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Items: 1 to 50 of 98

1.

Cerebral Corticoarterial Malformations : A Case Series of Unilateral Polymicrogyria and Ipsilateral Arterial Dysplasia.

Klostranec JM, Brinjikji W, Mathur S, Orru E, Andrade DM, Krings T.

Clin Neuroradiol. 2019 Aug 8. doi: 10.1007/s00062-019-00824-x. [Epub ahead of print] No abstract available.

PMID:
31396655
2.

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
3.

Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy.

Vlaskamp DRM, Bassett AS, Sullivan JE, Robblee J, Sadleir LG, Scheffer IE, Andrade DM.

Epilepsia. 2019 Mar;60(3):429-440. doi: 10.1111/epi.14678. Epub 2019 Mar 3.

PMID:
30828795
4.

Cryo-SOFI enabling low-dose super-resolution correlative light and electron cryo-microscopy.

Moser F, Pražák V, Mordhorst V, Andrade DM, Baker LA, Hagen C, Grünewald K, Kaufmann R.

Proc Natl Acad Sci U S A. 2019 Mar 12;116(11):4804-4809. doi: 10.1073/pnas.1810690116. Epub 2019 Feb 26.

5.

STXBP1 encephalopathy is associated with awake bruxism.

Rezazadeh A, Uddin M, Snead OC 3rd, Lira V, Silberberg A, Weiss S, Donner EJ, Zak M, Bradbury L, Scherer SW, Fasano A, Andrade DM.

Epilepsy Behav. 2019 Mar;92:121-124. doi: 10.1016/j.yebeh.2018.12.018. Epub 2019 Jan 14.

PMID:
30654231
6.

Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration.

Rezazadeh A, Bercovici E, Kiehl TR, Chow EW, Krings T, Bassett AS, Andrade DM.

Ann Clin Transl Neurol. 2018 Sep 23;5(11):1314-1322. doi: 10.1002/acn3.641. eCollection 2018 Nov.

7.

Training Load and Recovery in Volleyball During a Competitive Season.

Andrade DM, Fernandes G, Miranda R, Reis Coimbra D, Bara Filho MG.

J Strength Cond Res. 2018 Oct 12. doi: 10.1519/JSC.0000000000002837. [Epub ahead of print]

PMID:
30325790
8.

Global characterization of copy number variants in epilepsy patients from whole genome sequencing.

Monlong J, Girard SL, Meloche C, Cadieux-Dion M, Andrade DM, Lafreniere RG, Gravel M, Spiegelman D, Dionne-Laporte A, Boelman C, Hamdan FF, Michaud JL, Rouleau G, Minassian BA, Bourque G, Cossette P.

PLoS Genet. 2018 Apr 12;14(4):e1007285. doi: 10.1371/journal.pgen.1007285. eCollection 2018 Apr.

9.

Unilateral abdominal clonic seizures of parietal lobe origin: EEG findings.

Aljaafari D, Nascimento FA, Abraham A, Andrade DM, Wennberg RA.

Epileptic Disord. 2018 Apr 1;20(2):158-163. doi: 10.1684/epd.2018.0966.

10.

Age representation in antiepileptic drug trials: A systematic review and meta-analysis.

Desmarais P, Miville C, Milán-Tomás Á, Nguyen QD, Ojeda-López C, Masellis M, Black SE, Andrade DM, Herrmann N.

Epilepsy Res. 2018 May;142:9-15. doi: 10.1016/j.eplepsyres.2018.03.005. Epub 2018 Mar 6.

PMID:
29544171
11.

Radical Scavenger Capacity of Jabuticaba Fruit (Myrciaria cauliflora) and Its Biological Effects in Hypertensive Rats.

de Souza CG, de Andrade DML, Jordão JBR, de Ávila RI, Borges LL, Vaz BG, Valadares MC, de Souza Gil E, da Conceição EC, Rocha ML.

Oxid Med Cell Longev. 2017;2017:2383157. doi: 10.1155/2017/2383157. Epub 2017 Dec 20.

12.

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study, FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL.

Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi: 10.1016/j.ajhg.2017.09.008.

13.

De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures.

Myers CT, Stong N, Mountier EI, Helbig KL, Freytag S, Sullivan JE, Ben Zeev B, Nissenkorn A, Tzadok M, Heimer G, Shinde DN, Rezazadeh A, Regan BM, Oliver KL, Ernst ME, Lippa NC, Mulhern MS, Ren Z, Poduri A, Andrade DM, Bird LM, Bahlo M, Berkovic SF, Lowenstein DH, Scheffer IE, Sadleir LG, Goldstein DB, Mefford HC, Heinzen EL.

Am J Hum Genet. 2017 Oct 5;101(4):516-524. doi: 10.1016/j.ajhg.2017.08.013. Epub 2017 Sep 21.

14.

Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.

Borlot F, Regan BM, Bassett AS, Stavropoulos DJ, Andrade DM.

JAMA Neurol. 2017 Nov 1;74(11):1301-1311. doi: 10.1001/jamaneurol.2017.1775.

15.

Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force.

Andrade DM, Bassett AS, Bercovici E, Borlot F, Bui E, Camfield P, Clozza GQ, Cohen E, Gofine T, Graves L, Greenaway J, Guttman B, Guttman-Slater M, Hassan A, Henze M, Kaufman M, Lawless B, Lee H, Lindzon L, Lomax LB, McAndrews MP, Menna-Dack D, Minassian BA, Mulligan J, Nabbout R, Nejm T, Secco M, Sellers L, Shapiro M, Slegr M, Smith R, Szatmari P, Tao L, Vogt A, Whiting S, Carter Snead O 3rd.

Epilepsia. 2017 Sep;58(9):1502-1517. doi: 10.1111/epi.13832. Epub 2017 Jul 6.

16.

Convergence of lateral dynamic measurements in the plasma membrane of live cells from single particle tracking and STED-FCS.

Lagerholm BC, Andrade DM, Clausen MP, Eggeling C.

J Phys D Appl Phys. 2017 Feb 15;50(6):063001. doi: 10.1088/1361-6463/aa519e. Epub 2017 Jan 13. Review.

17.

22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.

Wither RG, Borlot F, MacDonald A, Butcher NJ, Chow EWC, Bassett AS, Andrade DM.

Epilepsia. 2017 Jun;58(6):1095-1101. doi: 10.1111/epi.13748. Epub 2017 Apr 27.

18.

Genetic generalized epilepsy in three siblings with 8q21.13-q22.2 duplication.

Rezazadeh A, Borlot F, Faghfoury H, Andrade DM.

Seizure. 2017 May;48:57-61. doi: 10.1016/j.seizure.2017.04.004. Epub 2017 Apr 11.

19.

The Missing Fellow: First Description of the Trypanoxyuris pigrae Male (Nematoda: Oxyuridae), a Parasite of the Black Howler Monkey (Alouatta pigra) in Mexico.

Solórzano-García B, Andrade DMG, de León GP.

J Parasitol. 2017 Aug;103(4):404-406. doi: 10.1645/17-8. Epub 2017 Mar 29.

PMID:
28355111
20.

Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues.

Nabbout R, Andrade DM, Bahi-Buisson N, Cross H, Desquerre I, Dulac O, Granata T, Hirsch E, Navarro V, Ouss L, Pearl PL, Schmidt D, Thiele E, Camfield PR, Camfield CS.

Epilepsy Behav. 2017 Apr;69:161-169. doi: 10.1016/j.yebeh.2016.11.010. Epub 2017 Feb 28. Review.

PMID:
28256379
21.

Treatment issues for children with epilepsy transitioning to adult care.

Nabbout R, Camfield CS, Andrade DM, Arzimanoglou A, Chiron C, Cramer JA, French JA, Kossoff E, Mula M, Camfield PR.

Epilepsy Behav. 2017 Apr;69:153-160. doi: 10.1016/j.yebeh.2016.11.008. Epub 2017 Feb 8. Review.

PMID:
28188045
22.

Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.

Aljaafari D, Fasano A, Nascimento FA, Lang AE, Andrade DM.

Epilepsia. 2017 Mar;58(3):e44-e48. doi: 10.1111/epi.13692. Epub 2017 Feb 10.

23.

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations.

Nascimento FA, Andrade DM.

Epileptic Disord. 2016 Sep 1;18(S2):135-138. Review.

PMID:
27629860
24.

Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries.

Andrade DM, Borges LL, Torres IM, Conceição EC, Rocha ML.

Arq Bras Cardiol. 2016 Sep;107(3):223-229. doi: 10.5935/abc.20160118. Epub 2016 Aug 11. English, Portuguese.

25.

Progressive myoclonus epilepsy associated with SACS gene mutations.

Nascimento FA, Canafoglia L, Aljaafari D, Muona M, Lehesjoki AE, Berkovic SF, Franceschetti S, Andrade DM.

Neurol Genet. 2016 Jun 23;2(4):e83. doi: 10.1212/NXG.0000000000000083. eCollection 2016 Aug.

26.

Which patients with epilepsy are at risk for psychogenic nonepileptic seizures (PNES)? A multicenter case-control study.

Wissel BD, Dwivedi AK, Gaston TE, Rodriguez-Porcel FJ, Aljaafari D, Hopp JL, Krumholz A, van der Salm SMA, Andrade DM, Borlot F, Moseley BD, Cavitt JL, Williams S, Stone J, LaFrance WC Jr, Szaflarski JP, Espay AJ.

Epilepsy Behav. 2016 Aug;61:180-184. doi: 10.1016/j.yebeh.2016.05.032. Epub 2016 Jun 27.

PMID:
27362440
27.

Reorganization of Lipid Diffusion by Myelin Basic Protein as Revealed by STED Nanoscopy.

Steshenko O, Andrade DM, Honigmann A, Mueller V, Schneider F, Sezgin E, Hell SW, Simons M, Eggeling C.

Biophys J. 2016 Jun 7;110(11):2441-2450. doi: 10.1016/j.bpj.2016.04.047.

28.

Epilepsy Transition: Let's start planting the seed.

Borlot F, Andrade DM.

Eur J Paediatr Neurol. 2016 Jul;20(4):684-5. doi: 10.1016/j.ejpn.2016.04.006. Epub 2016 Apr 19. No abstract available.

PMID:
27133781
29.

Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.

Nascimento FA, Borlot F, Cossette P, Minassian BA, Andrade DM.

Neurol Genet. 2015 Oct 15;1(4):e28. doi: 10.1212/NXG.0000000000000028. eCollection 2015 Dec.

30.

Omalizumab in Chronic Spontaneous Urticaria: A Brazilian Real-Life Experience.

Ensina LF, Valle SO, Juliani AP, Galeane M, Vieira dos Santos R, Arruda LK, Melo JM, de Souza PK, Serpa FS, de Andrade DM, França AT, Campos RA, Camelo-Nunes I, Solé D.

Int Arch Allergy Immunol. 2016;169(2):121-4. doi: 10.1159/000444985. Epub 2016 Apr 8.

31.

Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target.

Krishna V, King NK, Sammartino F, Strauss I, Andrade DM, Wennberg RA, Lozano AM.

Neurosurgery. 2016 Jun;78(6):802-11. doi: 10.1227/NEU.0000000000001197.

PMID:
26813858
32.

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability.

Vasli N, Ahmed I, Mittal K, Ohadi M, Mikhailov A, Rafiq MA, Bhatti A, Carter MT, Andrade DM, Ayub M, Vincent JB, John P.

Psychiatr Genet. 2016 Apr;26(2):66-73. doi: 10.1097/YPG.0000000000000114.

PMID:
26529358
33.

GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis.

Day GS, Prüss H, Benseler SM, Paton TA, Paterson AD, Andrade DM.

Neurol Neuroimmunol Neuroinflamm. 2015 Sep 24;2(5):e153. doi: 10.1212/NXI.0000000000000153. eCollection 2015 Oct.

34.

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

Merico D, Zarrei M, Costain G, Ogura L, Alipanahi B, Gazzellone MJ, Butcher NJ, Thiruvahindrapuram B, Nalpathamkalam T, Chow EW, Andrade DM, Frey BJ, Marshall CR, Scherer SW, Bassett AS.

G3 (Bethesda). 2015 Sep 16;5(11):2453-61. doi: 10.1534/g3.115.021345.

35.

Blocking the L-type Ca2+ channel (Cav 1.2) is the key mechanism for the vascular relaxing effect of Pterodon spp. and its isolated diterpene methyl-6α-acetoxy-7β-hydroxyvouacapan-17β-oate.

de Fátima Reis C, de Andrade DM, Junior Neves B, de Almeida Ribeiro Oliveira L, Pinho JF, da Silva LP, Dos Santos Cruz J, Bara MT, Andrade CH, Rocha ML.

Pharmacol Res. 2015 Oct;100:242-9. doi: 10.1016/j.phrs.2015.08.007. Epub 2015 Aug 17.

PMID:
26296533
36.

Cortical actin networks induce spatio-temporal confinement of phospholipids in the plasma membrane--a minimally invasive investigation by STED-FCS.

Andrade DM, Clausen MP, Keller J, Mueller V, Wu C, Bear JE, Hell SW, Lagerholm BC, Eggeling C.

Sci Rep. 2015 Jun 29;5:11454. doi: 10.1038/srep11454.

37.

Response to clozapine in a clinically identifiable subtype of schizophrenia.

Butcher NJ, Fung WL, Fitzpatrick L, Guna A, Andrade DM, Lang AE, Chow EW, Bassett AS.

Br J Psychiatry. 2015 Jun;206(6):484-91. doi: 10.1192/bjp.bp.114.151837. Epub 2015 Mar 5.

38.

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.

Boot E, Butcher NJ, van Amelsvoort TA, Lang AE, Marras C, Pondal M, Andrade DM, Fung WL, Bassett AS.

Am J Med Genet A. 2015 Mar;167A(3):639-45. doi: 10.1002/ajmg.a.36928. Epub 2015 Feb 13.

39.

Synovitis and tenosynovitis in Brazil: analysis of sickness benefit claims.

Andrade DM, Barbosa-Branco A.

Rev Bras Epidemiol. 2015 Jan-Mar;18(1):194-207. doi: 10.1590/1980-5497201500010015. Epub 2015 Mar 1. English, Portuguese.

40.

Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS.

Genet Med. 2015 Aug;17(8):599-609. doi: 10.1038/gim.2014.175. Epub 2015 Jan 8. Review.

41.

Dravet syndrome, lamotrigine, and personalized medicine.

Andrade DM.

Dev Med Child Neurol. 2015 Feb;57(2):118-9. doi: 10.1111/dmcn.12627. Epub 2014 Dec 8. No abstract available.

42.

Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.

Law R, Dixon-Salazar T, Jerber J, Cai N, Abbasi AA, Zaki MS, Mittal K, Gabriel SB, Rafiq MA, Khan V, Nguyen M, Ali G, Copeland B, Scott E, Vasli N, Mikhailov A, Khan MN, Andrade DM, Ayaz M, Ansar M, Ayub M, Vincent JB, Gleeson JG.

Am J Hum Genet. 2014 Dec 4;95(6):721-8. doi: 10.1016/j.ajhg.2014.10.016.

43.

Drug-induced anaphylaxis in children: nonsteroidal anti-inflammatory drugs and drug provocation test.

Ensina LF, de Lacerda AE, de Andrade DM, Machado L, Camelo-Nunes I, Solé D.

J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):825. doi: 10.1016/j.jaip.2014.08.016. Epub 2014 Nov 6. No abstract available.

PMID:
25439388
44.

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.

Muona M, Berkovic SF, Dibbens LM, Oliver KL, Maljevic S, Bayly MA, Joensuu T, Canafoglia L, Franceschetti S, Michelucci R, Markkinen S, Heron SE, Hildebrand MS, Andermann E, Andermann F, Gambardella A, Tinuper P, Licchetta L, Scheffer IE, Criscuolo C, Filla A, Ferlazzo E, Ahmad J, Ahmad A, Baykan B, Said E, Topcu M, Riguzzi P, King MD, Ozkara C, Andrade DM, Engelsen BA, Crespel A, Lindenau M, Lohmann E, Saletti V, Massano J, Privitera M, Espay AJ, Kauffmann B, Duchowny M, Møller RS, Straussberg R, Afawi Z, Ben-Zeev B, Samocha KE, Daly MJ, Petrou S, Lerche H, Palotie A, Lehesjoki AE.

Nat Genet. 2015 Jan;47(1):39-46. doi: 10.1038/ng.3144. Epub 2014 Nov 17.

45.

A pilot double-blind trial using verapamil as adjuvant therapy for refractory seizures.

Borlot F, Wither RG, Ali A, Wu N, Verocai F, Andrade DM.

Epilepsy Res. 2014 Nov;108(9):1642-51. doi: 10.1016/j.eplepsyres.2014.08.009. Epub 2014 Aug 30.

PMID:
25223728
46.

Epilepsy transition: challenges of caring for adults with childhood-onset seizures.

Borlot F, Tellez-Zenteno JF, Allen A, Ali A, Snead OC 3rd, Andrade DM.

Epilepsia. 2014 Oct;55(10):1659-66. doi: 10.1111/epi.12752. Epub 2014 Aug 28.

47.

Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan.

Vincent JB, Jamil T, Rafiq MA, Anwar Z, Ayaz M, Hameed A, Nasr T, Naeem F, Khattak NA, Carter M, Ahmed I, John P, Wiame E, Andrade DM, Schaftingen EV, Mir A, Ayub M.

Clin Genet. 2015 Mar;87(3):296-8. doi: 10.1111/cge.12445. Epub 2014 Jul 30. No abstract available.

PMID:
25080166
48.

Reply from the authors.

Steriade C, Andrade DM, Faghfoury H, Tarnopolsky MA, Tai P.

Pediatr Neurol. 2014 Aug;51(2):e5-6. doi: 10.1016/j.pediatrneurol.2014.05.024. Epub 2014 May 29. No abstract available.

PMID:
25079585
49.

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature.

Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS.

Genet Med. 2015 Feb;17(2):149-57. doi: 10.1038/gim.2014.83. Epub 2014 Jul 31. Review.

50.

Prevalence of asthma and allergic diseases in adolescents: nine-year follow-up study (2003-2012).

Solé D, Rosário Filho NA, Sarinho ES, Camelo-Nunes IC, Barreto BA, Medeiros ML, Franco JM, Camargos PA, Mallol J, Gurgel R, Andrade DM, Furlan FP, Silva AR, Cardozo C, Andrade C.

J Pediatr (Rio J). 2015 Jan-Feb;91(1):30-5. doi: 10.1016/j.jped.2014.05.002. Epub 2014 Jul 18.

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