Edwin H. Kolodny

发表

Spontaneous appearance of Tay-Sachs disease in an animal model.

J. Alroy, G. Pastores, S. Raghavan, 2008, Molecular genetics and metabolism.

Pathology of GM2 Gangliosidosis in Jacob Sheep

J. Alroy, B. Porter, E. Kolodny, 2011, Veterinary pathology.

Hematopoietic stem-cell transplantation in globoid-cell leukodystrophy.

J. Wagner, L. Lockman, D. Loes, 1998, The New England journal of medicine.

Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients.

P. Kaplan, J. Charrow, H. Andersson, 2004, Seminars in hematology.

Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry

P. Kaplan, J. Charrow, H. Andersson, 2017, American journal of hematology.

Late-onset Krabbe disease (globoid cell leukodystrophy): clinical and biochemical features of 15 cases.

W. Krivit, S. Raghavan, E. Kolodny, 1991, Developmental neuroscience.

Clinical Heterogeneity of Familial Spastic Paraplegia Linked to Chromosome 2p21

J. Haines, M. Pericak-Vance, M. Nance, 1998, Human Heredity.

Effects of Diet and Behavior Therapy on Social and Motor Behavior of Retarded Phenylketonuric Adults: An Experimental Analysis

E. Kolodny, P. Touchette, D. Marholin, 1978, Pediatric Research.

Molecular genetics of the beta-hexosaminidase isoenzymes: an introduction.

E. Kolodny, Edwin H. Kolodny, 2001, Advances in genetics.

Pathology of GM2 Gangliosidosis in Jacob Sheep

B. C. Lewis, B. Zeng, K. Bretzlaff, 2011, Veterinary pathology.

The autosomal dominant form of “pure” familial spastic paraplegia

M. Spence, M. Marazita, E. Kolodny, 1987, Neurology.