متابعة
Diogo Cordeiro de Queiroz Soares
Diogo Cordeiro de Queiroz Soares
Médico Titular do Departamento de Oncogenética, A.C. Camargo Cancer Center
بريد إلكتروني تم التحقق منه على accamargo.org.br
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
Natural history of 39 patients with Achondroplasia‏
JRM Ceroni, DCQ Soares, LC Testai, RSH Kawahira, GL Yamamoto, ...‏
Clinics 73, e324, 2018‏
262018
Prevalence of BRCA1 and BRCA2 pathogenic and likely pathogenic variants in non-selected ovarian carcinoma patients in Brazil‏
DP Cotrim, ARG Ribeiro, D Paixão, DC de Queiroz Soares, R Jbili, ...‏
BMC cancer 19, 1-9, 2019‏
242019
Clinical description of 41 Brazilian patients with oculo-auriculo-vertebral dysplasia‏
JRM Pegler, DCQ Soares, CRDAC Quaio, N Fernandes, LAN Oliveira, ...‏
Revista da Associação Médica Brasileira 62 (3), 202-206, 2016‏
182016
Short Communication Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings.‏
JF Franco, DC Soares, LC Torres, GN Leal, MT Cunha, RS Honjo, ...‏
Genetics and molecular research: GMR 15 (1), 2016‏
162016
Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy: results from a single-center case series study‏
JF da Silva Franco, R El Dib, A Agarwal, D Soares, NVM Milhan, ...‏
Intractable & rare diseases research 6 (3), 183-190, 2017‏
152017
Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance‏
AM Gómez, DC Soares, AAB Costa, DP Pereira, MI Achatz, MN Formiga‏
Archives of endocrinology and metabolism 63, 369-375, 2019‏
132019
CD4+ CD25highFoxp3+ Treg deficiency in a Brazilian patient with Gaucher disease and lupus nephritis‏
MC Matta, DC Soares, MS Kerstenetzky, ACP Freitas, CA Kim, LC Torres‏
Human Immunology 77 (2), 196-200, 2016‏
122016
Downregulation of genes outside the deleted region in individuals with 22q11. 2 deletion syndrome‏
AG Dantas, ML Santoro, N Nunes, CB de Mello, LSE Pimenta, VA Meloni, ...‏
Human genetics 138 (1), 93-103, 2019‏
112019
Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings‏
JF Franco, DC Soares, LC Torres, GN Leal, MT Cunha, RS Honjo, ...‏
Genet Mol Res 15 (1), 1-7, 2016‏
112016
NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene‏
LC Torres, DC de Queiroz Soares, LD Kulikowski, JF Franco, CA Kim‏
Clinical Immunology 154 (2), 100-104, 2014‏
92014
Role of SNAP29, LZTR1 and P2RXL1 genes on immune regulation in a patient with atypical 0.5 Mb deletion in 22q11. 2 region‏
DC de Queiroz Soares, RL Dutra, CRDC Quaio, MI Melaragno, ...‏
Clinical Immunology 145 (1), 55-58, 2012‏
82012
Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome‏
DC Soares, MN Stroparo, YC Lian, CY Takakura, S Wolf, R Betz, CA Kim‏
Journal of inherited metabolic disease 40, 461-462, 2017‏
72017
Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes‏
NA de Carvalho, KM Santiago, JML Maia, FDA Costa, MN Formiga, ...‏
Journal of Medical Genetics 61 (1), 61-68, 2024‏
42024
Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: an unusual presentation of 22q11. 2 deletion syndrome‏
DC Soares, AG Dantas, MC Matta, AC Pastorino, MI Melaragno, ...‏
Clinical Immunology 220, 108590, 2020‏
22020
Expanding the phenotype of 8p23. 1 deletion syndrome: eight new cases resembling the clinical spectrum of 22q11. 2 microdeletion‏
MM Montenegro, D Camilotti, CRDAC Quaio, Y Gasparini, ÉA Zanardo, ...‏
The Journal of Pediatrics 252, 56-60. e2, 2023‏
12023
Li–Fraumeni-associated pancreatic neuroendocrine tumour and XAF1 p. Glu134Ter risk modifier variant‏
RP Riechelmann, DC Soares, C Dias, DM Carraro, GT Torrezan‏
ecancermedicalscience 16, 2022‏
12022
Cowden Syndrome: a single institution case series and literature review‏
M Sonagli, RC Neto, MN da Cruz Formiga, DC de Queiroz Soares, ...‏
Revista de Senología y Patología Mamaria 33 (2), 57-60, 2020‏
12020
Intellectual performance profi le of a sample of children and adolescents from Brazil with 22q11. 2 Deletion Syndrome (22q11. 2DS) based on the Wechsler Scale‏
LSE Pimenta, CB Mello, DCQ Soares, AG Dantas, MI Melaragno, ...‏
Estudos de Psicologia (Campinas) 36, e180101, 2019‏
12019
Mucopolysaccharidosis type I, II and VI and response to enzyme replacement therapy‏
J FRANCO, R EL DIB, A AGARWAL, D SOARES, NVM MILHAN, ...‏
12017
Lipoid proteinosis: Rare case confirmed by ECM1 mutation detection‏
TF Almeida, DC Soares, CR Quaio, RS Honjo, DR Bertola, JA McGrath, ...‏
International Journal of Pediatric Otorhinolaryngology 78 (12), 2314-2315, 2014‏
12014
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مقالات 1–20