Zobrazeno 1 - 10
of 73
pro vyhledávání: '"T. T. Warner"'
Publikováno v:
Advances in Geosciences, Vol 12, Pp 159-164 (2008)
As a first step toward downscaling global model simulations of future climates for the eastern Mediterranean Sea and surrounding land area, mesoscale-model simulations with the Pennsylvania State University – National Center for Atmospheric Researc
Externí odkaz:
https://doaj.org/article/d96377122867485c9cc17eea0006135f
Autor:
M R Placzek, T T Warner
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 73:5ii-11
To the casual observer, the clinical neurologist and molecular geneticist would appear very different species. On closer inspection, however, they actually have a number of similarities: they both use a rather impenetrable language littered with abbr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe006062a9b5f9e9a67930e6bb9a10f2
https://doi.org/10.1136/jnnp.73.suppl_2.ii5
https://doi.org/10.1136/jnnp.73.suppl_2.ii5
Autor:
P R Jarman, T T Warner
Publikováno v:
Journal of Medical Genetics. 35:314-318
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::058f5f20a7a7b82709112961d8308e01
https://doi.org/10.1136/jmg.35.4.314
https://doi.org/10.1136/jmg.35.4.314
Autor:
Stanley Fahn, T. G. Nygaard, Ryan J. Uitti, Gary A. Heiman, Neil Risch, A. E. Harding, Demetrius M. Maraganore, T. T. Warner, Paul Greene, Susan B. Bressman, Patricia L. Kramer, D. Raymond, Blair Ford, Deborah de Leon, Laura Almasy
Publikováno v:
Annals of Neurology. 40:681-684
Clinical-genetic studies of idiopathic torsion dystonia (ITD) indicate that the DYT1 gene on chromosome 9q34 is responsible for most childhood limb-onset disease. The genetic basis of adult-onset ITD is less well studied. In most multiplex adult-onse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd5f4565f7bbfd606a03ad0589786594
https://doi.org/10.1002/ana.410400421
https://doi.org/10.1002/ana.410400421
Autor:
A, Granata, T T, Warner
Publikováno v:
European journal of neurology. 17
DYT1 dystonia is an autosomal-dominant movement disorder, characterised by early onset of involuntary sustained muscle contractions. It is caused by a 3-bp deletion in the DYT1 gene, which results in the deletion of a single glutamate residue in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::53b16729c1db03a158475694cfe29787
https://pubmed.ncbi.nlm.nih.gov/20590813
https://pubmed.ncbi.nlm.nih.gov/20590813
Publikováno v:
Meteorology and Atmospheric Physics. 49:209-227
The Penn State University/National Center for Atmospheric Research (PSU/NCAR) mesoscale model is a widely used research tool that has been applied in a wide variety of real-data, mesoalpha-scale applications. Recently a nonhydrostatic version of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14eb1e90d90f178d5f921c6ce028055c
https://doi.org/10.1007/bf01025408
https://doi.org/10.1007/bf01025408
Publikováno v:
Annals of neurology. 48(1)
We studied in vivo muscle energy metabolism in patients with Huntington's disease (HD) and dentatorubropallidoluysian atrophy (DRPLA) using 31P magnetic resonance spectroscopy (MRS). Twelve gene-positive HP patients (4 presymptomatic patients) and 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c725bb2e52cc3008536e6d47a2064fcb
https://pubmed.ncbi.nlm.nih.gov/10894218
https://pubmed.ncbi.nlm.nih.gov/10894218
Autor:
T T Warner, P Jarman
Since the introduction of the term dystonia by Oppenheim in 1911 to describe altering muscle tone and postural deformities seen in patients,1 there has been considerable controversy surrounding its aetiology, classification, and genetics. Dystonia ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9407e06043a3c69c8aa2f14489668214
https://europepmc.org/articles/PMC2170035/
https://europepmc.org/articles/PMC2170035/
Publikováno v:
Rheumatology. 39:1433-1434
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::858e8a841fcc6eecb2e968cff5b7baca
https://doi.org/10.1093/rheumatology/39.12.1433
https://doi.org/10.1093/rheumatology/39.12.1433
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 71:709-709
We read with interest the recent report by Castlenovo et al of the first reported case of Friedreich's ataxia presenting with a pure spastic paraparesis.1 Since the identification of the frataxin gene in 1996 the phenotypic range of Friedreich's atax
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f26d6a18cf770986bb4f675dc06eb302
https://doi.org/10.1136/jnnp.71.5.709
https://doi.org/10.1136/jnnp.71.5.709