S. DiMauro - Concepedia

Author

S. DiMauro

Columbia University

Also Known As

G Serratrice, S DIMAURO, S DiMauro, S Dimauro, S. DIMAURO, S. DiMauro, S. Dimauro, Salvatore DiMauro, Salvatore Dimauro

286

Publications

21.3K

Citations

H-Index

167

Concepts

All Affiliations

Columbia University NewYork–Presbyterian Hospital Muscular Dystrophy Association Columbia University Irving Medical Center

About

S. DiMauro is an author at Columbia University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	49	88	8.1K
2	Health Sciences	18	21	1.7K
3	Natural Sciences	13	14	2.1K
4	Education	1	1	153
5	Public Health	1	1	44

S. DiMauro

195

Publications

18.5K

Citations

H-Index

Page 1

	Year	Citations
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Massimo Zeviani, Carlos T. Moraes, S. DiMauro, Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderNatural Sciences	1988	735
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases. Carlos T. Moraes, Sara Shanske, Hans Tritschler, PubMed	1991	590
MELAS: Clinical features, biochemistry, and molecular genetics Emma Ciafaloni, Enzo Ricci, Sara Shanske, Annals of Neurology	1992	506
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy E. Arnaudo, Sarah Shanske, S. DiMauro, The Lancet	1991	505
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) Michio Hirano, Gabriella Silvestri, D. M. Blake, Neurology Mitochondrial MyopathyNeuromusculoskeletal DisorderPeripheral NeuropathyMitochondrial FunctionQuantitative Emg	1994	407
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Massimo Zeviani, Carlos T. Moraes, S. DiMauro, Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderNatural Sciences	1988	369
Dichloroacetate causes toxic neuropathy in MELAS P. Kaufmann, Kristin Engelstad, Ying Wei, Neurology	2006	355
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations Ichizo Nishino, Antonella Spinazzola, Alexandros Papadimitriou, Annals of Neurology	2000	342
Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome? Richard A. Berenberg, John M. Pellock, S. DiMauro, Annals of Neurology Ocular DiseaseShort StatureNeurological DisorderPathologyCommon Neurological Disorders	1977	317
The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome Filippo M. Santorelli, Sara Shanske, Alfons Macaya, Annals of Neurology	1993	256

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