Reuben Matalon - Concepedia

Author

Reuben Matalon

The University of Texas Medical Branch at Galveston

Also Known As

MATALON, R, Matalon R, Matalon, Reuben, R Matalon, R. MATALON, R. Matalon, REUBEN MATALON, Reuben K Matalon, Reuben K. Matalon, Reuben MATALON

344

Publications

10.8K

Citations

H-Index

223

Concepts

All Affiliations

The University of Texas Medical Branch at Galveston University of Illinois Chicago University of Chicago Miami Children's Hospital Children's Hospital of Los Angeles

About

Reuben Matalon is an author at The University of Texas Medical Branch at Galveston specializing in medicine, pathology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	92	4.4K
2	Natural Sciences	12	13	858
3	Engineering	6	6	169
4	Health Sciences	4	4	115
5	Language Studies	1	1	24

Reuben Matalon

167

Publications

9.5K

Citations

H-Index

Page 1

	Year	Citations
Aspartoacylase deficiency and N‐acetylaspartic aciduria in patients with canavan disease Reuben Matalon, K. Michals, Donald G. Sebesta, American Journal of Medical Genetics	1988	404
Multiple Phenotypes in Phosphoglucomutase 1 Deficiency Laura C. Tegtmeyer, Stephan Rust, Monique van Scherpenzeel, New England Journal of Medicine	2014	279
Treatment of Inborn Errors of Urea Synthesis Mark L. Batshaw, Saul W. Brusilow, Lewis Waber, New England Journal of Medicine	1982	264
Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease Chikkathur N. Madhavarao, Peethambaran Arun, John R. Moffett, Proceedings of the National Academy of Sciences	2005	232
Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease Rajinder Kaul, Guang Ping Gao, Kuppareddi Balamurugan, Nature Genetics GeneticsPathologyCanavan DiseaseMolecular GeneticsGenomics	1993	218
Aspartoacylase gene transfer to the mammalian central nervous system with therapeutic implications for Canavan disease Paola Leone, C. G. Janson, L. Bilianuk, Annals of Neurology	2000	177
Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture. Reuben Matalon, Albert Dorfman Proceedings of the National Academy of Sciences	1966	170
Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations Heidi Erlandsen, Ángel L. Pey, Alejandra Gámez, Proceedings of the National Academy of Sciences Protein ChemistryAldehyde DehydrogenaseAldo-keto ReductaseBiochemistryBlood Phenylalanine Levels	2004	169
Genetic polymorphisms of methylenetetrahydrofolate reductase (<i>MTHFR</i>) and methionine synthase reductase (<i>MTRR</i>) in ethnic populations in Texas; a report of a novel<i>MTHFR</i>polymorphic site, G1793A Peter L. Rady, Sylvia Szucs, James J. Grady, American Journal of Medical Genetics GeneticsGenetic EpidemiologyHuman PolymorphismPathologyEthnic Populations	2001	157
The Maternal Phenylketonuria International Study: 1984–2002 Richard Koch, William Hanley, Harvey L. Levy, PEDIATRICS	2003	152

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