decio brunoni
decio brunoni
Professor of Medical Genetics, Universidade Presbiteriana Mackenzie
E-mail confirmado em mackenzie.br
TítuloCitado porAno
Use of misoprostol during pregnancy and Möbius' syndrome in infants
AL Pastuszak, L Schüler, CE Speck-Martins, KEFA Coelho, SM Cordello, ...
New England Journal of Medicine 338 (26), 1881-1885, 1998
3051998
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome
J Marcelino, JD Carpten, WM Suwairi, OM Gutierrez, S Schwartz, ...
Nature genetics 23 (3), 319-322, 1999
2891999
Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy
CH Gonzalez, FR Vargas, ABA Perez, CA Kim, D Brunoni, ...
American Journal of Medical Genetics 47 (1), 59-64, 1993
2221993
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2
K Dathe, KW Kjaer, A Brehm, P Meinecke, P Nürnberg, JC Neto, ...
The American Journal of Human Genetics 84 (4), 483-492, 2009
1572009
Prenatal exposure to misoprostol and vascular disruption defects: A case‐control study
FR Vargas, L Schuler‐Faccini, D Brunoni, C Kim, VFA Meloni, ...
American Journal of Medical Genetics 95 (4), 302-306, 2000
1342000
Thalidomide, a current teratogen in South America
EE Castilla, P Ashton‐Prolla, E Barreda‐Mejia, D Brunoni, DP Cavalcanti, ...
Teratology 54 (6), 273-277, 1996
1281996
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes
A Splendore, EO Silva, LG Alonso, A Richieri‐Costa, N Alonso, A Rosa, ...
Human mutation 16 (4), 315-322, 2000
1162000
Relationship between polymorphisms in genes involved in homocysteine metabolism and maternal risk for Down syndrome in Brazil
LRJ da Silva, N Vergani, LC Galdieri, MP Ribeiro Porto, SB Longhitano, ...
American Journal of Medical Genetics Part A 135 (3), 263-267, 2005
1142005
Pregnancy outcome after exposure to misoprostol in Brazil: a prospective, controlled study
L Schüler, A Pastuszak, MTV Sanseverino, IM Orioliz, D Brunoni, ...
Reproductive Toxicology 13 (2), 147-151, 1999
901999
Prevalence of pervasive developmental disorder in Down’s syndrome
R Lowenthal, CS Paula, JS Schwartzman, D Brunoni, MT Mercadante
Journal of autism and developmental disorders 37 (7), 1394-1395, 2007
872007
Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome
JF Mazzeu, E Pardono, AM Vianna‐Morgante, A Richieri‐Costa, ...
American journal of medical genetics Part A 143 (4), 320-325, 2007
832007
Aconselhamento genético
D Brunoni
Ciência & Saúde Coletiva 7 (1), 101-107, 2002
792002
Ocular and clinical manifestations of Möbius' syndrome
MF Cronemberger, JB de Castro Moreira, D Brunoni, TS Mendonça, ...
Journal of pediatric ophthalmology and strabismus 38 (3), 156-162, 2001
722001
CFC index for the diagnosis of cardiofaciocutaneous syndrome
MI Kavamura, CA Peres, MMA Alchorne, D Brunoni
American journal of medical genetics 112 (1), 12-16, 2002
692002
Ring chromosome instability evaluation in six patients with autosomal rings
CP Sodré, RS Guilherme, VF Meloni, D Brunoni, Y Juliano, JA Andrade, ...
Genet Mol Res 9 (1), 134-143, 2010
642010
Impact of 5-HTTLPR and BDNF polymorphisms on response to sertraline versus transcranial direct current stimulation: implications for the serotonergic system
AR Brunoni, AH Kemp, P Shiozawa, Q Cordeiro, LCL Valiengo, ...
European Neuropsychopharmacology 23 (11), 1530-1540, 2013
592013
Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida
ABA Perez, V D'Almeida, N Vergani, AC de Oliveira, FT de Lima, ...
American Journal of Medical Genetics Part A 119 (1), 20-25, 2003
562003
Microcephaly and other Zika virus related events: the impact on children, families and health teams
D Brunoni, SM Blascovi-Assis, AAC Osório, AG Seabra, CAH Amato, ...
Ciencia & saude coletiva 21, 3297-3302, 2016
55*2016
Novel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta
D Pallos, PS Hart, JR Cortelli, S Vian, JT Wright, J Korkko, D Brunoni, ...
Archives of Oral Biology 46 (5), 459-470, 2001
532001
Genética do autismo
G Carvalheira, N Vergani, D Brunoni
Brazilian Journal of Psychiatry 26 (4), 270-272, 2004
492004
O sistema não pode executar a operação agora. Tente novamente mais tarde.
Artigos 1–20