Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 42

1.

Addressing travelers' perception of risk in pre-travel care: Reports from a travel clinic in Rio de Janeiro, Brazil.

Mesquita EC, Varela MC, Brasil PEAAD, Correa DF, Tuyama M, Carvalho F, Neves ES, Cerbino-Neto J, Lemos ADS, Costa MDD.

Rev Soc Bras Med Trop. 2019 May 16;52:e20180514. doi: 10.1590/0037-8682-0514-2018.

2.

VraSR and Virulence Trait Modulation during Daptomycin Resistance in Methicillin-Resistant Staphylococcus aureus Infection.

Taglialegna A, Varela MC, Rosato RR, Rosato AE.

mSphere. 2019 Feb 13;4(1). pii: e00557-18. doi: 10.1128/mSphere.00557-18.

3.

Activity of Telavancin against Staphylococcus aureus Isolates, Including Those with Decreased Susceptibility to Ceftaroline, from Cystic Fibrosis Patients.

Roch M, Varela MC, Taglialegna A, Rose WE, Rosato AE.

Antimicrob Agents Chemother. 2018 Aug 27;62(9). pii: e00956-18. doi: 10.1128/AAC.00956-18. Print 2018 Sep.

4.

Ageing with Chagas disease: an overview of an urban Brazilian cohort in Rio de Janeiro.

Vizzoni AG, Varela MC, Sangenis LHC, Hasslocher-Moreno AM, do Brasil PEAA, Saraiva RM.

Parasit Vectors. 2018 Jun 19;11(1):354. doi: 10.1186/s13071-018-2929-y.

5.

The draft genome sequence of cork oak.

Ramos AM, Usié A, Barbosa P, Barros PM, Capote T, Chaves I, Simões F, Abreu I, Carrasquinho I, Faro C, Guimarães JB, Mendonça D, Nóbrega F, Rodrigues L, Saibo NJM, Varela MC, Egas C, Matos J, Miguel CM, Oliveira MM, Ricardo CP, Gonçalves S.

Sci Data. 2018 May 22;5:180069. doi: 10.1038/sdata.2018.69.

6.

Seasonal changes in morphophysiological traits of two native Patagonian shrubs from Argentina with different drought resistance strategies.

Varela MC, Reinoso H, Luna V, Cenzano AM.

Plant Physiol Biochem. 2018 Jun;127:506-515. doi: 10.1016/j.plaphy.2018.03.018. Epub 2018 Mar 19.

PMID:
29709880
7.

Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity.

D'Angelo CS, Varela MC, de Castro CIE, Otto PA, Perez ABA, Lourenço CM, Kim CA, Bertola DR, Kok F, Garcia-Alonso L, Koiffmann CP.

Mol Cytogenet. 2018 Feb 5;11:14. doi: 10.1186/s13039-018-0363-7. eCollection 2018.

8.

Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twins.

Jehee FS, de Oliveira VT, Gurgel-Giannetti J, Pietra RX, Rubatino FVM, Carobin NV, Vianna GS, de Freitas ML, Fernandes KS, Ribeiro BSV, Brüggenwirth HT, Ali-Amin R; Baylor-Hopkins Center for Mendelian Genomics, White JJ, Akdemir ZC, Jhangiani SN, Gibbs RA, Lupski JR, Varela MC, Koiffmann C, Rosenberg C, Carvalho CMB.

Am J Med Genet A. 2017 Sep;173(9):2451-2455. doi: 10.1002/ajmg.a.38315. Epub 2017 Jun 20.

9.

Phenolic compounds as indicators of drought resistance in shrubs from Patagonian shrublands (Argentina).

Varela MC, Arslan I, Reginato MA, Cenzano AM, Luna MV.

Plant Physiol Biochem. 2016 Jul;104:81-91. doi: 10.1016/j.plaphy.2016.03.014. Epub 2016 Mar 18.

PMID:
27017434
10.

Characterization of the cork oak transcriptome dynamics during acorn development.

Miguel A, de Vega-Bartol J, Marum L, Chaves I, Santo T, Leitão J, Varela MC, Miguel CM.

BMC Plant Biol. 2015 Jun 25;15:158. doi: 10.1186/s12870-015-0534-1.

11.

Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes.

D'Angelo CS, Varela MC, de Castro CIe, Kim CA, Bertola DR, Lourenço CM, Perez AB, Koiffmann CP.

Mol Cytogenet. 2014 Oct 31;7(1):75. doi: 10.1186/s13039-014-0075-6. eCollection 2014.

12.

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.

D'Angelo CS, Kohl I, Varela MC, de Castro CI, Kim CA, Bertola DR, Lourenço CM, Perez AB, Koiffmann CP.

Am J Med Genet A. 2013 Mar;161A(3):479-86. doi: 10.1002/ajmg.a.35761. Epub 2013 Feb 7.

PMID:
23401328
13.

Angelman syndrome caused by deletion: a genotype-phenotype correlation determined by breakpoint.

Valente KD, Varela MC, Koiffmann CP, Andrade JQ, Grossmann R, Kok F, Marques-Dias MJ.

Epilepsy Res. 2013 Jul;105(1-2):234-9. doi: 10.1016/j.eplepsyres.2012.12.005. Epub 2013 Jan 23.

PMID:
23352739
14.

Dynamic conservation of forest genetic resources in 33 European countries.

Lefèvre F, Koskela J, Hubert J, Kraigher H, Longauer R, Olrik DC, Schüler S, Bozzano M, Alizoti P, Bakys R, Baldwin C, Ballian D, Black-Samuelsson S, Bednarova D, Bordács S, Collin E, de Cuyper B, de Vries SM, Eysteinsson T, Frýdl J, Haverkamp M, Ivankovic M, Konrad H, Koziol C, Maaten T, Notivol Paino E, Oztürk H, Pandeva ID, Parnuta G, Pilipovič A, Postolache D, Ryan C, Steffenrem A, Varela MC, Vessella F, Volosyanchuk RT, Westergren M, Wolter F, Yrjänä L, Zariŋa I.

Conserv Biol. 2013 Apr;27(2):373-84. doi: 10.1111/j.1523-1739.2012.01961.x. Epub 2012 Dec 12.

PMID:
23240629
15.

A clinical follow-up of 35 Brazilian patients with Prader-Willi syndrome.

Quaio CR, Almeida TF, Albano LM, Gomy I, Bertola DR, Varela MC, Koiffmann CP, Kim CA.

Clinics (Sao Paulo). 2012 Aug;67(8):917-21.

16.

Deletion of the RMGA and CHD2 genes in a child with epilepsy and mental deficiency.

Capelli LP, Krepischi AC, Gurgel-Giannetti J, Mendes MF, Rodrigues T, Varela MC, Koiffmann CP, Rosenberg C.

Eur J Med Genet. 2012 Feb;55(2):132-4. doi: 10.1016/j.ejmg.2011.10.004. Epub 2011 Nov 25.

PMID:
22178256
17.

[Burnt children care procedure: experience in family].

Varela MC, Vasconcelos Jde M, Santos IB, Pedrosa IL, de Sousa AT.

Rev Bras Enferm. 2009 Sep-Oct;62(5):723-8. Portuguese.

PMID:
20552831
18.

A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.

Pacanaro AN, Christofolini DM, Kulikowski LD, Belangero SI, da Silva Bellucco FT, Varela MC, Koiffmann CP, Yoshimoto M, Squire JA, Schiavon AV, Heck B, Melaragno MI.

Am J Med Genet A. 2010 Mar;152A(3):753-8. doi: 10.1002/ajmg.a.33308.

PMID:
20186782
19.

[Vaccination programmes].

Varela MC.

Rev Esp Salud Publica. 2009 Sep-Oct;83(5):639-43. Spanish.

20.

Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia.

D'Angelo CS, Kohl I, Varela MC, de Castro CI, Kim CA, Bertola DR, Lourenço CM, Koiffmann CP.

Am J Med Genet A. 2010 Jan;152A(1):102-10. doi: 10.1002/ajmg.a.33160.

PMID:
20034100
21.

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.

Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter K, Prigmore E, Krepischi-Santos AC, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, de Silva R, Carter NP.

Nat Genet. 2006 Sep;38(9):1032-7. Epub 2006 Aug 13.

PMID:
16906163
22.

A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.

Varela MC, Simões-Sato AY, Kim CA, Bertola DR, De Castro CI, Koiffmann CP.

Eur J Med Genet. 2006 Jul-Aug;49(4):298-305. Epub 2006 Jan 4.

PMID:
16829351
23.

A 17q21.31 microdeletion encompassing the MAPT gene in a mentally impaired patient.

Varela MC, Krepischi-Santos AC, Paz JA, Knijnenburg J, Szuhai K, Rosenberg C, Koiffmann CP.

Cytogenet Genome Res. 2006;114(1):89-92.

PMID:
16717456
24.

Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.

D'Angelo CS, Da Paz JA, Kim CA, Bertola DR, Castro CI, Varela MC, Koiffmann CP.

Eur J Med Genet. 2006 Nov-Dec;49(6):451-60. Epub 2006 Mar 10.

PMID:
16564757
25.

Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patterns.

Valente KD, Fridman C, Varela MC, Koiffmann CP, Andrade JQ, Grossmann RM, Kok F, Marques-Dias MJ.

Epilepsy Res. 2005 Dec;67(3):163-8. Epub 2005 Oct 14.

PMID:
16226874
26.

Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients.

Varela MC, Kok F, Setian N, Kim CA, Koiffmann CP.

Clin Genet. 2005 Jan;67(1):47-52.

PMID:
15617548
27.
28.

Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).

Varela MC, Lopes GM, Koiffmann CP.

Ann Genet. 2004 Jul-Sep;47(3):267-73. Review.

PMID:
15337472
29.

Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene.

Fridman C, Hosomi N, Varela MC, Souza AH, Fukai K, Koiffmann CP.

Am J Med Genet A. 2003 Jun 1;119A(2):180-3.

PMID:
12749060
31.

Cyclosporine-loaded polycaprolactone nanoparticles: immunosuppression and nephrotoxicity in rats.

Varela MC, Guzmán M, Molpeceres J, del Rosario Aberturas M, Rodríguez-Puyol D, Rodríguez-Puyol M.

Eur J Pharm Sci. 2001 Feb;12(4):471-8.

PMID:
11231114
32.

Prader-Willi syndrome: genetic tests and clinical findings.

Fridman C, Varela MC, Kok F, Setian N, Koiffmann CP.

Genet Test. 2000;4(4):387-92.

PMID:
11216664
33.

Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients.

Fridman C, Varela MC, Kok F, Diament A, Koiffmann CP.

Am J Med Genet. 2000 Jun 19;92(5):322-7.

PMID:
10861661
34.

Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15q.

Fridman C, Varela MC, Nicholls RD, Koiffmann CP.

Clin Genet. 1998 Oct;54(4):303-8.

PMID:
9831341
35.

Cyclosporine A-induced decrease in calbindin-D 28 kDa in rat kidney but not in cerebral cortex and cerebellum.

Varela MC, Arce A, Greiner B, Schwald M, Aicher L, Wahl D, Grenet O, Steiner S.

Biochem Pharmacol. 1998 Jun 15;55(12):2043-6.

PMID:
9714326
36.

The cyclosporine A-induced decrease in rat renal calbindin-D28kDa protein as a consequence of a decrease in its mRNA.

Grenet O, Varela MC, Staedtler F, Steiner S.

Biochem Pharmacol. 1998 Apr 1;55(7):1131-3.

PMID:
9605438
37.

[Image of pseudocapture caused by micro-dislodgment of the electrode in a VDD pacemaker].

Rodríguez Font E, Viñolas Prat X, Alegret JM, Varela MC, Torner P, Oter R.

Rev Esp Cardiol. 1997 Dec;50(12):909-12. Spanish.

38.

Decrease in kidney calbindin-D 28kDa as a possible mechanism mediating cyclosporine A- and FK-506-induced calciuria and tubular mineralization.

Aicher L, Meier G, Norcross AJ, Jakubowski J, Varela MC, Cordier A, Steiner S.

Biochem Pharmacol. 1997 Mar 7;53(5):723-31. Erratum in: Biochem Pharmacol 1997 Jun 15;53(12):1945.

PMID:
9113092
39.

Protein variability in male and female Wistar rat liver proteins.

Steiner S, Wahl D, Varela MC, Aicher L, Prieto P.

Electrophoresis. 1995 Oct;16(10):1969-76.

PMID:
8586072
40.

Comparable seropositivity for ascariasis and toxocariasis in tropical slum children.

Lynch NR, Hagel I, Vargas V, Rotundo A, Varela MC, Di Prisco MC, Hodgen AN.

Parasitol Res. 1993;79(7):547-50.

PMID:
8278336
41.

Modification of the methodology of stool culture for Salmonella detection.

Ruiz J, Sempere MA, Varela MC, Gomez J.

J Clin Microbiol. 1992 Feb;30(2):525-6.

42.

Presumptive identification of Salmonella enterica using two rapid tests.

Ruiz J, Varela MC, Sempere MA, Lopez ML, Gomez J, Oliva J.

Eur J Clin Microbiol Infect Dis. 1991 Aug;10(8):649-51.

PMID:
1660809

Supplemental Content

Loading ...
Support Center