F. A. Beemer - Concepedia

Author

F. A. Beemer

Wilhelmina Children's Hospital

Also Known As

F A Beemer, F Beemer, F. A. BEEMER, F. A. Beemer, F. Beemer, F.A Beemer, F.A. BEEMER, F.A. Beemer, FA Beemer

Publications

4.3K

Citations

H-Index

104

Concepts

All Affiliations

Wilhelmina Children's Hospital Utrecht University Cancer Genomics Centre University of Amsterdam University Medical Center Utrecht

About

F. A. Beemer is an author at Wilhelmina Children's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	25	2.2K
2	Natural Sciences	5	5	205
3	Health Sciences	4	4	326
4	Education	1	1	30
5	Engineering	1	1	27

F. A. Beemer

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. A K Ryan, Judith A. Goodship, David I. Wilson, Journal of Medical Genetics CytogeneticsGeneticsGenetic EpidemiologyEuropean Collaborative StudyPathology	1997	1.2K
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor. Jean L. Johnson, William R. Waud, K.V. Rajagopalan, Proceedings of the National Academy of Sciences PathologyMolybdenum CofactorPlasma Molybdenum ConcentrationRedox BiologyOxidative Stress	1980	167
Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport? M. Durán, F. A. Beemer, Colin van der Heiden, Journal of Inherited Metabolic Disease	1978	124
Symptomatology of patients with oligodontia Y. Schalk-van der Weide, F. A. Beemer, Jorge Faber, Journal of Oral Rehabilitation	1994	112
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism Rolf M.F. Berger, S. A. Stoker‐de Vries, S.K. Wadman, Clinica Chimica Acta UrologyPyrimidine MetabolismIodine Deficiency DisordersThyroid HormoneDihydropyrimidine Dehydrogenase Deficiency	1984	100
Non‐ocular cancer in patients with hereditary retinoblastoma and their relatives D. J. Derkinderen, Jan Willem Koten, N. J. D. Nagelkerke, International Journal of Cancer	1988	99
Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases J.M. Wit, F. A. Beemer, P. G. Barth, European Journal of Pediatrics NeuropsychologyCerebral GigantismNeurological DisorderClinical NeurologyBrain Injury	1985	84
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: Delineation of a new entity and review of lethal forms of multiple pterygium syndrome H. Chen, LaDonna Immken, Ralph Lachman, American Journal of Medical Genetics	1984	83
Osteogenesis Imperfecta in Childhood: Impairment and Disability Raoul Engelbert, Y. van der Graaf, R. van Empelen, PEDIATRICS	1997	78
Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase S.K. Wadman, M. Durán, F. A. Beemer, Journal of Inherited Metabolic Disease	1983	76

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