T. Baykal - Concepedia

Author

T. Baykal

Istanbul University

Also Known As

T Baykal, T. Baykal, Tolunay Baykal

Publications

596

Citations

H-Index

Concepts

All Affiliations

Istanbul University University Children's Hospital Zurich University of Connecticut Connecticut Children's Medical Center University Children’s Hospital Basel

About

T. Baykal is an author at Istanbul University specializing in medicine, molecular genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	269
2	Biochemistry	3	3	119
3	Natural Sciences	2	2	97
4	Public Health	2	2	33
5	Child Development	1	1	18

T. Baykal

Publications

552

Citations

H-Index

Page 1

	Year	Citations
Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population Steven F. Dobrowolski, Caroline Heintz, Trent Miller, Molecular Genetics and Metabolism Aldehyde DehydrogenaseCellular EnzymologyTurkish Pku PopulationBiochemistryNatural Sciences	2010	79
Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2 Ute Spiekerkoetter, G. Huener, T. Baykal, Journal of Inherited Metabolic Disease	2003	53
Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases T. Baykal, Gülden Gökçay, Yasemi̇n Gökdemi̇r, Journal of Inherited Metabolic Disease	2005	47
Novel mutations cause biotinidase deficiency in Turkish children Robert J. Pomponio, Turgay Coşkun, Mübeccel Demirkol, Journal of Inherited Metabolic Disease	2000	45
Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper Marcel R. Zurflüh, Marcello Giovannini, Laura M. Fiori, Molecular Genetics and Metabolism Dried Blood SpotsMedicineBioanalysisPathologyTetrahydrobiopterin Deficiencies	2005	38
Seventeen novel mutations that cause profound biotinidase deficiency Barry Wolf, Kevin P. Jensen, Gülden Hüner, Molecular Genetics and Metabolism Seventeen Novel MutationsGenetic DisorderGeneticsMolecular BiologyMolecular Genetics	2002	34
Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates Barry Wolf, Kevin P. Jensen, Bruce A. Barshop, Human Mutation	2005	33
Breastfeeding experience in inborn errors of metabolism other than phenylketonuria Gülden Hüner, T. Baykal, Fatih Demir, Journal of Inherited Metabolic Disease	2004	33
Consanguineous 3‐methylcrotonyl‐CoA carboxylase deficiency: Early‐onset necrotizing encephalopathy with lethal outcome T. Baykal, Gülden Gökçay, Zeynep İnce, Journal of Inherited Metabolic Disease	2005	29
Corticospinal Tract Involvement in a Patient With 3-HMG Coenzyme A Lyase Deficiency Yüksel Yýlmaz, Nihal Özdemir, Gazanfer Ekinci, Pediatric Neurology Mendelian DisorderGenetic DisorderMedicineCorticospinal Tract InvolvementDegenerative Disease	2006	24

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