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Items: 1 to 50 of 223

1.

Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.

Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus A, Trivisano M, Gill D, Sadleir LG, Specchio N, Guerrini R, Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE.

Ann Neurol. 2019 Oct 16. doi: 10.1002/ana.25619. [Epub ahead of print]

PMID:
31618474
2.

Torpedo Maculopathy Associated with NEXMIF Mutation.

Alarcon-Martinez T, Khan A, Myers KA.

Mol Syndromol. 2019 Jul;10(4):229-233. doi: 10.1159/000498835. Epub 2019 Mar 15.

3.

Xq26 duplications lead to undergrowth or overgrowth via competing pathways including GPC3/GPC4.

Karna GK, Myers KA.

Ann Hum Genet. 2019 Oct 3. doi: 10.1111/ahg.12357. [Epub ahead of print]

PMID:
31583675
4.

Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption.

Myers KA, van 't Hof FNG, Sadleir LG, Legault G, Simard-Tremblay E, Amor DJ, Scheffer IE.

Pediatrics. 2019 Sep;144(3). pii: e20190599. doi: 10.1542/peds.2019-0599. Epub 2019 Aug 22.

PMID:
31439621
5.

Adjuvant bevacizumab for melanoma patients at high risk of recurrence: survival analysis of the AVAST-M trial.

Corrie PG, Marshall A, Nathan PD, Lorigan P, Gore M, Tahir S, Faust G, Kelly CG, Marples M, Danson SJ, Marshall E, Houston SJ, Board RE, Waterston AM, Nobes JP, Harries M, Kumar S, Goodman A, Dalgleish A, Martin-Clavijo A, Westwell S, Casasola R, Chao D, Maraveyas A, Patel PM, Ottensmeier CH, Farrugia D, Humphreys A, Eccles B, Young G, Barker EO, Harman C, Weiss M, Myers KA, Chhabra A, Rodwell SH, Dunn JA, Middleton MR.

Ann Oncol. 2019 Aug 19. pii: mdz237. doi: 10.1093/annonc/mdz237. [Epub ahead of print] No abstract available.

PMID:
31430371
6.

Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability.

Borlot F, de Almeida BI, Combe SL, Andrade DM, Filloux FM, Myers KA.

Epilepsia. 2019 Aug;60(8):1661-1669. doi: 10.1111/epi.16273. Epub 2019 Jul 5.

PMID:
31273778
7.

Incorporation of fixation-removal with Fresnel glasses in a routine EEG protocol.

Alhajaj G, Myers KA.

Clin Neurophysiol. 2019 Aug;130(8):1185-1187. doi: 10.1016/j.clinph.2019.04.716. Epub 2019 May 24. No abstract available.

PMID:
31163362
8.

MRE11 as a Predictive Biomarker of Outcome After Radiation Therapy in Bladder Cancer.

Walker AK, Karaszi K, Valentine H, Strauss VY, Choudhury A, McGill S, Wen K, Brown MD, Ramani V, Bhattarai S, Teo MTW, Yang L, Myers KA, Deshmukh N, Denley H, Browning L, Love SB, Iyer G, Clarke NW, Hall E, Huddart R, James ND, Hoskin PJ, West CML, Kiltie AE.

Int J Radiat Oncol Biol Phys. 2019 Jul 15;104(4):809-818. doi: 10.1016/j.ijrobp.2019.03.015. Epub 2019 Mar 15.

9.

Ferrochelatase Deficiency Abrogated the Enhancement of Aminolevulinic Acid-mediated Protoporphyrin IX by Iron Chelator Deferoxamine.

Palasuberniam P, Kraus D, Mansi M, Braun A, Howley R, Myers KA, Chen B.

Photochem Photobiol. 2019 Jul;95(4):1052-1059. doi: 10.1111/php.13091. Epub 2019 Mar 15.

PMID:
30767226
10.

LANA oligomeric architecture is essential for KSHV nuclear body formation and viral genome maintenance during latency.

De Leo A, Deng Z, Vladimirova O, Chen HS, Dheekollu J, Calderon A, Myers KA, Hayden J, Keeney F, Kaufer BB, Yuan Y, Robertson E, Lieberman PM.

PLoS Pathog. 2019 Jan 25;15(1):e1007489. doi: 10.1371/journal.ppat.1007489. eCollection 2019 Jan.

11.

Sudden unexpected death in GEFS+ families with sodium channel pathogenic variants.

Myers KA, Shevell MI, S├ębire G.

Epilepsy Res. 2019 Feb;150:66-69. doi: 10.1016/j.eplepsyres.2019.01.009. Epub 2019 Jan 14.

PMID:
30660056
12.

PLCB1 Biallelic Point Mutations Cause West Syndrome.

Myers KA.

Pediatr Neurol. 2019 Feb;91:62-64. doi: 10.1016/j.pediatrneurol.2018.11.007. Epub 2018 Nov 22. No abstract available.

PMID:
30554916
13.

Hemiconvulsion-Hemiplegia-Epilepsy in a girl with cobalamin C deficiency.

Myers KA, Dudley RW, Srour M.

Epileptic Disord. 2018 Dec 1;20(6):545-550. doi: 10.1684/epd.2018.1017.

PMID:
30530444
14.

Rhythmic Sawtooth Electroencephalograph Waveforms in Neonatal Hypoxic-Ischemic/Hypoglycemic Encephalopathy.

Cinelli D, Lacroix C, Myers KA.

Pediatr Neurol. 2019 Feb;91:70-71. doi: 10.1016/j.pediatrneurol.2018.10.010. Epub 2018 Oct 24. No abstract available.

PMID:
30473260
15.

Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study.

Myers KA, Davey MJ, Ching M, Ellis C, Grinton BE, Roten A, Lightfoot PA, Scheffer IE.

J Clin Sleep Med. 2018 Oct 15;14(10):1697-1704. doi: 10.5664/jcsm.7376.

16.

Heart rate variability measurement in epilepsy: How can we move from research to clinical practice?

Myers KA, Sivathamboo S, Perucca P.

Epilepsia. 2018 Dec;59(12):2169-2178. doi: 10.1111/epi.14587. Epub 2018 Oct 21. Review.

PMID:
30345509
17.

Identification and characterization of agnuside, a natural proangiogenic small molecule.

Pillarisetti P, Myers KA.

Eur J Med Chem. 2018 Dec 5;160:193-206. doi: 10.1016/j.ejmech.2018.10.009. Epub 2018 Oct 5.

PMID:
30340142
18.

Live-cell imaging of small nucleolar RNA tagged with the broccoli aptamer in yeast.

Zinskie JA, Roig M, Janetopoulos C, Myers KA, Bruist MF.

FEMS Yeast Res. 2018 Dec 1;18(8). doi: 10.1093/femsyr/foy093.

PMID:
30137288
19.

Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170].

Myers KA, White SM, Mohammed S, Metcalfe KA, Fry AE, Wraige E, Vasudevan PC, Balasubramanian M, Scheffer IE.

Epilepsy Res. 2018 Nov;147:121. doi: 10.1016/j.eplepsyres.2018.07.019. Epub 2018 Aug 10. No abstract available.

PMID:
30104120
20.

Genetic literacy series: genetic epilepsy with febrile seizures plus.

Myers KA, Scheffer IE, Berkovic SF; ILAE Genetics Commission.

Epileptic Disord. 2018 Aug 1;20(4):232-238. doi: 10.1684/epd.2018.0985. Review.

21.

25-hydroxyvitamin D serum levels in patients with high risk resected melanoma treated in an adjuvant bevacizumab trial.

Lipplaa A, Fernandes R, Marshall A, Lorigan P, Dunn J, Myers KA, Barker E, Newton-Bishop J, Middleton MR, Corrie PG.

Br J Cancer. 2018 Oct;119(7):793-800. doi: 10.1038/s41416-018-0179-6. Epub 2018 Jul 23.

22.

Hybrid model intermediate between a laboratory and field study: A humane paradigm shift in feline research.

Fischer A, Benka VA, Briggs JR, Maki J, Morris KN, Myers KA, Rhodes L, Weedon GR, Levy JK.

J Feline Med Surg. 2018 Sep;20(9):803-810. doi: 10.1177/1098612X18791872. Epub 2018 Jul 19.

PMID:
30021502
23.

Adjuvant bevacizumab for melanoma patients at high risk of recurrence: survival analysis of the AVAST-M trial.

Corrie PG, Marshall A, Nathan PD, Lorigan P, Gore M, Tahir S, Faust G, Kelly CG, Marples M, Danson SJ, Marshall E, Houston SJ, Board RE, Waterston AM, Nobes JP, Harries M, Kumar S, Goodman A, Dalgleish A, Martin-Clavijo A, Westwell S, Casasola R, Chao D, Maraveyas A, Patel PM, Ottensmeier CH, Farrugia D, Humphreys A, Eccles B, Young G, Barker EO, Harman C, Weiss M, Myers KA, Chhabra A, Rodwell SH, Dunn JA, Middleton MR; AVAST-M Investigators.

Ann Oncol. 2018 Aug 1;29(8):1843-1852. doi: 10.1093/annonc/mdy229.

24.

Epilepsy genetics: Current knowledge, applications, and future directions.

Myers KA, Johnstone DL, Dyment DA.

Clin Genet. 2019 Jan;95(1):95-111. doi: 10.1111/cge.13414. Epub 2018 Aug 2. Review.

PMID:
29992546
25.

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk.

Myers KA, Bello-Espinosa LE, Symonds JD, Zuberi SM, Clegg R, Sadleir LG, Buchhalter J, Scheffer IE.

Epilepsia. 2018 Jul;59(7):1372-1380. doi: 10.1111/epi.14438. Epub 2018 Jun 6.

26.

A cell surface display fluorescent biosensor for measuring MMP14 activity in real-time.

Braun A, Farber MJ, Klase ZA, Berget PB, Myers KA.

Sci Rep. 2018 Apr 12;8(1):5916. doi: 10.1038/s41598-018-24080-0.

27.

Stiripentol efficacy and safety in Dravet syndrome: a 12-year observational study.

Myers KA, Lightfoot P, Patil SG, Cross JH, Scheffer IE.

Dev Med Child Neurol. 2018 Jun;60(6):574-578. doi: 10.1111/dmcn.13704. Epub 2018 Feb 23.

28.

Effectiveness of GonaCon as an immunocontraceptive in colony-housed cats.

Fischer A, Benka VA, Briggs JR, Driancourt MA, Maki J, Mora DS, Morris KN, Myers KA, Rhodes L, Vansandt LM, Weedon GR, Wolf J, Levy JK.

J Feline Med Surg. 2018 Aug;20(8):786-792. doi: 10.1177/1098612X18758549. Epub 2018 Feb 21.

PMID:
29463201
29.

Hemiconvulsion-hemiplegia-epilepsy evolving to contralateral hemi-Lennox-Gastaut-like phenotype.

Myers KA, Scheffer IE, Archer JS.

Brain Dev. 2018 May;40(5):425-428. doi: 10.1016/j.braindev.2018.01.005. Epub 2018 Feb 16.

PMID:
29459061
30.

Tuning microtubule dynamics to enhance cancer therapy by modulating FER-mediated CRMP2 phosphorylation.

Zheng Y, Sethi R, Mangala LS, Taylor C, Goldsmith J, Wang M, Masuda K, Karaminejadranjbar M, Mannion D, Miranda F, Herrero-Gonzalez S, Hellner K, Chen F, Alsaadi A, Albukhari A, Fotso DC, Yau C, Jiang D, Pradeep S, Rodriguez-Aguayo C, Lopez-Berestein G, Knapp S, Gray NS, Campo L, Myers KA, Dhar S, Ferguson D, Bast RC Jr, Sood AK, von Delft F, Ahmed AA.

Nat Commun. 2018 Feb 2;9(1):476. doi: 10.1038/s41467-017-02811-7.

31.

Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome.

Myers KA, White SM, Mohammed S, Metcalfe KA, Fry AE, Wraige E, Vasudevan PC, Balasubramanian M, Scheffer IE.

Epilepsy Res. 2018 Feb;140:166-170. doi: 10.1016/j.eplepsyres.2018.01.014. Epub 2018 Feb 3. Erratum in: Epilepsy Res. 2018 Aug 10;:.

PMID:
29367179
32.

KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood.

Myers KA, McGlade A, Neubauer BA, Lal D, Berkovic SF, Scheffer IE, Hildebrand MS.

PLoS One. 2018 Jan 19;13(1):e0191546. doi: 10.1371/journal.pone.0191546. eCollection 2018.

33.

Myoclonic absence seizures with complex gestural automatisms.

Myers KA, Scheffer IE.

Eur J Paediatr Neurol. 2018 May;22(3):532-535. doi: 10.1016/j.ejpn.2017.12.003. Epub 2017 Dec 19.

PMID:
29325826
34.

ADGRV1 is implicated in myoclonic epilepsy.

Myers KA, Nasioulas S, Boys A, McMahon JM, Slater H, Lockhart P, Sart DD, Scheffer IE.

Epilepsia. 2018 Feb;59(2):381-388. doi: 10.1111/epi.13980. Epub 2017 Dec 20.

35.

Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assay.

Myers KA, Bennett MF, Chow CW, Carden SM, Mandelstam SA, Bahlo M, Scheffer IE.

Am J Med Genet A. 2018 Jan;176(1):230-234. doi: 10.1002/ajmg.a.38549. Epub 2017 Nov 21.

PMID:
29160035
36.

Circulating tumor DNA predicts survival in patients with resected high-risk stage II/III melanoma.

Lee RJ, Gremel G, Marshall A, Myers KA, Fisher N, Dunn JA, Dhomen N, Corrie PG, Middleton MR, Lorigan P, Marais R.

Ann Oncol. 2018 Feb 1;29(2):490-496. doi: 10.1093/annonc/mdx717.

37.

Sudden Death After Febrile Seizure Case Report: Cerebral Suppression Precedes Severe Bradycardia.

Myers KA, McPherson RE, Clegg R, Buchhalter J.

Pediatrics. 2017 Nov;140(5). pii: e20162051. doi: 10.1542/peds.2016-2051. Epub 2017 Oct 5.

38.

CLASP1 regulates endothelial cell branching morphology and directed migration.

Myer NM, Myers KA.

Biol Open. 2017 Oct 15;6(10):1502-1515. doi: 10.1242/bio.028571.

39.

Blake's pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes.

Myers KA, Wallis MJ, Fitt GJ, Sarnat HB, Newton MR.

Am J Med Genet A. 2017 Sep;173(9):2442-2445. doi: 10.1002/ajmg.a.38346. Epub 2017 Jul 7. No abstract available.

PMID:
28686337
40.

Cytoplasmic Dynein Transports Axonal Microtubules in a Polarity-Sorting Manner.

Rao AN, Patil A, Black MM, Craig EM, Myers KA, Yeung HT, Baas PW.

Cell Rep. 2017 Jun 13;19(11):2210-2219. doi: 10.1016/j.celrep.2017.05.064.

41.

Systematic review of MRI findings in children with developmental delay or cognitive impairment.

Murias K, Moir A, Myers KA, Liu I, Wei XC.

Brain Dev. 2017 Sep;39(8):644-655. doi: 10.1016/j.braindev.2017.04.006. Epub 2017 Apr 27. Review.

PMID:
28457518
42.

The epileptology of Koolen-de Vries syndrome: Electro-clinico-radiologic findings in 31 patients.

Myers KA, Mandelstam SA, Ramantani G, Rushing EJ, de Vries BB, Koolen DA, Scheffer IE.

Epilepsia. 2017 Jun;58(6):1085-1094. doi: 10.1111/epi.13746. Epub 2017 Apr 25.

43.

DEPDC5 as a potential therapeutic target for epilepsy.

Myers KA, Scheffer IE.

Expert Opin Ther Targets. 2017 Jun;21(6):591-600. doi: 10.1080/14728222.2017.1316715. Epub 2017 Apr 13. Review.

PMID:
28406046
44.

Is a microRNA-328 binding site in PAX6 associated with Rolandic epilepsy?

McGlade A, Myers KA, Berkovic SF, Scheffer IE, Petrovski S, Hildebrand MS.

Ann Clin Transl Neurol. 2017 Mar 23;4(4):276-277. doi: 10.1002/acn3.401. eCollection 2017 Apr. No abstract available.

45.

Fatal Cerebral Edema With Status Epilepticus in Children With Dravet Syndrome: Report of 5 Cases.

Myers KA, McMahon JM, Mandelstam SA, Mackay MT, Kalnins RM, Leventer RJ, Scheffer IE.

Pediatrics. 2017 Apr;139(4). pii: e20161933. doi: 10.1542/peds.2016-1933. Epub 2017 Mar 22.

46.

MCAK-mediated regulation of endothelial cell microtubule dynamics is mechanosensitive to myosin-II contractility.

D'Angelo L, Myer NM, Myers KA.

Mol Biol Cell. 2017 May 1;28(9):1223-1237. doi: 10.1091/mbc.E16-05-0306. Epub 2017 Mar 15.

47.

Optic neuropathy in the context of leukemia or lymphoma: diagnostic approach to a neuro-oncologic emergency.

Myers KA, Nikolic A, Romanchuk K, Weis E, Brundler MA, Lafay-Cousin L, Costello F.

Neurooncol Pract. 2017 Mar;4(1):60-66. doi: 10.1093/nop/npw006. Epub 2016 Dec 9. Review.

48.

Myoclonic Absence Seizures in Dravet Syndrome.

Myers KA, Scheffer IE.

Pediatr Neurol. 2017 May;70:67-69. doi: 10.1016/j.pediatrneurol.2017.01.004. Epub 2017 Jan 24.

PMID:
28233668
49.

De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome.

Myers KA, Burgess R, Afawi Z, Damiano JA, Berkovic SF, Hildebrand MS, Scheffer IE.

Epilepsia. 2017 Feb;58(2):e26-e30. doi: 10.1111/epi.13649. Epub 2017 Jan 13.

50.

Familial Congenital Facial Synkinesis Due to 12q Duplication: A Case Report and Literature Review.

Myers KA, Innes AM, Mah JK.

Pediatrics. 2016 Dec;138(6). pii: e20161724. Epub 2016 Nov 17. Review.

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