Lawrence J. Schut - Concepedia

Author

Lawrence J. Schut

Also Known As

L J Schut, L Schut, L. J. Schut, L. Schut, L.J. Schut, LAWRENCE J. SCHUT, LAWRENCE SCHUT, Lawrence J Schut, Lawrence J. Schut, Lawrence Schut

Publications

4.7K

Citations

H-Index

Concepts

All Affiliations

University of Minnesota Montreal Neurological Institute and Hospital Clarke University Baycrest Hospital University of Toronto

About

Lawrence J. Schut is an author at University of Minnesota specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	2.9K
2	Social Sciences	5	5	2.1K
3	Health Sciences	2	2	42
4	Biochemistry	2	2	68
5	Engineering	1	1	12

Lawrence J. Schut

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome P Trouillas, T Takayanagi, Mark Hallett, Journal of the Neurological Sciences Neurobiology Of DiseaseNeurological DisorderClinical NeurologySocial SciencesRehabilitation	1997	1.3K
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) Michael D. Koob, Melinda L. Moseley, Lawrence J. Schut, Nature Genetics Molecular NeuroscienceNeurological DisorderNeuroanatomyGeneticsSpinocerebellar Ataxia	1999	636
Spectrin mutations cause spinocerebellar ataxia type 5 Yoshio Ikeda, Katherine A. Dick, Marcy R. Weatherspoon, Nature Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2006	382
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11 Laura P.W. Ranum, Lawrence J. Schut, Julie K. Lundgren, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsPresident LincolnNeuroscience	1994	324
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families Melinda L. Moseley, Kellie Benzow, Lawrence J. Schut, Neurology	1998	238
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset. Laura P.W. Ranum, Ming‐Yi Chung, Sandro Banfi, PubMed	1994	165
Spinocerebellar ataxia type 8 John Day, Lawrence J. Schut, Melinda L. Moseley, Neurology	2000	153
Cognitive deficits in olivopontocerebellar atrophy: Implications for the cholinergic hypothesis of Alzheimer's dementia Stephen J. Kish, Munir El‐Awar, Lawrence J. Schut, Annals of Neurology NeuropsychologyAgingCorticobasal DegenerationSocial SciencesAlzheimer's Disease	1988	140
Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia. Laura P.W. Ranum, Julie K. Lundgren, Lawrence J. Schut, PubMed	1995	139
Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype Yves Robitaille, Lawrence J. Schut, Stephen J. Kish Acta Neuropathologica BiologyGenetic DisorderMedicineGeneticsOlivopontocerebellar Atrophy	1995	136

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