F. Güttler - Concepedia

Author

F. Güttler

Kennedy Center

Also Known As

F Guttler, F Güttler, F. GUTTLER, F. Guttler, F. Güttler, F. GÜTTLER, F. GüTTLER, F. Güttler, Flemmlng Guttler

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Kennedy Center University of Copenhagen Howard Hughes Medical Institute Children's Hospital of Los Angeles Baylor College of Medicine

About

F. Güttler is an author at Kennedy Center specializing in medicine, genetics, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	518
2	Natural Sciences	1	1	26
3	Public Health	1	1	12
4	Social Sciences	1	1	13
5	Allergy	1	1	24

F. Güttler

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood. F. Güttler PubMed UrologyMedicineInherited Metabolic DiseasePediatricsPediatric Endocrinology	1980	197
Double blind placebo control trial of large neutral amino acids in treatment of PKU: Effect on blood phenylalanine Reuben Matalon, K. Michals‐Matalon, Gita Bhatia, Journal of Inherited Metabolic Disease	2007	101
Multiple origins for phenylketonuria in Europe. Randy C. Eisensmith, Y Okano, M. Dasovich, PubMed	1992	85
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study. Per Guldberg, Harvey L. Levy, WB Hanley, PubMed	1996	84
Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland. Per Guldberg, K. Henriksen, Ilkka Sipilä, Journal of Medical Genetics UrologyMolecular CharacterisationMendelian DisorderGenetic DisorderMutation R408w	1995	62
Brain phenylalanine concentration in the management of adults with phenylketonuria Rex Moats, Richard Koch, Kathryn Moseley, Journal of Inherited Metabolic Disease	2000	62
The international collaborative study of maternal phenylketonuria: status report 1994 Richard Koch, HL Levy, Reuben Matalon, Acta Paediatrica	1994	61
An occipito‐temporal syndrome in adolescents with optimally controlled hyperphenylalaninaemia H. Lou, Peter Bjerre Toft, Jente Andresen, Journal of Inherited Metabolic Disease	1991	52
Low frequency of <i>Parkin</i>, <i>Tyrosine Hydroxylase</i>, and <i>GTP Cyclohydrolase I</i> gene mutations in a Danish population of early‐onset Parkinson's Disease Jens Michael Hertz, Karen Østergaard, Inger Juncker, European Journal of Neurology GeneticsPathologyDisease Gene IdentificationPark2 MutationDanish Population	2006	37
Intellectual, Neurologic, and Neuropsychologic Outcome in Untreated Subjects with Nonphenylketonuria Hyperphenylalaninemia J. Weglage, Kurt Ullrich, Michael Pietsch, Pediatric Research NeuropsychologyPsychiatryNonphenylketonuria HyperphenylalaninemiaRenal PathologyUntreated Subjects	1997	34

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