Anatole S. Dekaban

National Institutes of Health — United States

Medicine · Health Sciences

31h-index3.9kcitations98works0.02yr avg
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Research Topics

Lysosomal Storage Disorders Research(15), Glycogen Storage Diseases and Myoclonus(13), Metabolism and Genetic Disorders(9), Carbohydrate Chemistry and Synthesis(7), Epilepsy research and treatment(6)

Publications98 total

CONTENT AND COMPOSITION OF URINARY GLYCOSAMINOGLYCANS IN THE PATIENTS WITH MYOCLONUS EPILEPSY WITH AND WITHOUT LAFORA BODIES
Acta Neurologica Scandinavica·2009· 2 cited
Author’s Erratum
Cytogenetics·2008· 1 citedOpen Access
Modified head-neck support for basilar invagination with brain-stem compression.
PubMed·1982· 9 citedOpen Access
Mucopolysaccharidosis Types IH, IS, II and IIIA: Glycosaminoglycans and Lipids of Isolated Brain Cells and Other Fractions from Autopsied Tissues
Journal of Neurochemistry·1980· 63 cited
Changes in brain weights during the span of human life: Relation of brain weights to body heights and body weights
Annals of Neurology·1978· 1.0k cited
NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN LIPIDS AND LYSOSOMAL ENZYMES IN PATIENTS WITH FOUR TYPES OF MUCOPOLYSACCHARIDOSIS AND IN NORMAL CONTROLS
Journal of Neurochemistry·1978· 76 citedOpen Access
Tables of cranial and orbital measurements, cranial volume, and derived indexes in males and females from 7 days to 20 years of age
Annals of Neurology·1977· 144 cited
Hyperlipoproteinemia and Cerebral Strokes
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques·1977· 2 citedOpen Access
Mucopolysaccharidosis types I, II, IIIA and V
Acta Neuropathologica·1977· 71 cited
Metabolic fate of phenobarbital. A quantitative study of p-hydroxyphenobarbital elimination in man.
Drug Metabolism and Disposition·1977· 44 cited
Familial Cerebellar Degeneration with Slow Eye‐movements, Mental Deterioration and Incidental Nevus of Ota (Oculo‐dermal Melanoeytosis)
Developmental Medicine & Child Neurology·1976· 15 cited
NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN GLYCOSAMINOGLYCANS IN NORMALS AND FOUR TYPES OF MUCOPOLYSACCHARIDOSES
Journal of Neurochemistry·1976· 44 cited
COMPARATIVE STUDIES OF THE BRAIN IN MUCOPOLYSACCHARIDOSES TYPES I, II, III AND V
Journal of Neuropathology & Experimental Neurology·1976
Mucopolysaccharidosis type V. (Scheie syndrome). A postmortem study by multidisciplinary techniques with emphasis on the brain.
PubMed·1976· 30 cited
Enzyme Replacement Therapy for the Sphingolipidoses
Advances in experimental medicine and biology·1976· 14 cited
EFFECTS OF DIFFERENT DOSAGES OF ANTICONVULSANT DRUGS ON MENTAL PERFORMANCE IN PATIENTS WITH CHRONIC EPILEPSY
Acta Neurologica Scandinavica·1975· 27 cited
Kinky Hair Disease
Archives of Neurology·1975· 32 cited
Chemical definition of the mucopolysaccharidoses
Clinica Chimica Acta·1975· 20 cited
Brain Dysfunction in Congenital Malformations of the Nervous System
1975· 4 cited
Replacement Therapy for Inherited Enzyme Deficiency
New England Journal of Medicine·1974· 291 cited
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Frequent Co-authors

George Constantopoulos(10), Roscoe O. Brady(3), Andrew E. Gal(3), Kenton R. Holden(3), John F. Tallman(2), Jane M. Quirk(2), Sue R. Hibbert(2), Doris A. Sadowsky(1), William G. Johnson(1), William R. Leahy(1), Peter G. Pentchev(1), Andrew W. Zimmerman(1), Edward O. Reiter(1), William R. Carroll(1), Khalid Iqbal(1), Rodney D. McComb(1), M P Whyte(1), Kenneth R. Magee(1), M. A. Bender(1), G.E. Economos(1)