Quem Somos

Publicações 2019

1. Aguiar TF, Barbosa-Teixeira AC, Costa SS, Ezquina S, Gimenez TM, Novak E, Cristofani LM, Rosenberg C, Odone Filho V, Krepischi AC. Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor. Pediatr Blood Cancer. 2019 Apr;66(4):e27566. doi: 10.1002/pbc.27566. Epub 2018 Dec 4.

2. Almeida LGD, Cruz DBD, Mingroni Netto RC, Batissoco AC, Oiticica J, Silva RS. Stem-cell therapy for hearing loss: are we there yet? Braz J Otorhinolaryngol. Braz J Otorhinolaryngol. 2019 Jul - Aug;85(4):520-529. doi: 10.1016/j.bjorl.2019.04.006. Epub 2019 May 18. 

3. Antonioli E, Torres N, Ferretti M, Piccinato CA, Sertie AL. Individual response to mTOR inhibition in delaying replicative senescence of mesenchymal stromal cells. PLoS One. 2019 Jan 31;14(1):e0204784. doi: 10.1371/journal.pone.0204784. eCollection 2019.

4. Batista AX, Bazán PR, Conforto AB, Martins MDGM, Hoshino M, Simon SS, Hampstead B, Figueiredo EG, Castro MP, Michelan D, Amaro E Jr, Miotto EC. Resting state functional connectivity and neural correlates of face-name encoding in patients with ischemic vascular lesions with and without the involvement of the left inferior frontal gyrus. Cortex. 2019 Apr;113:15-28. doi: 10.1016/j.cortex.2018.11.016. Epub 2018 Nov 26.

5. Bulubas L, Padberg F, Bueno PV, Duran F, Busatto G, Amaro E Jr, Benseñor IM, Lotufo PA, Goerigk S, Gattaz W, Keeser D, Brunoni AR. Antidepressant effects of tDCS are associated with prefrontal gray matter volumes at baseline: Evidence from the ELECT-TDCS trial. Brain Stimul. Brain Stimul. 2019 Sep - Oct;12(5):1197-1204. doi: 10.1016/j.brs.2019.05.006. Epub 2019 May 8

6. Burrage LC, Reynolds JJ, Baratang NV, Phillips JB, Wegner J, McFarquhar A, Higgs MR, Christiansen AE, Lanza DG, Seavitt JR, Jain M, Li X, Parry DA, Raman V, Chitayat D, Chinn IK, Bertuch AA, Karaviti L, Schlesinger AE, Earl D, Bamshad M, Savarirayan R, Doddapaneni H, Muzny D, Jhangiani SN, Eng CM, Gibbs RA, Bi W, Emrick L, Rosenfeld JA, Postlethwait J, Westerfield M, Dickinson ME, Beaudet AL, Ranza E, Huber C, Cormier-Daire V, Shen W, Mao R, Heaney JD, Orange JS; University of Washington Center for Mendelian Genomics; Undiagnosed Diseases Network, Bertola DR, Yamamoto GL, Baratela WAR, Butler MG, Ali A, Adeli M, Cohn DH, Krakow D, Jackson AP, Lees M, Offiah AC, Carlston CM, Carey JC, Stewart GS, Bacino CA, Campeau PM, Lee B. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 Mar 7;104(3):422-438. doi: 10.1016/j.ajhg.2019.01.007. Epub 2019 Feb 14.

7. Ceroni JRM, Spolador GM, Bermeo DS, Honjo RS, de Oliveira LAN, Bertola DR, Kim CA. Clinical and radiological findings in Brazilian patients with mucolipidosis types II/III . Skeletal Radiol. 2019 Aug;48(8):1201-1207. doi: 10.1007/s00256-019-3159-x. Epub 2019 Feb 2

8. Ceroni JRM, Spolador GM, Bermeo DS, Honjo RS, de Oliveira LAN, Bertola DR, Kim CA. Natural history of 39 patients with Achondroplasia. Skeletal Radiol. 2019 Aug;48(8):1201-1207. doi: 10.1007/s00256-019-3159-x. Epub 2019 Feb 2.

9. Chaves NA, Alegria TGP, Dantas LS, Netto LES, Miyamoto S, Bonini Domingos CR, da Silva DGH. Impaired antioxidant capacity causes a disruption of metabolic homeostasis in sickle erythrocytes. Free Radic Biol Med. 2019 Sep;141:34-46. doi: 10.1016/j.freeradbiomed.2019.05.034. Epub 2019 Jun 1

10. Coatti GC, Cavaçana N, Zatz M. The Role of Pericytes in Amyotrophic Lateral Sclerosis. Adv Exp Med Biol. 2019;1147:137-146. Adv Exp Med. Biol. 2019;1147:137-146. doi: 10.1007/978-3-030-16908-4_

11. Comim CM, Ventura L, Freiberger V, Dias P, Bragagnolo D, Dutra ML, Amaral RA, Camargo-Fagundes ALS, Reis PA, Castro-Faria-Neto HC, Vainzof M, Rosa MI. Neurocognitive Impairment in mdx Mice . Mol Neurobiol. 2019 Nov;56(11):7608-7616. doi: 10.1007/s12035-019-1573-7. Epub 2019 May 10.

12. Conforto AB, Servinsckins L, de Paiva JPQ, Amaro E Jr, Dos Santos DG, Soares P, Pires DS, Meltzer J, Plow EB, de Freitas PF, Speciali DS, Lopes P, Peres MFP, Silva GS, Lacerda S, Boasquevisque DS. Safety of cathodal transcranial direct current stimulation early after ischemic stroke. Brain Stimul. 2019 Mar - Apr;12(2):374-376. doi: 10.1016/j.brs.2018.11.009. Epub 2018 Nov 20. No abstract available.

13. Costantini A, Valta H, Baratang NV, Yap P, Bertola DR, Yamamoto GL, Kim CA, Chen J, Wierenga KJ, Fanning EA, Escobar L, McWalter K, McLaughlin H, Willaert R, Begtrup A, Alm JJ, Reinhardt DP, Mäkitie O, Campeau PM. Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures". Bone. 2019 Apr;121:163-171. doi: 10.1016/j.bone.2018.12.020.

14. Cotta A, Paim JF, Carvalho E, Valicek J, da Cunha Junior AL, Navarro MM, Vargas AP, Lima MI, de Almeida CF, Takata RI, Vainzof M. LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability. J Mol Neurosci. 2019 Dec;69(4):623-627. doi: 10.1007/s12031-019-01390-0. Epub 2019 Aug 13.

15. De Armas MI, Esteves R, Viera N, Reyes AM, Mastrogiovanni M, Alegria TGP, Netto LES, Tórtora V, Radi R, Trujillo M. Rapid peroxynitrite reduction by human peroxiredoxin 3: Implications for the fate of oxidants in mitochondria. Free Radic Biol Med. 2019 Jan;130:369-378. doi: 10.1016/j.freeradbiomed.2018.10.451.

16. de Oliveira JF, do Prado PFV, da Costa SS, Sforça ML, Canateli C, Ranzani AT, Maschietto M, de Oliveira PSL, Otto PA, Klevit RE, Krepischi ACV, Rosenberg C, Franchini KG. Mechanistic insights revealed by a UBE2A mutation linked to intellectual disability. Nat Chem Biol. 2019 Jan;15(1):62-70. doi: 10.1038/s41589-018-0177-2.

17. Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni-Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans . J Hum Genet. 2019 Mar;64(3):257-260. doi: 10.1038/s10038-018-0546-4.

18. Dufner-Almeida LG, do Carmo RT, Masotti C, Haddad LA. Understanding human DNA variants affecting pre-mRNA splicing in the NGS era. Adv Genet. 2019;103:39-90. doi: 10.1016/bs.adgen.2018.09.002. Epub 2019 Jan 17.

19. Dufner-Almeida LG, Cruz DBD, Mingroni Netto RC, Batissoco AC, Oiticica J, Salazar-Silva R. Stem-cell therapy for hearing loss: are we there yet? Braz J Otorhinolaryngol. 2019 Jul - Aug;85(4):520-529. doi: 10.1016/j.bjorl.2019.04.006. Epub 2019 May 18. Review.

20. El-Sayed ZA, Abramova I, Aldave JC, Al-Herz W, Bezrodnik L, Boukari R, Bousfiha AA, Cancrini C, Condino-Neto A, Dbaibo G, Derfalvi B, Dogu F, Edgar JDM, Eley B, El-Owaidy RH, Espinosa-Padilla SE, Galal N, Haerynck F, Hanna-Wakim R, Hossny E, Ikinciogullari A, Kamal E, Kanegane H, Kechout N, Lau YL, Morio T, Moschese V, Neves JF, Ouederni M, Paganelli R, Paris K, Pignata C, Plebani A, Qamar FN, Qureshi S, Radhakrishnan N, Rezaei N, Rosario N, Routes J, Sanchez B, Sediva A, Seppanen MR, Serrano EG, Shcherbina A, Singh S, Siniah S, Spadaro G, Tang M, Vinet AM, Volokha A, Sullivan KE. X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world. World.Allergy Organ J. 2019 Mar 22;12(3):100018. doi: 10.1016/j.waojou.2019.100018. eCollection 2019.

21. França TT, Barreiros LA, Al-Ramadi BK, Ochs HD, Cabral-Marques O, Condino-Neto A. CD40 ligand deficiency: treatment strategies and novel therapeutic perspectives. Expert Rev Clin Immunol. 2019 May;15(5):529-540. doi: 10.1080/1744666X.2019.1573674. Epub 2019 Feb 18.

22. Gimenez M, Veríssimo-Filho S, Wittig I, Schickling BM, Hahner F, Schürmann C, Netto LES, Rosa JC, Brandes RP, Sartoretto S, De Lucca Camargo L, Abdulkader F,Miller FJ Jr, Lopes LR. Redox Activation of Nox1 (NADPH Oxidase 1) Involves na Intermolecular isulfide Bond Between Protein Disulfide Isomerase and p47(phox) in Vascular Smooth Muscle Cells. Arterioscler Thromb Vasc Biol. 2019Feb;39(2):224-236. doi: 10.1161/ATVBAHA.118.311038. PubMed PMID: 30580571; PubMedCentral PMCID: PMC6344286.

23. Godoy JAP, Paiva RMA, Souza AM, Kondo AT, Kutner JM, Okamoto OK. Clinical Translation of Mesenchymal Stromal Cell Therapy for Graft Versus Host Disease. Front Cell Dev Biol. 2019 Nov 21;7:255. doi: 10.3389/fcell.2019.00255. eCollection 2019. Review.

24. Gomes LR, Rocha CRR, Martins DJ, Fiore APZP, Kinker GS, Bruni-Cardoso A, Menck CFM. ATR mediates cisplatin resistance in 3D-cultured breast cancer cells via translesion DNA synthesis modulation. Cell Death Dis. 2019 Jun 12;10(6):459. doi: 10.1038/s41419-019-1689-8

25. Gomes, F,C, Melo-Neto JS, Ferrari MF, Carlos, C,P, Goloni-Bertollo EM, Pavarino EC. Vitamin D3 increases the caspase-3 p12, MTHFR, and p-glycoprotein reducing amyloid-beta 42 in the kidney of a mouse model for Down syndrome. Life Sci. 2019 Aug 15;231:116537. doi: 10.1016/j.lfs.2019.06.012. Epub 2019 Jun 6.

26. Goulart E, de Caires-Junior LC, Telles-Silva KA, Araujo BHS, Rocco SA, Sforca M, de Sousa IL, Kobayashi GS, Musso CM, Assoni AF, Oliveira D, Caldini E, Raia S, Lelkes PI, Zatz M. 3D bioprinting of liver spheroids derived from human induced pluripotent stem cells sustain liver function and viability in vitro. Biofabrication. 2019 Nov 27;12(1):015010. doi: 10.1088/1758-5090/ab4a30.

27. Guo L, Bertola DR, Takanohashi A, Saito A, Segawa Y, Yokota T, Ishibashi S, Nishida Y, Yamamoto GL, Franco JFDS, Honjo RS, Kim CA, Musso CM, Timmons M, Pizzino A, Taft RJ, Lajoie B, Knight MA, Fischbeck KH, Singleton AB, Ferreira CR, Wang Z, Yan L, Garbern JY, Simsek-Kiper PO, Ohashi H, Robey PG, Boyde A, Matsumoto N, Miyake N, Spranger J, Schiffmann R, Vanderver A, Nishimura G, Passos-Bueno MR, Simons C, Ishikawa K, Ikegawa S. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation. Am J Hum Genet. 2019 May 2;104(5):925-935. doi: 10.1016/j.ajhg.2019.03.004. Epub 2019 Apr 11.

28. Howe LJ, Richardson TG, Arathimos R, Alvizi L, Passos-Bueno MR, Stanier P, Nohr E, Ludwig KU, Mangold E, Knapp M, Stergiakouli E, Pourcain BS, Smith GD, Sandy J, Relton CL, Lewis SJ, Hemani G, Sharp GC. Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. Epigenomics. 2019 Feb;11(2):133-145. doi: 10.2217/epi-2018-0091. Epub 2019 Jan 14.

29. Ishiba R, Santos ALF, Almeida CF, Caires LC Jr, Ribeiro AF Jr, Ayub-Guerrieri D, Fernandes SA, Souza LS, Vainzof M. Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse. J Mol Histol. 2019 Aug;50(4):375-387. doi: 10.1007/s10735-019-09834-y. Epub 2019 Jun 19.

30. Kaid C, Jordan D, Bueno HMS, Araujo BHS, Assoni A, Okamoto OK. miR-367 as a therapeutic target in stem-like cells from embryonal central nervous system tumor. Mol Oncol. 2019 Aug 11. doi: 10.1002/1878-0261.12562. [Epub ahead of print]

31. Leme JMM, Ohara E, Santiago VF, Barros MH, Netto LES, Pimenta DC, Mariano DOC, Oliveira CLP, Bicev RN, Barreto-Chaves MLM, Lino CA, Demasi M. Mutations of Cys and Ser residues in the α5-subunit of the 20S proteasome from Saccharomyces cerevisiae affects gating and chronological lifespan. Arch Biochem Biophys . 2019 May 15;666:63-72. doi: 10.1016/j.abb.2019.03.012. Epub 2019 Mar 30.

32. Lima SOA, Farias AA, Albino VA, Marques-Alves YK, Olinda R, Santos-Silva TA, Alves LU, Zatz M, Santos S. A population-based study of inter-generational attitudes towards consanguineous marriages in north-eastern Brazil. J Biosoc Sci. 2019 Mar 13:1-15. doi: 10.1017/S0021932018000433. [Epub ahead of print]

33. Malaquias AC, Noronha RM, Souza TTO, Homma TK, Funari MFA, Yamamoto GL, Silva FV, Moraes MB, Honjo RS, Kim CA, Nesi-França S, Carvalho JAR, Quedas EPS, Bertola DR, Jorge AAL. Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome. Horm Res Paediatr. 2019;91(4):252-261. doi: 10.1159/000500264. Epub 2019 May 27.

34. Mazzonetto PC, Ariza CB, Ocanha SG, de Souza TA, Ko GM, Menck CFM, Massironi SMG, Porcionatto MA. Mutation in NADPH oxidase 3 (NOX3) impairs SHH signaling and increases cerebellar neural stem/progenitor cell proliferation. Biochim Biophys Acta Mol Basis Dis. 2019 Jun 1;1865(6):1502-1515. doi: 10.1016/j.bbadis.2019.02.022. Epub 2019 Mar 8.

35. Melo KP, Silva CM, Almeida MF, Chaves RS, Marcourakis T, Cardoso SM, Demasi M, Netto LES, Ferrari MF. Mild Exercise Differently Affects Proteostasis and Oxidative Stress on Motor Areas During Neurodegeneration: A Comparative Study of Three Treadmill Running Protocols  Neurotox Res. 2019 Feb;35(2):410-420. doi: 10.1007/s12640-018-9966-3.

36. Melo-Hanchuk TD, Slepicka PF, Pelegrini AL, Menck CFM, Kobarg J. NEK5 interacts with topoisomerase IIβ and is involved in the DNA damage response induced by etoposide. J Cell Biochem. 2019 May 15. doi: 10.1002/jcb.28943. [Epub ahead of print]

37. Mingroni-Netto RC . Aconselhamento Genético: Será que eu preciso ? Genética na Escola (on line), v.14, p.34 - 43, 2019.

38. Misawa MYO, Silvério Ruiz KG, Nociti FH Jr, Albiero ML, Saito MT, Nóbrega Stipp R, Condino-Neto A, Holzhausen M, Palombo H, Villar CC. Periodontal ligament-derived mesenchymal stem cells modulate neutrophil responses via paracrine mechanisms. J Periodontol. 2019 Jan 15. doi: 10.1002/JPER.18-0220. [Epub ahead of print]

39. Moura LM, Luccas R, de Paiva JPQ, Amaro E Jr, Leemans A, Leite CDC, Otaduy MCG, Conforto AB. Diffusion Tensor Imaging Biomarkers to Predict Motor Outcomes in Stroke: A Narrative Review . Front Neurol. 2019 May 8;10:445. doi: 10.3389/fneur.2019.00445. eCollection 2019. Review.

40. Nolin SL, Glicksman A, Tortora N, Allen E, Macpherson J, Mila M, Vianna-Morgante AM, Sherman SL, Dobkin C, Latham GJ, Hadd AG. Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles. Am J Med Genet A. 2019 Jul;179(7):1148-1156. doi: 10.1002/ajmg.a.61165. Epub 2019 May 2.

41. Oliveira D, Leal GF, Sertié AL, Caires LC Jr, Goulart E, Musso CM, Oliveira JRM, Krepischi AC, Vianna-Morgante AM, Zatz M. 10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly. J Med Genet. 2019 Aug;56(8):543-547. doi: 10.1136/jmedgenet-2018-105471. Epub 2018 Oct 9.

42. Oliveira LF, Pinheiro DJLL, Rodrigues LD, Reyes-Garcia SZ, Nishi EE, Ormanji MS, Faber J, Cavalheiro EA. Behavioral, electrophysiological and neuropathological characteristics of the occurrence of hypertension in pregnant rats. Sci Rep. 2019 Mar 11;9(1):4051. doi: 10.1038/s41598-019-40969-w.

43. O'Sullivan S, Heinsen H, Grinberg LT, Chimelli L, Amaro E Jr, do Nascimento Saldiva PH, Jeanquartier F, Jean-Quartier C, da Graça Morais Martin M, Sajid MI, Holzinger A. The role of artificial intelligence and machine learning in harmonization of high-resolution post-mortem MRI (virtopsy) with respect to brain microstructure. Brain Inform. 2019 Mar 7;6(1):3. doi: 10.1186/s40708-019-0096-3.

44. Pereira LV, Bento RF, Cruz DB, Marchi C, Salomone R, Oiticicca J, Costa MP, Haddad LA, Mingroni-Netto RC, Costa HJZR. Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration. Cell Transplant. 2019 Jan;28(1):55-64. doi: 10.1177/0963689718809090.

45. Raices JB, Otto PA, Vibranovski MD. Haploid selection drives new gene male germline expression. Genome Res. 2019 Jul; 29(7): 1115–1122. doi: 10.1101/gr.238824.118

46. Ramos LLP, Monteiro FP, Sampaio LPB, Costa LA, Ribeiro MDO, Freitas EL, Kitajima JP, Kok F. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment. Clin Case Rep. 2019 Jul 11;7(8):1582-1584. doi: 10.1002/ccr3.2260. eCollection 2019 Aug.

47. Reyes-Garcia SZ, Scorza CA, Ortiz-Villatoro NN, Cavalheiro EA. Losartan fails to suppress epileptiform activity in brain slices from resected tissues of patients with drug resistant epilepsy. J Neurol Sci. 2019 Feb 15;397:169-171. doi: 10.1016/j.jns.2019.01.008. Epub 2019 Jan 8. No abstract available.

48. Ribeiro AF Jr, Souza LS, Almeida CF, Ishiba R, Fernandes SA, Guerrieri DA, Santos ALF, Onofre-Oliveira PCG, Vainzof M. Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies. Sci Rep. 2019 Aug 14;9(1):11842. doi: 10.1038/s41598-019-48156-7.

49. Rivas MP, Marques TF, Fernandes GR, Caires-Jr LC, Goulart E, Telles-Silva KA, Cypriano M, Toledo SRC, Rosenberg C, Carraro DM, Costa CML, cunha IW, Krepishci ACV. TET Upregulation Leads to 5-Hydroxymethylation Enrichment in Hepatoblastoma. Front Genet. 2019 Jun 12;10:553. doi: 10.3389/fgene.2019.00553. eCollection 2019.

50. Romanelli Tavares VL, Kague E, Musso CM, Alegria TGP, Freitas RS, Bertola DR, Twigg SRF, Passos-Bueno MR. Craniofrontonasal Syndrome Caused by Introduction of a Novel uATG in the 5'UTR of EFNB1. Mol Syndromol. 2019 Feb;10(1-2):40-47. doi: 10.1159/000490635

51. Samogy-Costa CI, Varella-Branco E, Monfardini F, Ferraz H, Fock RA, Barbosa RHA, Pessoa ALS, Perez ABA, Lourenço N,Vibranovski M, Krepischi A, Rosenberg C, Passos-Bueno MR. A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case. J Neurodev Disord. 2019 Jul 18;11(1):13. doi: 10.1186/s11689-019-9273-1.

52. Sarasin A, Quentin S, Droin N, Sahbatou M, Saada V, Auger N, Boursin Y, Dessen P, Raimbault A, Asnafi V, Schmutz JL, Taïeb A, Menck CFM, Rosselli F, La Rochelle LD, Robert C, Sicre de Fontbrune F, Sébert M, Leblanc T, Kannouche P, De Botton S, Solary E, Soulier J. Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum. Blood. 2019 Jun 20;133(25):2718-2724. doi: 10.1182/blood-2019-01-895698. Epub 2019 Mar 26.

53. Sato JR, Biazoli CE Jr, Moura LM, Crossley N, Zugman A, Picon FA, Hoexter MQ, Amaro E Jr, Miguel EC, Rohde LA, Bressan RA, Jackowski AP. Association Between Fractional Amplitude of Low-Frequency Spontaneous Fluctuation and Degree Centrality in Children and Adolescents. Brain Connect. 2019 Jun;9(5):379-387. doi: 10.1089/brain.2018.0628. Epub 2019 May 1.

54. Simões PSR, Zanelatto AO, Assis MC, Varella PPV, Yacubian EM, Carrete H, Centeno R, Araujo MS, Cavalheiro EA, Tersariol ILS, Motta G, Naffah-Mazzacoratti MDG. Plasma kallikrein-kinin system contributes to peripheral inflammation in temporal lobe epilepsy. J Neurochem. 2019 Aug;150(3):296-311. doi: 10.1111/jnc.14793. Epub 2019 Jul 10.

55. Simon SS, Hampstead BM, Nucci MP, Duran FLS, Fonseca LM, Martin MDGM, Ávila R, Porto FHG, Brucki SMD, Martins CB, Tascone LS, Amaro E Jr, Busatto GF, Bottino CMC. Training gains and transfer effects after mnemonic strategy training in mild cognitive impairment: A fMRI study. Int J Psychophysiol . 2019 Mar 29. pii: S0167-8760(18)30961-9. doi: 10.1016/j.ijpsycho.2019.03.014. [Epub ahead of print]

56. Souza DC, Abreu HLV, Oliveira PV, Capelo LP, Passos-Bueno MR, Catalani LH. A fast degrading PLLA composite with a high content of functionalized octacalcium phosphate mineral phase induces stem cells differentiation. J Mech Behav Biomed Mater. 2019 May;93:93-104. doi: 10.1016/j.jmbbm.2019.02.003. Epub 2019 Feb 6.

57. Tofoli FA, Semeano ATS, Oliveira-Giacomelli Á, Gonçalves MCB, Ferrari MF, Veiga Pereira L, Ulrich H. Midbrain Dopaminergic Neurons Differentiated from Human-Induced Pluripotent Stem Cells. Methods Mol Biol. 2019;1919:97-118. doi: 10.1007/978-1-4939-9007-8_8.

58. Trancozo M, Moraes MVD, Silva DA, Soares JAM, Barbirato C, Almeida MG, Santos LR, Rebouças MRGO, Akel AN Jr, Sipolatti V, Nunes VRR, Errera FIV, Aguena M, Passos-Bueno MR, Paula F. Osteogenesis imperfecta in Brazilian patients. Genet Mol Biol. 2019 Aug 15. pii: S1415-47572019005033102. doi: 10.1590/1678-4685-GMB-2018-0043.

59. Vitor T, Kozasa EH, Bressan RA, Lacerda SS, Campos Neto GC, Batista IR, Gebrim LH, Cohen L, Amaro E Jr, Felicio AC. Impaired brain dopamine transporter in chemobrain patients submitted to brain SPECT imaging using the technetium-99m labeled tracer TRODAT-1. Ann Nucl Med. 2019 Apr;33(4):269-279. doi: 10.1007/s12149-019-01331-2. Epub 2019 Mar 7.

60. Walker CP, Pessoa ALS, Figueiredo T, Rafferty M, Melo US, Nóbrega PR, Murphy N, Kok F, Zatz M, Santos S, Cho RY. Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG.Orphanet J Rare Dis. 2019 Jan 7;14(1):3. doi: 10.1186/s13023-018-0977-1.

61. Yamamoto PK, de Souza TA, Antiorio ATFB, Zanatto DA, Garcia-Gomes MSA, Alexandre-Ribeiro SR, Oliveira NS, Menck CFM, Bernardi MM, Massironi SMG, Mori CMC. Genetic and behavioral characterization of a Kmt2d mouse mutant, a new model for Kabuki Syndrome. Genes Brain Behav. 2019 Nov;18(8):e12568. doi: 10.1111/gbb.12568. Epub 2019 Apr 23.