Zobrazeno 1 - 6
of 6
pro vyhledávání: '"J. L. Steckley"'
Publikováno v:
Scopus-Elsevier
The authors report an autosomal dominant episodic ataxia that is clinically distinct from the other episodic ataxias. Vestibular ataxia, vertigo, tinnitus, and interictal myokymia are prominent; attacks are diminished by acetazolamide. Linkage analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06cfd63fe0bde55349c1e5ffbf28d5a6
https://ora.ox.ac.uk/objects/uuid:a8e9c0d6-2426-4f05-afad-3edeb026b1ee
https://ora.ox.ac.uk/objects/uuid:a8e9c0d6-2426-4f05-afad-3edeb026b1ee
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 35:98-101
A 68-year-old Caucasian male presented to emergency with a spontaneous sudden onset headache localized behind the left eye. Pain was severe and associated with vomiting, agitation, anxiety, memory loss, and word-finding difficulty. There was no prece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b01235484966b355726079e0ab6194e
https://doi.org/10.1017/s0317167100007642
https://doi.org/10.1017/s0317167100007642
Autor:
Shih-Han S. Huang, Maria Carmela Tartaglia, J. L. Steckley, Robert Hammond, C. Hyson, Hasini Reddy
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 36(1)
A 40-year old female presented to the emergency room at London Health Sciences Centre with a one week history of gradually progressive right leg weakness which had caused several falls. She also described numbness of the right arm and leg. In the two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577ffda0ec53449ea228419f398c159d
https://pubmed.ncbi.nlm.nih.gov/19294898
https://pubmed.ncbi.nlm.nih.gov/19294898
Publikováno v:
Neurology. 65(1)
Episodic ataxias are ion channel disorders characterized by attacks of incoordination. The authors performed a genome-wide screen in a large pedigree segregating a novel episodic ataxia and found significant linkage on 1q42 with a multipoint lod scor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8295f1b6868b878a5546051d80523a92
http://ora.ox.ac.uk/objects/uuid:eec2924b-6c23-4bc3-8389-faf12cefa487
http://ora.ox.ac.uk/objects/uuid:eec2924b-6c23-4bc3-8389-faf12cefa487
Autor:
Neil Risch, Gabriele C. DeLuca, K Morrison, David A. Dyment, J L Steckley, G C Ebers, Cristen J. Willer, M Z Cader, A D Sadovnick
Publikováno v:
Genes and immunity. 5(5)
A total of 267 families with two or more siblings with multiple sclerosis (MS) were genotyped with 14 restriction fragment length polymorphisms at the TCR beta locus. A nonparametric linkage analysis of the data showed no evidence for linkage to this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3dd93e45b5396a65ca2c84031733d24
https://pubmed.ncbi.nlm.nih.gov/15175643
https://pubmed.ncbi.nlm.nih.gov/15175643
Publikováno v:
Scopus-Elsevier
Article abstract The objective of this study was to investigate genes involved in the metabolism and function of vitamin D as candidate genes for genetic susceptibility to MS. Restriction fragment length polymorphisms and highly polymorphic microsate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b425263f856a46529c3215c2c52e712
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034620555&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034620555&partnerID=MN8TOARS