decio brunoni
decio brunoni
Professor of Medical Genetics, Universidade Presbiteriana Mackenzie
E-mail confirmado em
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
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
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
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
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
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
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
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
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
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
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
Aconselhamento genético
D Brunoni
Ciência & Saúde Coletiva 7 (1), 101-107, 2002
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
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
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
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
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
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
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
Genética do autismo
G Carvalheira, N Vergani, D Brunoni
Brazilian Journal of Psychiatry 26 (4), 270-272, 2004
O sistema não pode executar a operação agora. Tente novamente mais tarde.
Artigos 1–20