Starling ALP - Search Results

1

Body fat percentage in adolescents with phenylketonuria and associated factors.

Camatta GC, Kanufre VC, Alves MRA, Soares RDL, Norton RC, de Aguiar MJB, Starling ALP. Camatta GC, et al. Among authors: starling alp. Mol Genet Metab Rep. 2020 May 12;23:100595. doi: 10.1016/j.ymgmr.2020.100595. eCollection 2020 Jun. Mol Genet Metab Rep. 2020. PMID: 32426233 Free PMC article.

2

Overweight/obesity in adolescents with phenylketonuria: protective and predisposing factors.

Silveira AM, Lima PL, Alves MRA, Soares RDL, Kanufre VC, Rodrigues VM, Starling ALP, Norton RC, Aguiar MJB. Silveira AM, et al. Among authors: starling alp. J Pediatr (Rio J). 2022 Jan-Feb;98(1):104-110. doi: 10.1016/j.jped.2021.04.009. Epub 2021 Jun 16. J Pediatr (Rio J). 2022. PMID: 34144002 Free PMC article.

3

Nonalcoholic fatty liver disease in adolescents with phenylketonuria.

Silveira AM, Lima PL, Alves MRA, de Jesus RP, Pinto-Silva RA, Rodrigues VM, Starling ALP, Norton RC, de Aguiar MJB. Silveira AM, et al. Among authors: starling alp. J Pediatr (Rio J). 2023 Mar-Apr;99(2):174-180. doi: 10.1016/j.jped.2022.08.003. Epub 2022 Oct 12. J Pediatr (Rio J). 2023. PMID: 36243033 Free PMC article.

4

BH₄ deficiency identified in a neonatal screening program for hyperphenylalaninemia.

Souza CAA, Alves MRA, Soares RDL, Kanufre VC, Rodrigues VM, Norton RC, Starling ALP, Aguiar MJB. Souza CAA, et al. Among authors: starling alp. J Pediatr (Rio J). 2018 Mar-Apr;94(2):170-176. doi: 10.1016/j.jped.2017.04.005. Epub 2017 Aug 9. J Pediatr (Rio J). 2018. PMID: 28801146 Free article.

5

Frequency of biotinidase gene variants and incidence of biotinidase deficiency in the Newborn Screening Program in Minas Gerais, Brazil.

Carvalho NO, Januário JN, Felix GLP, Nolasco DM, Ladeira RVP, Del Castillo DM, Starling ALP, Norton RC, Viana MB. Carvalho NO, et al. Among authors: starling alp. J Med Screen. 2020 Sep;27(3):115-120. doi: 10.1177/0969141319892298. Epub 2019 Dec 4. J Med Screen. 2020. PMID: 31801038

6

Relationships between phenylalanine levels, intelligence and socioeconomic status of patients with phenylketonuria.

Castro IP, Borges JM, Chagas HA, Tibúrcio J, Starling AL, Aguiar MJ. Castro IP, et al. J Pediatr (Rio J). 2012 Jul;88(4):353-6. doi: 10.2223/JPED.2175. Epub 2012 Mar 28. J Pediatr (Rio J). 2012. PMID: 22456753

7

Children with phenylketonuria treated early: basic audiological and electrophysiological evaluation.

Mancini PC, Durrant JD, Starling AL, Iório MC. Mancini PC, et al. Ear Hear. 2013 Mar-Apr;34(2):236-44. doi: 10.1097/AUD.0b013e31826a1c99. Ear Hear. 2013. PMID: 23038064

8

Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil.

Santos LL, Magalhães Mde C, Reis Ade O, Starling AL, Januário JN, Fonseca CG, Aguiar MJ, Carvalho MR. Santos LL, et al. Genet Mol Res. 2006 Mar 31;5(1):16-23. Genet Mol Res. 2006. PMID: 16755493 Free article.

9

Novel mutations causing biotinidase deficiency in individuals identified by the newborn screening program in Minas Gerais, Brazil.

Carvalho NO, Del Castillo DM, Januário JN, Starling ALP, Arantes RR, Norton RC, Viana MB. Carvalho NO, et al. Among authors: starling alp. Am J Med Genet A. 2019 Jun;179(6):978-982. doi: 10.1002/ajmg.a.61137. Epub 2019 Mar 26. Am J Med Genet A. 2019. PMID: 30912303

10

Metabolic syndrome in children and adolescents with phenylketonuria.

Kanufre VC, Soares RD, Alves MR, Aguiar MJ, Starling AL, Norton RC. Kanufre VC, et al. J Pediatr (Rio J). 2015 Jan-Feb;91(1):98-103. doi: 10.1016/j.jped.2014.06.006. Epub 2014 Oct 25. J Pediatr (Rio J). 2015. PMID: 25458873 Free article.

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