Philip P. Dembure - Concepedia

Concepedia

Author

Philip P. Dembure

Emory University

Also Known As

P Dembure, P P Dembure, P. Dembure, P. P. Dembure, P.P. Dembure, PHILIP P. DEMBURE, Philip Dembure, Philip P Dembure, Philip P. DEMBURE, Philip P. Dembure

33

Publications

1.3K

Citations

18

H-Index

65

Concepts

All Affiliations

Emory University University at Buffalo, State University of New York

PP

About

Philip P. Dembure is an author at Emory University specializing in medicine, urology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	804
2	Biochemistry	5	5	202
3	Natural Sciences	3	3	83
4	Health Sciences	1	1	141
5	Social Sciences	1	1	194

Philip P. Dembure

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20

Publications

1.3K

Citations

17

H-Index

	Year	Citations
Biochemical and neuropsychological effects of elevated plasma phenylalanine in patients with treated phenylketonuria. A model for the study of phenylalanine and brain function in man. WL Krause, Margaret Halminski, L McDonald, Journal of Clinical Investigation NeuropsychologyUrine Dopamine ExcretionPsychopharmacologySocial SciencesNeuropsychological Effects	1985	194
Sickle-Cell Anemia and Other Hemoglobinopathies Michael D. Garrick, Philip P. Dembure, Robert Guthrie New England Journal of Medicine ImmunohematologyDiagnosisPathologyBlood SpotsDisease Detection	1973	141
A prevalent mutation for galactosemia among black Americans Kent Lai, Sharon D. Langley, Rani H. Singh, The Journal of Pediatrics Human VariationPrevalent MutationGeneticsDiabetesGenetic Epidemiology	1996	117
A common mutation associated with the Duarte galactosemia allele. Louis J. Elsas, Philip P. Dembure, Sharon D. Langley, PubMed	1994	98
Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypes. Louis J. Elsas, Sharon D. Langley, Ernest C. Steele, PubMed	1995	98
Neural-tube defects are associated with low concentrations of cobalamin (vitamin B12) in amniotic fluid Mårten Steen, A. M. Boddie, A. J. Fisher, Prenatal Diagnosis	1998	75
Molecular basis for Duarte and Los Angeles variant galactosemia. Sharon D. Langley, Kent Lai, Philip P. Dembure, PubMed	1997	68
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency Fernando Scaglia, Yuhuan Wang, Rani H. Singh, Genetics in Medicine UrologyBiochemistryPrimary Carnitine DeficiencyPhysiologyMetabolism	1998	60
A molecular approach to galactosemia Louis J. Elsas, Sharon D. Langley, Elizabeth M. Paulk, European Journal of Pediatrics BiosynthesisBiochemistryGlycobiologyPolysaccharideMolecular Approach	1995	59
Phospholipid‐Sensitive Ca<sup>2+</sup>‐Dependent Protein Kinase Preferentially Phosphorylates Serine‐115 of Bovine Myelin Basic Protein Raymond Scott Turner, C H Chou, Gonzalo J. Mazzei, Journal of Neurochemistry	1984	57

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