A. Dalton - Concepedia

Author

A. Dalton

Sheffield Children's Hospital

Also Known As

A Dalton, A. DALTON, A. Dalton, Amy E Dalton, Saxena

Publications

739

Citations

H-Index

Concepts

All Affiliations

Sheffield Children's Hospital University of Sheffield Sheffield Children's NHS Foundation Trust

About

A. Dalton is an author at Sheffield Children's Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	127
2	Molecular Genetics	2	2	45
3	Health Sciences	1	1	18
4	Biochemistry	1	1	22
5	Cell Biology	1	1	22

A. Dalton

Publications

518

Citations

H-Index

Page 1

	Year	Citations
Clinical features of hereditary spastic paraplegia due to spastin mutation Christopher McDermott, Christine Burness, Janine Kirby, Neurology	2006	136
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK. Jayne Leggo, A. Dalton, Patrick J. Morrison, Journal of Medical Genetics	1997	78
High frequency of missense mutations in glycogen storage disease type VI Nicholas Beauchamp, Joanna Taybert, M. P. Champion, Journal of Inherited Metabolic Disease	2007	56
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency S. E. Olpin, Amal Afifi, S. Clark, Journal of Inherited Metabolic Disease	2003	52
Neonatal Screening for Cystic Fibrosis in the Trent Region (UK): Two-Stage Immunoreactive Trypsin Screening Compared with a Three-Stage Protocol with DNA Analysis as an Intermediate Step R. J. Pollitt, A. Dalton, Steve O. Evans, Journal of Medical Screening	1997	38
Infantile hereditary spastic paraparesis due to codominant mutations in the <i>spastin</i> gene Patrick F. Chinnery, Sharon Keers, M. J. Holden, Neurology	2004	31
Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation Sarah T. Pendlebury, P M Rothwell, A. Dalton, Neurology GeneticsPathologySudden OnsetMolecular GeneticsDisease Gene Identification	2004	24
Time-Course of Hypericin Phototoxicity and Effect on Mitochondrial Energies in EMT6 Mouse Mammary Carcinoma Cells Sandra A.S Johnson, A. Dalton, Ronald S. Pardini Free Radical Biology and Medicine Mitochondrial EnergiesTumor BiologyBiochemistryPhotochemistryMitochondrial Function	1998	22
<i>HSP60</i> IS A RARE CAUSE OF HEREDITARY SPASTIC PARAPARESIS, BUT MAY ACT AS A GENETIC MODIFIER Channa Hewamadduma, Janine Kirby, Christopher J. Kershaw, Neurology Rare DiseasesMendelian DisorderBroad Clinical VariabilityGenetic DisorderGenetics	2008	21
Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth H.Z. Blades, Paul Arundel, W. Carlino, Bone Bone DiseaseBone Mass AcquisitionBone HealthGenetic EpidemiologyBone Metabolism	2010	21

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