Zobrazeno 1 - 10
of 268
pro vyhledávání: '"J. Brismar"'
Publikováno v:
Acta Radiologica. 37:512-516
Purpose: To assess frequency, location, and appearance of peripheral osteoarticular and soft-tissue tuberculosis (TB). Material and Methods: Twenty-five of 503 patients with TB had peripheral osteoarticular TB and 5 had soft-tissue TB. Chest radiogra
Publikováno v:
Acta Radiologica. 37:496-505
Purpose: To show that intracranial tuberculosis (TB) often masquerades as brain tumour. Material and Methods: Forty-six patients with intracranial TB, who after CT at the local hospital were referred for surgery or radiotherapy of brain tumour, are p
Publikováno v:
Acta Radiologica. 36:485-490
A series of 458 consecutive ultrasound-guided biopsies in 347 patients − 171 fine-needle aspiration biopsies (FNABs) and 287 1.2-mm needle core biopsies (NCBs) − was analysed for diagnostic yield and complications. FNAB was diagnostic in 107 (64%
Publikováno v:
Acta Radiologica. 36:485-490
A series of 458 consecutive ultrasound-guided biopsies in 347 patients - 171 fine-needle aspiration biopsies (FNABs) and 287 1.2-mm needle core biopsies (NCBs) - was analysed for diagnostic yield and complications. FNAB was diagnostic in 107 (64%) bi
Autor:
B. Stigsby, Zuhair Rahbeeni, O. Dabbagh, S.M. Yarworth, Generoso G. Gascon, Pinar Ozand, J. Brismar, N. Abdo, C. de Gier Munk
Publikováno v:
Brain and Development. 16:125-144
The files of 107 patients with 19 different types of organic acidemia were reviewed retrospectively. Approximately 50% of the patients had abnormal electroencephalogram (EEG) at the time of initial study. In patients who had serial studies, the EEG d
Publikováno v:
Brain and Development. 16:72-80
Ten patients with biotin-dependent, chronic progressive encephalopathies were studied retrospectively. In four patients, the underlying disease was either total or partial deficiency of biotinidase. In one patient, the disease was caused by a lack of
Autor:
Mohamed S. Rashed, O. Dabbagh, A. Al Odaib, Pinar Ozand, A. Al Aqeel, Generoso G. Gascon, J. Brismar
Publikováno v:
Brain and Development. 16:23-32
3-Methylglutaconic aciduria is an organic aciduria with diverse phenotypic presentations. In more than half of the cases it is a 'neurologic or silent organic aciduria', and, except for one subtype, the biochemical defect is unknown. This report desc
Autor:
Pinar Ozand, J. Brismar, Mohamed S. Rashed, M. Amoudi, A. Al Odaib, S. Al Garawi, M. N. Al Nasser, M. Nester, Generoso G. Gascon, Zuhair Rahbeeni
Publikováno v:
Brain and Development. 16:64-71
The clinical findings in six patients from three families with 4-hydroxybutyric aciduria are described. The onset of disease was in early infancy in all cases. All infants presented with severe global delay and severe hypotonia, and all patients had
Autor:
N.G. Youssef, A. Al Odaib, Nadia Sakati, A. Mazrou, Mohamed S. Rashed, Pinar Ozand, S. Hazzaa, Zuhair Rahbeeni, Generoso G. Gascon, David S. Millington, J. Brismar
Publikováno v:
Brain and Development. 16:12-22
Five infants from 3 families, one Egyptian, two Yemeni, are described with a progressive encephalopathy, four of whom have been studied in detail. All patients showed vascular lesions of the skin, characterized by waxing and waning petechiae and ecch
Publikováno v:
Neuroradiology. 35:130-133
Eight patients with Wilson's disease (WD) were studied by magnetic resonance imaging (MRI) of the brain; seven also underwent X-ray computed tomography (CT) of the brain. We describe the changes in the brain and try to correlate them with the clinica