DongWangMD

Neurology Duluth, GA

Epilepsy, Neurophysiology, Child Neurology

Attending Neurologist at SRMC, Georgia Neurodiagnostic and Treatment Center( Riverdale, GA), and LaGrange Neurology

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Office Address

3790 Pleasant Hill Rd, Suite 250
30096
Duluth, GA 30096
Phone
(678) 878-2989

Fax
(678) 878-2990
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Education & Training

Drexel University - Hahnemann University HospitalFellowship
Albert Einstein College of MedicineResidency
New York Presbyterian Hospital - Columbia CampusResidency
New York Presbyterian HospitalFellowship
Shandong Medical UniversityMedicalSchool

Certifications & Licensure

PA State Medical License 2012 - 2014
GA State Medical License 2012 - 2020
American Board of Psychiatry and Neurology Neurology

Awards, Honors, & Recognition

The recipient of American Academy of Neurology Alliance Awards: S. Weir Mitchell Award American Academy of Neurology, 2011
Third prize awarded in the Science Poster Competition American Chinese Medical Association (ACMA) annual meeting, 1999
Annual Outstanding Scholastic Achievement Award Shandong Medical University, 1984

Publications & Presentations

PubMed
The role of extracellular-5'-nucleotidase/CD73 in glioma peritumoural brain edema. Wang B, Wang D, Zhu Z, Wang W, Zhang X, Tang F, Zhou Y, Wang H, Liu M, Yao X, Yan X> ;Neurol. Sci.. 2016-04-01
Endoscopic Closure for EUS and ERCP Related Duodenal Perforation by Endoclips. Liu Y, Wang D, Li Z> ;Gastroenterol Res Pract. 2016-01-01
Complex Learning in Bio-plausible Memristive Networks. Deng L, Li G, Deng N, Wang D, Zhang Z, He W, Li H, Pei J, Shi L> ;Sci Rep. 2015-06-19
Relationship between abnormal NOS expression and the pathogenesis of cerebral aneurysm. Liu WS, Geng HJ, Wang CD, Li AJ, Cao PC, Wang DK, Li G> ;Genet. Mol. Res.. 2015-04-28
Pioglitazone reduces lipid droplets in cholesterolosis of the gallbladder by increasing ABCA1 and NCEH1 expression. Wang J, Wang D, Tan Y, Zhao G, Ji Z> ;Mol. Cell. Biochem.. 2015-01-01
YM155, a selective survivin inhibitor, reverses chronic hypoxic pulmonary hypertension in rats via upregulating voltage-gated potassium channels. Fan Z, Liu B, Zhang S, Liu H, Li Y, Wang D, Liu Y, Li J, Wang N, Liu Y, Zhang B> ;Clin. Exp. Hypertens.. 2015-01-01
Preventive Effects of Aspirin on Cardiovascular Complications in Prostate Cancer Cases after Endocrinotherapy. Li X, Zhang Y, Wang D, Chen Y, Shan Y> ;Asian Pac. J. Cancer Prev.. 2015-01-01
Upregulation of pronociceptive mediators and downregulation of opioid peptide by adrenomedullin following chronic exposure to morphine in rats. Wang D, Li J, Chen P, Hong Y> ;Neuroscience. 2014-11-07
New phenylpropanoid-substituted flavan-3-ols from Pu-er ripe tea. Tao M, Xu M, Zhu H, Cheng R, Wang D, Yang C, Zhang Y> ;Nat Prod Commun. 2014-08-01
Rac1 regulates skin tumors by regulation of keratin 17 through recruitment and interaction with CD11b+Gr1+ cells. Chen R, Fu M, Zhang G, Zhou Y, Zhu S, Liu J, Wang D, Deng A, Wang Z> ;Oncotarget. 2014-06-30
Long-term decoding stability of local field potentials from silicon arrays in primate motor cortex during a 2D center out task. Wang D, Zhang Q, Li Y, Wang Y, Zhu J, Zhang S, Zheng X> ;J Neural Eng. 2014-06-01
Optical properties of secondary organic aerosols generated by photooxidation of aromatic hydrocarbons. Li K, Wang W, Ge M, Li J, Wang D> ;Sci Rep. 2014-05-12
Functional analysis of the involvement of apurinic/apyrimidinic endonuclease 1 in the resistance to melphalan in multiple myeloma. Xie J, Zhang L, Li M, Du J, Zhou L, Yang S, Zeng L, Li Z, Wang G, Wang D> ;BMC Cancer. 2014-01-08
Highly diastereo- and enantioselective [3+2] annulation of isatin-derived Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by tertiary amines. Zhong N, Wei F, Xuan Q, Liu L, Wang D, Chen Y> ;Chem. Commun. (Camb.). 2013-12-07
The effect of CXCR4 silencing on epithelial-mesenchymal transition related genes in glioma U87 cells. Zhu Y, Yang P, Wang Q, Hu J, Xue J, Li G, Zhang G, Li X, Li W, Zhou C, Zhao M, Wang D> ;Anat Rec (Hoboken). 2013-12-01
Mechanical comparison between lengthened and short sacroiliac screws in sacral fracture fixation: a finite element analysis. Zhao Y, Zhang S, Sun T, Wang D, Lian W, Tan J, Zou D, Zhao Y> ;Orthop Traumatol Surg Res. 2013-09-01
Membrane trafficking in neuronal maintenance and degeneration. Wang, D.,Chan, C. C.,Cherry, S.,Hiesinger, P. R.> ;Cell. Mol. Life Sci.. 2012 Nov 08
PP-1α and PP-1γ display antagonism and differential roles in tumorigenicity of lung cancer cells. Chen P, Li C, Wang D, Luo Z, Fu S, Li X, Li Z, Chen X, Li L, Huang Z, Ji W, Hu W, Hu X, Deng M, Gong L, Chen H, Liu J, Li DW> ;Curr. Mol. Med.. 2013-01-01
Formononetin attenuates IL-1β-induced apoptosis and NF-κB activation in INS-1 cells. Wang Y, Zhu Y, Gao L, Yin H, Xie Z, Wang D, Zhu Z, Han X> ;Molecules. 2012-08-24
Allelic variations of glut-1 deficiency syndrome: the chinese experience. Liu Y Bao X Wang D Fu N Zhang X Cao G Song F Wang S Zhang Y Qin J Yang H Engelstad K De Vivo DC Wu X> ;Pediatr Neurol. 2012 Jul
Autophagy, neuron-specific degradation and neurodegeneration. Wang, D.,Hiesinger, P. R.> ;Autophagy. 2012 Apr 14
Progesterone increases circulating endothelial progenitor cells and induces neural regeneration after traumatic brain injury in aged rats. Li Z, Wang B, Kan Z, Zhang B, Yang Z, Chen J, Wang D, Wei H, Zhang J, Jiang R> ;J. Neurotrauma. 2012-01-20
Glut1 deficiency syndrome and erythrocyte glucose uptake assay. Yang H Wang D Engelstad K Bagay L Wei Y Rotstein M Aggarwal V Levy B Ma L Chung WK De Vivo DC> ;Ann Neurol. 2011 Dec
3D-conformal RT, fixed-field IMRT and RapidArc, which one is better for esophageal carcinoma treated with elective nodal irradiation. Wang D, Yang Y, Zhu J, Li B, Chen J, Yin Y> ;Technol. Cancer Res. Treat.. 2011-10-01
[Comparative research on the NIR and MIR micro-imaging of two similar plastic materials]. Wang D, Ma Z, Zhao L, Pan L, Li X, Wang J> ;Guang Pu Xue Yu Guang Pu Fen Xi. 2011-09-01
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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
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
Methylprednisolone for Status Migrainous Vertigo and Cephalic Status Migrainosus Robbins MS, Wang D,DeOrchis VS, Headache, 1/1/2009
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
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
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
Glut1 Deficiency: CSF Glucose How low is too low? De Vivo,Wang D, Revue Neurologique, 1/1/2008
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
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
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
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
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
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
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
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
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
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
Glucose transporter proteindeficiency syndromes De Vivo DC, Wang D, Pascual JM, Ho Y-Y, Int Rev Neurobiol, 1/1/2002
Glut-1 Deficiency Syndrome and Other Glycolytic Defects De VivoDC, Leary L, Wang D, J Child Neurol, 1/1/2002
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
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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
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
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
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
Molecular genetics of Glut1 Deficiency Syndrome. Wang D, Yang H, Engelstad K, Min-Wei C, De Vivo DC, Neurology, 1/1/2007
Pyruvate carboxylase deficiency: Mosaicism correlates with prolonged survival. Wang D, Yang H, Lu JS, De Vivo DC, Am Acad Neurol, 1/1/2007
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
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
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
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
KmtA, A putative novel potassium transporter gene. Yang R, Wang D, Yang H, De Vivo DC, Pascaul JM, 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
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
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
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
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
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
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): 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
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

Grant Support

Neurological Sciences Academic Development Award (NSADA) (K12)National Institution of Health2005–2008

Research History

Associated Research Scientist1998 - 2008

Professional Memberships

American Academy of Neurology - AANMember

Other Languages

Chinese (Mandarin)

Hospital Affiliations

Gwinnett Hospital SystemLawrenceville, Georgia

External Links

websitehttps://neurologyspecialistsofga.com/