Shifteh Sattar • UCSD Profiles (original) (raw)

  1. Response: "Incidental interictal epileptiform discharges in infants with nonepileptic events". Epilepsia. 2026 Feb; 67(2):1010-1011. Montenegro MA, Tsuha M, Baccin F, Sattar S. PMID: 41387716.
    View in: PubMed Mentions: Fields:
  2. Epilepsy in children and adolescents with B-cell acute lymphoblastic leukemia. Epilepsy Res. 2025 Dec; 218:107671. Choi SA, Trivedi A, Unwalla D, Jindal A, Montenegro MA, Sattar S. PMID: 41110283.
    View in: PubMed Mentions: Fields:
    Translation:Humans
  3. Factors Associated With More Medication Trials Before Surgical Evaluation and Postsurgical Outcomes in Pediatric Drug-Resistant Epilepsy. Neurology. 2025 Nov 11; 105(9):e214198. Samanta D, Newell G, Caraway AR, Brock E, Albert GW, Novotny EJ, Depositario Cabacar DF, Oluigbo CO, Gaillard WD, Tatachar P, Bolton JB, Wong-Kisiel L, Romanowski EF, Mcnamara NA, Eschbach K, Alexander AL, Auguste KI, Gonzalez-Giraldo E, Bernardo D, Ostendorf AP, Coryell J, Karia S, Karakas C, Javarayee PK, Pichon PD, Olaya J, Shrey DW, Reddy SB, Ganesh A, Hauptman JS, Singh RK, Ciliberto M, Marashly A, Grinspan ZM, Nangia S, Arredondo K, Miller DJ, Sattar S, Montenegro M, Agarwal N, Galan FN, Wagner J, Abel TJ, Knox AT, Perry MS. PMID: 41056528.
    View in: PubMed Mentions: Fields:
    Translation:Humans
  4. Vigabatrin Versus Adrenocorticotropic Hormone After High-Dose Prednisolone Failure for the Treatment of Epileptic Spasms. J Child Neurol. 2026 Mar; 41(3):359-364. Layton A, Sattar S, Rho JM, Yang JH, Gold J, Zimbric M, Bui J, Sahagian M, Kim-McManus O, Frederick A, Guido-Estrada N, Jindal A, Wiegand S, Dove K, Sweat M, Nespeca M, Montenegro MA. PMID: 40754938.
    View in: PubMed Mentions: Fields:
  5. The development of aperiodic neural activity in the human brain. Nat Hum Behav. 2025 Dec; 9(12):2548-2563. Cross ZR, Gray SM, Dede AJO, Rivera YM, Yin Q, Vahidi P, Rau EMB, Cyr C, Holubecki AM, Asano E, Lin JJ, Kim McManus O, Sattar S, Saez I, Girgis F, King-Stephens D, Weber PB, Laxer KD, Schuele SU, Rosenow JM, Wu JY, Lam SK, Raskin JS, Chang EF, Shaikhouni A, Brunner P, Roland JL, Braga RM, Knight RT, Ofen N, Johnson EL. PMID: 40670699; PMCID: PMC12818177.
    View in: PubMed Mentions: 2 Fields:
    Translation:Humans
  6. Incidental interictal epileptiform discharges in infants with nonepileptic events. Epilepsia. 2025 Sep; 66(9):3571-3577. Montenegro MA, Tsuha M, Sattar S. PMID: 40394879.
    View in: PubMed Mentions: Fields:
    Translation:Humans
  7. Status Epilepticus Protocol Variation Across Accredited National Association of Epilepsy Centers Members. Neurology. 2025 06 10; 104(11):e213689. Lamberta LK, Asmar M, Fredwall MM, Ahrens SM, Bai S, Eisner M, Lado FA, Schuele SU, Clarke DF, Abdelmoity AT, Davis KA, Hopp JL, Koubeissi MZ, Bensalem Owen MK, Herman ST, Ostendorf AP, NAEC Center Director Study Group. PMID: 40378375; PMCID: PMC12089659.
    View in: PubMed Mentions: 2 Fields:
    Translation:Humans
  8. Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies. Pediatr Neurol. 2025 Jul; 168:67-81. Samanta D, Bhatia S, Hunter SE, Rao CK, Xiong K, Karakas C, Reeders PC, Erdemir G, Sattar S, Axeen E, Sandoval Karamian AG, Fine AL, Keator CG, Nolan D, Schreiber JM. PMID: 40381457.
    View in: PubMed Mentions: 5 Fields:
    Translation:Humans
  9. Reinstatement and transformation of memory traces for recognition. Sci Adv. 2025 Feb 21; 11(8):eadp9336. Rau EMB, Fellner MC, Heinen R, Zhang H, Yin Q, Vahidi P, Kobelt M, Asano E, Kim-McManus O, Sattar S, Lin JJ, Auguste KI, Chang EF, King-Stephens D, Weber PB, Laxer KD, Knight RT, Johnson EL, Ofen N, Axmacher N. PMID: 39970226; PMCID: PMC11838014.
    View in: PubMed Mentions: 4 Fields:
    Translation:Humans
  10. Laser Interstitial Thermal Therapy for the Treatment of Mesial Temporal Lobe Epilepsy in Children. J Child Neurol. 2025 May; 40(5):342-347. Trivedi AM, Montenegro MA, Gonda D, Kim-McManus O, Rismanchi N, Frederick A, Guido-Estrada N, Jindal A, Sattar S. PMID: 39887192.
    View in: PubMed Mentions: 1 Fields:
    Translation:Humans
  11. De novo cerebral pseudoaneurysm formation: a rare delayed complication of stereotactic electroencephalography in children. Childs Nerv Syst. 2024 May; 40(5):1501-1506. Daniel M, Stone LE, Plonsker JH, Sattar S, Ravindra V, Gonda D. PMID: 38240787.
    View in: PubMed Mentions: Fields:
    Translation:Humans
  12. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development. Nat Genet. 2023 02; 55(2):209-220. Chung C, Yang X, Bae T, Vong KI, Mittal S, Donkels C, Westley Phillips H, Li Z, Marsh APL, Breuss MW, Ball LL, Garcia CAB, George RD, Gu J, Xu M, Barrows C, James KN, Stanley V, Nidhiry AS, Khoury S, Howe G, Riley E, Xu X, Copeland B, Wang Y, Kim SH, Kang HC, Schulze-Bonhage A, Haas CA, Urbach H, Prinz M, Limbrick DD, Gurnett CA, Smyth MD, Sattar S, Nespeca M, Gonda DD, Imai K, Takahashi Y, Chen HH, Tsai JW, Conti V, Guerrini R, Devinsky O, Silva WA, Machado HR, Mathern GW, Abyzov A, Baldassari S, Baulac S, Focal Cortical Dysplasia Neurogenetics Consortium, Brain Somatic Mosaicism Network, Gleeson JG. PMID: 36635388; PMCID: PMC9961399.
    View in: PubMed Mentions: 51 Fields:
    Translation:Humans
  13. Spatiotemporal dynamics of human high gamma discriminate naturalistic behavioral states. PLoS Comput Biol. 2022 08; 18(8):e1010401. Alasfour A, Gabriel P, Jiang X, Shamie I, Melloni L, Thesen T, Dugan P, Friedman D, Doyle W, Devinsky O, Gonda D, Sattar S, Wang S, Halgren E, Gilja V. PMID: 35939509; PMCID: PMC9387937.
    View in: PubMed Mentions: 1 Fields:
    Translation:Humans
  14. Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes. Hum Mutat. 2022 03; 43(3):305-315. Yang JH, Friederich MW, Ellsworth KA, Frederick A, Foreman E, Malicki D, Dimmock D, Lenberg J, Prasad C, Yu AC, Anthony Rupar C, Hegele RA, Manickam K, Koboldt DC, Crist E, Choi SS, Farhan SMK, Harvey H, Sattar S, Karp N, Wong T, Haas R, Van Hove JLK, Wigby K, Wigby K. PMID: 35026043; PMCID: PMC8863643.
    View in: PubMed Mentions: 4 Fields:
    Translation:HumansCells
  15. Successful Treatment of Pediatric FIRES With Anakinra. Pediatr Neurol. 2021 01; 114:60-61. Yang JH, Nataraj S, Sattar S. PMID: 33227629.
    View in: PubMed Mentions: 9 Fields:
    Translation:Humans
  16. Telehealth in pediatric epilepsy care: A rapid transition during the COVID-19 pandemic. Epilepsy Behav. 2020 10; 111:107282. Sattar S, Kuperman R. PMID: 32759065; PMCID: PMC7386847.
    View in: PubMed Mentions: 15 Fields:
    Translation:HumansCellsPHPublic Health
  17. Neural correlates of unstructured motor behaviors. J Neural Eng. 2019 10 30; 16(6):066026. Gabriel PG, Chen KJ, Alasfour A, Pailla T, Doyle WK, Devinsky O, Friedman D, Dugan P, Melloni L, Thesen T, Gonda D, Sattar S, Wang SG, Gilja V. PMID: 31342926.
    View in: PubMed Mentions: 6 Fields:
    Translation:Humans
  18. Correction: The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 Aug; 21(8):1896. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks EH, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30262923; PMCID: PMC7608233.
    View in: PubMed Mentions: 4 Fields:
  19. Correction to: The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 Jul; 21(7):1671. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, Martin AS, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen F, Braun K, Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, NordliJr DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30158694; PMCID: PMC7608347.
    View in: PubMed Mentions: Fields:
  20. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Am J Hum Genet. 2019 06 06; 104(6):1210-1222. O'Donnell-Luria AH, Pais LS, Faundes V, Wood JC, Sveden A, Luria V, Abou Jamra R, Accogli A, Amburgey K, Anderlid BM, Azzarello-Burri S, Basinger AA, Bianchini C, Bird LM, Buchert R, Carre W, Ceulemans S, Charles P, Cox H, Culliton L, Currò A, Deciphering Developmental Disorders (DDD) Study, Demurger F, Dowling JJ, Duban-Bedu B, Dubourg C, Eiset SE, Escobar LF, Ferrarini A, Haack TB, Hashim M, Heide S, Helbig KL, Helbig I, Heredia R, Héron D, Isidor B, Jonasson AR, Joset P, Keren B, Kok F, Kroes HY, Lavillaureix A, Lu X, Maas SM, Maegawa GHB, Marcelis CLM, Mark PR, Masruha MR, McLaughlin HM, McWalter K, Melchinger EU, Mercimek-Andrews S, Nava C, Pendziwiat M, Person R, Ramelli GP, Ramos LLP, Rauch A, Reavey C, Renieri A, Rieß A, Sanchez-Valle A, Sattar S, Saunders C, Schwarz N, Smol T, Srour M, Steindl K, Syrbe S, Taylor JC, Telegrafi A, Thiffault I, Trauner DA, van der Linden H, van Koningsbruggen S, Villard L, Vogel I, Vogt J, Weber YG, Wentzensen IM, Widjaja E, Zak J, Baxter S, Banka S, Rodan LH. PMID: 31079897; PMCID: PMC6556837.
    View in: PubMed Mentions: 45 Fields:
    Translation:Humans
  21. Laser Ablation of a Nonlesional Cingulate Gyrus Epileptogenic Zone Using Robotic-Assisted Stereotactic EEG Localization: A Case Report. Stereotact Funct Neurosurg. 2019; 97(1):10-17. Upadhyayula PS, Rennert RC, Hoshide R, Sattar S, Gonda DD. PMID: 30943498.
    View in: PubMed Mentions: Fields:
    Translation:Humans
  22. Coarse behavioral context decoding. J Neural Eng. 2019 02; 16(1):016021. Alasfour A, Gabriel P, Jiang X, Shamie I, Melloni L, Thesen T, Dugan P, Friedman D, Doyle W, Devinsky O, Gonda D, Sattar S, Wang S, Halgren E, Gilja V. PMID: 30523860.
    View in: PubMed Mentions: 5 Fields:
    Translation:Humans
  23. Patient-Specific Pose Estimation in Clinical Environments. IEEE J Transl Eng Health Med. 2018; 6:2101111. Chen K, Gabriel P, Alasfour A, Gong C, Doyle WK, Devinsky O, Friedman D, Dugan P, Melloni L, Thesen T, Gonda D, Sattar S, Wang S, Gilja V. PMID: 30483453; PMCID: PMC6255526.
    View in: PubMed Mentions: 17 Fields:
  24. The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 02; 21(2):398-408. Baldassari S, Picard F, Verbeek NE, van Kempen M, Brilstra EH, Lesca G, Conti V, Guerrini R, Bisulli F, Licchetta L, Pippucci T, Tinuper P, Hirsch E, de Saint Martin A, Chelly J, Rudolf G, Chipaux M, Ferrand-Sorbets S, Dorfmüller G, Sisodiya S, Balestrini S, Schoeler N, Hernandez-Hernandez L, Krithika S, Oegema R, Hagebeuk E, Gunning B, Deckers C, Berghuis B, Wegner I, Niks E, Jansen FE, Braun K, de Jong D, Rubboli G, Talvik I, Sander V, Uldall P, Jacquemont ML, Nava C, Leguern E, Julia S, Gambardella A, d'Orsi G, Crichiutti G, Faivre L, Darmency V, Benova B, Krsek P, Biraben A, Lebre AS, Jennesson M, Sattar S, Marchal C, Nordli DR, Lindstrom K, Striano P, Lomax LB, Kiss C, Bartolomei F, Lepine AF, Schoonjans AS, Stouffs K, Jansen A, Panagiotakaki E, Ricard-Mousnier B, Thevenon J, de Bellescize J, Catenoix H, Dorn T, Zenker M, Müller-Schlüter K, Brandt C, Krey I, Polster T, Wolff M, Balci M, Rostasy K, Achaz G, Zacher P, Becher T, Cloppenborg T, Yuskaitis CJ, Weckhuysen S, Poduri A, Lemke JR, Møller RS, Baulac S. PMID: 30093711; PMCID: PMC6292495.
    View in: PubMed Mentions: 119 Fields:
    Translation:HumansCells
  25. Neurological Outcomes After Presumed Childhood Encephalitis. Pediatr Neurol. 2015 Sep; 53(3):200-6. Rismanchi N, Gold JJ, Sattar S, Glaser C, Sheriff H, Proudfoot J, Mower A, Nespeca M, Crawford JR, Wang SG. PMID: 26220354.
    View in: PubMed Mentions: 6 Fields:
    Translation:Humans
  26. Epilepsy After Resolution of Presumed Childhood Encephalitis. Pediatr Neurol. 2015 Jul; 53(1):65-72. Rismanchi N, Gold JJ, Sattar S, Glaser CA, Sheriff H, Proudfoot J, Mower A, Crawford JR, Nespeca M, Wang SG. PMID: 26092415.
    View in: PubMed Mentions: 4 Fields:
    Translation:Humans
  27. Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiers. Am J Med Genet A. 2011 Dec; 155A(12):3042-9. Zaki MS, Sattar S, Massoudi RA, Gleeson JG. PMID: 22002901; PMCID: PMC3415794.
    View in: PubMed Mentions: 23 Fields:
    Translation:Humans
  28. New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect. Am J Med Genet A. 2011 Dec; 155A(12):3035-41. Zaki MS, Salam GM, Saleem SN, Dobyns WB, Issa MY, Sattar S, Gleeson JG. PMID: 22002884; PMCID: PMC3415795.
    View in: PubMed Mentions: 4 Fields:
    Translation:Humans
  29. The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disorders. Dev Med Child Neurol. 2011 Sep; 53(9):793-798. Sattar S, Gleeson JG. PMID: 21679365; PMCID: PMC3984879.
    View in: PubMed Mentions: 70 Fields:
    Translation:HumansCells
  30. Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families. Neurology. 2011 Jan 25; 76(4):373-82. Hanna RM, Marsh SE, Swistun D, Al-Gazali L, Zaki MS, Abdel-Salam GM, Al-Tawari A, Bastaki L, Kayserili H, Rajab A, Boglárka B, Dietrich RB, Dobyns WB, Truwit CL, Sattar S, Chuang NA, Sherr EH, Gleeson JG. PMID: 21263138; PMCID: PMC3034417.
    View in: PubMed Mentions: 20 Fields:
    Translation:Humans
  31. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum. Eur J Med Genet. 2011 Jan-Feb; 54(1):82-5. Abdel Aleem A, Abu-Shahba N, Swistun D, Silhavy J, Bielas SL, Sattar S, Gleeson JG, Zaki MS. PMID: 20971220; PMCID: PMC3073376.
    View in: PubMed Mentions: 6 Fields:
    Translation:HumansCells

Start with: newest oldestInclude: line numbers double spacing all authors publication IDs