Zobrazeno 1 - 10
of 124
pro vyhledávání: '"B. Emeryk-Szajewska"'
Publikováno v:
Acta Neurologica Scandinavica. 60:170-177
This paper presents two juvenile cases of familial amyotrophic lateral sclerosis. They are the first and fourth child in a family with seven children from the eastern part of Finland. All seven children, as well as the parents, were examined by our g
Autor:
Angela Vincent, Anna Kostera-Pruszczyk, B. Emeryk-Szajewska, M. H. Strugalska-Cynowska, M. Dutkiewicz, Hubert Kwieciński, Anna Kamińska
Publikováno v:
European Journal of Neurology. 15:720-724
Background and purpose: MuSK-positive myasthenia gravis (MG) is diagnosed in 0–48% of cases with generalized seronegative MG in different populations. The presence of anti-MuSK antibodies generally relates to a severe course and lack of response to
Autor:
B. Emeryk-Szajewska, A. Karwańska, Katarzyna Rowińska-Marcińska, Anna Kostera-Pruszczyk, Irena Niebroj-Dobosz
Publikováno v:
Acta Neurologica Scandinavica. 106:34-38
Objectives– Electrophysiological studies of amyotrophic lateral sclerosis (ALS) patients reveal not only lower motor neuron involvement, but also widespread signs of its hyperexcitability. They might be the consequence of changes in the level of am
Autor:
B, Emeryk-Szajewska, J, Kopeć
Publikováno v:
Electromyography and clinical neurophysiology. 48(6-7)
The study was aimed to evaluate the EMG pattern in myopathy, in the muscles with early, slight abnormalities and in the muscles severely affected, and to analyze the sequence of abnormalities appearing with the progress of the impairment.Fifty one bo
Autor:
B, Emeryk-Szajewska, J, Kopeć
Publikováno v:
Electromyography and clinical neurophysiology. 48(6-7)
The aim of this study was to compare the electromyographic pattern in Becker muscular dystrophy (BMD) with that found in Duchenne muscular dystrophy (DMD).Fourteen men with BMD and 51 boys with DMD were investigated. Proximal muscles were examined: m
Autor:
A, Kostera-Pruszczyk, A, Kamińska, M, Dutkiewicz, B, Emeryk-Szajewska, M H, Strugalska-Cynowska, A, Vincent, H, Kwieciński
Publikováno v:
European journal of neurology. 15(7)
MuSK-positive myasthenia gravis (MG) is diagnosed in 0-48% of cases with generalized seronegative MG in different populations. The presence of anti-MuSK antibodies generally relates to a severe course and lack of response to thymectomy. We analyzed f
Autor:
B, Emeryk-Szajewska
Publikováno v:
Supplements to Clinical neurophysiology. 53
Autor:
J, Kopec, B, Emeryk-Szajewska
Publikováno v:
Electromyography and clinical neurophysiology. 42(8)
In classical quantitative analysis motor unit action potentials (MUAPs) parameters are useful in establishing diagnosis, but not in monitoring the functional status as expressed by clinical sings. This drawback is overcome by our new method called "F
Autor:
A, Kostera-Pruszczyk, I, Niebroj-Dobosz, B, Emeryk-Szajewska, A, Karwańska, K, Rowińska-Marcińska
Publikováno v:
Acta neurologica Scandinavica. 106(1)
Electrophysiological studies of amyotrophic lateral sclerosis (ALS) patients reveal not only lower motor neuron involvement, but also widespread signs of its hyperexcitability. They might be the consequence of changes in the level of amino acids acti
Autor:
B Emeryk-Szajewska, Anna Kostera-Pruszczyk, T Nowak-Michalska, Beata Szyluk, Halina Strugalska-Cynowska, Katarzyna Rowińska-Marcińska, J Switalska
Publikováno v:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 113(4)
Objectives : Approximately 50% of patients treated with thymectomy have a chance for symptom-free life. However, immunological and neurophysiological abnormalities may be detected in patients with clinical remission. Although improvement usually para