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of 74
pro vyhledávání: '"H J, Gdynia"'
Publikováno v:
Fortschritte der Neurologie · Psychiatrie. 82:695-697
Beim Posterioren Reversiblen Enzephalopathiesyndrom (PRES) handelt es sich in der Regel um eine gutartige und potenziell ruckbildungsfahige Erkrankung. In der Literatur wurden dennoch Falle mit schwerwiegendem Krankheitsverlauf beschrieben, genauere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e176d9fdbcb5f4105bda0f780974f48
https://doi.org/10.1055/s-0034-1385441
https://doi.org/10.1055/s-0034-1385441
Akademický článek
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Publikováno v:
Fortschritte der Neurologie-Psychiatrie. 82(12)
Posterior reversible encephalopathy syndrome (PRES) is widely held to be a benign and potentially reversible disease. However, severe cases have been described in the literature. Data on the long-term outcome of these severe cases are scarce. Further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45aacddc9659381df8c2daf79a6b125f
https://pubmed.ncbi.nlm.nih.gov/25489757
https://pubmed.ncbi.nlm.nih.gov/25489757
Publikováno v:
Der Nervenarzt. 85(2)
The diagnosis of intensive care unit acquired weakness (ICUAW) in the setting of neurological rehabilitation is steadily increasing. This is due to the fact that the intensive care of patients with sepsis or after cardiac or abdominal surgery is impr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1fa4e73dacf345f47594996de00d40af
https://pubmed.ncbi.nlm.nih.gov/24463649
https://pubmed.ncbi.nlm.nih.gov/24463649
Publikováno v:
Fortschritte der Neurologie-Psychiatrie. 80(6)
Since valosin-containing protein mutations were reported as a cause of hereditary inclusion body myositis associated with Paget's disease of the bone and frontotemporal dementia, many new mutations have been described in the last decade. We report on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa7f404169fb2dc2f3f421234cd041f5
https://pubmed.ncbi.nlm.nih.gov/22644520
https://pubmed.ncbi.nlm.nih.gov/22644520
Publikováno v:
European journal of neurology. 19(5)
Tick-borne encephalitis (TBE) is caused by a RNA-virus and is in about 50% of cases characterized by a biphasic clinical course in adults. Different clinical syndromes have been described, including meningitis, meningoencephalitis, meningoencephalomy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b602b53ab9f662688c07980cbf4a50e8
https://pubmed.ncbi.nlm.nih.gov/22289138
https://pubmed.ncbi.nlm.nih.gov/22289138
Publikováno v:
Fortschritte der Neurologie-Psychiatrie. 77(2)
With higher age, monoclonal gammopathies are more frequently diagnosed as the underlying cause of polyneuropathies. Whereas in approximately one-third of the patients, the gammopathy is related to multiple myeloma, lymphoma, other lymphoproliferative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a7b00b62c8a7473dc501978a47b06b3
https://pubmed.ncbi.nlm.nih.gov/19221974
https://pubmed.ncbi.nlm.nih.gov/19221974
Publikováno v:
European journal of medical research. 13(10)
Progressive infantile spastic tetraparesis spans a wide spectrum of partially rare differential diagnoses. Based on a clinical example the differential diagnostic thoughts are discussed in detail. Though juvenile motor neuron disease is a rare entity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f66e5fd8cb43ced1eaa458d630d9f15b
https://pubmed.ncbi.nlm.nih.gov/19008170
https://pubmed.ncbi.nlm.nih.gov/19008170
Publikováno v:
Der Nervenarzt. 79(4)
Granulomatous myositis is a rare neuromuscular disorder histologically characterized by the development of endomyseal and/or perimyseal granulomas. Clinical hallmarks are generalized muscle weakness, myalgias, and bulbar symptoms. The association of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8ccbace034850ef8ac28dce4dadc8d9
https://pubmed.ncbi.nlm.nih.gov/18210045
https://pubmed.ncbi.nlm.nih.gov/18210045
Publikováno v:
Der Internist. 49(1)
Cerebral toxoplasmosis nearly exclusively affects immunodeficient or immunocompromised patients. Mostly, it is a reactivation of latent toxoplasmosis. The pathogens, persisting in the reticuloendothelial system of heart and skeletal muscle cells, are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c67cd20fc0e2a0100cc3846874198d31
https://pubmed.ncbi.nlm.nih.gov/18060332
https://pubmed.ncbi.nlm.nih.gov/18060332