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Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network.
Genet Mol Biol. 2014 Mar;37(1):23-9. doi: 10.1590/s1415-47572014000100006. Epub 2013 Feb 28.
Genet Mol Biol. 2014.
PMID: 24688287
Free PMC article.
What syndrome is this? Oculocerebral hypopigmentation syndrome of preus.
de Oliveira Sobrinho RP, Steiner CE.
de Oliveira Sobrinho RP, et al.
Pediatr Dermatol. 2007 May-Jun;24(3):313-5. doi: 10.1111/j.1525-1470.2007.00410.x.
Pediatr Dermatol. 2007.
PMID: 17542888
No abstract available.
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Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis.
de Oliveira-Sobrinho RP, Appenzeller S, Holanda IP, Heleno JL, Jorente J, On Behalf Of The Rare Genomes Project Consortium, Vieira TP, Steiner CE.
de Oliveira-Sobrinho RP, et al.
Genes (Basel). 2024 Apr 19;15(4):513. doi: 10.3390/genes15040513.
Genes (Basel). 2024.
PMID: 38674447
Free PMC article.
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Metacarpophalangeal pattern profile in Marfan syndrome and Marfan-like patients.
de Oliveira Sobrinho RP, Moretti-Ferreira D, Contini A, Norato DY.
de Oliveira Sobrinho RP, et al.
Am J Med Genet. 1997 Oct 17;72(2):159-63.
Am J Med Genet. 1997.
PMID: 9382136
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Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances.
de Souza LC, Dos Santos AP, Sgardioli IC, Viguetti-Campos NL, Marques Prota JR, de Oliveira-Sobrinho RP, Vieira TP, Gil-da-Silva-Lopes VL.
de Souza LC, et al. Among authors: de oliveira sobrinho rp.
J Intellect Disabil Res. 2019 Nov;63(11):1379-1389. doi: 10.1111/jir.12615. Epub 2019 Mar 21.
J Intellect Disabil Res. 2019.
PMID: 30900361
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