Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hanna Jedrzejowska"'
Autor:
William W. Pendlebury, Lester S. Adelman, Reid Taylor, Hanna Jedrzejowska, Hanna Drac, Irena Hausmanowa-Petruzewicz, Margaret Jenkison, Walter G. Bradley, David R. Rice
Publikováno v:
Archives of Neurology. 47:1013-1017
A progressive degenerative myopathy has been well described in hypokalemic periodic paralysis but is not as widely recognized in hyperkalemic periodic paralysis. We studied four families with the latter disease in which some members developed a progr
[Charcot-Marie Tooth type X (CMTX) disease: clinical and genetic characteristics of eleven patients]
Publikováno v:
Neurologia i neurochirurgia polska. 36(6)
Charcot-Marie-Tooth type X disease (CMTX) is the second most frequent inherited neuropathy, after CMT1A type associated with 17p11.2-p12 duplication. CMTX is inherited as X dominant trait and is caused by point mutations in Cx32 gene. In the study th
Autor:
Anatol Mickielewicz, Stanislaw Lopaciuk, Winnie Schröder, Ksenia Bykowska, Tadeusz Mendel, Jerzy Windyga, Hubert Kwiecinski, Anna Czlcankawska, Arletta Kuczynska-Zardzewialy, Dorota Szelagowska, Hanna Jedrzejowska, Falko H. Herrmann
Publikováno v:
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 7(4)
Ischemic stroke in young adults is a well-known disease, but despite extensive clinical and laboratory investigations, its etiology remains unclear in approximately half of the cases. We examined the prevalence of factor V Leiden, the prothrombin G20
Autor:
Andrzej Kochanski, Ann Lofgren, Hanna Jedrzejowska, Barbara Ryniewicz, Malwina Czarny-Ratajczak, Anna-Maria Barciszewska, Joanna Samocko, Irena Hausmanowa-Petrusewicz, Peter De Jonghe, Vincent Timmerman, Anna Latos-Bielenska
Publikováno v:
Human Mutation. 17:157
Autor:
Vincent Timmerman, Joanna Samocko, Malwina Czarny-Ratajczak, Barbara Ryniewicz, Ann Löfgren, Hanna Jedrzejowska, Peter De Jonghe, Anna-Maria Barciszewska, Andrzej Kochański, Irena Hausmanowa-Petrusewicz, Anna Latos-Bielenska
Publikováno v:
Human mutation
Mutation and Polymorphism Report Authors: Andrzej Kochanski, Ann Lofgren, Hanna Jedrzejowska, Barbara Ryniewicz, Malwina CzarnyRatajczak, Anna-Maria Barciszewska, Joanna Samocko, Irena Hausmanowa-Petrusewicz, Peter De Jonghe, Vincent Timmerman, and A
Autor:
Hanna Jedrzejowska, Hanna Drac
Publikováno v:
Acta Neuropathologica. 37:213-217
An 8-year-old boy with a slowly progressive motor neuropathy is described. The first signs appeared at the age of 3 years. Histological examination of the sural nerve showed the presence of numerous segmental axonal swellings and features of demyelin
Publikováno v:
Acta Neuropathologica. 49:163-168
A case of intoxication with Phytosol (an insecticide) in a 29-year-old man is described. Ingestion of Phytosol (suicide attempt) produced signs of cholinergic crisis followed, after 16 days, by features of peripheral neuropathy and later, with the re
Publikováno v:
Italian journal of neurological sciences. 2(3)
A case of hereditary neuropathy with liability to pressure palsies is described. The main histological findings in sural nerve were focal thickenings of myelin-"sausages", "tomaculae"-and wide variability of internodal length. Numerous fibers with si
Autor:
Hanna Jedrzejowska
Publikováno v:
Acta neuropathologica. 37(2)
Two sporadic cases of amyloid polyneuropathy with clinical features corresponding to the Portuguese type of this disease were studied. Histological examination of sural nerve demonstrated a marked loss of myelinated and unmyelinated fibres in the cas
Autor:
Hanna Jedrzejowska
Publikováno v:
Life sciences (1962). 3
The literature concerning the pathologic changes of the intramuscular nerve fibers in muscular dystrophy is scanty. The common opinion is that lesions in the motor nerve fibers occur during the advanced stage of the disease. The Coers and Woolf (1) i