R. Surtees - Concepedia

Author

R. Surtees

Also Known As

R A H Surtees, R A Surtees, R Surtees, R. A H Surtees, R. A. H. Surtees, R. A. Surtees, R. A.H. Surtees, R. SURTEES, R. Surtees, Rachel Surtees

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University College London Great Ormond Street Hospital Institute of Child Health Royal Manchester Children's Hospital National Hospital for Neurology and Neurosurgery

About

R. Surtees is an author at University College London specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	1.1K
2	Health Sciences	3	3	76
3	Public Health	2	2	266
4	Social Sciences	2	2	82
5	Natural Sciences	1	1	149

R. Surtees

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members NiCole A. Finch, Matthew B. Baker, Richard Crook, Brain	2009	377
Recommendations on the dietary management of phenylketonuria. Report of Medical Research Council Working Party on Phenylketonuria. D. P. Brenton, Jean Chapple, B. J. Clark, Archives of Disease in Childhood NutritionUrologyClinical NutritionDietary ManagementMedical Nutrition Therapy	1993	253
Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway R. Surtees, J. Leonard, Stephanie Austin The Lancet Cerebrospinal-fluid S-adenosylmethionineInborn ErrorsNeurological DisorderMedicineCerebrospinal Fluid	1991	234
The effect of genotype on the natural history of eIF2B-related leukodystrophies Anne Fogli, Raphael Schiffmann, Enrico Bertini, Neurology	2004	166
GAMT deficiency Saadet Mercimek‐Mahmutoglu, Sylvia Stoeckler-Ipsiroglu, A. Adami, Neurology	2006	156
Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism? Kevin Talbot, Chris P. Ponting, Aspasia Theodosiou, Human Molecular Genetics GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsDisease Gene Identification	1997	149
Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I) S. Kölker, E. Christensen, James V. Leonard, Journal of Inherited Metabolic Disease	2007	145
Neurological outcome of methylmalonic acidaemia Paola Nicolaides, James V. Leonard, R. Surtees Archives of Disease in Childhood	1998	132
Dopa‐responsive dystonia: A clinical and molecular genetic study Oliver Bandmann, Enza Maria Valente, Peter Holmans, Annals of Neurology	1998	125
Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) Tracy A. Briggs, Ghada M. H. Abdel‐Salam, Maryagnes R. Balicki, American Journal of Medical Genetics Part A	2007	103

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