SCOPUS 정보 검색 플랫폼

Movement Disorders

Volumn 26, Issue 12, 2011, Pages 2296-2297

Expanding the phenomenology of benign hereditary chorea: Evolution from chorea to myoclonus and dystonia

(5) Armstrong, Melissa J a Shah, Binit B a Chen, Robert a Angel, Michael J a Lang, Anthony E a

a UNIVERSITY OF TORONTO (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

THYROID TRANSCRIPTION FACTOR 1;

ADULT; CASE REPORT; DISEASE COURSE; DYSTONIA; ELECTROMYOGRAM; ELECTROPHYSIOLOGY; FEMALE; HUMAN; HUNTINGTON CHOREA; INTRON; INVOLUNTARY MOVEMENT; LETTER; MYOCLONUS; PHENOMENOLOGY; PRIORITY JOURNAL;

CHOREA; DISEASE PROGRESSION; DYSTONIA; ELECTROMYOGRAPHY; FEMALE; HUMANS; MYOCLONUS; NUCLEAR PROTEINS; TRANSCRIPTION FACTORS; YOUNG ADULT;

EID: 80055091462 PISSN: 08853185 EISSN: 15318257 Source Type: Journal
DOI: 10.1002/mds.23822 Document Type: Letter

Times cited : (16)

References (8)

1
- 0034073531
- Benign hereditary chorea-entity or syndrome?
- Schrag A, Quinn NP, Bhatia KP, Marsden CD. Benign hereditary chorea-entity or syndrome? Mov Disord 2000; 15: 280-288.
- (2000) Mov Disord , vol.15 , pp. 280-288
- Schrag, A.¹ Quinn, N.P.² Bhatia, K.P.³ Marsden, C.D.⁴

2
- 0042845864
- Benign hereditary chorea: clinical, genetic, and pathological findings
- Kleiner-Fisman G, Rogaeva E, Halliday W, et al. Benign hereditary chorea: clinical, genetic, and pathological findings. Ann Neurol 2003; 54: 244-247.
- (2003) Ann Neurol , vol.54 , pp. 244-247
- Kleiner-Fisman, G.¹ Rogaeva, E.² Halliday, W.³

3
- 20444412260
- A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa
- Asmus F, Horber V, Pohlenz J, et al. A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa. Neurology 2005; 64: 1952-1954.
- (2005) Neurology , vol.64 , pp. 1952-1954
- Asmus, F.¹ Horber, V.² Pohlenz, J.³

4
- 28344435213
- Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea
- do Carmo Costa M, Costa C, Silva AP, et al. Nonsense mutation in TITF1 in a Portuguese family with benign hereditary chorea. Neurogenetics 2005; 6: 209-215.
- (2005) Neurogenetics , vol.6 , pp. 209-215
- do Carmo Costa, M.¹ Costa, C.² Silva, A.P.³

5
- 57049181326
- Psychosis, short stature in benign hereditary chorea: a novel thyroid transcription factor-1 mutation
- Glik A, Vuillaume I, Devos D, Inzelberg R. Psychosis, short stature in benign hereditary chorea: a novel thyroid transcription factor-1 mutation. Mov Disord 2008; 23: 1744-1747.
- (2008) Mov Disord , vol.23 , pp. 1744-1747
- Glik, A.¹ Vuillaume, I.² Devos, D.³ Inzelberg, R.⁴

6
- 37549028382
- Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia
- Asmus F, Devlin A, Munz M, Zimprich A, Gasser T, Chinnery PF. Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia. Mov Disord 2007; 22: 2104-2109.
- (2007) Mov Disord , vol.22 , pp. 2104-2109
- Asmus, F.¹ Devlin, A.² Munz, M.³ Zimprich, A.⁴ Gasser, T.⁵ Chinnery, P.F.⁶

7
- 36649028914
- Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea
- Provenzano C, Veneziano L, Appleton R, Frontali M, Civitareale D. Functional characterization of a novel mutation in TITF-1 in a patient with benign hereditary chorea. J Neurol Sci 2008; 264: 56-62.
- (2008) J Neurol Sci , vol.264 , pp. 56-62
- Provenzano, C.¹ Veneziano, L.² Appleton, R.³ Frontali, M.⁴ Civitareale, D.⁵

8
- 67651146609
- "Jerky" dystonia in children: spectrum of phenotypes and genetic testing
- Asmus F, Langseth A, Doherty E, et al. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing. Mov Disord 2009; 24: 702-709.
- (2009) Mov Disord , vol.24 , pp. 702-709
- Asmus, F.¹ Langseth, A.² Doherty, E.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.