carnitine has been researched along with Motor Neuron Disease in 2 studies
Motor Neuron Disease: Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Foley, AR | 1 |
| Menezes, MP | 1 |
| Pandraud, A | 1 |
| Gonzalez, MA | 1 |
| Al-Odaib, A | 1 |
| Abrams, AJ | 1 |
| Sugano, K | 1 |
| Yonezawa, A | 1 |
| Manzur, AY | 1 |
| Burns, J | 1 |
| Hughes, I | 1 |
| McCullagh, BG | 1 |
| Jungbluth, H | 1 |
| Lim, MJ | 1 |
| Lin, JP | 1 |
| Megarbane, A | 1 |
| Urtizberea, JA | 1 |
| Shah, AH | 1 |
| Antony, J | 1 |
| Webster, R | 1 |
| Broomfield, A | 1 |
| Ng, J | 1 |
| Mathew, AA | 1 |
| O'Byrne, JJ | 1 |
| Forman, E | 1 |
| Scoto, M | 1 |
| Prasad, M | 1 |
| O'Brien, K | 1 |
| Olpin, S | 1 |
| Oppenheim, M | 1 |
| Hargreaves, I | 1 |
| Land, JM | 1 |
| Wang, MX | 1 |
| Carpenter, K | 1 |
| Horvath, R | 1 |
| Straub, V | 1 |
| Lek, M | 1 |
| Gold, W | 1 |
| Farrell, MO | 1 |
| Brandner, S | 1 |
| Phadke, R | 1 |
| Matsubara, K | 1 |
| McGarvey, ML | 1 |
| Scherer, SS | 1 |
| Baxter, PS | 1 |
| King, MD | 1 |
| Clayton, P | 1 |
| Rahman, S | 1 |
| Reilly, MM | 1 |
| Ouvrier, RA | 1 |
| Christodoulou, J | 1 |
| Züchner, S | 1 |
| Muntoni, F | 1 |
| Houlden, H | 1 |
| Bonne, G | 1 |
| Benelli, C | 1 |
| De Meirleir, L | 1 |
| Lissens, W | 1 |
| Chaussain, M | 1 |
| Diry, M | 1 |
| Clot, JP | 1 |
| Ponsot, G | 1 |
| Geoffroy, V | 1 |
| Leroux, JP | 1 |
2 other studies available for carnitine and Motor Neuron Disease
| Article | Year |
|---|---|
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
Topics: Adolescent; Brain; Bulbar Palsy, Progressive; Carnitine; Child; Child, Preschool; Exome; Female; Gen | 2014 |
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy.
Topics: Base Sequence; Carnitine; Child; DNA; DNA Mutational Analysis; Drug Therapy, Combination; Humans; Ly | 1993 |