- American Academy of Neurology
- Child Neurology Society
- Functional Neurological Disorders Society
Biography
Jeff Waugh, M.D., Ph.D., is an Associate Professor in the Department of Pediatrics at UT Southwestern Medical Center.
Dr. Waugh earned his medical degree and a doctoral degree in neuroscience and molecular psychiatry through the Medical Scientist Training Program at UT Southwestern. He completed a residency in pediatrics at Children’s Medical Center Dallas and a residency in pediatric neurology at Boston Children’s Hospital. He received advanced training through a fellowship in pediatric movement disorders at Boston Children’s Hospital, a fellowship in mood and motor control at Massachusetts General Hospital and Harvard University, and a fellowship in computational radiology at Boston Children’s and Harvard.
Certified by the American Board of Psychiatry and Neurology in child neurology, he joined the UT Southwestern faculty in 2017. He serves as Director of the Pediatric Movement Disorders Program and Co-Director of the Pediatric Functional Neurological Disorders Clinic at Children's Medical Center Dallas.
Dr. Waugh is a member of the American Academy of Neurology, the Child Neurology Society, and the Functional Neurological Disorders Society.
Education & Training
- Medical School - UT Southwestern Medical School (1999-2007)
- Fellowship - Massachusetts General Hospital (2012-2014), Pediatric Movement Disorders
- Residency - UT Southwestern/Children's Medical Center (2007-2009), Pediatrics
- Residency - Harvard Medical School/Boston Childrens Hospital (2009-2012), Pediatric Neurology
Professional Associations & Affiliations
Honors & Awards
- Golden Boot Award 2022, UT Southwestern Child Neurology Residents
- Early-Stage Investigator Award 2021, Network for Excellence in Neuroscience Clinical Trials
- D Magazine Best Pediatric Specialist 2020-2021
- Invited Member, Practice Committee, Child Neurology Society 2014
- Silverman Family Fellowship, Bachman-Strauss Dystonia Parkinson Foundation 2012-2014
- Invited Member, Medical Economics and Management Committee, American Academy of Neurology 2013
- Member, Clinical Documentation Integrity Committee, Boston Children's Hospital 2013
Books & Publications
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Publications
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Striatal compartment and white matter alterations in focal dystonia Subtypes: An MRI study
Marques Paulo AJ, Waugh JL, Winkler AM, Queiroz de Paiva JP, de Faria DD, Borges V, Silva Sd, de Ferraz HB, Aguiar Pd Parkinsonism and Related Disorders 2025 Dec 141 -
The striatal matrix compartment is expanded in autism spectrum disorder
Waugh JL, Hassan AO, Funk AT, Maldjian JA Journal of neurodevelopmental disorders 2025 Dec 17 -
Chronic Striatal Cholinergic Interneuron Excitation Causes Cerebral Palsy-Related Dystonic Behavior in Mice
Gemperli K, Lu X, Chintalapati K, Rust A, Bajpai R, Suh N, Blackburn J, Gelineau-Morel R, Kruer MC, Mingbunjerdsuk D, O'Malley J, Tochen L, Waugh JL, Wu S, Feyma T, Perlmutter J, Mennerick S, McCall JG, Aravamuthan BR Annals of Neurology 2025 Oct 98 726-740 -
Globally Reduced Brain Volume in Rett Syndrome
Dy-Hollins ME, Kapur K, Prohl AK, Sharma N, Yang E, Warfield SK, Waugh JL Pediatric Neurology 2025 Jul 168 60-66 -
The striatal compartments, striosome and matrix, are embedded in largely distinct resting-state functional networks
Sadiq A, Funk AT, Waugh JL Frontiers in Neural Circuits 2025 19 -
Depression-associated reductions in putaminal volume are accompanied by a shift from matrix-like to striosome-like structural connectivity
Tieu AN, Waugh JL Frontiers in Psychiatry 2025 16 -
Analysis of striatal connectivity corresponding to striosomes and matrix in de novo Parkinson’s disease and isolated REM behavior disorder
Marecek S, Krajca T, Krupicka R, Sojka P, Nepozitek J, Varga Z, Mala C, Keller J, Waugh JL, Zogala D, Trnka J, Sonka K, Ruzicka E, Dusek P npj Parkinson's Disease 2024 Dec 10 -
In Humans, Insulo-striate Structural Connectivity is Largely Biased Toward Either Striosome-like or Matrix-like Striatal Compartments
Funk AT, Hassan AA, Waugh JL Neuroscience Insights 2024 Jan 19 -
Emerging Subspecialties: Pediatric Movement Disorders Neurology
Kahlon S, Barton CR, Abu Libdeh A, O'Malley JA, Pearson T, Waugh JL, Wu SW, Zea Vera AG, Kruer MC Neurology 2024 Jan 102 -
Cachexia, chorea, and pain in chronic nonbacterial osteitis and inflammatory bowel disease: a case report
Agharokh L, Mamola K, Yu AG, Medina AL, Gurram B, Fuller J, Park JY, Chen W, Rajaram V, Hammer MR, Waugh JL Journal of Medical Case Reports 2023 Dec 17 -
Functional Neurological Disorder Among Sexual and Gender Minority People
Lerario MP, Rosendale N, Waugh JL, Turban J, Maschi T Neurologic Clinics 2023 Nov 41 759-781 -
A Case Series of Transgender and Gender-Nonconforming Patients in a Pediatric Functional Neurologic Disorder Clinic
Wilkinson-Smith A, Lerario MP, Klindt KN, Waugh JL Journal of child neurology 2023 Oct 38 631-641 -
A Network Imaging Biomarker of X-Linked Dystonia-Parkinsonism
Niethammer M, Tang CC, Jamora RD, Vo A, Nguyen N, Ma Y, Peng S, Waugh JL, Westenberger A, Eidelberg D Annals of Neurology 2023 Oct 94 684-695 -
Expanding Knowledge of the Causes of Childhood Chorea
Kern HM, Waugh JL Seminars in Pediatric Neurology 2023 Oct 47 -
Functional symptoms in children may be much more common than previously believed
Waugh JL Developmental Medicine and Child Neurology 2023 Sep 65 1138-1139 -
Subdural Hemorrhage and Focal Motor Status Epilepticus in Cobalamin Metabolism Disorder
Choudhari PR, Waugh JL, Lowden A Pediatric Neurology 2023 Mar 140 47-49 -
In humans, striato-pallido-thalamic projections are largely segregated by their origin in either the striosome-like or matrix-like compartments
Funk AT, Hassan AA, Brüggemann N, Sharma N, Breiter HC, Blood AJ, Waugh JL Frontiers in Neuroscience 2023 17 -
An MRI method for parcellating the human striatum into matrix and striosome compartments in vivo
Waugh JL, Hassan AA, Kuster JK, Levenstein JM, Warfield SK, Makris N, Brüggemann N, Sharma N, Breiter HC, Blood AJ NeuroImage 2022 Feb 246 -
Movement Disorders
Kern H, Waugh J 2022 Jan 75-84 -
Functional movement disorder gender, age and phenotype study: a systematic review and individual patient meta-analysis of 4905 cases
Author Collaboration FG, Lidstone SC, Costa-Parke M, Robinson EJ, Ercoli T, Stone J, Ahmad O, Akbaripanahi S, Albanese A, Aybek S, Baizabal-Carvallo JF, Beek PJ, Bhatia KP, Cabreira V, Carson AJ, Castagna A, Dale RC, Dallocchio C, Defazio G, Degos B, Demartini B, Deuschl G, Diukova G, Duque KR, Edwards MJ, Epstein SA, Espay AJ, Factor SA, Garcin B, Geroin C, Hagenaars M, Hallett M, Hassa T, Hassan A, Herbert LD, Holden SK, Jankovic J, Kanaan RA, Kempe CA, Kojovic M, Kompoliti K, Kostić VS, Kyle K, LaFaver K, Lang AE, Martino D, Massano J, Maurer CW, McWhirter L, Mehanna R, Waugh JL Journal of Neurology, Neurosurgery and psychiatry 2022 93 609-616 -
Functional Movement Disorder in Children
Wilkinson-Smith A, Waugh JL 2022 183-195 -
When neurologists diagnose functional neurological disorder, why don't they code for it?
Herbert LD, Kim R, Hassan AA, Wilkinson-Smith A, Waugh JL CNS spectrums 2021 Dec 26 664-674 -
Anti-Myelin Oligodendrocyte Glycoprotein (MOG) antibody disease presenting with severe dystonia
Khan TR, Waugh JL, Wang C Neuroimmunology Reports 2021 Dec 1 -
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy (Nature Genetics, (2020), 52, 10, (1046-1056), 10.1038/s41588-020-0695-1)
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MS, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC Nature genetics 2021 Mar 53 412 -
Segmental Myoclonus Following Hepatorenal Transplant and Tacrolimus Immunosuppression
McLaughlin AM, Khan TR, Lauritsen J, Batley K, Waugh JL Pediatric Neurology 2021 Jan 114 40-41 -
Changing the culture of care for children and adolescents with functional neurological disorder
Kozlowska K, Sawchuk T, Waugh JL, Helgeland H, Baker J, Scher S, Fobian AD Epilepsy and Behavior Reports 2021 Jan 16 -
Role of child neurologists and neurodevelopmentalists in the diagnosis of cerebral palsy: A survey study
Aravamuthan BR, Shevell M, Kim YM, Wilson JL, O'Malley JA, Pearson TS, Kruer MC, Fahey M, Waugh JL, Russman B, Shapiro B, Tilton A Neurology 2020 Nov 95 962-972 -
Management of Infantile Spasms During the COVID-19 Pandemic
Grinspan ZM, Mytinger JR, Baumer FM, Ciliberto MA, Cohen BH, Dlugos DJ, Harini C, Hussain SA, Joshi SM, Keator CG, Knupp KG, McGoldrick PE, Nickels KC, Park JT, Pasupuleti A, Patel AD, Shahid AM, Shellhaas RA, Shrey DW, Singh RK, Wolf SM, Yozawitz EG, Yuskaitis CJ, Waugh JL, Pearl PL Journal of child neurology 2020 Oct 35 828-834 -
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Heim J, Webber DL, Frank MS, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC Nature genetics 2020 Oct 52 1046-1056 -
Advanced MRI techniques for transcranial high intensity focused ultrasound targeting
Shah BR, Lehman VT, Kaufmann TJ, Blezek D, Waugh J, Imphean D, Yu FF, Patel TR, Chitnis S, Dewey RB, Maldjian JA, Chopra R Brain 2020 Sep 143 2664-2672 -
Crisis Standard of Care: Management of Infantile Spasms during COVID-19
Grinspan ZM, Mytinger JR, Baumer FM, Ciliberto MA, Cohen BH, Dlugos DJ, Harini C, Hussain SA, Joshi SM, Keator CG, Knupp KG, McGoldrick PE, Nickels KC, Park JT, Pasupuleti A, Patel AD, Pomeroy SL, Shahid AM, Shellhaas RA, Shrey DW, Singh RK, Wolf SM, Yozawitz EG, Yuskaitis CJ, Waugh JL, Pearl PL Annals of Neurology 2020 Aug 88 215-217 -
Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity
Cheng H, Capponi S, Wakeling E, Marchi E, Li Q, Zhao M, Weng C, Stefan PG, Ahlfors H, Kleyner R, Rope A, Lumaka A, Lukusa P, Devriendt K, Vermeesch J, Posey JE, Palmer EE, Murray L, Leon E, Diaz J, Worgan L, Mallawaarachchi A, Vogt J, de Munnik SA, Dreyer L, Baynam G, Ewans L, Stark Z, Lunke S, Gonçalves AR, Soares G, Oliveira J, Fassi E, Willing M, Waugh JL, Faivre L, Riviere JB, Moutton S, Mohammed S, Payne K, Walsh L, Begtrup A, Guillen Sacoto MJ, Douglas G, Alexander N, Buckley MF, Mark PR, Adès LC, Sandaradura SA, Lupski JR, Roscioli T, Agrawal PB, Kline AD, Wang K, Timmers HT, Lyon GJ Human mutation 2020 Feb 41 449-464 -
KMT2B-related disorders: Expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation
Cif L, Demailly D, Lin JP, Barwick KE, Sa M, Abela L, Malhotra S, Chong WK, Steel D, Sanchis-Juan A, Ngoh A, Trump N, Meyer E, Vasques X, Rankin J, Allain MW, Applegate CD, Isfahani SA, Baleine J, Balint B, Bassetti JA, Baple EL, Bhatia KP, Blanchet C, Burglen L, Cambonie G, Seng EC, Bastaraud SC, Cyprien F, Coubes C, d’Hardemare V, Doja A, Dorison N, Doummar D, Dy-Hollins ME, Farrelly E, Fitzpatrick DR, Fearon C, Fieg EL, Fogel BL, Forman EB, Fox RG, Gahl WA, Galosi S, Gonzalez V, Graves TD, Gregory A, Hallett M, Hasegawa H, Hayflick SJ, Hamosh A, Hully M, Jansen S, Jeong SY, Krier JB, Krystal S, Kumar KR, Laurencin C, Lee H, Lesca G, François LL, Lynch T, Mahant N, Martinez-Agosto JA, Milesi C, Mills KA, Mondain M, Morales-Briceno H, Ostergaard JR, Pal S, Pallais JC, Pavillard F, Perrigault PF, Petersen AK, Polo G, Poulen G, Rinne T, Roujeau T, Rogers C, Roubertie A, Sahagian M, Schaefer E, Selim L, Selway R, Sharma N, Signer R, Soldatos AG, Stevenson DA, Stewart F, Tchan M, Verma IC, de Vries BB, Wilson JL, Wong DA, Zaitoun R, Zhen D, Znaczko A, Dale RC, de Gusmão CM, Friedman J, Fung VS, King MD, Mohammad SS, Rohena L, Waugh JL, Toro C, Raymond FL, Topf M, Coubes P, Gorman KM, Kurian MA Brain 2020 143 3242-3261 -
VAC14 Gene-Related Parkinsonism-Dystonia With Response to Deep Brain Stimulation
de Gusmao CM, Stone S, Waugh JL, Yang E, Lenk GM, Rodan LH Movement Disorders Clinical Practice 2019 Jul 6 494-497 -
Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia
Wagner F, Titelbaum DS, Engisch R, Coskun EK, Waugh JL Clinical Neuroradiology 2019 Jun 29 215-221 -
A registration method for improving quantitative assessment in probabilistic diffusion tractography
Waugh JL, Kuster JK, Makhlouf ML, Levenstein JM, Multhaupt-Buell TJ, Warfield SK, Sharma N, Blood AJ NeuroImage 2019 Apr 189 288-306 -
How should we normalize regional volume abnormalities in childhood neurodegenerative disorders?
Waugh JL, Dure LS Neurology 2019 Apr 92 779-780 -
Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region
Author Collaboration UD, Kelly M, Park M, Mihalek I, Rochtus A, Gramm M, Pérez-Palma E, Axeen ET, Hung CY, Olson H, Swanson L, Anselm I, Briere LC, High FA, Sweetser DA, Kayani S, Snyder M, Calvert S, Scheffer IE, Yang E, Waugh JL, Lal D, Bodamer O, Poduri A Epilepsia 2019 Mar 60 406-418 -
White matter changes in cervical dystonia relate to clinical effectiveness of botulinum toxin treatment
Blood AJ, Kuster JK, Waugh JL, Levenstein JM, Multhaupt-Buell TJ, Sudarsky LR, Breiter HC, Sharma N Frontiers in Neurology 2019 10 -
Autoimmune Movement Disorders in Children
Stredny CM, Waugh JL Seminars in Pediatric Neurology 2018 Apr 25 92-112 -
Inherited and Acquired Choreas
de Gusmao CM, Waugh JL Seminars in Pediatric Neurology 2018 Apr 25 42-53 -
PURA syndrome: Clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
Reijnders MR, Janowski R, Alvi M, Self JE, Van Essen TJ, Vreeburg M, Rouhl RP, Stevens SJ, Stegmann AP, Schieving J, Pfundt R, Van Dijk K, Smeets E, Stumpel CT, Bok LA, Cobben JM, Engelen M, Mansour S, Whiteford M, Chandler KE, Douzgou S, Cooper NS, Tan EC, Foo R, Lai AH, Rankin J, Green A, Lönnqvist T, Isohanni P, Williams S, Ruhoy I, Carvalho KS, Dowling JJ, Lev DL, Sterbova K, Lassuthova P, Neupauerová J, Waugh JL, Keros S, Clayton-Smith J, Smithson SF, Brunner HG, Van Hoeckel C, Anderson M, Clowes VE, Siu VM, Ddd Study T, Selber P, Leventer RJ, Nellaker C, Niessing D, Hunt D, Baralle D Journal of medical genetics 2018 Feb 55 104-113 -
Increased insula-putamen connectivity in X-linked dystonia-parkinsonism
Blood AJ, Waugh JL, Münte TF, Heldmann M, Domingo A, Klein C, Breiter HC, Lee LV, Rosales RL, Brüggemann N NeuroImage: Clinical 2018 17 835-846 -
Deep brain stimulation for monogenic dystonia
Aravamuthan BR, Waugh JL, Stone SS Current opinion in pediatrics 2017 Dec 29 691-696 -
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Author Collaboration GH, Author Collaboration DD, Author Collaboration UD, Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HA, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BW, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KL, Juusola J, Foss K American Journal of Human Genetics 2017 Nov 101 768-788 -
Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective
Dy ME, Waugh JL, Sharma N, O'Leary H, Kapur K, D'Gama AM, Sahin M, Urion DK, Kaufmann WE Pediatric Neurology 2017 Oct 75 91-95 -
Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression
Brüggemann N, Rosales RL, Waugh JL, Blood AJ, Domingo A, Heldmann M, Jamora RD, Münchau A, Münte TF, Lee LV, Buchmann I, Klein C European Journal of Neurology 2017 May 24 680-686 -
Treatment of ADCY5 -Associated Dystonia, Chorea, and Hyperkinetic Disorders with Deep Brain Stimulation
Dy ME, Chang FC, Jesus SD, Anselm I, Mahant N, Zeilman P, Rodan LH, Foote KD, Tan WH, Eskandar E, Sharma N, Okun MS, Fung VS, Waugh JL Journal of child neurology 2016 Jul 31 1027-1035 -
Thalamic volume is reduced in cervical and laryngeal dystonias
Waugh JL, Kuster JK, Levenstein JM, Makris N, Multhaupt-Buell TJ, Sudarsky LR, Breiter HC, Sharma N, Blood AJ PloS one 2016 May 11 -
Benign hereditary chorea related to NKX2-1 with ataxia and dystonia
De Gusmao CM, Kok F, Casella EB, Waugh JL Neurology: Genetics 2016 Feb 2 -
Localization of Basal Ganglia and Thalamic Damage in Dyskinetic Cerebral Palsy
Aravamuthan BR, Waugh JL Pediatric Neurology 2016 Jan 54 11-21 -
Education in medical billing benefits both neurology trainees and academic departments
Waugh JL Neurology 2014 Nov 83 1856-1861 -
Increased pediatric functional neurological symptom disorders after the boston marathon bombings: A case series
Guerriero RM, Pier DB, De Gusmão CM, Bernson-Leung ME, Maski KP, Urion DK, Waugh JL Pediatric Neurology 2014 Nov 51 619-623 -
Functional neurological symptom disorders in a pediatric emergency room: Diagnostic accuracy, features, and outcome
De Gusmão CM, Guerriero RM, Bernson-Leung ME, Pier D, Ibeziako PI, Bujoreanu S, Maski KP, Urion DK, Waugh JL Pediatric Neurology 2014 Aug 51 233-238 -
Progressive multifocal leukoencephalopathy in pediatric patients: Case report and literature review
Schwenk H, Ramirez-Avila L, Sheu SH, Wuthrich C, Waugh J, Was A, Degirolami U, Burchett S, Koralnik IJ, Ahmed A Pediatric Infectious Disease Journal 2014 Apr 33 e99-e105 -
Clinical Neurogenetics: Dystonia From Phenotype to Genotype
Waugh JL, Sharma N Neurologic Clinics 2013 Nov 31 969-986 -
Acute dyskinetic reaction in a healthy toddler following methylphenidate ingestion
Waugh JL Pediatric Neurology 2013 Jul 49 58-60 -
Prolonged direct catheter thrombolysis of cerebral venous sinus thrombosis in children: A case series
Waugh J, Plumb P, Rollins N, Dowling MM Journal of child neurology 2012 Mar 27 337-345 -
Association between regulator of G protein signaling 9-2 and body weight
Waugh JL, Celver J, Sharma M, Dufresne RL, Terzi D, Risch SC, Fairbrother WG, Neve RL, Kane JP, Malloy MJ, Pullinger CR, Gu HF, Tsatsanis C, Hamilton SP, Gold SJ, Zachariou V, Kovoor A PloS one 2011 Nov 6 -
Clinical reasoning: A 16-year-old girl with fixed unilateral grimace
Waugh J, Prabhu SP, Bourgeois B, Kothare S Neurology 2011 Sep 77 e61-e64 -
Juvenile Huntington disease exacerbated by methylphenidate: Case report
Waugh JL, Miller VS, Chudnow RS, Dowling MM Journal of child neurology 2008 Jul 23 807-809 -
RGS9-2 negatively modulates L-3,4-dihydroxyphenylalanine-induced dyskinesia in experimental Parkinson's disease
Gold SJ, Hoang CV, Potts BW, Porras G, Pioli E, Ki WK, Nadjar A, Qin C, LaHoste GJ, Li Q, Bioulac BH, Waugh JL, Gurevich E, Neve RL, Bezard E Journal of Neuroscience 2007 Dec 27 14338-14348 -
Regional, cellular, and subcellular localization of RGS10 in rodent brain
Waugh JL, Lou AC, Eisch AJ, Monteggia LM, Muly EC, Gold SJ Journal of Comparative Neurology 2005 Jan 481 299-313
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Striatal compartment and white matter alterations in focal dystonia Subtypes: An MRI study
Research
- Functional consequences of dystonia treatment, such as deep brain stimulation
- Neurophysiology of the neostraitum
- Structural basis of dystonia
Results: 1 Locations
Children's Medical Center of Dallas
1935 Medical District DriveDallas, Texas 75235 214-730-5437 Directions to Children's Medical Center of Dallas at Children's Medical Center of Dallas, Dallas