Judith Bluvstein, MD

  • Specialties: Pediatric Epilepsy, Epilepsy, Neurology, Pediatric Neurology
  • Languages: English, Portuguese, Spanish
  • Phone: 646-558-0808
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About Me

Conditions and Treatments

epilepsy, electroencephalography, child developmental disability, autism, Asperger syndrome, attention deficit hyperactivity disorder, infantile spasms, child developmental delay, infantile spasms, epileptic encephalopathy, Angelman syndrome, tuberous sclerosis, autism, Landau Kleffner syndrome, Landau Kleffner syndrome, epilepsy, sturge-weber syndrome, epileptic encephalopathy, electroencephalography
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Credentials

Positions
  • Clinical Associate Professor, Department of Neurology
  • Clinical Associate Professor, Department of Pediatrics
  • Co-Director of Pediatric Special Procedure for Epilepsy
Board Certifications
  • American Board of Psychiatry & Neurology (Epilepsy), 2013
  • American Board of Psychiatry & Neurology - w/Spec Qual"s In Child Neurolo, 2009
  • American Board of Psychiatry & Neurology - Neurology, 2009
Education and Training
  • Fellowship, Montefiore Medical Center, Neurophysiology, 2009
  • Fellowship, Montefiore Medical Center, Pediatric Neurology, 2002
  • Residency, St. Vincent's Hospital, Pediatrics, 1999
Departments

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Locations and Appointments

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  • Aetna
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NYU Langone Comprehensive Epilepsy Center

223 East 34th Street
New York, NY 10016

Research Academic Contact

Academic office

225 East 34th Street

First Floor

New York, NY 10016

Phone

646-558-0808

Research Interests Timeline

These focus areas and their associated publications are derived from PubMed and the MeSH term library.
represents one publication
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Publications

  • Abou-Khalil, Bassel; Afawi, Zaid; Allen, Andrew S; Bautista, Jocelyn F; Bellows, Susannah T; Berkovic, Samuel F; Bluvstein, Judith; Burgess, Rosemary; Cascino, Gregory; Cops, Elisa J; Cossette, Patrick; Cristofaro, Sabrina; Crompton, Douglas E; Delanty, Norman; Devinsky, Orrin; Dlugos, Dennis; Epstein, Michael P; Fountain, Nathan B; Freyer, Catharine; Garry, Sarah I; Geller, Eric B; Glauser, Tracy; Glynn, Simon; Goldberg-Stern, Hadassa; Goldstein, David B; Gravel, Micheline; Haas, Kevin; Haut, Sheryl; Heinzen, Erin L; Kirsch, Heidi E; Kivity, Sara; Knowlton, Robert; Korczyn, Amos D; Kossoff, Eric; Kuzniecky, Ruben; Loeb, Rebecca; Lowenstein, Daniel H; Marson, Anthony G; McCormack, Mark; McKenna, Kevin; Mefford, Heather C; Motika, Paul; Mullen, Saul A; O'Brien, Terence J; Ottman, Ruth; Paolicchi, Juliann; Parent, Jack M; Paterson, Sarah; Petrovski, Slave; Pickrell, William Owen; Poduri, Annapurna; Rees, Mark I; Sadleir, Lynette G; Scheffer, Ingrid E; Shih, Jerry; Singh, Rani; Sirven, Joseph; Smith, Michael; Smith, Phil EM; Thio, Liu Lin; Thomas, Rhys H; Venkat, Anu; Vining, Eileen; Von Allmen, Gretchen; Weisenberg, Judith; Widdess-Walsh, Peter; Winawer, Melodie R; Epi4K Consortium

    Brain. 2017 AUG; 140:2144-2156

  • Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data

    Allen, A S; Berkovic, S F; Bridgers, J; Cossette, P; Dlugos, D; Epstein, M P; Glauser, T; Goldstein, D B; Heinzen, E L; Jiang, Y; Johnson, M R; Kuzniecky, R; Lowenstein, D H; Marson, A G; Mefford, H C; O'Brien, T J; Ottman, R; Petrou, S; Petrovski, S; Poduri, A; Ren, Z; Scheffer, I E; Sherr, E; Wang, Q; Balling, R; Barisic, N; Baulac, S; Caglayan, H; Craiu, D; De, Jonghe P; Depienne, C; Guerrini, R; Helbig, I; Hjalgrim, H; Hoffman-Zacharska, D; Jahn, J; Klein, K M; Koeleman, B; Komarek, V; Krause, R; Leguern, E; Lehesjoki, A -E; Lemke, J R; Lerche, H; Linnankivi, T; Marini, C; May, P; Moller, R S; Muhle, H; Pal, D; Palotie, A; Rosenow, F; Selmer, K; Serratosa, J M; Sisodiya, S; Stephani, U; Sterbova, K; Striano, P; Suls, A; Talvik, T; Von, Spiczak S; Weber, Y; Weckhuysen, S; Zara, F; Abou-Khalil, B; Alldredge, B K; Amrom, D; Andermann, E; Andermann, F; Bautista, J F; Bluvstein, J; Cascino, G D; Consalvo, D; Crumrine, P; Devinsky, O; Fiol, M E; Fountain, N B; French, J; Friedman, D; Haas, K; Haut, S R; Hayward, J; Joshi, S; Kanner, A; Kirsch, H E; Kossoff, E H; Kuperman, R; McGuire, S M; Motika, P V; Novotny, E J; Paolicchi, J M; Parent, J; Park, K; Shellhaas, R A; Sirven, J; Smith, M C; Sullivan, J; Thio, L L; Venkat, A; Vining, E P G; Von, Allmen G K; Weisenberg, J L; Widdess-Walsh, P; Winawer, M R

    European journal of human genetics. 2017 Jun 01; 25(7):894-899

  • Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

    Allen, Andrew S; Bellows, Susannah T; Berkovic, Samuel F; Bridgers, Joshua; Burgess, Rosemary; Cavalleri, Gianpiero; Chung, Seo-Kyung; Cossette, Patrick; Delanty, Norman; Dlugos, Dennis; Epstein, Michael P; Freyer, Catharine; Goldstein, David B; Heinzen, Erin L; Hildebrand, Michael S; Johnson, Michael R; Kuzniecky, Ruben; Lowenstein, Daniel H; Marson, Anthony G; Mayeux, Richard; Mebane, Caroline; Mefford, Heather C; O'Brien, Terence J; Ottman, Ruth; Petrou, Steven; Petrovski, Slave; Pickrell, William O; Poduri, Annapurna; Radtke, Rodney A; Rees, Mark I; Regan, Brigid M; Ren, Zhong; Scheffer, Ingrid E; Sills, Graeme J; Thomas, Rhys H; Wang, Quanli; Abou-Khalil, Bassel; Alldredge, Brian K; Amrom, Dina; Andermann, Eva; Andermann, Frederick; Bautista, Jocelyn F; Berkovic, Samuel F; Bluvstein, Judith; Boro, Alex; Cascino, Gregory D; Consalvo, Damian; Crumrine, Patricia; Devinsky, Orrin; Dlugos, Dennis; Epstein, Michael P; Fiol, Miguel; Fountain, Nathan B; French, Jacqueline; Freyer, Catharine; Friedman, Daniel; Geller, Eric B; Glauser, Tracy; Glynn, Simon; Haas, Kevin; Haut, Sheryl R; Hayward, Jean; Helmers, Sandra L; Joshi, Sucheta; Kanner, Andres; Kirsch, Heidi E; Knowlton, Robert C; Kossoff, Eric H; Kuperman, Rachel; Kuzniecky, Ruben; Lowenstein, Daniel H; Motika, Paul V; Novotny, Edward J; Ottman, Ruth; Paolicchi, Juliann M; Parent, Jack M; Park, Kristen; Poduri, Annapurna; Sadleir, Lynette G; Scheffer, Ingrid E; Shellhaas, Renee A; Sherr, Elliott H; Shih, Jerry J; Shinnar, Shlomo; Singh, Rani K; Sirven, Joseph; Smith, Michael C; Sullivan, Joseph; Thio, Liu Lin; Venkat, Anu; Vining, Eileen PG; Von Allmen, Gretchen K; Weisenberg, Judith L; Widdess-Walsh, Peter; Winawer, Melodie R; Epi4k Consortium; Epi4k Consortium; Epilepsy Phenome-Genome Proj

    Lancet. Neurology. 2017 Feb; 16(2):135-143

Read All Publications (11)

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