Zobrazeno 1 - 10
of 802
pro vyhledávání: '"Hedera P"'
Autor:
Hacker ML, Ploucher S, Naik AG, Turchan M, Meystedt JC, Harper K, Hedera P, Pirtle CJ, Stubblefield K, Charles D
Publikováno v:
Clinical Interventions in Aging, Vol Volume 15, Pp 655-662 (2020)
Mallory L Hacker,1,2 Shelby Ploucher,1,3 Aaditi G Naik,1,4 Maxim Turchan,1 Jacqueline C Meystedt,1 Kelly Harper,1 Peter Hedera,1 Claude J Pirtle,5 Kassandra Stubblefield,1 David Charles1 1Department of Neurology, Vanderbilt University Medical Center,
Externí odkaz:
https://doaj.org/article/61efc2398b9f4691b5a3dc838c25a6e2
Autor:
Hedera P
Publikováno v:
The Application of Clinical Genetics, Vol Volume 10, Pp 9-19 (2017)
Peter Hedera Department of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA Abstract: Wilson’s disease (WD), albeit relatively rare, is an important genetic metabolic disease because of highly effective therapies that can be life
Externí odkaz:
https://doaj.org/article/916b3e269378409eba3e8e85e41546c4
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Wilson disease (WD) is a rare disorder of copper metabolism, causing copper accumulation mainly in the liver and the brain. The prevalence of WD was previously estimated around 20 to 33.3 patients per million for the United States
Externí odkaz:
https://doaj.org/article/6bee8a7810134c238a92a9c16191f466
Autor:
Fabiola Di Dato, Peter Hedera
Publikováno v:
European Medical Journal, Pp 84-95 (2024)
Externí odkaz:
https://doaj.org/article/0d36099440074b36acc805812fa08903
Role of Botulinum Toxin in Treatment of Secondary Dystonia: A Case Series and Overview of Literature
Publikováno v:
Toxins, Vol 16, Iss 7, p 286 (2024)
Introduction: Dystonia can present in primary and secondary forms, depending on co-occurring symptoms and syndromic associations. In contrast to primary dystonia, secondary forms of dystonia are often associated with lesions in the putamen or globus
Externí odkaz:
https://doaj.org/article/e6eb781ea29242c68820fbce1e468df7
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-12 (2023)
Abstract Background Wilson disease (WD) is a genetic disorder of copper metabolism that leads to copper accumulation in various organs, primarily the liver and brain, resulting in heterogenous hepatic, neurologic, and psychiatric symptoms. Diagnosis
Externí odkaz:
https://doaj.org/article/3f9638a3b9774c02bf3f47133bacb39d
Akademický článek
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Akademický článek
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Autor:
Hedera Peter, Xiao Jianfeng, Puschmann Andreas, Momčilović Dragana, Wu Steve W, LeDoux Mark S
Publikováno v:
BMC Neurology, Vol 12, Iss 1, p 93 (2012)
Abstract Background Recently, heterozygous mutations in PRRT2 (Chr 16p11.2) have been identified in Han Chinese, Japanese and Caucasians with paroxysmal kinesigenic dyskinesia. In previous work, a paroxysmal kinesigenic dyskinesia locus was mapped to
Externí odkaz:
https://doaj.org/article/32012e44ca0b44f485e04acf62e00d1f
Publikováno v:
BMC Neurology, Vol 10, Iss 1, p 66 (2010)
Abstract Background There is an ongoing debate whether essential tremor (ET) represents a monosymptomatic disorder or other neurologic symptoms are compatible with the diagnosis of ET. Many patients with clinically definite ET develop dystonia. It re
Externí odkaz:
https://doaj.org/article/2f0c1db45d444529a1957b5c0e57c367