Dong Wang MD

PubMed

• A Distinct Down-to-Up Transition Assembly in the Retrosplenial Cortex during Slow-Wave Sleep.
  Ashley N Opalka, Kimberly J Dougherty, Dong V Wang
  The Journal of Neuroscience. 2025-04-02
• A cortical-hippocampal communication undergoes rebalancing after new learning.
  Arron F Hall, Dong V Wang
  Biorxiv. 2025-03-29
• Tau and MAP6 establish labile and stable domains on microtubules.
  Koray Kirimtay, Wenqiang Huang, Xiaohuan Sun, Liang Qiang, Dong V Wang
  Iscience. 2025-03-21

Journal Articles

• Allelic Variations of Glut1 Deficiency Syndrome: The Chinese Experience  
  Liu Y, Bao XH, Wang D, Fu N, Zhang XY, Cao GN, Song FY, Wang S, Zhang YH, QinJ, Yang H, Engelstad K, De Vivo DC, Wu XR, Pediatr Neurol, 1/1/2012
• T295M associated glut-1 deficiency syndrome with normal erythrocyte 3-OMG uptake  
  Fuji T, Morimoto M, Yoshioka H, Ho YY, Law PY, Wang D, De Vivo DC, Brain Dev, 1/1/2011
• Uncovering Microdeletions in Patients with Severe Glut-1 Deficiency Syndrome Using SNP Oligonucleotide Microarray Analysis  
  Levy B, Wang D, Ullner PM, Engelstad K, Yang H, Nahum O, Chung WK, De Vivo DC, Molecular Genetics and Metabolism, 1/1/2010
• Murine Glut-1 transporter haploinsufficiency: postnatal deceleration of brain weight and reactive astrocytosis  
  Ullner PM, Di Nardo A, Goldman JE,Schobel S, Yang H, Engelstad K, Wang D,Sahin M, De Vivo DC, Neurobiology of Disease, 1/1/2009
• Methylprednisolone for Status Migrainous Vertigo and Cephalic Status Migrainosus  
  Robbins MS, Wang D,DeOrchis VS, Headache, 1/1/2009
• Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency  
  Akman CI, Engelstad K, Hinton VJ, Ullner P, Koenigsberger D, Leary L, Wang D, De Vivo DC, Annals of Neurology, 1/1/2009
• Functional studies of the T295M mutation Causing Glut1 Deficiency: Glucose efflux preferentially affected by T295M  
  Wang D, Yang H, Shi L, Ma L, Fujii T, Engelstad K, Pascual JM, and De Vivo DC, Ped Res, 1/1/2008
• Glut 1 deficiency without epilepsy- yet another case  
  Joshi C, Greenberg CR, De Vivo DC, Wang D, Chan-Lui W and Booth F, J Child Neurol, 1/1/2008
• Membrane helix 4 and other crucial structural signatures of Glut-1: Inferences from blood brain glucose transport mutants  
  Pascual JM, Wang D, Yang R, Shi L, Yang H, and Darryl DC, JBC, 1/1/2008
• A Novel tRNAVal Mitochondrial DNA Mutation Causing MELAS  
  Tanji K, Kaufmann K, Naini AB, Parsons TC, Wang D, Wiley J, Lu JS, Shanske S, Hirano M, Khandji AJ, DiMauro S and Rowland LP, J NeurolSci, 1/1/2008
• Glut1 Deficiency: CSF Glucose How low is too low?  
  De Vivo,Wang D, Revue Neurologique, 1/1/2008
• Brain glucose supply and the syndrome of infantile neuroglycopenia  
  Pascual JM, Wang D, Hinton V, Engelstad K, Saxena CM, Van Heertum RL, De Vivo DC, Archives of Neurology, 1/1/2007
• Three Japanese patients with glucose transporter type 1 deficiency syndrome  
  Fujii T, Ho YY, Wang D, De Vivo DC, Miyajima T, Wong HY, Tsang PT, Shirasaka Y, Kudo T and Ito M, Brain & Dev, 1/1/2007
• Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiencysyndrome  
  Coman DJ, Sinclair KG, Burke CJ, Appleton DB, Pelekanos JT, O'Neil CM, Wallace GB, Bowling FG, Wang D, De Vivo DC, McGill JJ, J Paediatr Child Health, 1/1/2006
• Atypical GLUT1 Deficiency: Movement Disorder and Sleep Disturbance Responsive to Ketogenic Diet  
  Friedman JR, Thiele EA, Wang D, Levine KB, Cloherty EK, Pfeifer H, De Vivo DC, Carruthers A,Natowicz M, MovDisord, 1/1/2006
• Glucose transporter protein syndromes (In Chinese)  
  Wang D,Sun RP, Wang X, Yang R, Yang H, Pascual JM, De Vivo DC, J. Chinese Pediatrics, 1/1/2005
• Type 1 glucose transporter (Glut1) deficiency: manifestations of a hereditary neurological syndrome (In Spanish)  
  Pascual JM, Lecumberri B,Wang D, Yang R, Engelstad K, De Vivo DC, Rev Neurol, 1/1/2004
• GLUT1 deficiency without epilepsy -an exceptional case  
  Overweg-Plandsoen WCG, Groener JEM, Wang D, Onkenhout P, Brouwer OF, Bakker HD, De Vivo DC, J. Inherit. Metab. Dis., 1/1/2003
• Functional studies of Thr310 mutations in Glut-1: T310I is a pathogenic mutation of Glut-1 deficiency  
  Wang D, Pascual JM, Iserovich P, Yang H, Ma L, Kuang K, Kranz-Eble P, Fischbarg J, De Vivo DC, J Biol Chem, 1/1/2003
• Seizure characterization and electrographic features in Glut-1 deficiency syndrome  
  Leary LD, Wang D, Nordli DR, Engelstad K, De vivo DC, Epilepsia, 1/1/2003
• Changes in glucose transport and water permeability resulting from the T310I pathogenic mutation in Glut1 are consistent with two transport channels per monomer  
  Wang D, Iserovich P, Ma L, Yang H, Zuniga FA, Shi G, Haller JF, Wen Q, Pascual JM, Kuang K, De Vivo DC, Fischbarg J, J. Biol. Chem., 1/1/2002
• Glut-1 Deficiency Syndrome and Other Glycolytic Defects  
  De VivoDC, Leary L, Wang D, J Child Neurol, 1/1/2002
• Glucose transporter proteindeficiency syndromes  
  De Vivo DC, Wang D, Pascual JM, Ho Y-Y, Int Rev Neurobiol, 1/1/2002
• Imaging the metabolic footprint of Glut1 deficiency on the brain  
  Pascual JM, van Heertum RL, Wang D, Engelstad K, De Vivo DC, Ann Neurol, 1/1/2002
• EEG Features of Glut-1 Deficiency Syndrome  
  von Moers A, Brockmann K, Wang D, Korenke CG, Huppke P, De Vivo DC, and Hanefeld F, Epilepsia, 1/1/2002
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Abstracts/Posters

• Functional Studies Confirm Relative Pathogenicity of Serine 66 Mutations in Glut1 Deficiency.
  Wang D, Yang H, De Vivo DC, Neurology, (poster presentation to be presented at 65th AAN Annual Meeting), 1/1/2013
• Glut1 Deficiency Syndrome -An Emerging Realization of Protean Phenotypes.
  Wang D, Yang H, Bagay L, Engelstad K, Bao XH, De Vivo DC, Neurology, (poster presentation at 63rd AAN Annual Meeting), 1/1/2012
• Glut1 Deficiency Syndrome: The Diagnostic Value of the Erythrocyte 3-O-Methyl-D-Glucose Uptake Assay.
  Wang D, Yang H, Bagay L, Engelstad K, Wei Y, Rotstein M, Chung W, De Vivo DC, Neurology, 63rd AAN Annual Meeting, 1/1/2011
• Voxel based brain mapping of glucose metabolism in children with glucose transporter Type 1 Deficiency.
  Akman CI, Provazano F, Wang D, Engelstad K, Rikofsky R, Van Heertum RL, De Vivo DC, Neurology, 1/1/2008
• GLUT1 Deficiency without Epilepsy: Yet another case.
  Joshi C, Greenberg CR, De Vivo D, Wang D, Chan-Lui W, Booth FA, J Child Neurol, 1/1/2008
• A novel mutation in pyruvate carboxylase deficiency Type C.
  Lang TF, Wang D, De Vivo DC and Loughrey CL, J Inherited Metab Dis, 1/1/2008
• Pyruvate carboxylase deficiency: Mosaicism correlates with prolonged survival.
  Wang D, Yang H, Lu JS, De Vivo DC, Am Acad Neurol, 1/1/2007
• Molecular genetics of Glut1 Deficiency Syndrome.
  Wang D, Yang H, Engelstad K, Min-Wei C, De Vivo DC, Neurology, 1/1/2007
• Glucose transporter type 1 deficiency syndrome (Glut1 DS). (Platform presentation)
  Wang D, Pascual JM and De Vivo DC, 10th International Child Neurology Congress, Montreal, Canada, 1/1/2006
• Aminoglycoside enhancement of glucose transport in GLUT1 Deficiency Syndrome.
  Pascual JM, Zhang XM, Wang D, and De Vivo DC, Neuropediatrics, 1/1/2006
• Glucose transporter Type 1 deficiency syndrome (Glut 1 DS): the relationship with glucose transport to brain function during development.
  De Vivo DC, Engelstad K, Pascual JM, Wang D, Neurometabolic Disease Symposium Section, 10th International Child Neurology Congress, Montreal, Canada, 1/1/2006
• Glucose Transporter Type 1 Deficiency Syndrome (GLUT 1 DS).
  De Vivo DC, Wang D, Pascual J, Neuropediatrics, 1/1/2006
• GLUT-1 Deficiency Syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins.
  Henneke M, Wang D, Korinthenberg R, Pascual J, Yang H, Engelstad K, Brockmann K, De Vivo DC, Gartner J, Neuropediatrics, 1/1/2005
• Effects of valproic acid on GLUT-1 gene expression.
  Mao X, Wang D, Pascaul JM, Yang H, Stiener D, De Vivo DC, Soc Neurosci, 1/1/2004
• Pyruvate carboxylase deficiency: genotype-phenotype correlations.
  Wang D,Pascaul JM, Yang H, Steiner D, Di Mauro S, De Vivo DC, Soc Neurosci, 1/1/2004
• KmtA, A putative novel potassium transporter gene.
  Yang R, Wang D, Yang H, De Vivo DC, Pascaul JM, Soc Neurosci, 1/1/2004
• Functional studies of disease-associated R126 mutations in GLUT1.
  Yang R, Wang D, Yang H, Pascaul JM, De Vivo DC, Soc Neurosci, 1/1/2004
• Pyruvate dehydrogenase deficiency: clinical and molecular analysis.
  GarciaAlvarez M, Wang D, Kranz-Eble P, De Vivo DC, The Joint Congress of ICNA and AOCNA, 1/1/2002
• Early onset dystonia /choreoathetosls/ataxia secondary to GLUT-1 deficiency, responsible to Ketogenic diet.
  FriedmanJR, Thiele E A, Wang D, De Vivo DC, Penny P, Heidi, P, Movement disorders, 1/1/2002
• Genotype-phenotype correlation of Glut-1 deficiency syndrome.
  Wang D, Pascual JM, Kranz-Eble P, Yang H, Alvarez MG, Sun RP, De Vivo DC, The Joint Congress of ICNA and AOCNA, 1/1/2002
• Water permeability of pathogenic mutants of human facilitative glucose transporter Glut-1.
  Ma L, Wang D, Zuniga F, Wang D, Kuang K, Yang H, Iserovich P, De Vivo DC, Fischbarg J, ARVO (The Association for Research in Vision and Ophthalmology) meeting, 1/1/2002
• Glut-1 deficiency syndrome (Glut-1DS): A severe phenotype associated with compound heterozygosity in trans.
  Wang D, Pascual JM, Yang H, Ho YY, Hinton V, Yang H, Engelstad K, Jhung S, Miller C, Kranz-Eble P, De Vivo DC, Ann Neurol, 1/1/2001
• Water passage across a water-filled pore in the Glut1 glucose transporter pathogenic mutant T310I.
  Ma L, Wang D, Kuang K, Yang H, Iserovich P, Wen Q, Pauscal JM, De Vivo DC and Fischbarg J, IOVS, 1/1/2001
• Glut-1 deficiency syndrome (Glut-1DS): Autosomal dominant transmission of the R126H missense mutation.
  Wang D, Brockmann K, Korenke CG, Moers AV, Ho YY, Pascual JM, Kuang K, Yang H, Ma L, Kranz-Eble P, Fischbarg J, Hanefeld F and De Vivo DC, Ann Neurol, 1/1/2001
• Glut-1 deficiency syndrome (Glut-1DS): R333W genotype and paternal mosaicism.
  Wang D, Ho Y-Y, Pascual JM, Hinton V, Yang H, Anolik M, Kranz-Eble P, Jhung S, Engelstad K, De Vivo DC, Ann Neurol, 1/1/2001
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Other

• Glucose Transporter Type 1 Deficiency Syndrome. 
  Wang D, Pascual JM, De Vivo D; Pagon RA, Bird TD, Dolan CR, et al., eds., GeneReviews™ [Internet]
  University of Washington, Seattle, Seattle, WA - 8/9/2012
• Pyruvate Carboxylase Deficiency. 
  Wang D, De Vivo D; Pagon RA, Bird TD, Dolan CR, et al., eds., GeneReviews™ [Internet]
  University of Washington, Seattle, Seattle, WA - 7/21/2011