abnormalities, Multiple; Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatinine; Dementi | 2004 |
MRI of a family with leukoencephalypathy with vanishing white matter.
Topics: Adolescent; Amino Acid Substitution; Aspartic Acid; Brain; Case-Control Studies; Cerebellar Ataxia; | 2005 |
Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome.
Topics: Aspartic Acid; Atrophy; Brain Diseases; Brain Edema; Cerebellum; Child; Choline; Creatine; Diffusion | 2006 |