Browsing "Comunicações em Eventos - FM/MPE" by Title
Showing results 149 to 168 of 250
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| Issue Date | Title | Author(s) |
|---|---|---|
| 2014 | Macrophage Activation Macrophage Activation Syndrome: A Severe and Frequent Manifestation of Acute Pancreatitis in Childhood-Onset Compared to Adult Systemic Lupus Erythematosus Patients | SPELLING, Natali W.; OTSUZI, Carini I.; BARROS, Diego L.; SILVA, Mariana A. da; PEREIRA, Rosa M. R.; CAMPOS, Lucia M. A.; BORBA, Eduardo F.; BONFA, Eloisa; SILVA, Clovis A. |
| 2022 | MALNUTRITION AND OBESITY PREVALENCE IN CRITICALLY ILL LATIN AMERICAN CHILDREN: A PRELIMINARY REPORT OF THE NUTRIPIC STUDY | MINO, S. Campos; DELGADO, A. Figueiredo; ZARATE, P.; ZAMBERLAN, P.; BENAVIDES, E. Munoz; BU, J. A. Coss |
| 2020 | MEG3 and MEG8 aberrant methylation associated with worst prognosis in an infant with neuroblastoma | NOVAK, Estela M.; GIMENEZ, Thamiris Magalhaes; NEVES, Nathalia Halley; VINCE, Carolina Sgarioni Camargo; KREPISCHI, Ana Cristina Victorino; LAPA, Rainer Marco Lopez; CRISTOFANI, Lilian M.; BENDIT, Israel; ODONE FILHO, Vicente |
| 2023 | MENTAL HEALTH ISSUES AND LIFE CONDITIONS OF ADOLESCENTS WITH JUVENILE DERMATOMYOSITIS AND OTHER AUTOIMMUNE RHEUMATIC DISEASES DURING COVID-19 QUARANTINE | IHARA, Bianca; ELIAS, Adriana; SIMON, Juliana; VIANA, Vivianne; STRABELLI, Claudia; PEREIRA, Rosa; AIKAWA, Nadia; KOZU, Katia; BUSCATTI, Izabel; FERREIRA, Juliana, et al |
| 2023 | METABOLIC ALTERATIONS AND GROWTH DISORDERS IN CHILDREN BORN WITH VERY LOW BIRTH WEIGHT AND PRETERM INFANTS SMALL FOR GESTATIONAL AGE AT 36 MONTHS OF CORRECTED GESTATIONAL AGE | ATHAYDE, D.; COMINATO, L.; ATHAYDE, G.; FIRMINO, S.; SADECK, L.; DINIZ, E.; DAMIANI, D. |
| 2012 | Misdiagnosis in Wilms tumor: Concerns on the use of preoperative chemotherapy | DUARTE, R. J.; CRISTOFANI, L. M.; DENES, F. T.; GIRON, A. M.; ODONE-FILHO, V; SROUGI, M. |
| 2016 | Mixed Gonadal Disgenesia: Patients of Instituto da Crianca, HC-FMUSP | FERREIRA, Marianna; PINHEIRO, Claudia; QUEIROZ, Edjane; BRIGATTI, Nathalia; ITO, Simone; STEINMETZ, Leandra; COMINATO, Louise; SETIAN, Nuvarte; DICHTCHEKENIAN, Vae; MENEZES FILHO, Hamilton, et al |
| 2017 | Model of Short Bowel Syndrome and Segmental Intestinal Autotransplantation in Swine | GALVAO, Flavio; TANNURI, Ana; JABUR, Gabriel; LEE, Andre; CRUZ, Ruy; ARANTES, Rubens; LOPES, Liliana; CHAIB, Eleazar; UENIS, Tannuri; D'ALBUQUERQUE, Luiz |
| 2014 | Modular Transcriptional Repertoire Analysis in Down Syndrome Thymus | MOREIRA-FILHO, C.; BANDO, S. Y.; BERTONHA, F. B.; SILVA, F. N.; COSTA, L. D. A. F.; CARNEIRO-SAMPAIO, M. |
| 2015 | MODULAR TRANSCRIPTIONAL REPERTOIRE AND microRNA-TARGET ANALYSES IN THYMIC TISSUE OF DOWN SYNDROME INFANTS | MOREIRA-FILHO, Carlos Alberto; BANDO, Silvia Yumi; BERTONHA, Fernanda Bernardi; SILVA, Filipi Nascimento; COSTA, Luciano da Fontoura; FEREIRA, Leandro Rodrigues; CARNEIRO-SAMPAIO, Magda |
| 2019 | Molecular autopsy reveals clues for genetic basis of congenital valve defect | MADIA, F. A. R.; DIAS, A. T.; ZANARDO, E. A.; DAMASCENO, J. G.; NASCIMENTO, A. M.; COSTA, T. V. M. M.; CHEHIMI, S. N.; NOVO-FILHO, G. M.; MONTENEGRO, M. M.; OLIVEIRA, Y. G., et al |
| 2013 | MOLECULAR CHARACTERIZATION OF COMPLEMENT C1Q, C2, AND C4 GENES IN JUVENILE SYSTEMIC LUPUS ERYTHEMATOSUS | LIPHAUS, B. L.; UMETSU, N.; BANDO, S.; JESUS, A. A.; ANDRADE, L. E. C.; SILVA, C. A.; CARNEIRO-SAMPAIO, M. |
| 2012 | MUCOPOLYSSACCHARIDOSES TYPE IV: CASE OF A PATIENT WITH HUMORAL RESPONSE DEFICIENCY | TORRES, L. C.; SOARES, D. C.; QUAIO, C. R. D. C.; FRANCO, J. F.; GOMY, I.; KULIKOWSKI, L. D.; BERTOLA, D. R.; SAMPAIO, M. Carneiro; KIM, C. A. |
| 2012 | MUTATION SCREENING IN STAT1, CARD9 AND PKC-DELTA IN PATIENTS WITH CHRONIC MUCOCUTANEOUS CANDIDIASIS | DEPNER, M.; VEERDONK, F. van de; WANDERS, J.; STAUSS, H.; RAABE, J.; ATKINSON, T. P.; SCHROEDER JR., H. W.; NIEHUES, T.; DUECKERS, G.; PUCK, J., et al |
| 2012 | NATURAL KILLER CELL DEFICIENCY IN PATIENTS WITH MUCOPOLYSACCHARIDOSES | TORRES, L. C.; QUAIO, C. R. D. C.; FRANCO, J. F.; GOMY, I.; BERTOLA, D. R.; KULIKOWSKI, L. D.; SAMPAIO, M. Carneiro; KIM, C. A. |
| 2019 | Next-generation sequencing (NGS) of nine candidate genes with custom AmpliSeq in 22q11.2 deletion syndrome patients | DANTAS, A. G.; NUNES, N.; KIM, C. A.; SOARES, D. C. Q.; MELONI, V. A.; BELANGERO, S. I.; CARVALHEIRA, G. G.; MELARAGNO, M. I. |
| 2017 | NO DIFFERENCES BETWEEN THE INTAKES OF MACRO AND MICRONUTRIENTS IN PRESCHOOL CHILDREN, WITH AND WITHOUT EXCESS WEIGHT, CARED AT HEALTH SCHOOL CENTER BUTANTA/COLLEGE OF MEDICINE UNIVERSITY OF SAO PAULO | MARTINS, Tomaz Bruna Cabral Ribas; RAMOS, Bianca Prado de Lima; ANGELIS, Karina Guimaraes de; LIMA, Victoria Kupper; OMORI, Luciana Harumi Miranda; FERNANDES, Maria Teresa Bechere |
| 2018 | Novel mutations in fibronectin associated with metaphyseal fractures - Expanding the phenotype of patients with a subtype of spondylomethaphyseal dysplasia with ""corner fractures"" | ALM, Jessica J.; COSTANTINI, Alice; VALTA, Helena; BARATANG, Nissan Vida; YAP, Patrick; BERTOLA, Debora; YAMAMOTO, Guilherme; KIM, Chong A.; CHEN, Jiani; WIERENGA, Klaas J., et al |
| 2014 | Novel Mutations in MVK Associated with Hyperimmunoglobulinemia D with Periodic Fever Syndrome Phenotype | VASCONCELOS, D. Moraes; FUJIHIRA, E.; OLIVEIRA, J. B.; JESUS, A. A.; SILVA, C.; CASTRO, A. P. M.; DORNA, M. B.; WATANABE, L.; PONTILLO, A.; CHUFFI-BARROS, N., et al |
| 2023 | NUTRITIONAL ASSESSMENT, BODY COMPOSITION AND PHASE ANGLE IN JUVENILE DERMATOMYOSITIS PATIENTS | PUGLIESE, Camila; KOZU, Katia T.; CAMPOS, Lucia M. A.; AIKAWA, Nadia E.; SILVA, Clovis A. A.; ELIAS, Adriana M. |