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Artigo de periodico
Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment (2019)
Ramos, Luiza L. P; Monteiro, Fabiola P; Sampaio, Leticia P. B; Costa, Larissa A; Ribeiro, Mara D. O; Freitas, Erika L; Kitajima, Joao P; Kok, Fernando
Source: Clinical case reports. Unidade: FM
Subjects: PESSOAS COM DEFICIÊNCIA INTELECTUAL, EPILEPSIA, TRANSTORNOS DA LINGUAGEM, PROTEÍNAS NUCLEARES, MUTAÇÃO GENÉTICA, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Luiza L. P et al. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment. Clinical case reports, v. 7, n. 8, p. 1582-1584, 2019Tradução . . Disponível em: https://doi.org/10.1002/ccr3.2260. Acesso em: 07 nov. 2024.
APA
Ramos, L. L. P., Monteiro, F. P., Sampaio, L. P. B., Costa, L. A., Ribeiro, M. D. O., Freitas, E. L., et al. (2019). Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment. Clinical case reports, 7( 8), 1582-1584. doi:10.1002/ccr3.2260
NLM
Ramos LLP, Monteiro FP, Sampaio LPB, Costa LA, Ribeiro MDO, Freitas EL, Kitajima JP, Kok F. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment [Internet]. Clinical case reports. 2019 ; 7( 8): 1582-1584.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ccr3.2260
Vancouver
Ramos LLP, Monteiro FP, Sampaio LPB, Costa LA, Ribeiro MDO, Freitas EL, Kitajima JP, Kok F. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment [Internet]. Clinical case reports. 2019 ; 7( 8): 1582-1584.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ccr3.2260
Artigo de periodico
Transient abnormal myelopoiesis with pericardial effusion in Down syndrome: case report (2019)
Falasco, Bianca Francisco; Durante, Brenda; Faria, Daniel Kanaan; Faria, Caroline Silveri; Rosolen, Debora Cristina Batista; Antonangelo, Leila
Source: Clinical case reports. Unidade: FM
Subjects: HEMATOPOESE, DOENÇAS CARDIOVASCULARES, SÍNDROME DE DOWN, RECÉM-NASCIDO, ESTUDO DE CASO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FALASCO, Bianca Francisco et al. Transient abnormal myelopoiesis with pericardial effusion in Down syndrome: case report. Clinical case reports, v. 7, n. 7, p. 1280-1284, 2019Tradução . . Disponível em: https://doi.org/10.1002/ccr3.2184. Acesso em: 07 nov. 2024.
APA
Falasco, B. F., Durante, B., Faria, D. K., Faria, C. S., Rosolen, D. C. B., & Antonangelo, L. (2019). Transient abnormal myelopoiesis with pericardial effusion in Down syndrome: case report. Clinical case reports, 7( 7), 1280-1284. doi:10.1002/ccr3.2184
NLM
Falasco BF, Durante B, Faria DK, Faria CS, Rosolen DCB, Antonangelo L. Transient abnormal myelopoiesis with pericardial effusion in Down syndrome: case report [Internet]. Clinical case reports. 2019 ; 7( 7): 1280-1284.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ccr3.2184
Vancouver
Falasco BF, Durante B, Faria DK, Faria CS, Rosolen DCB, Antonangelo L. Transient abnormal myelopoiesis with pericardial effusion in Down syndrome: case report [Internet]. Clinical case reports. 2019 ; 7( 7): 1280-1284.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ccr3.2184

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