Passos-Bueno MR - Search Results

1

HTR1B and HTR2C in autism spectrum disorders in Brazilian families.

Orabona GM, Griesi-Oliveira K, Vadasz E, Bulcão VL, Takahashi VN, Moreira ES, Furia-Silva M, Ros-Melo AM, Dourado F, Matioli SR, Otto P, Passos-Bueno MR. Orabona GM, et al. Brain Res. 2009 Jan 23;1250:14-9. doi: 10.1016/j.brainres.2008.11.007. Epub 2008 Nov 12. Brain Res. 2009. PMID: 19038234

2

Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy.

Passos-Bueno MR, Otto PA, Zata M. Passos-Bueno MR, et al. Hum Hered. 1989;39(4):202-11. doi: 10.1159/000153861. Hum Hered. 1989. PMID: 2583732

3

Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region.

Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SK, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A, et al. Passos-Bueno MR, et al. Genomics. 1995 May 1;27(1):192-5. doi: 10.1006/geno.1995.1024. Genomics. 1995. PMID: 7665169

4

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.

Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M. Passos-Bueno MR, et al. Hum Mol Genet. 1996 Jun;5(6):815-20. doi: 10.1093/hmg/5.6.815. Hum Mol Genet. 1996. PMID: 8776597

5

A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3.

Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. Sertié AL, et al. Hum Mol Genet. 1996 Jun;5(6):843-7. doi: 10.1093/hmg/5.6.843. Hum Mol Genet. 1996. PMID: 8776601

6

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M. Passos-Bueno MR, et al. J Med Genet. 1996 Feb;33(2):97-102. doi: 10.1136/jmg.33.2.97. J Med Genet. 1996. PMID: 8929943 Free PMC article.

7

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.

Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, Anderson LV, Bonnemann CG, McNally EM, Nigro V, Kunkel LM, Zatz M. Vainzof M, et al. Hum Mol Genet. 1996 Dec;5(12):1963-9. doi: 10.1093/hmg/5.12.1963. Hum Mol Genet. 1996. PMID: 8968750

8

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.

Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR. Moreira ES, et al. Am J Hum Genet. 1997 Jul;61(1):151-9. doi: 10.1086/513889. Am J Hum Genet. 1997. PMID: 9245996 Free PMC article.

9

Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophy.

Vainzof M, Costa CS, Marie SK, Moreira ES, Reed U, Passos-Bueno MR, Beggs AH, Zatz M. Vainzof M, et al. Neuropediatrics. 1997 Aug;28(4):223-8. doi: 10.1055/s-2007-973704. Neuropediatrics. 1997. PMID: 9309713

10

Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophrenia.

Mendes de Oliveira JR, Otto PA, Vallada H, Lauriano V, Elkis H, Lafer B, Vasquez L, Gentil V, Passos-Bueno MR, Zatz M. Mendes de Oliveira JR, et al. Am J Med Genet. 1998 May 8;81(3):225-7. doi: 10.1002/(sici)1096-8628(19980508)81:3<225::aid-ajmg4>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9603609

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