Allan M. Lund - Concepedia

Author

Allan M. Lund

Also Known As

A Lund, A M Lund, A Meldgaard Lund, A. Lund, A. M Lund, A. M. Lund, A.M. Lund, ALLAN M. LUND, AM Lund, AM Lund, M Hansen, G Kollerup, A Juul,

285

Publications

7.5K

Citations

H-Index

167

Concepts

All Affiliations

Rigshospitalet Copenhagen University Hospital University of Copenhagen University Children's Hospital Zurich Children's Memorial Health Institute

About

Allan M. Lund is an author at Rigshospitalet specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	44	2.1K
2	Health Sciences	9	9	631
3	Natural Sciences	5	5	308
4	Public Health	5	5	108
5	Social Sciences	2	2	62

Allan M. Lund

118

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg, Pediatric Research NutritionMetabolic DisorderPediatric HematologyTreatment EfficacyHematology	2006	266
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation Stefan Kölker, Ángeles García Cazorla, Vassili Valayannopoulos, Journal of Inherited Metabolic Disease	2015	242
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype Stefan Kölker, Vassili Valayannopoulos, Alberto Burlina, Journal of Inherited Metabolic Disease	2015	229
Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease Maurizio Scarpa, Zsuzsanna Almássy, Michael Beck, Orphanet Journal of Rare Diseases	2011	223
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5 Peter R. Baker, Marisa W. Friederich, Michael A. Swanson, Brain GeneticsPathologyMolecular GeneticsDisease Gene IdentificationInsulin Signaling	2013	219
Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence Gunilla Malm, Allan M. Lund, Jan‐Eric Månsson, Acta Paediatrica	2008	123
Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the <i>IFITM5</i> c.−14C>T mutation in all patients Frank Rauch, Pierre Moffatt, Moira Cheung, Journal of Medical Genetics	2012	113
Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III Jessica de Ruijter, Minke H. de Ru, Tom Wagemans, Molecular Genetics and Metabolism Sensitive MarkersMolecular Diagnostic TechniquesImmunodeficienciesBioanalysisPathogenesis	2012	102
Hyperglucagonemia correlates with plasma levels of non-branched-chain amino acids in patients with liver disease independent of type 2 diabetes Nicolai J. Wewer Albrechtsen, Anders Junker, Mette Christensen, American Journal of Physiology-Gastrointestinal and Liver Physiology	2017	98
Chromosomal deletion unmasking a recessive disease: 22q13 deletion syndrome and metachromatic leukodystrophy A‐M. Bisgaard, M. Kirchhoff, JE Nielsen, Clinical Genetics	2009	94

Page 1