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Refinado por: Base de dados/Biblioteca: ROAD: Directory of Open Access Scholarly Resources remover tipo de recurso: Reports remover
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1
2D Virtual Reality-Based Exercise Improves Spatial Navigation in Institutionalized Non-robust Older Persons: A Preliminary Data Report of a Single-Blind, Randomized, and Controlled Study
2D Virtual Reality-Based Exercise Improves Spatial Navigation in Institutionalized Non-robust Older Persons: A Preliminary Data Report of a Single-Blind, Randomized, and Controlled Study
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2D Virtual Reality-Based Exercise Improves Spatial Navigation in Institutionalized Non-robust Older Persons: A Preliminary Data Report of a Single-Blind, Randomized, and Controlled Study

Oliveira, Luciana Mendes ; Evangelista E Souza, Eric Hudson ; Alves, Mariana Rocha ; Carneiro, Lara S F ; Fagundes, Daniel Ferreira ; de Paula, Alfredo Maurício Batista ; Engedal, Knut ; Nascimento, Osvaldo J M ; Monteiro-Junior, Renato Sobral

Frontiers in neurology, 2020, Vol.11, p.609988-609988

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2
Apical periodontitis associated with a calculus-like deposit: A case report of a rare fan-shaped manifestation
Apical periodontitis associated with a calculus-like deposit: A case report of a rare fan-shaped manifestation
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Apical periodontitis associated with a calculus-like deposit: A case report of a rare fan-shaped manifestation

Toubes, Kênia M ; Tonelli, Stéphanie Q ; Oliveira, Bruno J de ; Duarte, Graziele ; Nunes, Eduardo ; Silveira, Frank F

Annals of medicine and surgery (2012), 2019, Vol.41, p.1-5

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3
ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26
ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26
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ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26

Perez Botero, J ; Oliveira, J L ; Chen, D ; Reichard, K K ; Viswanatha, D S ; Nguyen, P L ; Pruthi, R K ; Majerus, J ; Gada, P ; Gangat, N ; Tefferi, A ; Patnaik, M M

Blood cancer journal, 2015, Vol.5, p.e315-e315

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4
Benign fasciculations and corticosteroid use: possible association? An update
Benign fasciculations and corticosteroid use: possible association? An update
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Benign fasciculations and corticosteroid use: possible association? An update

Orsini, Marco ; Sztajnbok, Flavio R ; Oliveira, Acary Bulle ; Araújo Leite, Marco Antonio ; Júnior, Salem Peter ; de Freitas, Marcos R G ; Nascimento, Osvaldo J M ; Silva, Júlio Guilherme ; Sholer, Marzia Puccioni ; Guimarães, Fernando Silva ; Pereira, Alessandra Cardoso ; de Menezes, Sara Lúcia Silveira ; da Silva Catharino, Antonio Marcos ; Bino, Fabrício

Neurology international, 2011, Vol.3 (2), p.e11-e11

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5
Bevacizumab-associated osteonecrosis of the femur and tibia
Bevacizumab-associated osteonecrosis of the femur and tibia
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Bevacizumab-associated osteonecrosis of the femur and tibia

Oliveira, Leandro J C ; Canedo, Felipe S N A ; Sacardo, Karina P ; Alessi, João V M ; Barbosa, Felipe G ; Shimada, Andrea K ; Katz, Artur

Oxford medical case reports, 2019, Vol.2019 (5), p.omz040-omz040

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6
Bladder Urothelial Carcinoma in a Child: Case Report and Review of Literature
Bladder Urothelial Carcinoma in a Child: Case Report and Review of Literature
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Bladder Urothelial Carcinoma in a Child: Case Report and Review of Literature

Oda, Marian Hanae ; Dos Santos, Danilo Vicente ; Farias, Adria Karina ; de Oliveira, Leilane ; Falcão, Bruno Pinheiro ; Ahn, Nicholas J ; Amarante, Antônio Carlos ; Losso, Graziele Moraes ; Dias, Andre Ivan Bradley Dos Santos ; Agulham, Miguel Angelo ; Fachin, Camila Girardi

Frontiers in pediatrics, 2019, Vol.7, p.385-385

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7
Blinatumomab-induced lineage switch of B-ALL with t(4:11)(q21;q23) KMT2A/AFF1 into an aggressive AML: pre- and post-switch phenotypic, cytogenetic and molecular analysis
Blinatumomab-induced lineage switch of B-ALL with t(4:11)(q21;q23) KMT2A/AFF1 into an aggressive AML: pre- and post-switch phenotypic, cytogenetic and molecular analysis
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Blinatumomab-induced lineage switch of B-ALL with t(4:11)(q21;q23) KMT2A/AFF1 into an aggressive AML: pre- and post-switch phenotypic, cytogenetic and molecular analysis

Haddox, C L ; Mangaonkar, A A ; Chen, D ; Shi, M ; He, R ; Oliveira, J L ; Litzow, M R ; Al-Kali, A ; Hogan, W J ; Elliott, M A

Blood cancer journal, 2017, Vol.7 (9), p.e607-e607

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8
Brazilian Group of Gastrointestinal Tumours' consensus guidelines for the management of oesophageal cancer
Brazilian Group of Gastrointestinal Tumours' consensus guidelines for the management of oesophageal cancer
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Brazilian Group of Gastrointestinal Tumours' consensus guidelines for the management of oesophageal cancer

Rocha-Filho, Duilio R ; Peixoto, Renata D'Alpino ; Weschenfelder, Rui F ; Rego, Juliana F M ; Riechelmann, Rachel ; Coutinho, Anelisa K ; Fernandes, Gustavo S ; Jacome, Alexandre A ; Andrade, Aline C ; Murad, Andre M ; Mello, Celso A L ; Miguel, Diego S C G ; Gomes, Diogo B D ; Racy, Douglas J ; Moraes, Eduardo D ; Akaishi, Eduardo H ; Carvalho, Elisangela S ; Mello, Evandro S ; Filho, Fauze Maluf ; Coimbra, Felipe J F ; Capareli, Fernanda C ; Arruda, Fernando F ; Vieira, Fernando M A C ; Takeda, Flavio R ; Cotti, Guilherme C C ; Pereira, Guilherme L S ; Paulo, Gustavo A ; Ribeiro, Héber S C ; Lourenco, Laercio G ; Crosara, Marcela ; Toneto, Marcelo G ; Oliveira, Marcos B ; de Lourdes Oliveira, Maria ; Begnami, Maria Dirlei ; ones, Nora M ; Yagi, Osmar ; Ashton-Prolla, Patricia ; Aguillar, Patricia B ; Amaral, Paulo C G ; Hoff, Paulo M ; Araujo, Raphael L C ; Di Paula Filho, Raphael P ; Gansl, Rene C ; Gil, Roberto A ; Pfiffer, Tulio E F ; Souza, Tulio ; Ribeiro, Ulysses ; Jesus, Victor Hugo F ; Costa, Wilson L ; Prolla, Gabriel

Ecancermedicalscience, 2021, Vol.15, p.1195-1195

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9
Cecum perforation in intestinal malrotation setting in a patient with chromosome 12p deletion syndrome: A case report
Cecum perforation in intestinal malrotation setting in a patient with chromosome 12p deletion syndrome: A case report
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Cecum perforation in intestinal malrotation setting in a patient with chromosome 12p deletion syndrome: A case report

Oliveira, João T ; Marques, Paula ; Preza Fernandes, J M ; Teixeira, Tânia ; Santos, Marisa D ; Povo, Ana ; Castro Alves, Eurico

International journal of surgery case reports, 2020, Vol.66, p.342-345

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10
Chyloperitoneum due to gastric carcinoma: a case report
Chyloperitoneum due to gastric carcinoma: a case report
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Chyloperitoneum due to gastric carcinoma: a case report

Pinto, J C ; Oliveira, S ; Duarte, L ; Ferreira, M ; Marques, C ; Casimiro, C

Oxford medical case reports, 2022, Vol.2022 (6), p.omac062-omac062

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