"Edwin H. Kolodny" appeared in Books and Chapters

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"Edwin H. Kolodny" appeared in Books and Chapters

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Book	Author(s)	Year	Publisher
Neurology of hereditary metabolic diseases of children /	Lyon, Gilles.; Adams, Raymond D.; Kolodny, Edwin H.	[1996], ©1996.	McGraw-Hill, Health Professions Division,
Bioimaging in Neurodegeneration	Patricia A. Broderick; David N. Rahni; Edwin H. Kolodny	2005	Humana Press
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Chapter	Author(s)	Book	Book Authors	Year	Publisher
Sandhoff’s Disease: Studies on the Enzyme Defect in Homozygotes and Detection of Heterozygotes	Edwin H. Kolodny	Sphingolipids, Sphingolipidoses and Allied Disorders: Proceedings of the Symposium on Sphingolipidoses and Allied Disorders held in Brooklyn, New York, October 25–27, 1971	Bruno W. Volk; Stanley M. Aronson	1972	Springer US
Lysosomal Storage Diseases	Edwin H. Kolodny	Mental Retardation and Developmental Disabilities: Volume 13	Joseph Wortis	1984	Springer US
Overview of the Leukoencephalopathies	Edwin H. Kolodny	Bioimaging in Neurodegeneration	Patricia A. Broderick; David N. Rahni; Edwin H. Kolodny	2005	Humana Press
10. Molecular genetics of the βxosaminidase isoenzymes: An introduction	Edwin H. Kolodny	Tay-Sachs Disease	Michael M. Kaback	2001	Academic Press
19. The G[subscript M2] Gangliosidoses	Edwin H. Kolodny	The molecular and genetic basis of neurologic and psychiatric disease /	Rosenberg, Roger N.	c2008.	Wolters Kluwer Health/Lippincott Williams & Wilkins,
51. Fabry disease	Edwin H. Kolodny	Stroke syndromes /	Bogousslavsky, Julien.; Caplan, Louis R.	[1995], ©1995.	Cambridge University Press,
Chapter 13 Dementia in Young Adults	Marcin Sadowski; Edwin H. Kolodny	The Dementias 2		2007	Butterworth-Heinemann
Inherited neurodegenerative diseases	Edwin H. Kolodny; Swati Sathe	Oxford Textbook of Medicine		2010	Oxford University Press
Chapter 29 - Lysosomal disorders and Menkes syndrome	Edwin H. Kolodny; Swati Sathe	The Causes of Epilepsy: Common and Uncommon Causes in Adults and Children	Simon D. Shorvon; Frederick Andermann; Renzo Guerrini	2011-04	Cambridge University Press
Arylsulfatases A and B in Metachromatic Leukodystrophy and Maroteaux-Lamy Syndrome: Studies with 4-Methylumbelliferyl Sulfate	Edwin H. Kolodny; Richard A. Mumford	Current Trends in Sphingolipidoses and Allied Disorders	Bruno Volk	1976	Springer US
20. Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency: Sulfatide Lipidosis	Edwin H. Kolodny and Swati Sathe	The molecular and genetic basis of neurologic and psychiatric disease /	Rosenberg, Roger N.	c2008.	Wolters Kluwer Health/Lippincott Williams & Wilkins,
Ch. 21. The Gm2-Gangliosidoses	Edwin H. Kolodny and Orit Neudorfer	The molecular and genetic basis of neurologic and psychiatric disease /	Rosenberg, Roger N.	[2003], ©2003.	Butterworth-Heinemann,
Ch. 22. Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency: Sulfatide Lipidosis	Edwin H. Kolodny and Orit Neudorfer	The molecular and genetic basis of neurologic and psychiatric disease /	Rosenberg, Roger N.	[2003], ©2003.	Butterworth-Heinemann,
Seizures in Hereditary Metabolic Disease	Claude Sansaricq; Gilles Lyon; Edwin H. Kolodny	The Epilepsies	Prakash Kotagal and Hans O. Lüders	1999	Academic Press
Chapter	Author(s)	Book	Book Authors	Year	Publisher

Showing 1 to 14 of 14 entries

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