| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| N Hemanth Kumar, K Joy Mounika, N V Sundarachar. Adolescent/Adult-Onset Leukodystrophy with MTHFR Deficiency - A Treatable Cause. Neurology India. vol 71. issue 2. 2023-05-06. PMID:37148062. |
patients typically present with a progressive syndrome including various combinations of cognitive impairment, movement disorders, ataxia, and upper motor neuron signs. |
2023-05-06 |
2023-08-14 |
Not clear |
| Daniel Moo. Disorders of Movement due to Acquired and Traumatic Brain Injury. Current physical medicine and rehabilitation reports. 2022-09-27. PMID:36164499. |
thus, these patients may exhibit signs of both upper motor neuron syndrome and movement disorder simultaneously which can further complicate diagnosis and management. |
2022-09-27 |
2023-08-14 |
Not clear |
| David S Lynch, Charles Wade, Anderson Rodrigues Brandão de Paiva, Nevin John, Justin A Kinsella, Áine Merwick, Rebekah M Ahmed, Jason D Warren, Catherine J Mummery, Jonathan M Schott, Nick C Fox, Henry Houlden, Matthew E Adams, Indran Davagnanam, Elaine Murphy, Jeremy Chatawa. Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era. Journal of neurology, neurosurgery, and psychiatry. vol 90. issue 5. 2020-03-19. PMID:30467211. |
patients typically present with a progressive syndrome including various combinations of cognitive impairment, movement disorders, ataxia and upper motor neuron signs. |
2020-03-19 |
2023-08-13 |
Not clear |
| David S Lynch, Anderson Rodrigues Brandão de Paiva, Wei Jia Zhang, Enrico Bugiardini, Fernando Freua, Leandro Tavares Lucato, Lucia Inês Macedo-Souza, Rahul Lakshmanan, Justin A Kinsella, Aine Merwick, Alexander M Rossor, Nin Bajaj, Brian Herron, Paul McMonagle, Patrick J Morrison, Deborah Hughes, Alan Pittman, Matilde Laurà, Mary M Reilly, Jason D Warren, Catherine J Mummery, Jonathan M Schott, Matthew Adams, Nick C Fox, Elaine Murphy, Indran Davagnanam, Fernando Kok, Jeremy Chataway, Henry Houlde. Clinical and genetic characterization of leukoencephalopathies in adults. Brain : a journal of neurology. vol 140. issue 5. 2017-10-30. PMID:28334938. |
they are associated with a spectrum of clinical phenotypes dominated by dementia, psychiatric changes, movement disorders and upper motor neuron signs. |
2017-10-30 |
2023-08-13 |
Not clear |
| Lucas R Smith, Henry G Chambers, Shankar Subramaniam, Richard L Liebe. Transcriptional abnormalities of hamstring muscle contractures in children with cerebral palsy. PloS one. vol 7. issue 8. 2013-01-21. PMID:22956992. |
cerebral palsy (cp) is an upper motor neuron disease that results in a spectrum of movement disorders. |
2013-01-21 |
2023-08-12 |
Not clear |
| Rebecca M Wolf Gilbert, Stanley Fahn, Hiroshi Mitsumoto, Lewis P Rowlan. Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes. Movement disorders : official journal of the Movement Disorder Society. vol 25. issue 12. 2010-12-28. PMID:20669307. |
by using the columbia university division of movement disorders database, we reviewed data from 5,500 cases of parkinsonism and recorded the presence of upper motor neuron (umn) dysfunction, lower motor neuron (lmn) dysfunction, or both. |
2010-12-28 |
2023-08-12 |
Not clear |
| Lucas R Smith, Eva Pontén, Yvette Hedström, Samuel R Ward, Henry G Chambers, Shankar Subramaniam, Richard L Liebe. Novel transcriptional profile in wrist muscles from cerebral palsy patients. BMC medical genomics. vol 2. 2009-12-14. PMID:19602279. |
cerebral palsy (cp) is an upper motor neuron disease that results in a progressive movement disorder. |
2009-12-14 |
2023-08-12 |
Not clear |
| Cindy B Ivanhoe, Timothy A Reistette. Spasticity: the misunderstood part of the upper motor neuron syndrome. American journal of physical medicine & rehabilitation. vol 83. issue 10 Suppl. 2004-11-02. PMID:15448572. |
contracture, hypertonia, weakness, and movement disorders can all coexist as a result of the upper motor neuron syndrome. |
2004-11-02 |
2023-08-12 |
Not clear |
| D A Maschka, N M Bauman, P B McCray, H T Hoffman, M P Karnell, R J Smit. A classification scheme for paradoxical vocal cord motion. The Laryngoscope. vol 107. issue 11 Pt 1. 1997-12-16. PMID:9369385. |
we propose that pvcm be classified according to its underlying etiology and recognize the following causes of the disorder: 1. brainstem compression; 2. cortical or upper motor neuron injury; 3. nuclear or lower motor neuron injury; 4. movement disorder; 5. gastroesophageal reflux; 6. factitious or malingering disorder; 7. somatization/conversion disorder. |
1997-12-16 |
2023-08-12 |
Not clear |
| W Cordell, H Feue. Premonitory neurologic signs in a patient with an acute vertex epidural hematoma. The American journal of emergency medicine. vol 1. issue 3. 1985-03-15. PMID:6680633. |
prior to the onset of signs of midbrain compression, the patient developed an excrutiating headache, a movement disorder, and upper motor neuron signs. |
1985-03-15 |
2023-08-12 |
Not clear |
| H D Langoh. [Biochemical studies on muscles in neurogenic atrophies and central paralysis. Studies of the trophic functions of neurons]. Fortschritte der Medizin. vol 98. issue 39. 1981-01-26. PMID:7429410. |
we assume that this reduction is due to general inactivity which is caused by the movement disorder rather than to the particular influence of the upper motor neuron. |
1981-01-26 |
2023-08-12 |
Not clear |