A. Dekaban

The Contribution of George W. Bartelmez to the American School of Neurology and Biological Science
20150 citationsauthor #1
Hippircle
20150 citationsauthor #7
Neurology of Infancy
20120 citationsauthor #1
Retardation in a child with an extra submetacentric chromosome fragment and partial mongolism.
20087 citationsauthor #1
Modified head-neck support for basilar invagination with brain-stem compression.
19828 citationsauthor #2
Mucopolysaccharidosis Types IH, IS, II and IIIA: Glycosaminoglycans and Lipids of Isolated Brain Cells and Other Fractions from Autopsied Tissues
198065 citationsauthor #3
NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN LIPIDS AND LYSOSOMAL ENZYMES IN PATIENTS WITH FOUR TYPES OF MUCOPOLYSACCHARIDOSIS AND IN NORMAL CONTROLS
197877 citationsauthor #2
Changes in brain weights during the span of human life: Relation of brain weights to body heights and body weights
19781,055 citationsauthor #1
Tables of cranial and orbital measurements, cranial volume, and derived indexes in males and females from 7 days to 20 years of age
1977157 citationsauthor #1
Hyperlipoproteinemia and Cerebral Strokes
19774 citationsauthor #1
CONTENT AND COMPOSITION OF URINARY GLYCOSAMINOGLYCANS IN THE PATIENTS WITH MYOCLONUS EPILEPSY WITH AND WITHOUT LAFORA BODIES
19772 citationsauthor #2
Mucopolysaccharidosis types I, II, IIIA and V
197736 citationsauthor #1
Metabolic fate of phenobarbital. A quantitative study of p-hydroxyphenobarbital elimination in man.
197743 citationsauthor #2
Mucopolysaccharidosis type I, II, IIIA and V. Pathological and biochemical abnormalities in the neural and mesenchymal elements of the brain.
197741 citationsauthor #1
Therapeutic approaches to selected disorders of inborn errors of metabolism with neurological involvement.
19760 citationsauthor #1
Familial Cerebellar Degeneration with Slow Eye‐movements, Mental Deterioration and Incidental Nevus of Ota (Oculo‐dermal Melanoeytosis)
197617 citationsauthor #2
Mucopolysaccharidosis type V. (Scheie syndrome). A postmortem study by multidisciplinary techniques with emphasis on the brain.
197631 citationsauthor #1
Enzyme replacement therapy for the sphingolipidoses.
197612 citationsauthor #9
COMPARATIVE STUDIES OF THE BRAIN IN MUCOPOLYSACCHARIDOSES TYPES I, II, III AND V: 129
19760 citationsauthor #1
Chemical definition of the mucopolysaccharidoses.
197521 citationsauthor #2
Kinky Hair Disease: Study of Copper Metabolism With Use of 67Cu
197530 citationsauthor #1
EFFECTS OF DIFFERENT DOSAGES OF ANTICONVULSANT DRUGS ON MENTAL PERFORMANCE IN PATIENTS WITH CHRONIC EPILEPSY
197531 citationsauthor #1
Brain Dysfunction in Congenital Malformations of the Nervous System
19754 citationsauthor #1
Letter: Menkes' kinky hair disease treated with subcutaneous copper sulphate.
197432 citationsauthor #1
Study of copper metabolism in kinky hair disease (Menkes' disease) and in hepatolenticular degeneration (Wilson's disease) utilizing 67Cu and radioactivity counting in the total body and various tissues.
19749 citationsauthor #1
PROTEINS OF HUMAN BRAIN TISSUE OBTAINED DURING SURGICAL PROCEDURES
19746 citationsauthor #3
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease.
1974275 citationsauthor #5
Childhood, juvenile, and adult cerebral lipidoses. Are these different nosological entities?
197411 citationsauthor #1
Wilson's Disease and Menkes' Disease—A Contrast in Chronogenetics
19740 citationsauthor #2
Comparison of serum levels and urinary excretion of three major anticonvulsants as between children and adults (Japanese)
19742 citationsauthor #2
The effects of different dosages of combined antiepileptic drugs on their metabolism and their levels in body fluids
19741 citationsauthor #1
Mucopolysaccharidoses: relation of elevated CSF mucopolysaccharides to brain involvement.
19730 citationsauthor #1
Acid mucopolysaccharides (glycosaminoglycans) in normal human kidneys and in kidneys of patients with mucopolysaccharidoses.
197314 citationsauthor #3
[Anatomo-pathology and study of lipids in Hurler's and Sanfilippo's mucopolysaccharidosis].
19730 citationsauthor #1
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's disease.
1973298 citationsauthor #7
Medroxprogesterone acetate in the treatment of seizures associated with menstruation.
197383 citationsauthor #4
BRAIN PROTEINS: QUALITATIVE AND QUANTITATIVE CHANGES, SYNTHESIS AND DEGRADATION DURING FETAL DEVELOPMENT OF THE RABBIT
197219 citationsauthor #3
Laurence-Moon syndrome: evaluation of endocrinological function and phenotypic concordance and report of cases.
19722 citationsauthor #1
Mental Retardation and Neurologic Involvement in Patients with Congenital Retinal Blindness
197235 citationsauthor #1
Neurological involvement in nevus unis lateris and nevus linearis sebaceus
197277 citationsauthor #2
Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis.
197248 citationsauthor #1
Urinary acid mucopolysaccharides in cystic fibrosis.
19714 citationsauthor #2
Correlation of brain proteins in degenerative diseases, encephalitis, gliomas and focal epilepsy.
19710 citationsauthor #2
STRUCTURAL AND BIOCHEMICAL MATURATION OF THE CEREBRAL PALLIUM IN RABBIT FETUSES: MORPHOGENESIS AND LIPIDS
197112 citationsauthor #1
Maitland Baldwin
19711 citationsauthor #2
Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study.
19718 citationsauthor #2
Content and distribution of molecular weights of mucopolysaccharides in the brain and other organs of Hurler's patients.
19711 citationsauthor #2
Acid mucopolysaccharides in the cerebrospinal fluid of patients with Hunter–Hurler's syndrome
197021 citationsauthor #2
Late form of congenital rubella syndrome; thoughts on pathogenesis.
19701 citationsauthor #1
Optical rotatory dispersion of mucopolysaccharides. IV. Optical rotatory dispersion and circular dichroism of glycosaminoglycans and heparan sulfate fractions from the urine of patients with mucopolysaccharidosis (Hurler syndrome).
197019 citationsauthor #4
Neurology of early childhood
197035 citationsauthor #1
Hereditary syndrome of congenital retinal blindness (Leber), polycystic kidneys and maldevelopment of the brain.
1969113 citationsauthor #1
Familial occurrence of congenital retinal blindness and developmental renal lesions.
19697 citationsauthor #1
Determination of molecular weight distribution of acid mucopolysaccharides by sephadex gel filtration.
196969 citationsauthor #2
Effects of x-radiation on mouse fetus during gesttion: emphasis on distribution of cerebral lesions, Part II.
196923 citationsauthor #1
Biological behavior of lymphocytes in Hunter-Hurler's disease.
19694 citationsauthor #2
IN CH1LDREN EXPOSED TO X-RADIATION DURING VARIOUS STAGES OF GESTATION: TENTATIVE TIMETABLE OF RADIA TION INJURY TO THE HUMAN FETUS, PART I
19681 citationsauthor #1
Abnormalities in children exposed to x-radiation during various stages of gestation: tentative timetable of radiation injury to the human fetus. I.
1968164 citationsauthor #1
Studies in the Hunter-Hurler's syndrome.
19680 citationsauthor #1
NEUROLOGICAL COMPLICATIONS OF IDIOPATHIC HYPOGLYCEMIA IN CHILDREN
19672 citationsauthor #1
Regional Development of the Brain in Early Life: A Symposium
196710 citationsauthor #1
Histological, histochemical and chemical studies in Hurler's disease.
19671 citationsauthor #1
Hunter-Hurler Syndrome: clinical and biochemical study. Combined clinical staff conference at th National Institutes of Health.
19661 citationsauthor #1
Modification of urinary mucopolysaccharide excretion in patients with Hurler's syndrome
196612 citationsauthor #2
Chromosomal Aberrations in Irradiated Blood and Blood Cultures of Normal Subjects and of Selected Patients with Chromosomal Abnormality
196630 citationsauthor #1
Congenital amaurosis of retinal origin. Frequent association with neurological disorders.
196626 citationsauthor #1
Plasma lipids in epileptic children treated with the high fat diet.
196666 citationsauthor #1
Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation.
196614 citationsauthor #1
Metabolic and chromosomal studies in leprechaunism.
196530 citationsauthor #1
Cephalopagus twins seven years after separation. Follow-up of a case.
19659 citationsauthor #2
Large Defects in Cerebral Hemispheres Associated with Cortical Dysgenesis
196588 citationsauthor #1
Persisting clone of cells with an abnormal chromosome in a woman previously irradiated.
196571 citationsauthor #1
Leprechaunism--a syndrome.
19652 citationsauthor #1
Author’s Erratum
19651 citationsauthor #1
Twins, probably monozygotic: one mongoloid with 48 chromosomes, the other normal.
196525 citationsauthor #1
COMPLETE DYSRAPHISM IN 14 SOMITE HUMAN EMBRYO. A CONTRIBUTION TO NORMAL AND ABNORMAL MORPHOGENESIS.
196430 citationsauthor #1
PLASMA LIPIDS, GLUCOSE AND KETONES IN YOUNG CHILDREN ON A HIGH FAT DIET.
19643 citationsauthor #1
CLINICAL PATHOLOGICAL CONFERENCE: THE DANDY-WALKER SYNDROME.
19641 citationsauthor #1
FAMILIAL SYNDROME OF DYSPLASTIC BODY BUILD, MENTAL RETARDATION AND CHOROIDO-RETINAL COLOBOMA.
19632 citationsauthor #2
ANENCEPHALY IN EARLY HUMAN EMBRYOS
196356 citationsauthor #1
CHROMOSOME STUDIES IN MONGOLOIDS AND THEIR FAMILIES.
196333 citationsauthor #1
Correlation of fetal wastage and condition of offspring with maternal state during gestation, and circumstances of delivery in 4,156 pregnancies. I. Demographic characteristics and summarized results of data.
19622 citationsauthor #1
Familial idiopathic hypoglycemia: neurological complications.
19628 citationsauthor #1
Correlation of fetal wastage and condition of offspring with maternal stage during gestation, and circumstances of delivery in 4,156 pregnancies. II. Analysis of the main distribution of the outcome of 4,156 pregnancies.
19622 citationsauthor #1
Neurological complications of familial idiopathic hypoglycemia in children.
19610 citationsauthor #2
Idiopathic epilepsy in early infancy. The question of frequent daily attacks causing undifferentiated type of mental deficiency.
19602 citationsauthor #1
Metastases of the Retinoblastoma to the Central Nervous System: Advisability of a Combined Intraorbital and Intracranial Removal of the Affected Optic Nerve
19593 citationsauthor #1
ARHINENCEPHALY IN AN INFANT BORN TO A DIABETIC MOTHER
195931 citationsauthor #1
The outcome of pregnancy in diabetic women. I. Fetal wastage, mortality, and morbidity in the offspring of diabetic and normal control mothers.
195921 citationsauthor #1
The outcome of pregnancy in diabetic women. II. Analysis of clinical abnormalities and pathologic lesions in offspring of diabetic mothers.
19598 citationsauthor #1
Occurrence of neurologic abnormalities in infants of diabetic mothers
195828 citationsauthor #1
Abnormalities in offspring related to maternal rubella during pregnancy
195820 citationsauthor #1
HEMIPLEGIA IN EARLY LIFE ASSOCIATED WITH THROMBOSIS OF THE SAGITTAL SINUS AND ITS TRIBUTARY VEINS IN ONE HEMISPHERE
195815 citationsauthor #1
Progressive cerebral degenerations of childhood
19580 citationsauthor #2
Is needle puncture of the brain entirely harmless?
195813 citationsauthor #1
THE SURGICAL SEPARATION OF SIAMESE TWINS CONJOINED BY THE HEADS (CEPHALOPAGUS FRONTALIS) FOLLOWED BY NORMAL DEVELOPMENT
195821 citationsauthor #2
Long survival in juvenile essential hypertension complicated by bilateral hemiplegia.
19550 citationsauthor #1
Failure in treatment of multiple sclerosis patients with isoniazid.
19551 citationsauthor #1
Investigation into the possible infective etiology of multiple sclerosis.
19552 citationsauthor #1
Book Reviews / Personalia
19550 citationsauthor #7

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