Zobrazeno 1 - 10
of 79
pro vyhledávání: '"A S, Dekaban"'
Publikováno v:
Acta Neurologica Scandinavica. 56:291-298
Content, composition and molecular weight distribution of the urinary glycosaminoglycans (GAG) were determined in five patients with progressive myoclonus epilepsy (PME). In one patient (Family B) this syndrome was associated with cerebral Lafora bod
Autor:
Anatole S. Dekaban
Publikováno v:
Developmental Medicine & Child Neurology. 14:436-444
SUMMARY Congenital retinal blindness is a recessively inherited disorder which occurs in about 10 per cent of blind children. The salient features are blindness or near-blindness since birth or early months of life, absent or attenuated electroretino
Autor:
J. Zelson, A. S. Dekaban
Publikováno v:
Journal of Intellectual Disability Research. 12:216-225
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 4:13-17
Determination of lipoprotein patterns and of major plasma lipids was carried out in 171 patients with strokes. Of these, 22 had hyperlipoproteinemia (HLIPR) by paper electrophoresis and by elevation of principal plasma lipids (either cholesterol over
Publikováno v:
Clinica Chimica Acta. 59:321-336
Glycosaminoglycans were isolated from the urines of 46 patients with mucopolysaccharidosis; 11 with Type I (Hurler), 8 with Type II (Hunter), 16 with Type III (Sanfilippo A and B), 9 with Type V (Scheie), one with Type VI (Marateaux-Lamy), and one un
Autor:
Elyse J. B. Lehman, Anatole S. Dekaban
Publikováno v:
Acta Neurologica Scandinavica. 52:319-330
Fifteen epileptic patients had their dose of anticonvulsant drugs changed twice, each time by 30-50 per cent of the initial medication. Before the dose change, the patients were given six especially adapted mental performance tests, which were design
Publikováno v:
Journal of Neurochemistry. 34:1399-1411
Brain cellular fractions were prepared in bulk from four non-neurological patients and from five patients with mucopolysaccharidosis (MPS). Glycosaminoglycans and lipids were isolated and chemically analyzed. Results of the present study: in the norm
Autor:
Anatole S. Dekaban, Doris Sadowsky
Publikováno v:
Annals of Neurology. 4:345-356
More than 20,000 autopsy reports from several general hospitals were surveyed for the purpose of selecting brains without a pathological lesion that had been weighed in the fresh condition. From this number, 2,773 males and 1,963 females were chosen
Publikováno v:
Journal of Neurochemistry. 30:965-973
— Lipids and certain lysosomal enzymes were measured in the cerebral gray and white matter and in the liver of unaffected controls and six patients with mucopolysaccharidosis (MPS). Three of the patients had MPS Type I (Hurler), one Type II (Hunter
Autor:
A. Zanchetti, E. Chiarugi, Anatole S. Dekaban, Richard Kayser, John E. Callagan, G.F. Rossi, John W. Lovett Doust
Publikováno v:
Stereotactic and Functional Neurosurgery. 15:323-326