Zobrazeno 1 - 10
of 149
pro vyhledávání: '"H, Skre"'
Autor:
H. Skre
Publikováno v:
Clinical Genetics. 5:163-172
A scoring system for neurological signs based on the clinical examination was applied to a randomized population sample of adults and to three kindreds with hereditary neurological disease. To achieve qualitative properties of the system, nine subtes
Autor:
Kristian Berg, H. Skre
Publikováno v:
Clinical Genetics. 11:57-66
Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism were observed in two kindreds, and they were found to occur togetherin 9 out of 10 affected individuals. The last patient had Marinesco-Sjøgren syndrome without manifestations of hypogon
Publikováno v:
Clinical Genetics. 5:196-204
In a sibship occurring in a kindred with a high degree of inbreeding, four persons with an auto-somal recessive type of cerebellar ataxia all had total albinism (tyrosinase-negative, as judged from investigation of the prohand). Of the five healthy s
Autor:
H. Skre
Publikováno v:
Clinical Genetics. 7:287-298
Friedreich's ataxia (FA) was investigated in Western Norway, an area comprising several isolated communities and with a population of 725,000 as at 1 January 1968. The prevalence of FA was estimated to be 1/100,000 in this population. An autosomal re
Autor:
H. Skre
Publikováno v:
Acta Neurologica Scandinavica. 46:288-289
Autor:
S E Johnson, H Skre
Publikováno v:
Stroke. 17:662-666
During an investigation of coronary risk factors, a population 20 to 54 years old in Tromsø, Northern Norway was screened for transient ischemic cerebral attacks. Three simple screening questions were used. Sixteen thousand six hundred and twenty-on
Autor:
R. Matre, J. Fagius, H. Jacobsen, H. Skre, Harald Nyland, Christian A. Vedeler, Johan A. Aarli, P. O. Osterman, R. W. C. Janzen
Publikováno v:
Journal of Neurology. 228:59-64
The mixed haemagglutination technique was used to demonstrate IgG antibodies to peripheral nerve tissue in sera from patients with the Guillain-Barré syndrome. The clinical effect and the effect on the antibodies of plasma exchange were examined in
Autor:
D.E. Wilson, P. Shaffer-Berman, E. Solomon, N. Shimizu, S. Goss, P. DeBona, A.G. Steinberg, R.M. Siervogel, A.S. Henderson, T.-S. Chan, J.E. Anderson, A.B. Deisseroth, J.A. Anderson, D. Weil, A.D. Merritt, M. Velivasakis, D. Cox, P. Meera Khan, K.M. Overton, G.B. Côté, E. Lovrien, J.A. Brown, S. Chen, C. Finaz, R.H. Schwartz, I.W. Craig, J. Courval, B. Olaisen, P. Teisberg, J.A. Robinson, P.L. Pearson, M.C. DuVal, N. Busby, M. Ray, T.P. Webb, R.H. Kennett, C.J. Chern, P.J. Davies, I. Schreuder, B. Kaiser McCaw, H. Wyandt, J. Mohr, A. Icén, K.E. Buckton, A.R. Dunn, A.W. Nienhuis, J.V. Higgins, R.G. Worton, P.J.L. Cook, G. Spowart, J.A. Norton, J.E. Noades, R.S. Kucherlapati, W.S. Volkers, T.B. Shows, H. Wang, R.A. Raeburn, Matthew Parks, R.E. Magenis, M. Bobrow, S. Hansen, H.M. Dick, S.H. Boyer, S.H. Hsu, Veronica van Heyningen, K.R.M. Pai, R.A. Fisher, D.P. Aden, C.A. Slaughter, A.B. Bijnen, R.D. Koler, S. Guttormsen, R. Sanger, D. Linder, F. Hecht, D. Bacon, R.B. Surana, P.L. Yu, L.A. Klobutcher, O. Smithies, T.T. Puck, D.A. Hopkinson, D. Warburton, D. Shaw, K. Berg, S.J. Goss, L.L.L. Wijnen, D.A. Meyers, A. Heiberg, T. Gedde-Dahl, E. Hackel, C. Cochet, J. Frézal, C.M. Giles, A.A. Biegel, I.P. Gormley, M. Smith, F.-T. Kao, P. Vuopio, B. Schacter, B. Clark, J.D. Minna, T.A. Tedesco, M.G. Brown, C.J. Glueck, K.G. Orkwiszewski, H. Skre, K. Hirschhorn, N. Van Cong, W.F. Bodmer, W.G. Burgerhout, B.A. Doppert, W. Bodmer, G. Skude, A. Boué, E.A. Jones, K.C. Atwood, S. McDonald, C.M. Croce, E. Eicher, E.S. Seravalli, R.C.P. Go, C.G. Palmer, E.B. Robson, K. Bender, D.A. Aitken, R.P. Creagan, W.F. Anderson, P.H. Gallimore, J.B. Dossetor, W. Putt, M. Lewis, V. Lewis, F.H. Ruddle, J. Ott, H. Eiberg, M. Rivas, T.H. Marshall, M.E. Hodes, K.D. Smith, P. Bowen, A.P.M. Jongsma, R. Bigley, N. Lea, G.F. Brooks, H. Kaita, L. Wisniewski, E.R. Giblett, H.E. Faber, R.C. Elston, P. Couillin, W.B. Bias, H. Koprowski, R. Rebourcet, C.T. Falk, M.T. Yu, L.J. Stevens, U. Francke, J.J. van Rood, G. Pontecorvo, P.E. Polani, D. Patterson, E.W. Lovrien, E.A. Nichols, J.L. Hamerton, D.P. Singal, J.K. McDougall, M.L. Rivas, T. Reber, B.H. Petersen, S. Povey, Erik Thorsby, G. Khoury, E. Tolley, W.R. Breg, T. Hassold, L. Kunkel, R.L. Eddy, L.L. Haley, J. Shuster, M.A. Ferguson-Smith, D.W. Buck, R.M. Denney, K. Lange, F.H. Allen, B.R. Migeon, P. Goodfellow, R. Kucherlapati, L.R. Weitkamp, J. de Grouchy, B.M. Turner, S.S. Wachtel, T. Mohandas, P.M. Conneally, M. Siniscalco, M.D. Poulik, R. Velez, A. Hershberg, B. Moore, G.C. Koo, V.M. Chapman, A. Westerveld, B. Hellkuhl, H.P. Klinger, D. Bootsma, K.K. Namboodiri, G. Wullems, O.J. Miller, P. Gold, P. Perry, P.J. McAlpine, P.A. Lalley, A. Brøgger, J. Schlaut, M.W. Thompson, A. de la Chapelle, B. Chown, A.G. Searle, I. Pagan-Charry, C. Jones, J. van der Horst, H. van Someren, K. Willecke, E. Johnston, J.H. Edwards, W.J. Mellman, K.-H. Grzeschik, S. Ohno, P. Teesdale, C.S.N. Lee, L. Wang, V.S. Turner
Publikováno v:
Cytogenetic and Genome Research. 16:449-452
Publikováno v:
European Neurology. 18:73-78
A 51-year-old man who died of Creutzfeldt-Jakob disease (CJD), had transient dyskinesias with intention myoclonus and exaggerated startle reaction in early life. This may suggest a link between myoclonic encephalopathy of infants and CJD, and an incu
Autor:
H. Skre
Publikováno v:
Acta Neurologica Scandinavica. 48:575-606
The prevalence of neurological signs in the normal population was investigated in order to establish their significance when found in patients. The traditional neurological examination is characterized by the registration of various reflexes, motor a