Iughetti P[au] - Search Results

Year	Number of Results
1995	1
1996	3
1997	1
1998	1
2000	1
2001	2
2003	1
2023	0

1

Capurro Mde L, Iughetti P, Ribolla PE, de Bianchi AG. Capurro Mde L, et al. Among authors: iughetti p. Arch Insect Biochem Physiol. 1996;32(2):197-207. doi: 10.1002/(SICI)1520-6327(1996)32:2<197::AID-ARCH4>3.0.CO;2-W. Arch Insect Biochem Physiol. 1996. PMID: 8785419

2

Waardenburg syndrome: clinical differentiation between types I and II.

Pardono E, van Bever Y, van den Ende J, Havrenne PC, Iughetti P, Maestrelli SR, Costa F O, Richieri-Costa A, Frota-Pessoa O, Otto PA. Pardono E, et al. Among authors: iughetti p. Am J Med Genet A. 2003 Mar 15;117A(3):223-35. doi: 10.1002/ajmg.a.10193. Am J Med Genet A. 2003. PMID: 12599185

3

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17.

Nitrini R, Teixeira da Silva LS, Rosemberg S, Caramelli P, Carrilho PE, Iughetti P, Passos-Bueno MR, Zatz M, Albrecht S, LeBlanc A. Nitrini R, et al. Among authors: iughetti p. Arq Neuropsiquiatr. 2001 Jun;59(2-A):161-4. doi: 10.1590/s0004-282x2001000200001. Arq Neuropsiquiatr. 2001. PMID: 11400017 Free article.

4

Familial spongiform encephalopathy associated with a novel prion protein gene mutation.

Nitrini R, Rosemberg S, Passos-Bueno MR, da Silva LS, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBlanc A. Nitrini R, et al. Among authors: iughetti p. Ann Neurol. 1997 Aug;42(2):138-46. doi: 10.1002/ana.410420203. Ann Neurol. 1997. PMID: 9266722

5

Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) families.

Iughetti P, Otto PA, Zatz M, Passos Bueno MR, Marie SK. Iughetti P, et al. Am J Med Genet. 1998 May 18;77(3):246-8. Am J Med Genet. 1998. PMID: 9605593 No abstract available.

6

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. Among authors: iughetti p. Genomics. 1995 May 1;27(1):192-5. doi: 10.1006/geno.1995.1024. Genomics. 1995. PMID: 7665169

7

A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma.

Iughetti P, Suzuki O, Godoi PH, Alves VA, Sertié AL, Zorick T, Soares F, Camargo A, Moreira ES, di Loreto C, Moreira-Filho CA, Simpson A, Oliva G, Passos-Bueno MR. Iughetti P, et al. Cancer Res. 2001 Oct 15;61(20):7375-8. Cancer Res. 2001. PMID: 11606364

8

Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia.

Iughetti P, Alonso LG, Wilcox W, Alonso N, Passos-Bueno MR. Iughetti P, et al. Am J Med Genet. 2000 Dec 18;95(5):482-91. doi: 10.1002/1096-8628(20001218)95:5<482::aid-ajmg14>3.0.co;2-x. Am J Med Genet. 2000. PMID: 11146471

9

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. Among authors: iughetti p. 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.

10

Different origins of mutations at the Machado-Joseph locus (MJD1).

Iughetti P, Zatz M, Bueno MR, Marie SK. Iughetti P, et al. J Med Genet. 1996 May;33(5):439. doi: 10.1136/jmg.33.5.439. J Med Genet. 1996. PMID: 8733063 Free PMC article. No abstract available.

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