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Items: 1 to 50 of 221

1.

Postoperative Cataract Endophthalmitis Masquerading as Hemorrhagic Occlusive Retinal Vasculitis (HORV): A Case Report.

Greenberg E, Dedeker C, Olson HJ, Montezuma RS.

Ocul Immunol Inflamm. 2019 Aug 15:1-4. doi: 10.1080/09273948.2019.1634216. [Epub ahead of print]

PMID:
31414916
2.

CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.

Demarest ST, Olson HE, Moss A, Pestana-Knight E, Zhang X, Parikh S, Swanson LC, Riley KD, Bazin GA, Angione K, Niestroj LM, Lal D, Juarez-Colunga E, Benke TA.

Epilepsia. 2019 Aug;60(8):1733-1742. doi: 10.1111/epi.16285. Epub 2019 Jul 16.

PMID:
31313283
3.

Severity Assessment in CDKL5 Deficiency Disorder.

Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, Utley K, Jaksha A, Amin S, Khwaja O, Devinsky O, Neul JL, Percy AK, Benke TA.

Pediatr Neurol. 2019 Aug;97:38-42. doi: 10.1016/j.pediatrneurol.2019.03.017. Epub 2019 Mar 27.

PMID:
31147226
4.

Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review.

Olson HE, Demarest ST, Pestana-Knight EM, Swanson LC, Iqbal S, Lal D, Leonard H, Cross JH, Devinsky O, Benke TA.

Pediatr Neurol. 2019 Aug;97:18-25. doi: 10.1016/j.pediatrneurol.2019.02.015. Epub 2019 Feb 23. Review.

PMID:
30928302
5.

Cannabis for refractory epilepsy in children: A review focusing on CDKL5 Deficiency Disorder.

Dale T, Downs J, Olson H, Bergin AM, Smith S, Leonard H.

Epilepsy Res. 2019 Mar;151:31-39. doi: 10.1016/j.eplepsyres.2019.02.001. Epub 2019 Feb 5. Review.

PMID:
30771550
6.

Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.

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; Undiagnosed Diseases Network, Kayani S, Snyder M, Calvert S, Scheffer IE, Yang E, Waugh JL, Lal D, Bodamer O, Poduri A.

Epilepsia. 2019 Mar;60(3):406-418. doi: 10.1111/epi.14653. Epub 2019 Jan 25.

PMID:
30682224
7.

PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.

Johnstone DL, Al-Shekaili HH, Tarailo-Graovac M, Wolf NI, Ivy AS, Demarest S, Roussel Y, Ciapaite J, van Roermund CWT, Kernohan KD, Kosuta C, Ban K, Ito Y, McBride S, Al-Thihli K, Abdelrahim RA, Koul R, Al Futaisi A, Haaxma CA, Olson H, Sigurdardottir LY, Arnold GL, Gerkes EH, Boon M, Heiner-Fokkema MR, Noble S, Bosma M, Jans J, Koolen DA, Kamsteeg EJ, Drögemöller B, Ross CJ, Majewski J, Cho MT, Begtrup A, Wasserman WW, Bui T, Brimble E, Violante S, Houten SM, Wevers RA, van Faassen M, Kema IP, Lepage N; Care4Rare Canada Consortium, Lines MA, Dyment DA, Wanders RJA, Verhoeven-Duif N, Ekker M, Boycott KM, Friedman JM, Pena IA, van Karnebeek CDM.

Brain. 2019 Mar 1;142(3):542-559. doi: 10.1093/brain/awy346.

PMID:
30668673
8.

Characterizing the molecular epidemiology of Staphylococcus aureus across and within fitness facility types.

Dalman M, Bhatta S, Nagajothi N, Thapaliya D, Olson H, Naimi HM, Smith TC.

BMC Infect Dis. 2019 Jan 18;19(1):69. doi: 10.1186/s12879-019-3699-7.

9.

A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis.

Olson HE, Jean-Marçais N, Yang E, Heron D, Tatton-Brown K, van der Zwaag PA, Bijlsma EK, Krock BL, Backer E, Kamsteeg EJ, Sinnema M, Reijnders MRF, Bearden D, Begtrup A, Telegrafi A, Lunsing RJ, Burglen L, Lesca G, Cho MT, Smith LA, Sheidley BR, El Achkar CM, Pearl PL, Poduri A, Skraban CM, Tarpinian J, Nesbitt AI, Fransen van de Putte DE, Ruivenkamp CAL, Rump P, Chatron N, Sabatier I, De Bellescize J, Guibaud L, Sweetser DA, Waxler JL, Wierenga KJ; DDD Study, Donadieu J, Narayanan V, Ramsey KM; C4RCD Research Group, Nava C, Rivière JB, Vitobello A, Mau-Them FT, Philippe C, Bruel AL, Duffourd Y, Thomas L, Lelieveld SH, Schuurs-Hoeijmakers J, Brunner HG, Keren B, Thevenon J, Faivre L, Thomas G, Thauvin-Robinet C.

Am J Hum Genet. 2018 Oct 4;103(4):631. doi: 10.1016/j.ajhg.2018.09.002. No abstract available.

10.

Nothing to Be Sniffed At: Anosmin1 Tunes Fgf Diffusivity.

Olson HM, Nechiporuk AV.

Dev Cell. 2018 Sep 24;46(6):674-676. doi: 10.1016/j.devcel.2018.09.004.

11.

Using Zebrafish to Study Collective Cell Migration in Development and Disease.

Olson HM, Nechiporuk AV.

Front Cell Dev Biol. 2018 Aug 17;6:83. doi: 10.3389/fcell.2018.00083. eCollection 2018. Review.

12.

Lariat sign: An MRI finding associated with common peroneal nerve rupture.

Morris BL, Grinde AS, Olson H, Brubacher JW, Schroeppel JP, Everist BM.

Radiol Case Rep. 2018 May 30;13(3):743-746. doi: 10.1016/j.radcr.2018.03.015. eCollection 2018 Jun.

13.

Increased levels of RECQ5 shift DNA repair from canonical to alternative pathways.

Olson HC, Davis L, Kiianitsa K, Khoo KJ, Liu Y, Knijnenburg TA, Maizels N.

Nucleic Acids Res. 2018 Oct 12;46(18):9496-9509. doi: 10.1093/nar/gky727.

14.

Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.

Gardner JF, Cushion TD, Niotakis G, Olson HE, Grant PE, Scott RH, Stoodley N, Cohen JS, Naidu S, Attie-Bitach T, Bonnières M, Boutaud L, Encha-Razavi F, Palmer-Smith SM, Mugalaasi H, Mullins JGL, Pilz DT, Fry AE.

Brain Sci. 2018 Aug 7;8(8). pii: E145. doi: 10.3390/brainsci8080145.

15.

The TEACH trial: Tailored education to assist label comprehension and health literacy.

Lee S, Khare MM, Olson HR, Chen AMH, Law AV.

Res Social Adm Pharm. 2018 Sep;14(9):839-845. doi: 10.1016/j.sapharm.2018.05.015. Epub 2018 Jun 7.

PMID:
29937110
16.

A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis.

Olson HE, Jean-Marçais N, Yang E, Heron D, Tatton-Brown K, van der Zwaag PA, Bijlsma EK, Krock BL, Backer E, Kamsteeg EJ, Sinnema M, Reijnders MRF, Bearden D, Begtrup A, Telegrafi A, Lunsing RJ, Burglen L, Lesca G, Cho MT, Smith LA, Sheidley BR, Moufawad El Achkar C, Pearl PL, Poduri A, Skraban CM, Tarpinian J, Nesbitt AI, Fransen van de Putte DE, Ruivenkamp CAL, Rump P, Chatron N, Sabatier I, De Bellescize J, Guibaud L, Sweetser DA, Waxler JL, Wierenga KJ; DDD Study, Donadieu J, Narayanan V, Ramsey KM; C4RCD Research Group, Nava C, Rivière JB, Vitobello A, Tran Mau-Them F, Philippe C, Bruel AL, Duffourd Y, Thomas L, Lelieveld SH, Schuurs-Hoeijmakers J, Brunner HG, Keren B, Thevenon J, Faivre L, Thomas G, Thauvin-Robinet C.

Am J Hum Genet. 2018 May 3;102(5):995-1007. doi: 10.1016/j.ajhg.2018.03.005. Epub 2018 Apr 12. Erratum in: Am J Hum Genet. 2018 Oct 4;103(4):631.

17.

Neonatal epilepsy genetics.

Axeen EJT, Olson HE.

Semin Fetal Neonatal Med. 2018 Jun;23(3):197-203. doi: 10.1016/j.siny.2018.01.003. Epub 2018 Jan 31. Review.

PMID:
29426807
18.

Should patients with complex febrile seizure be admitted for further management?

Olson H, Rudloe T, Loddenkemper T, Harper MB, Kimia AA.

Am J Emerg Med. 2018 Aug;36(8):1386-1390. doi: 10.1016/j.ajem.2017.12.059. Epub 2017 Dec 28.

PMID:
29317153
19.

An Expanded Role for the RFX Transcription Factor DAF-19, with Dual Functions in Ciliated and Nonciliated Neurons.

De Stasio EA, Mueller KP, Bauer RJ, Hurlburt AJ, Bice SA, Scholtz SL, Phirke P, Sugiaman-Trapman D, Stinson LA, Olson HB, Vogel SL, Ek-Vazquez Z, Esemen Y, Korzynski J, Wolfe K, Arbuckle BN, Zhang H, Lombard-Knapp G, Piasecki BP, Swoboda P.

Genetics. 2018 Mar;208(3):1083-1097. doi: 10.1534/genetics.117.300571. Epub 2018 Jan 3.

20.

Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency.

Sacharow SJ, Dudenhausen EE, Lomelino CL, Rodan L, El Achkar CM, Olson HE, Genetti CA, Agrawal PB, McKenna R, Kilberg MS.

Mol Genet Metab. 2018 Mar;123(3):317-325. doi: 10.1016/j.ymgme.2017.12.433. Epub 2017 Dec 20.

21.

Understanding and managing sleep disruption in children with fetal alcohol spectrum disorder.

Hanlon-Dearman A, Chen ML, Olson HC.

Biochem Cell Biol. 2018 Apr;96(2):267-274. doi: 10.1139/bcb-2017-0064. Epub 2017 Oct 4. Review.

PMID:
28977761
22.

Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part I: review of experience at Boston Children's Hospital.

Yang E, Storey A, Olson HE, Soul J, Estroff JA, Trenor CC, Cooper BK, Smith ER, Orbach DB.

J Neurointerv Surg. 2018 May;10(5):467-470. doi: 10.1136/neurintsurg-2017-013344. Epub 2017 Sep 30. Review.

PMID:
28965107
23.

Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part II: synthesis of the literature and patient management.

Yang E, Storey A, Olson HE, Soul J, Estroff JA, Trenor CC, Cooper BK, Smith ER, Orbach DB.

J Neurointerv Surg. 2018 May;10(5):471-475. doi: 10.1136/neurintsurg-2017-013343. Epub 2017 Sep 30. Review.

PMID:
28965104
24.

A randomized controlled trial of levodopa in patients with Angelman syndrome.

Tan WH, Bird LM, Sadhwani A, Barbieri-Welge RL, Skinner SA, Horowitz LT, Bacino CA, Noll LM, Fu C, Hundley RJ, Wink LK, Erickson CA, Barnes GN, Slavotinek A, Jeremy R, Rotenberg A, Kothare SV, Olson HE, Poduri A, Nespeca MP, Chu HC, Willen JM, Haas KF, Weeber EJ, Rufo PA.

Am J Med Genet A. 2018 May;176(5):1099-1107. doi: 10.1002/ajmg.a.38457. Epub 2017 Sep 25.

25.

PMA2020: Rapid Turn-Around Survey Data to Monitor Family Planning Service and Practice in Ten Countries.

Zimmerman L, Olson H; PMA2020 Principal Investigators Group, Tsui A, Radloff S.

Stud Fam Plann. 2017 Sep;48(3):293-303. doi: 10.1111/sifp.12031. Epub 2017 Aug 28. No abstract available.

26.

Use of the ketogenic diet to manage refractory epilepsy in CDKL5 disorder: Experience of >100 patients.

Lim Z, Wong K, Olson HE, Bergin AM, Downs J, Leonard H.

Epilepsia. 2017 Aug;58(8):1415-1422. doi: 10.1111/epi.13813. Epub 2017 Jun 12.

27.

Prevalence and profile of Neurodevelopment and Fetal Alcohol Spectrum Disorder (FASD) amongst Australian Aboriginal children living in remote communities.

Fitzpatrick JP, Latimer J, Olson HC, Carter M, Oscar J, Lucas BR, Doney R, Salter C, Try J, Hawkes G, Fitzpatrick E, Hand M, Watkins RE, Tsang TW, Bower C, Ferreira ML, Boulton J, Elliott EJ.

Res Dev Disabil. 2017 Jun;65:114-126. doi: 10.1016/j.ridd.2017.04.001. Epub 2017 May 9.

PMID:
28499185
28.

An investigation of intra-individual variability in children with fetal alcohol spectrum disorder (FASD).

Ali S, Kerns KA, Mulligan BP, Olson HC, Astley SJ.

Child Neuropsychol. 2018 Jul;24(5):617-637. doi: 10.1080/09297049.2017.1302579. Epub 2017 Mar 16.

29.

Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.

Olson HE, Kelly M, LaCoursiere CM, Pinsky R, Tambunan D, Shain C, Ramgopal S, Takeoka M, Libenson MH, Julich K, Loddenkemper T, Marsh ED, Segal D, Koh S, Salman MS, Paciorkowski AR, Yang E, Bergin AM, Sheidley BR, Poduri A.

Ann Neurol. 2017 Mar;81(3):419-429. doi: 10.1002/ana.24883. Epub 2017 Feb 14.

30.

A Model Program for Translational Medicine in Epilepsy Genetics.

Smith LA, Ullmann JF, Olson HE, Achkar CM, Truglio G, Kelly M, Rosen-Sheidley B, Poduri A.

J Child Neurol. 2017 Mar;32(4):429-436. doi: 10.1177/0883073816685654. Epub 2017 Jan 6.

31.

Chiropractic Management of a Patient With Perineal Numbness After Arthroscopic Hip Surgery: A Case Report.

Olson HM, Zetocha AJ, Olson CA.

J Chiropr Med. 2016 Dec;15(4):305-309. Epub 2016 Oct 13.

32.

Chiropractic Management of Musculoskeletal Symptoms in a 14-Year-Old Hockey Player With Postconcussion Symptoms: A Case Report.

Olson HM, Tunning MJ, Boesch RJ.

J Chiropr Med. 2016 Sep;15(3):208-13. doi: 10.1016/j.jcm.2016.04.006. Epub 2016 May 27.

33.

A Renewed Call to Action: The Need for Systematic Research on Interventions for FASD.

Olson HC.

Alcohol Clin Exp Res. 2016 Sep;40(9):1817-21. doi: 10.1111/acer.13150. Epub 2016 Jul 25. No abstract available.

PMID:
27453398
34.

BRAT1 mutations present with a spectrum of clinical severity.

Srivastava S, Olson HE, Cohen JS, Gubbels CS, Lincoln S, Davis BT, Shahmirzadi L, Gupta S, Picker J, Yu TW, Miller DT, Soul JS, Poretti A, Naidu S.

Am J Med Genet A. 2016 Sep;170(9):2265-73. doi: 10.1002/ajmg.a.37783. Epub 2016 Jun 9. Review.

35.

Far-field head-media optical interaction in heat-assisted magnetic recording.

Yang R, Jones P, Klemmer T, Olson H, Zhang D, Perry T, Scholz W, Yin H, Hipwell R, Thiele JU, Tang H, Seigler M.

Appl Opt. 2016 Feb 20;55(6):1241-8. doi: 10.1364/AO.55.001241.

PMID:
26906574
36.

Developmental validation of the PowerPlex(®) Fusion 6C System.

Ensenberger MG, Lenz KA, Matthies LK, Hadinoto GM, Schienman JE, Przech AJ, Morganti MW, Renstrom DT, Baker VM, Gawrys KM, Hoogendoorn M, Steffen CR, Martín P, Alonso A, Olson HR, Sprecher CJ, Storts DR.

Forensic Sci Int Genet. 2016 Mar;21:134-44. doi: 10.1016/j.fsigen.2015.12.011. Epub 2015 Dec 22.

37.

Pediatric anti-Hu-associated encephalitis with clinical features of Rasmussen encephalitis.

Aravamuthan BR, Sánchez Fernández I, Zurawski J, Olson H, Gorman M, Takeoka M.

Neurol Neuroimmunol Neuroinflamm. 2015 Sep 24;2(5):e150. doi: 10.1212/NXI.0000000000000150. eCollection 2015 Oct. No abstract available.

38.

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.

Howell KB, McMahon JM, Carvill GL, Tambunan D, Mackay MT, Rodriguez-Casero V, Webster R, Clark D, Freeman JL, Calvert S, Olson HE, Mandelstam S, Poduri A, Mefford HC, Harvey AS, Scheffer IE.

Neurology. 2015 Sep 15;85(11):958-66. doi: 10.1212/WNL.0000000000001926. Epub 2015 Aug 19.

39.

A Military Transitional Year Professionalism Curriculum.

Edwards M, Sterbis JR, Olson HL.

J Grad Med Educ. 2014 Sep;6(3):571-3. doi: 10.4300/JGME-D-13-00399.1.

40.

Neurobehavioral Disorder Associated with Prenatal Alcohol Exposure (ND-PAE): Proposed DSM-5 Diagnosis.

Kable JA, O'Connor MJ, Olson HC, Paley B, Mattson SN, Anderson SM, Riley EP.

Child Psychiatry Hum Dev. 2016 Apr;47(2):335-46. doi: 10.1007/s10578-015-0566-7. Review.

PMID:
26202432
41.

The genetics of the epilepsies.

El Achkar CM, Olson HE, Poduri A, Pearl PL.

Curr Neurol Neurosci Rep. 2015 Jul;15(7):39. doi: 10.1007/s11910-015-0559-8. Review.

PMID:
26008807
42.

Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.

Olson HE, Tambunan D, LaCoursiere C, Goldenberg M, Pinsky R, Martin E, Ho E, Khwaja O, Kaufmann WE, Poduri A.

Am J Med Genet A. 2015 Sep;167A(9):2017-25. doi: 10.1002/ajmg.a.37132. Epub 2015 Apr 25.

43.

Evaluation and treatment of autoimmune neurologic disorders in the pediatric intensive care unit.

Benson LA, Olson H, Gorman MP.

Semin Pediatr Neurol. 2014 Dec;21(4):284-90. doi: 10.1016/j.spen.2014.12.008. Epub 2014 Dec 18. Review.

PMID:
25727510
44.

Genetic forms of epilepsies and other paroxysmal disorders.

Olson HE, Poduri A, Pearl PL.

Semin Neurol. 2014 Jul;34(3):266-79. doi: 10.1055/s-0034-1386765. Epub 2014 Sep 5. Review.

45.

Safety and retention rate of rufinamide in 300 patients: a single pediatric epilepsy center experience.

Thome-Souza S, Kadish NE, Ramgopal S, Sánchez Fernández I, Bergin AM, Bolton J, Harini C, Libenson M, Olson H, Peters J, Poduri A, Rotenberg A, Takeoka M, Kothare SV, Kapur K, Bourgeois BF, Loddenkemper T.

Epilepsia. 2014 Aug;55(8):1235-44. doi: 10.1111/epi.12689. Epub 2014 Jul 28.

46.

Copy number variation plays an important role in clinical epilepsy.

Olson H, Shen Y, Avallone J, Sheidley BR, Pinsky R, Bergin AM, Berry GT, Duffy FH, Eksioglu Y, Harris DJ, Hisama FM, Ho E, Irons M, Jacobsen CM, James P, Kothare S, Khwaja O, Lipton J, Loddenkemper T, Markowitz J, Maski K, Megerian JT, Neilan E, Raffalli PC, Robbins M, Roberts A, Roe E, Rollins C, Sahin M, Sarco D, Schonwald A, Smith SE, Soul J, Stoler JM, Takeoka M, Tan WH, Torres AR, Tsai P, Urion DK, Weissman L, Wolff R, Wu BL, Miller DT, Poduri A.

Ann Neurol. 2014 Jun;75(6):943-58. doi: 10.1002/ana.24178. Epub 2014 Jun 13.

47.

Root and Stem Rot of Begonia Caused by Phytopythium helicoides in Virginia.

Yang X, Richardson PA, Olson HA, Hong CX.

Plant Dis. 2013 Oct;97(10):1385. doi: 10.1094/PDIS-05-13-0472-PDN.

PMID:
30722172
48.

Clinical application and evaluation of the Bien diagnostic criteria for Rasmussen encephalitis.

Olson HE, Lechpammer M, Prabhu SP, Ciarlini PD, Poduri A, Gooty VD, Anjum MW, Gorman MP, Loddenkemper T.

Epilepsia. 2013 Oct;54(10):1753-60. doi: 10.1111/epi.12334. Epub 2013 Aug 23.

49.

Functional handwriting performance in school-age children with fetal alcohol spectrum disorders.

Duval-White CJ, Jirikowic T, Rios D, Deitz J, Olson HC.

Am J Occup Ther. 2013 Sep-Oct;67(5):534-42. doi: 10.5014/ajot.2013.008243.

50.

Diversity and Mefenoxam Sensitivity of Phytophthora spp. Associated with the Ornamental Horticulture Industry in the Southeastern United States.

Olson HA, Jeffers SN, Ivors KL, Steddom KC, Williams-Woodward JL, Mmbaga MT, Benson DM, Hong CX.

Plant Dis. 2013 Jan;97(1):86-92. doi: 10.1094/PDIS-04-12-0348-RE.

PMID:
30722305

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