Matte U - Search Results

1

Ontogenetic changes in serum S100B in Down syndrome patients.

Netto CB, Portela LV, Ferreira CT, Kieling C, Matte U, Felix T, da Silveira TR, Souza DO, Gonçalves CA, Giugliani R. Netto CB, et al. Among authors: matte u. Clin Biochem. 2005 May;38(5):433-5. doi: 10.1016/j.clinbiochem.2004.12.014. Clin Biochem. 2005. PMID: 15820773

2

Study on possible increase in twinning rate at a small village in south Brazil.

Matte U, Le Roux MG, Bénichou B, Moisan JP, Giugliani R. Matte U, et al. Acta Genet Med Gemellol (Roma). 1996;45(4):431-7. doi: 10.1017/s0001566000000829. Acta Genet Med Gemellol (Roma). 1996. PMID: 9181177

3

Unique frequency of known mutations in Brazilian MPS I patients.

Matte U, Leistner S, Lima L, Schwartz I, Giugliani R. Matte U, et al. Am J Med Genet. 2000 Jan 17;90(2):108-9. doi: 10.1002/(sici)1096-8628(20000117)90:2<108::aid-ajmg3>3.0.co;2-y. Am J Med Genet. 2000. PMID: 10607946

4

Molecular analysis of the Pi*Z allele in patients with liver disease.

Lima LC, Matte U, Leistner S, Bopp AR, Scholl VC, Giugliani R, da Silveira TR. Lima LC, et al. Among authors: matte u. Am J Med Genet. 2001 Dec 15;104(4):287-90. doi: 10.1002/ajmg.10069. Am J Med Genet. 2001. PMID: 11754061

5

Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients.

Matte U, Yogalingam G, Brooks D, Leistner S, Schwartz I, Lima L, Norato DY, Brum JM, Beesley C, Winchester B, Giugliani R, Hopwood JJ. Matte U, et al. Mol Genet Metab. 2003 Jan;78(1):37-43. doi: 10.1016/s1096-7192(02)00200-7. Mol Genet Metab. 2003. PMID: 12559846

6

CNS involvement in Fabry disease: clinical and imaging studies before and after 12 months of enzyme replacement therapy.

Jardim L, Vedolin L, Schwartz IV, Burin MG, Cecchin C, Kalakun L, Matte U, Aesse F, Pitta-Pinheiro C, Marconato J, Giugliani R. Jardim L, et al. Among authors: matte u. J Inherit Metab Dis. 2004;27(2):229-40. doi: 10.1023/B:BOLI.0000028794.04349.91. J Inherit Metab Dis. 2004. PMID: 15159654 Clinical Trial.

7

The Latin-American network of human genetics.

Giugliani R, Matte U. Giugliani R, et al. Among authors: matte u. Community Genet. 2004;7(2-3):74-5. doi: 10.1159/000080775. Community Genet. 2004. PMID: 15539821

8

Infected and noninfected ascites in pediatric patients.

Vieira SM, Matte U, Kieling CO, Barth AL, Ferreira CT, Souza AF, Taniguchi A, da Silveira TR. Vieira SM, et al. Among authors: matte u. J Pediatr Gastroenterol Nutr. 2005 Mar;40(3):289-94. doi: 10.1097/01.mpg.0000154659.54735.1d. J Pediatr Gastroenterol Nutr. 2005. PMID: 15735482

9

Nonviral in vivo gene transfer in the mucopolysaccharidosis I murine model.

Camassola M, Braga LM, Delgado-Cañedo A, Dalberto TP, Matte U, Burin M, Giugliani R, Nardi NB. Camassola M, et al. Among authors: matte u. J Inherit Metab Dis. 2005;28(6):1035-43. doi: 10.1007/s10545-005-0070-5. J Inherit Metab Dis. 2005. PMID: 16435197

10

Further cases of "neighbor" mutations in mucopolysaccharidosis type II.

Schwartz IV, Lima LC, Tylee K, Sobrinho RP, Norato DY, Duarte AR, Besley G, Burin MG, Matte U, Giugliani R, Leistner-Segal S. Schwartz IV, et al. Among authors: matte u. Am J Med Genet A. 2006 Aug 1;140(15):1684-6. doi: 10.1002/ajmg.a.31317. Am J Med Genet A. 2006. PMID: 16770800 No abstract available.

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