Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Donald R, McLean"'
Publikováno v:
Clinical Neurophysiology. 111:1320-1329
Objectives : To compare neurological involvement in Behcet's disease as documented by transcranial magnetic stimulation (TMS) with clinical, neuroradiological, somatosensory (SEP) and auditory evoked potential (BAEP) findings. Methods : Forty-four pa
Publikováno v:
European Journal of Neurology. 5:411-416
We describe two patients with post-partum cerebral angiopathy. (Case 1) A 24-year-old patient developed vaginal bleeding 1 day post-partum. She received blood transfusion and ergometrine. Four days later she experienced severe occipital headache, los
Publikováno v:
Neuromuscular Disorders. 8:321-326
Miyoshi myopathy (MM) is a rare autosomal recessive distal myopathy linked to chromosome 2p12–14 that has not been described in Saudi Arabia. A Saudi family with five siblings aged 3–25 years, an unrelated 18-year-old woman and a 40-year-old man
Autor:
Ibrahim Althubaiti, Abdulaziz Alsemari, Mona AlKhawajah, David B. MacDonald, Donald R. McLean
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 40(4)
Publikováno v:
Neurosciences (Riyadh, Saudi Arabia). 8(1)
Neurobrucellosis is chronic brucellosis affecting the nervous system. It may mimic many neurological diseases but it rarely presents as polyradiculopathy. Brucellar radiculopathy was diagnosed in 6 patients who presented with weakness of the lower ex
Autor:
Saeed Bohlega, Mohammed Zuheir Al-Kawi, P. Coates, Donald R. McLean, P. Ozand, Bent Stigsby, Omer Sm
Publikováno v:
Movement Disorders. 10:513-517
We report two families with a disorder, probably autosomal recessive, characterized by tremor of juvenile onset, dystonia, and myoclonus with preserved cognitive, cerebellar, and peripheral nervous system functions. During 4 years' follow-up, mild sp
Autor:
Saeed Bohlega, M. Zuheir Al Kawi, Peter Ernst, Robert Coates, Salah Omer, Hugh M. Clink, Donald R. McLean
Publikováno v:
Cancer. 73:3037-3040
Background. Paraplegia caused by intrathecal chemotherapy has no known pathognomonic features and is a diagnosis of exclusion. Methods. The authors reported the clinical and neuroimaging findings in one patient with this syndrome. Results. The patien
Autor:
Saeed Bohlega, Donald R. McLean
Publikováno v:
Clinical Neurology and Neurosurgery. 99:217-219
A 24 year-old woman developed acute hemiplegia and a seizure following accidental catheterization of the right common carotid artery and total parenteral nutrition infusion. Magnetic resonance imaging of the brain showed lesions in the frontal lobe a
Publikováno v:
Muscle & Nerve. 20:514-516
Publikováno v:
Annals of Saudi medicine. 12(1)
The neuroleptic malignant syndrome (NMS) is a relatively uncommon, sometimes fatal, idiosyncratic drug reaction usually associated with the administration of neuroleptic drugs. The syndrome is characterized by generalized rigidity, fever, altered con