Dong Wang

发表

Murine Glut-1 transporter haploinsufficiency: Postnatal deceleration of brain weight and reactive astrocytosis

M. Sahin, P. Ullner, A. Nardo, 2009, Neurobiology of Disease.

Imaging the metabolic footprint of Glut1 deficiency on the brain

R. V. Van Heertum, K. Engelstad, Dong Wang, 2002, Annals of neurology.

Functional Studies of Threonine 310 Mutations in Glut1

Hong Yang, Dong Wang, J. Pascual, 2003, Journal of Biological Chemistry.

Structural Signatures and Membrane Helix 4 in GLUT1

Lei Shi, Hong Yang, Dong Wang, 2008, Journal of Biological Chemistry.

Defective Glucose Transport Across Brain Tissue Barriers: A Newly Recognized Neurological Syndrome

J. Vera, Dong Wang, D. D. De Vivo, 1999, Neurochemical Research.

Atypical GLUT1 deficiency with prominent movement disorder responsive to ketogenic diet

E. Thiele, J. Friedman, Dong Wang, 2006, Movement disorders : official journal of the Movement Disorder Society.

Glucose Transporter Type 1 Deficiency Syndrome

Dong Wang, D. Vivo, J. Pascual, 2015 .

GLUT1 deficiency and other glucose transporter diseases.

Hong Yang, Dong Wang, J. Pascual, 2004, European journal of endocrinology.

Autosomal dominant Glut‐1 deficiency syndrome and familial epilepsy

F. Hanefeld, Hong Yang, Dong Wang, 2001, Annals of neurology.

Glucose Transporter Type 1 Deficiency Syndrome (Glut1DS): Methylxanthines Potentiate GLUT1 Haploinsufficiency In Vitro

Hong Yang, Dong Wang, D. Vivo, 2001, Pediatric Research.

GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier

N. Spinner, M. Birnbaum, J. Yeh, 1998, Nature Genetics.

A mouse model for Glut-1 haploinsufficiency.

J. Noebels, Hong Yang, K. Engelstad, 2006, Human molecular genetics.

Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement

Wei Zhang, Zhaoxia Wang, Yun Yuan, 2019, Neuromuscular Disorders.

Glut1 deficiency: Inheritance pattern determined by haploinsufficiency

W. Chung, B. Levy, Hong Yang, 2010, Annals of neurology.

Allelic variations of glut-1 deficiency syndrome: the chinese experience.

Hong Yang, K. Engelstad, Dong Wang, 2012, Pediatric neurology.

A mouse model for Glut1 haploinsufficiency

J. Noebels, Hong Yang, K. Engelstad, 2006 .

Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysis.

W. Chung, B. Levy, P. Ullner, 2010, Molecular genetics and metabolism.

The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.

Hong Yang, Dong Wang, P. Briones, 2008, Molecular genetics and metabolism.

Changes in Glucose Transport and Water Permeability Resulting from the T310I Pathogenic Mutation in Glut1 Are Consistent with Two Transport Channels per Monomer*

Hong Yang, Dong Wang, J. Pascual, 2002, The Journal of Biological Chemistry.

Seizure Characterization and Electroencephalographic Features in Glut‐1 Deficiency Syndrome

K. Engelstad, Dong Wang, D. Nordli, 2003, Epilepsia.

EEG Features of Glut‐1 Deficiency Syndrome

P. Huppke, F. Hanefeld, Dong Wang, 2002, Epilepsia.

Mutational analysis of GLUT1 (SLC2A1) in Glut‐1 Deficiency Syndrome

Dong Wang, D. D. De Vivo, Darryl C. De Vivo, 2000, Human mutation.

Mutational Analysis of GLUT 1 ( SLC 2 A 1 ) in Glut1 Deficiency Syndrome

Dong Wang, D. Vivo, P. Kranz-Eble, 2022 .

Glut‐1 deficiency syndrome: Clinical, genetic, and therapeutic aspects

Hong Yang, K. Engelstad, Dong Wang, 2005, Annals of neurology.

Glut1 deficiency syndrome and erythrocyte glucose uptake assay

Ying Wei, V. Aggarwal, B. Levy, 2011, Annals of neurology.

Topography of brain glucose hypometabolism and epileptic network in glucose transporter 1 deficiency

R. Tikofsky, F. Provenzano, K. Engelstad, 2015, Epilepsy Research.

Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency

P. Ullner, K. Engelstad, Dong Wang, 2010, Annals of neurology.

Brain glucose supply and the syndrome of infantile neuroglycopenia.

R. V. Van Heertum, K. Engelstad, Dong Wang, 2007, Archives of neurology.

Glucose transporter 1 deficiency syndrome and other glycolytic defects.

Dong Wang, L. Leary, D. D. De Vivo, 2002, Journal of child neurology.

Erythrocyte 3‐O‐methyl‐D‐glucose uptake assay for diagnosis of glucose‐transporter‐protein syndrome

Dong Wang, D. D. De Vivo, Y. Ho, 1999, Journal of clinical laboratory analysis.

Glucose transporter type I deficiency and other glucose flux disorders

Dong Wang, D. Vivo, J. Pascual, 2020, Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease.

Three Japanese patients with glucose transporter type 1 deficiency syndrome

T. Kudo, Dong Wang, D. Vivo, 2007, Brain and Development.

T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake

Dong Wang, D. Vivo, M. Morimoto, 2011, Brain and Development.

Functional Studies of the T295M Mutation Causing Glut1 Deficiency: Glucose Efflux Preferentially Affected by T295M

Lei Shi, Hong Yang, K. Engelstad, 2008, Pediatric Research.

GLUT1-Deficiency: Barbiturates Potentiate Haploinsufficiency in Vitro

J. Vera, Dong Wang, D. Vivo, 1999, Pediatric Research.

GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins

K. Engelstad, Dong Wang, M. Henneke, 2005 .

Glucose transporter protein syndromes.

Dong Wang, J. Pascual, D. D. De Vivo, 2002, International review of neurobiology.

A novel tRNAVal mitochondrial DNA mutation causing MELAS

S. Dimauro, A. Khandji, J. Willey, 2008, Journal of the Neurological Sciences.

Glucose Transporter Type 1 Deficiency Syndrome

Dong Wang, D. Vivo, J. Pascual, 2015 .

Glut1 deficiency: CSF glucose. How low is too low?

Dong Wang, D. Vivo, D. D. De Vivo, 2008, Revue neurologique.

GLUT-1 deficiency without epilepsy—an exceptional case

Dong Wang, D. Vivo, O. Brouwer, 2003, Journal of Inherited Metabolic Disease.