D. M. Danks - Concepedia

Author

D. M. Danks

Royal Children's Hospital

Also Known As

D DANKS, D Danks, D M Danks, D. DANKS, D. Danks, D. M. DANKS, D. M. Danks, D.M Danks, D.M. Danks, David M. Danks

109

Publications

6.9K

Citations

H-Index

114

Concepts

All Affiliations

Royal Children's Hospital The University of Melbourne Hospital Research Foundation Universitätskinderklinik

About

D. M. Danks is an author at Royal Children's Hospital specializing in medicine, pathology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	37	5.7K
2	Health Sciences	4	4	191
3	Natural Sciences	2	2	38
4	Education	1	1	41
5	Engineering	1	1	26

D. M. Danks

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Genetic heterogeneity in osteogenesis imperfecta. David Sillence, A Senn, D. M. Danks Journal of Medical Genetics OsteopathyPresenile DeafnessOsteogenesisOsteoporosisOrthopaedic Surgery	1979	2.2K
Leigh syndrome: Clinical features and biochemical and DNA abnormalities S. Rahman, Rozanne B. Blok, H H Dahl, Annals of Neurology Down SyndromeComplex Iv-deficient SibshipsGenetic TestingMendelian DisorderGenetic Disorder	1996	776
International nosology of heritable disorders of connective tissue, Berlin, 1986 Peter Beighton, A. De Paepe, D. M. Danks, American Journal of Medical Genetics Gross AnatomyMendelian DisorderHistopathologyInternational NosologyPathology	1988	729
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1 David Ravine, LJ Sheffield, D. M. Danks, The Lancet UrologyMedicineKidney FailureRenal PathologyDiagnosis	1994	562
MENKES' KINKY-HAIR SYNDROME D. M. Danks, P E Campbell, J A Walker‐Smith, The Lancet Kinky-hair SyndromeMendelian DisorderMendelian InheritanceDisorders Of Sex DevelopmentMasculinity	1972	422
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease David Ravine, Sue Forrest, L. J. Sheffield, The Lancet GlomerulonephritisRenal DiseaseGenetic DisorderMedicineGenetics	1992	177
Clinical variability in osteogenesis imperfecta-variable expressivity or genetic heterogeneity. David Sillence, D L Rimoin, D. M. Danks PubMed Bone DiseaseBone RemodelingOrthopaedicsOsteogenesisGenetic Heterogeneity	1979	152
Malignant hyperphenylalaninaemia—Current status (June 1977) D. M. Danks, K. Bartholomé, B. E. Clayton, Journal of Inherited Metabolic Disease MedicineAdrenal DiseasePathologyMalignant Hyperphenylalaninaemia—current Status	1978	107
?Cerebral? lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis Garry K. Brown, Eric Haan, Denise M. Kirby, European Journal of Pediatrics Lactic AcidosisEnergy MetabolismPyruvate MetabolismNeurophysiologyMedicine	1988	103
Patient with Defect in Leucine Metabolism K. Faull, Patrick Bolton, B. Halpern, New England Journal of Medicine Leucine MetabolismMetabolic DiseaseMetabolismMedicineEndocrine Disease	1976	87

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