Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2001 2
2002 2
2003 1
2011 1
2014 1
2018 1
2019 1
2021 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

10 results

Results by year

Filters applied: . Clear all
Page 1
Dystonia: an update on phenomenology, classification, pathogenesis and treatment.
Balint B, Bhatia KP. Balint B, et al. Curr Opin Neurol. 2014 Aug;27(4):468-76. doi: 10.1097/WCO.0000000000000114. Curr Opin Neurol. 2014. PMID: 24978640 Review.
Clinical and genetic heterogeneity underlie myoclonus-dystonia, dopa-responsive dystonia and deafness-dystonia syndrome. ALS2 gene mutations are a newly recognized cause for combined dystonia. ...
Clinical and genetic heterogeneity underlie myoclonus-dystonia, dopa-responsive dystonia and deafness-dystonia syndrome …
The genetics of primary dystonias and related disorders.
Németh AH. Németh AH. Brain. 2002 Apr;125(Pt 4):695-721. doi: 10.1093/brain/awf090. Brain. 2002. PMID: 11912106 Review.
Conditions discussed in detail include idiopathic torsion dystonia (DYT1), focal dystonias (DYT7) and mixed dystonias (DYT6 and DYT13), dopa-responsive dystonia, myoclonus dystonia, rapid-onset dystonia parkinsonism, Fahr disease, Aicardi-Goutieres syndrome, Hallervorden-Spatz sy …
Conditions discussed in detail include idiopathic torsion dystonia (DYT1), focal dystonias (DYT7) and mixed dystonias (DYT6 and DYT13), dopa …
Protein import into mitochondria.
Paschen SA, Neupert W. Paschen SA, et al. IUBMB Life. 2001 Sep-Nov;52(3-5):101-12. doi: 10.1080/15216540152845894. IUBMB Life. 2001. PMID: 11798021 Free article. Review.
In addition, the molecular basis of a new human mitochondrial disorder is discussed, the Mohr-Tranebjaerg syndrome. This is the first known disease, which is caused by an impaired mitochondrial protein import machinery leading to progressive neurodegeneration …
In addition, the molecular basis of a new human mitochondrial disorder is discussed, the Mohr-Tranebjaerg syndrome. Thi …
Underappreciated Roles of the Translocase of the Outer and Inner Mitochondrial Membrane Protein Complexes in Human Disease.
Heinemeyer T, Stemmet M, Bardien S, Neethling A. Heinemeyer T, et al. DNA Cell Biol. 2019 Jan;38(1):23-40. doi: 10.1089/dna.2018.4292. Epub 2018 Nov 27. DNA Cell Biol. 2019. PMID: 30481057 Review.
Pathogenic mutations have been identified in the TIMM8A (DDP) and DNAJC19 (TIMM14) genes and are linked to Mohr-Tranebjaerg syndrome and dilated cardiomyopathy syndrome (with and without ataxia), respectively. ...
Pathogenic mutations have been identified in the TIMM8A (DDP) and DNAJC19 (TIMM14) genes and are linked to Mohr-Tranebjaerg …
The mitochondrial connection in auditory neuropathy.
Cacace AT, Pinheiro JM. Cacace AT, et al. Audiol Neurootol. 2011;16(6):398-413. doi: 10.1159/000323276. Epub 2011 Jan 22. Audiol Neurootol. 2011. PMID: 21266802 Review.
These observations are based on the expression of AN in known mitochondrial-based neurological diseases (Friedreich's ataxia, Mohr-Tranebjaerg syndrome), in conditions where defects in axonal transport, protein trafficking, and fusion processes perturb and/or …
These observations are based on the expression of AN in known mitochondrial-based neurological diseases (Friedreich's ataxia, Mohr- …
Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene.
Binder J, Hofmann S, Kreisel S, Wöhrle JC, Bäzner H, Krauss JK, Hennerici MG, Bauer MF. Binder J, et al. Brain. 2003 Aug;126(Pt 8):1814-20. doi: 10.1093/brain/awg174. Epub 2003 Jun 4. Brain. 2003. PMID: 12805099 Review.
The Mohr-Tranebjaerg syndrome (MTS) is a rare neurodegenerative disorder characterized by early-onset deafness, dystonia and further neurological abnormalities such as cortical blindness, spasticity, dementia and mental retardation. ...
The Mohr-Tranebjaerg syndrome (MTS) is a rare neurodegenerative disorder characterized by early-onset deafness, dystoni …
[Mohr-Tranebjaerg syndrome].
Yamamoto K, Ikeda S. Yamamoto K, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:385-8. Nihon Rinsho. 2002. PMID: 12013893 Review. Japanese. No abstract available.
Protein translocation into mitochondria: the role of TIM complexes.
Bauer MF, Hofmann S, Neupert W, Brunner M. Bauer MF, et al. Trends Cell Biol. 2000 Jan;10(1):25-31. doi: 10.1016/s0962-8924(99)01684-0. Trends Cell Biol. 2000. PMID: 10603473 Review.
This review discusses recent advances in understanding the structure and function of the translocases of the inner membrane and the possible role of Tim proteins in the development of the Mohr-Tranebjaerg syndrome, a mitochondrial disorder leading to neurodeg …
This review discusses recent advances in understanding the structure and function of the translocases of the inner membrane and the possible …
[Mohr-Tranebjaerg syndrome].
Ohkoshi N. Ohkoshi N. Ryoikibetsu Shokogun Shirizu. 2001;(36):213-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596373 Review. Japanese. No abstract available.