Zobrazeno 1 - 10
of 29
pro vyhledávání: '"G T Bots"'
Clinical and neuropathological findings are reported in 63 patients with hereditary cerebral haemorrhage with amyloid angiopathy. Patients had mostly recurrent strokes, and at least 80% of these were haemorrhages. Almost a third of the patients died
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fad9627c1bc9b0fd86f086ee22218cc
https://europepmc.org/articles/PMC1073548/
https://europepmc.org/articles/PMC1073548/
Publikováno v:
Neuroscience letters. 140(2)
With immunohistochemical staining methods on cryostat sections we investigated the brains of three patients with hereditary cerebral hemorrhage with amyloidosis-Dutch type, one of the cerebral beta/A4 amyloid diseases. Immunostaining for beta/A4 prot
Autor:
G T, Bots
Publikováno v:
Clinical neurology and neurosurgery.
Cerebral hemorrhages with amyloidosis and dementia of the Alzheimer type have many neuropathological findings in common, but there are also marked quantitative and qualitative differences. That makes it highly improbably that the B-protein amyloid de
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 44:144-147
Computed tomography fails to ascertain, or exclude, the presence of intracranial haemorrhage in a considerable number of cases, especially in subarachnoid haemorrhage and haemorrhagic infarcts. A number of other methods, including cerebrospinal fluid
Autor:
G T Bots, R G Willighagen
Publikováno v:
British Journal of Cancer
Images Fig.
Publikováno v:
Journal of clinical pathology. 41(5)
A three step method using microwave irradiation enabled microscopic slides of human brain tissue to be obtained within one working day: steps 1 and 2 hardened and solidified brain tissue; step 3 completed formalin fixation. The efficacy and precision
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 123(35)
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 121(52)
Publikováno v:
The American journal of gastroenterology. 81(1)
A patient is reported who presented with a typical intestinal pseudoobstruction syndrome. Before this illness, the patient had suffered from measles encephalitis at the age of 15 months. A postencephalitic syndrome was present which included severe m
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 130(43)