Schwartz IVD - Search Results

1

Prevalence and causes of congenital microcephaly in the absence of a Zika virus outbreak in southern Brazil.

Herber S, Silva AA, Sanseverino MTV, Friedrich L, Ranieri TMS, Favreto C, Fraga LR, Terra AP, Schwartz IVD, Schuler-Faccini L. Herber S, et al. Among authors: schwartz ivd. J Pediatr (Rio J). 2019 Sep-Oct;95(5):600-606. doi: 10.1016/j.jped.2018.05.013. Epub 2018 Jul 4. J Pediatr (Rio J). 2019. PMID: 31340900 Free article.

2

Glycogen storage disease type I: clinical and laboratory profile.

Santos BL, Souza CF, Schuler-Faccini L, Refosco L, Epifanio M, Nalin T, Vieira SM, Schwartz IV. Santos BL, et al. J Pediatr (Rio J). 2014 Nov-Dec;90(6):572-9. doi: 10.1016/j.jped.2014.02.005. Epub 2014 Jul 11. J Pediatr (Rio J). 2014. PMID: 25019649 Free article.

3

Atypical macrocephaly-cutis marmorata telangiectatica congenita with retinoblastoma.

Schwartz IV, Felix TM, Riegel M, Schüler-Faccini L. Schwartz IV, et al. Clin Dysmorphol. 2002 Jul;11(3):199-202. doi: 10.1097/00019605-200207000-00010. Clin Dysmorphol. 2002. PMID: 12072801

4

DNA damage in leukocytes from pretreatment mucopolysaccharidosis type II patients; protective effect of enzyme replacement therapy.

Filippon L, Wayhs CA, Atik DM, Manfredini V, Herber S, Carvalho CG, Schwartz IV, Giugliani R, Vargas CR. Filippon L, et al. Mutat Res. 2011 Apr 3;721(2):206-10. doi: 10.1016/j.mrgentox.2011.02.005. Epub 2011 Feb 18. Mutat Res. 2011. PMID: 21334454

5

Prospective study of 11 Brazilian patients with mucopolysaccharidosis II.

Pinto LL, Schwartz IV, Puga AC, Vieira TA, Munoz MV, Giugliani R. Pinto LL, et al. J Pediatr (Rio J). 2006 Jul-Aug;82(4):273-8. doi: 10.2223/JPED.1512. J Pediatr (Rio J). 2006. PMID: 16912829

6

[Report of a Brazilian patient with Wolfram Syndrome].

Zen PR, Pinto LL, Schwartz IV, Barrett TG, Paskulin G. Zen PR, et al. J Pediatr (Rio J). 2002 Nov-Dec;78(6):529-32. J Pediatr (Rio J). 2002. PMID: 14647736 Portuguese.

7

Infant mortality in Brazil attributable to inborn errors of metabolism associated with sudden death: a time-series study (2002-2014).

de Bitencourt FH, Schwartz IVD, Vianna FSL. de Bitencourt FH, et al. Among authors: schwartz ivd. BMC Pediatr. 2019 Feb 8;19(1):52. doi: 10.1186/s12887-019-1421-y. BMC Pediatr. 2019. PMID: 30736757 Free PMC article.

8

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): assessment of joint mobility and grip and pinch strength.

Cardoso-Santos A, Azevedo AC, Fagondes S, Burin MG, Giugliani R, Schwartz IV. Cardoso-Santos A, et al. J Pediatr (Rio J). 2008 Mar-Apr;84(2):130-5. doi: 10.2223/JPED.1743. Epub 2008 Mar 18. J Pediatr (Rio J). 2008. PMID: 18338089

9

Gaucher disease type I: assessment of basal metabolic rate in patients from southern Brazil.

Doneda D, Lopes AL, Oliveira AR, Netto CB, Moulin CC, Schwartz IV. Doneda D, et al. Blood Cells Mol Dis. 2011 Jan 15;46(1):42-6. doi: 10.1016/j.bcmd.2010.10.008. Epub 2010 Nov 13. Blood Cells Mol Dis. 2011. PMID: 21075022

10

Prevalence of the most common pathogenic variants in three genes for inborn errors of metabolism associated with sudden unexpected death in infancy: a population-based study in south Brazil.

Randon DN, Sperb-Ludwig F, Vianna FSL, Becker APP, Vargas CR, Sitta A, Sant'Ana AN, Schwartz IVD, Bitencourt FH. Randon DN, et al. Among authors: schwartz ivd. Genet Mol Biol. 2020 Jul 24;43(3):20190298. doi: 10.1590/1678-4685-GMB-2019-0298. Genet Mol Biol. 2020. PMID: 32706845 Free PMC article.

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