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- Publisher Website: 10.1016/j.clineuro.2020.106258
- Scopus: eid_2-s2.0-85092026567
- PMID: 33031988
- WOS: WOS:000598721700008
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Article: Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype
Title | Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype |
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Authors | |
Keywords | TPK1 Dystonia Tremor Spasticity Movement disorders |
Issue Date | 2020 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/clineuro |
Citation | Clinical Neurology and Neurosurgery, 2020, v. 199, p. article no. 106258 How to Cite? |
Persistent Identifier | http://hdl.handle.net/10722/293870 |
ISSN | 2023 Impact Factor: 1.8 2023 SCImago Journal Rankings: 0.608 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Au, LWC | - |
dc.contributor.author | Lee, HCH | - |
dc.contributor.author | Sheng, B | - |
dc.contributor.author | Chan, KY | - |
dc.contributor.author | Yau, EKC | - |
dc.contributor.author | Mak, MC | - |
dc.contributor.author | Chan, AYW | - |
dc.contributor.author | Chan, AYY | - |
dc.contributor.author | Lau, CKY | - |
dc.contributor.author | Mok, VCT | - |
dc.contributor.author | Lam, CW | - |
dc.date.accessioned | 2020-11-23T08:22:59Z | - |
dc.date.available | 2020-11-23T08:22:59Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Clinical Neurology and Neurosurgery, 2020, v. 199, p. article no. 106258 | - |
dc.identifier.issn | 0303-8467 | - |
dc.identifier.uri | http://hdl.handle.net/10722/293870 | - |
dc.language | eng | - |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/clineuro | - |
dc.relation.ispartof | Clinical Neurology and Neurosurgery | - |
dc.subject | TPK1 | - |
dc.subject | Dystonia | - |
dc.subject | Tremor | - |
dc.subject | Spasticity | - |
dc.subject | Movement disorders | - |
dc.title | Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype | - |
dc.type | Article | - |
dc.identifier.email | Mak, MC: chloemak@HKUCC-COM.hku.hk | - |
dc.identifier.email | Lam, CW: ching-wanlam@pathology.hku.hk | - |
dc.identifier.authority | Lam, CW=rp00260 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.clineuro.2020.106258 | - |
dc.identifier.pmid | 33031988 | - |
dc.identifier.scopus | eid_2-s2.0-85092026567 | - |
dc.identifier.hkuros | 318967 | - |
dc.identifier.volume | 199 | - |
dc.identifier.spage | article no. 106258 | - |
dc.identifier.epage | article no. 106258 | - |
dc.identifier.isi | WOS:000598721700008 | - |
dc.publisher.place | Netherlands | - |
dc.identifier.issnl | 0303-8467 | - |