Bai J Zeng, M.D.

Krabbe disease: Clinical, biochemical and molecular information on six new patients and successful retrospective diagnosis using stored newborn screening cards
Puckett R.L.; Orsini J.J.; Pastores G.M.; Wang R.Y.; Chang R.; Saavedra-Matiz C.A.; Torres P.A.; Zeng B.; Caggana M.; Lorey F.; Abdenur J.E.
2012 ;105(1):126-131, Molecular genetics & metabolism
— id: 149818, year: 2012, vol: 105, page: 126, stat: Journal Article,

Pathology of GM2 gangliosidosis in Jacob sheep
Porter, B F; Lewis, B C; Edwards, J F; Alroy, J; Zeng, B J; Torres, P A; Bretzlaff, K N; Kolodny, E H
2011 Jul;48(4):807-813, Veterinary pathology
— id: 141329, year: 2011, vol: 48, page: 807, stat: Journal Article,

Krabbe disease: Clinical, biochemical and molecular information on six new patients and successful retrospective diagnosis using stored newborn screening cards
Puckett, R. L.; Orsini, J. J.; Pastores, G. M.; Saavedra, C. A.; Torres, P. A.; Zeng, B.; Chang, R.; Wang, R. Y.; Caggana, M.; Lorey, F.; Abdenur, J. E.
2011 MAR ;102(3):309-310, Molecular genetics & metabolism
— id: 127193, year: 2011, vol: 102, page: 309, stat: Journal Article,

Tay-Sachs disease in Jacob sheep
Torres, Paola A; Zeng, Bai Jin; Porter, Brian F; Alroy, Joseph; Horak, Fred; Horak, Joan; Kolodny, Edwin H
2010 Dec;101(4):357-363, Molecular genetics & metabolism
— id: 114819, year: 2010, vol: 101, page: 357, stat: Journal Article,

Multiple sulfatase deficiency: clinical report and description of two novel mutations in a Brazilian patient
Artigalas, Osvaldo Alfonso; da Silva, Luiz Roberto; Burin, Maira; Pastores, Gregory M; Zeng, Bai; Macedo, Nivea; Schwartz, Ida Vanessa Doederlein
2009 Sep;24(3):493-500, Metabolic brain disease
— id: 109087, year: 2009, vol: 24, page: 493, stat: Journal Article,

A novel GM2-activator deficiency mutation as a cause of AB variant GM2-gangliosidosis
Kolodny, E; Sathe, S; Zeng, BJ; Torres, P; Alroy, J; Pastores, G
2008 FEB ;93(2):S27-S28, Molecular genetics & metabolism
— id: 87125, year: 2008, vol: 93, page: S27, stat: Journal Article,

Juvenile-onset g(m2)-gangliosidosis in an african-american child with nystagmus
Paciorkowski, Alex R; Sathe, Swati; Zeng, Bei-Jin; Torres, Paola; Rosengren, Sally S; Kolodny, Edwin
2008 Apr;38(4):284-286, Pediatric neurology
— id: 77798, year: 2008, vol: 38, page: 284, stat: Journal Article,

Novel mutations in juvenile Sandhoff disease presenting as motor neuron disease
Pierson, TM; Zeng, BJ; Torres, P; Pastores, G; Finkel, R; Mahuran, D; Kolodny, E; Tennekoon, G
2008 FEB ;93(2):S33-S33, Molecular genetics & metabolism
— id: 87128, year: 2008, vol: 93, page: S33, stat: Journal Article,

Spontaneous appearance of Tay-Sachs disease in an animal model
Zeng, B J; Torres, P A; Viner, T C; Wang, Z H; Raghavan, S S; Alroy, J; Pastores, G M; Kolodny, E H
2008 Sep-Oct;95(1-2):59-65, Molecular genetics & metabolism
— id: 93349, year: 2008, vol: 95, page: 59, stat: Journal Article,

Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene
Janson, Christopher G; Kolodny, Edwin H; Zeng, Bai-Jin; Raghavan, Srinivasa; Pastores, Gregory; Torres, Paola; Assadi, Mitra; McPhee, Scott; Goldfarb, Olga; Saslow, Beth; Freese, Andrew; Wang, D J; Bilaniuk, Larissa; Shera, David; Leone, Paola
2006 Feb;59(2):428-431, Annals of neurology
— id: 62683, year: 2006, vol: 59, page: 428, stat: Journal Article,

Spontaneous appearance of Tay-Sachs disease in American flamingos
Kolodny, EH; Zeng, BJ; Viner, T; Torres, PA; Wang, ZH; Raghavan, SS
2006 MAR 14 ;66(5):274-274, Neurology
— id: 74924, year: 2006, vol: 66, page: 274, stat: Journal Article,

Rapid detection of three large novel deletions of the aspartoacylase gene in non-Jewish patients with Canavan disease
Zeng, B J; Wang, Z H; Torres, P A; Pastores, G M; Leone, P; Raghavan, S S; Kolodny, E H
2006 Sep-Oct;89(1-2):156-163, Molecular genetics & metabolism
— id: 69024, year: 2006, vol: 89, page: 156, stat: Journal Article,

Mutation analysis of the aspartoacylase gene in non-Jewish patients with Canavan disease
Zeng, Bai-Jin; Pastores, Gregory M; Leone, Paola; Raghavan, Srinivasa; Wang, Zhao-Hui; Ribeiro, Lucilene A; Torres, Paola; Ong, Elton; Kolodny, Edwin H
2006 ;576:165-73; discussion 361, Advances in experimental medicine & biology
— id: 67534, year: 2006, vol: 576, page: 165, stat: Journal Article,

Late-onset Tay-Sachs disease: Phenotypic characterization and genotypic correlations in 21 affected patients
Neudorfer, Orit; Pastores, Gregory M; Zeng, Bai J; Gianutsos, John; Zaroff, Charles M; Kolodny, Edwin H
2005 Feb;7(2):119-123, Genetics in medicine
— id: 48748, year: 2005, vol: 7, page: 119, stat: Journal Article,

Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations
Raghavan, S; Zeng, B; Torres, P A; Pastores, G M; Kolodny, E H; Kurtzberg, J; Krivit, W
2005 ;28(6):1005-1009, Journal of inherited metabolic disease
— id: 64662, year: 2005, vol: 28, page: 1005, stat: Journal Article,

Late-onset Tay-Sachs disease: natural history and treatment with OGT 918 (Zavesca (TM))
Kolodny, EH; Neudorfer, O; Gianutsos, J; Zaroff, C; Barnett, N; Zeng, B; Raghavan, S; Torres, P; Pastores, G
2004 AUG ;90(5):54-54, Journal of neurochemistry
— id: 46902, year: 2004, vol: 90, page: 54, stat: Journal Article,

Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations
Krivit, WC; Kurtzberg, J; Zeng, B; Torres, P; Pastores, G; Raghavan, S
2004 AUG ;90(5):95-95, Journal of neurochemistry
— id: 46903, year: 2004, vol: 90, page: 95, stat: Journal Article,

Therapeutic effects of astrocytes expressing both tyrosine hydroxylase and brain-derived neurotrophic factor on a rat model of Parkinson's disease
Wang, Z H; Ji, Y; Shan, W; Zeng, B; Raksadawan, N; Pastores, G M; Wisniewski, T; Kolodny, E H
2002 ;113(3):629-640, Neuroscience
— id: 39612, year: 2002, vol: 113, page: 629, stat: Journal Article,

Identification and characterization of novel mutations of the aspartoacylase gene in non-Jewish patients with Canavan disease
Zeng, B J; Wang, Z H; Ribeiro, L A; Leone, P; De Gasperi, R; Kim, S J; Raghavan, S; Ong, E; Pastores, G M; Kolodny, E H
2002 Nov;25(7):557-570, Journal of inherited metabolic disease
— id: 39272, year: 2002, vol: 25, page: 557, stat: Journal Article,

Rapid detection of the two common mutations in Ashkenazi Jewish patients with mucolipidosis type IV
Wang ZH; Zeng B; Pastores GM; Raksadawan N; Ong E; Kolodny EH
2001 Summer;5(2):87-92, Genetic testing
— id: 39483, year: 2001, vol: 5, page: 87, stat: Journal Article,

The major mutation in mucolipidosis IV among Ashkenazi Jewish individuals requires further clarification. (vol 5, pg 87, 2001)
Wang, ZH; Zeng, B; Pastores, GM; Raksadawan, N; Ong, E; Kolodny, EH
2001 ;5(3):273-273 FAL, Genetic testing
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