Zobrazeno 1 - 10
of 62
pro vyhledávání: '"M. Bornebroek"'
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 161
Zoledronic acid is a nitrogen-containing bisphosphonate that is frequently used in the treatment of osteoporosis. Many patients experience a so-called acute-phase reaction during initial treatment; this is characterized by flu-like symptoms and fever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69848df0908d3ab890cde590a89a8fed
https://pubmed.ncbi.nlm.nih.gov/29125079
https://pubmed.ncbi.nlm.nih.gov/29125079
Autor:
M. Bornebroek, Joost Haan, Rivka van den Boom, Michel D. Ferrari, Sjoerd G. van Duinen, Saskia A J Lesnik Oberstein, Mark A. van Buchem
Publikováno v:
Radiology. 224:791-796
To assess the prevalence and distribution of subcortical lacunar lesions (SLLs) in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), to determine whether SLLs are an abnormal finding b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffa6e9a5d33b9c49863fecd1f0c59bba
https://doi.org/10.1148/radiol.2243011123
https://doi.org/10.1148/radiol.2243011123
Autor:
J. B. K. Lanser, Ronald Brand, M.A. van Buchem, M. Bornebroek, R A C Roos, Joost Haan, F. T. de Bruïne
Publikováno v:
Alzheimer Disease & Associated Disorders. 10:224-231
Summary: The relationship between cognitive deterioration and abnormalities detected by magnetic resonance imaging (MRI) was investigated to determine the radiological correlates of cognitive deterioration in hereditary cerebral hemorrhage with amylo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::661d46b6e0948f918f6c5cffd25782f1
https://doi.org/10.1097/00002093-199601040-00008
https://doi.org/10.1097/00002093-199601040-00008
Autor:
Egbert Bakker, Joost Haan, C. Van Broeckhoven, M. Bornebroek, H Backhovens, R. A. C. Roos, M.A. van Buchem, P. Deutz, M Van den Broeck
Publikováno v:
Annals of Neurology. 42:108-110
Hereditary cerebral hemorrhage with amyloidosis, Dutch type, caused by a mutation at codon 693 of the amyloid beta precursor protein gene, is characterized by amyloid beta deposition resulting in recurrent strokes and dementia. Recent data suggest th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e62456a156d703f61a8c6c44c299f5cb
https://doi.org/10.1002/ana.410420116
https://doi.org/10.1002/ana.410420116
Autor:
Joost Haan, M. Bornebroek, A. A. van den Berg-Huysmans, M.A. van Buchem, R. van den Boom, F. Behloul
Publikováno v:
Neurology. 64(7)
In a hereditary variant of cerebral amyloid angiopathy (CAA), cerebral hemorrhage with amyloidosis-Dutch type, supratentorial microbleeds were found to occur independently of the presence of hypertension, whereas hypertension probably contributed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f57102873c0fe166bc62584315ea529
https://pubmed.ncbi.nlm.nih.gov/15824369
https://pubmed.ncbi.nlm.nih.gov/15824369
Autor:
M BORNEBROEK
Publikováno v:
Clinical Neuroscience Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19a20de67557aa165afb58e7f377b067
https://doi.org/10.1016/s1566-2772(04)00003-9
https://doi.org/10.1016/s1566-2772(04)00003-9
Publikováno v:
Annals of neurology. 50(6)
Cerebral amyloid angiopathy is frequently found in demented and nondemented elderly persons, but its contribution to the causation of dementia is unknown. Therefore, we investigated the relation between the amount of cerebral amyloid angiopathy and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f7afe48ed91f18913ddf6df2e8f2c45
https://pubmed.ncbi.nlm.nih.gov/11761474
https://pubmed.ncbi.nlm.nih.gov/11761474
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 145(34)
Hereditary cerebral haemorrhage with amyloidosis-Dutch type (HCHWA-D) is an autosomal dominant disease caused by a mutation in the amyloid precursor protein gene on chromosome 21. The disease is characterised by amyloid deposition in cerebral blood v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::657e22ff00e05aa36a1fc4232b392441
https://pubmed.ncbi.nlm.nih.gov/11552366
https://pubmed.ncbi.nlm.nih.gov/11552366
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 6(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8414a6e4b933c184b13e099e7418bfb
https://pubmed.ncbi.nlm.nih.gov/10524288
https://pubmed.ncbi.nlm.nih.gov/10524288
Autor:
M, Bornebroek, J, Haan, H, Backhovens, P, Deutz, M A, Van Buchem, M, van den Broeck, E, Bakker, R A, Roos, C, Van Broeckhoven
Publikováno v:
Annals of neurology. 42(1)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type, caused by a mutation at codon 693 of the amyloid beta precursor protein gene, is characterized by amyloid beta deposition resulting in recurrent strokes and dementia. Recent data suggest th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cde0c88b3af9512e53dd06503d6d3beb
https://pubmed.ncbi.nlm.nih.gov/9225691
https://pubmed.ncbi.nlm.nih.gov/9225691