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Page 1
Schizophreniform presentation and abrupt neurologic decline in a patient with late-onset mucopolysaccharidosis type IIIB.
Psychiatr Genet. 2021 Oct 1;31(5):199-204. doi: 10.1097/YPG.0000000000000294.
Psychiatr Genet. 2021.
PMID: 34347683
Review.
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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Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network.
Dornelles AD, de Camargo Pinto LL, de Paula AC, Steiner CE, Lourenço CM, Kim CA, Horovitz DD, Ribeiro EM, Valadares ER, Goulart I, Neves de Souza IC, da Costa Neri JI, Santana-da-Silva LC, Silva LR, Ribeiro M, de Oliveira Sobrinho RP, Giugliani R, Schwartz IV.
Dornelles AD, et al. Among authors: de oliveira sobrinho rp.
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.
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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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