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Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
D'Angelo CS, Da Paz JA, Kim CA, Bertola DR, Castro CI, Varela MC, Koiffmann CP. D'Angelo CS, et al. Among authors: da paz ja. Eur J Med Genet. 2006 Nov-Dec;49(6):451-60. doi: 10.1016/j.ejmg.2006.02.001. Epub 2006 Mar 10. Eur J Med Genet. 2006. PMID: 16564757
Asymptomatic MRI lesions in pediatric-onset AQP4-IgG positive NMOSD.
Paolilo RB, Rimkus CM, da Paz JA, Apostolos-Pereira SL, Callegaro D, Sato DK. Paolilo RB, et al. Among authors: da paz ja. Mult Scler Relat Disord. 2022 Dec;68:104215. doi: 10.1016/j.msard.2022.104215. Epub 2022 Oct 4. Mult Scler Relat Disord. 2022. PMID: 36257150
Treatment and outcome of aquaporin-4 antibody-positive NMOSD: A multinational pediatric study.
Paolilo RB, Hacohen Y, Yazbeck E, Armangue T, Bruijstens A, Lechner C, Apostolos-Pereira SL, Martynenko Y, Breu M, de Medeiros Rimkus C, Wassmer E, Baumann M, Papetti L, Capobianco M, Kornek B, Rostásy K, da Paz JA, Ciccarelli O, Lim M, Saiz A, Neuteboom R, Marignier R, Hemingway C, Sato DK, Deiva K. Paolilo RB, et al. Among authors: da paz ja. Neurol Neuroimmunol Neuroinflamm. 2020 Jul 30;7(5):e837. doi: 10.1212/NXI.0000000000000837. Print 2020 Sep. Neurol Neuroimmunol Neuroinflamm. 2020. PMID: 32732259 Free PMC article.
18 results