Harold M. Nitowsky - Concepedia

Author

Harold M. Nitowsky

Also Known As

H M NITOWSKY, H M Nitowsky, H NITOWSKY, H Nitowsky, H. M. NITOWSKY, H. M. Nitowsky, H.M Nitowsky, H.M. Nitowsky, HAROLD M. NITOWSKY, Harold M Nitowsky

108

Publications

3.8K

Citations

H-Index

171

Concepts

All Affiliations

Albert Einstein College of Medicine Johns Hopkins University Sinai Hospital Johns Hopkins Medicine John F. Kennedy Center for the Performing Arts

About

Harold M. Nitowsky is an author at Albert Einstein College of Medicine specializing in medicine, pediatrics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	50	3.1K
2	Health Sciences	10	12	495
3	Natural Sciences	7	7	192
4	Education	1	1	73
5	Law	1	1	11

Harold M. Nitowsky

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
An association between low maternal serum α-fetoprotein and fetal chromosomal abnormalities Irwin R. Merkatz, Harold M. Nitowsky, James N. Macri, American Journal of Obstetrics and Gynecology GeneticsFetal Chromosomal AbnormalitiesReproductive HealthGenetic EpidemiologyGynecology	1984	739
DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS Ronald G. Davidson, Harold M. Nitowsky, Barton Childs Proceedings of the National Academy of Sciences GeneticsMolecular GeneticsMetabolismMedicineCell Biology	1963	369
Genetic polymorphisms of methylenetetrahydrofolate reductase (<i>MTHFR</i>) and methionine synthase reductase (<i>MTRR</i>) in ethnic populations in Texas; a report of a novel<i>MTHFR</i>polymorphic site, G1793A Peter L. Rady, Sylvia Szucs, James J. Grady, American Journal of Medical Genetics GeneticsGenetic EpidemiologyHuman PolymorphismPathologyEthnic Populations	2001	157
PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPING M S Pollack, L S Levine, Songya Pang, The Lancet Developmental AnomalyAdrenal GlandBy Hla TypingMedicineInherited Metabolic Disease	1979	128
A new gene, EVC2, is mutated in Ellis–van Creveld syndrome Marzena Galdzicka, Sujatha Patnala, M.G Hirshman, Molecular Genetics and Metabolism Developmental BiologyGenetic DisorderGeneticsPathogenesisNew Gene	2002	127
Amniotic Fluid Concentrations of Δ5 and Δ4 Steroids in Fetuses with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Deficiency and in Anencephalic Fetuses* Songya Pang, L S Levine, Lars L. Cederqvist, The Journal of Clinical Endocrinology & Metabolism Amniotic Fluidδ4 SteroidsMale FetusFetal MedicineGynecology	1980	118
Studies of Jocopherol Deficiency in Infants and Children Harold M. Nitowsky A M A Journal of Diseases of Children NutritionJocopherol DeficiencyPositive Hemolysis TestsBody CompositionHematology	1956	104
Kinetic and electrophoretic evidence for multiple forms of glucose-ATP phosphotransferase activity from human cell cultures and rat liver Howard M. Katzen, Denis D. Soderman, Harold M. Nitowsky Biochemical and Biophysical Research Communications Energy MetabolismCellular EnzymologyBiochemistryBioenergeticsPhysiology	1965	92
STUDIES ON THE EPIDEMIOLOGY OF SARCOIDOSIS IN THE UNITED STATES: THE RELATIONSHIP TO SOIL AREAS AND TO URBAN-RURAL RESIDENCE John T. Gentry, Harold M. Nitowsky, Max Michael Journal of Clinical Investigation	1955	89
The Prenatal Diagnosis of Adrenoleukodystrophy. Demonstration of Increased Hexacosanoic Acid Levels in Cultured Amniocytes and Fetal Adrenal Gland Hugo W. Moser, Ann B. Moser, James M. Powers, Pediatric Research Adrenal GlandFetal Adrenal GlandFetal MedicinePediatricsGynecology	1982	87

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