choline has been researched along with Neuronal Ceroid-Lipofuscinoses in 4 studies
Neuronal Ceroid-Lipofuscinoses: A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Late juvenile neuronal ceroid lipofuscinosis (NCL) is a lysosomal neurodegenerative disorder caused by the accumulation of lipopigment in neurons." | 1.30 | MR imaging and localized proton MR spectroscopy in late infantile neuronal ceroid lipofuscinosis. ( Grodd, W; Klose, U; Nägele, T; Schwab, A; Seeger, U; Seitz, D, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Vanhanen, SL | 1 |
| Puranen, J | 2 |
| Autti, T | 2 |
| Raininko, R | 1 |
| Liewendahl, K | 1 |
| Nikkinen, P | 1 |
| Santavuori, P | 2 |
| Suominen, P | 1 |
| Vuori, K | 1 |
| Häkkinen, AM | 2 |
| Sitter, B | 1 |
| Tyynelä, J | 1 |
| Sonnewald, U | 1 |
| Bathen, TF | 1 |
| Haltia, MJ | 1 |
| Paetau, A | 1 |
| Polvikoski, T | 1 |
| Gribbestad, IS | 1 |
| Brockmann, K | 1 |
| Pouwels, PJ | 1 |
| Christen, HJ | 1 |
| Frahm, J | 1 |
| Hanefeld, F | 1 |
| Seitz, D | 1 |
| Grodd, W | 1 |
| Schwab, A | 1 |
| Seeger, U | 1 |
| Klose, U | 1 |
| Nägele, T | 1 |
4 other studies available for choline and Neuronal Ceroid-Lipofuscinoses
| Article | Year |
|---|---|
Neuroradiological findings (MRS, MRI, SPECT) in infantile neuronal ceroid-lipofuscinosis (infantile CLN1) at different stages of the disease.
Topics: Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatinine; Humans; Infant; Infant, Newborn; | 2004 |
High-resolution magic angle spinning and 1H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3.
Topics: Adolescent; Adult; Analysis of Variance; Aspartic Acid; Brain; Brain Chemistry; Child; Child, Presch | 2004 |
Localized proton magnetic resonance spectroscopy of cerebral metabolic disturbances in children with neuronal ceroid lipofuscinosis.
Topics: Aspartic Acid; Brain; Brain Diseases, Metabolic; Brain Mapping; Child; Child, Preschool; Choline; Cr | 1996 |
MR imaging and localized proton MR spectroscopy in late infantile neuronal ceroid lipofuscinosis.
Topics: Aspartic Acid; Brain; Brain Diseases; Case-Control Studies; Cerebellum; Cerebral Ventricles; Child; | 1998 |