Zobrazeno 1 - 10
of 339
pro vyhledávání: '"Samir K, Ballas"'
Autor:
Viviane Teixeira de Sousa, Samir K. Ballas, Júlia Mota Leite, Maria Cristina Albe Olivato, Rodolfo D. Cancado
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 3, Pp 369-373 (2022)
Introduction: The aim of this study was to describe maternal and perinatal outcomes in pregnant women with sickle cell disease (SCD) followed at Santa Casa de Sao Paulo over a 10-year period (between 2010 and 2019). Method: Fifty-five records of preg
Externí odkaz:
https://doaj.org/article/945190fa2a1b4118aa62c99efc6813f4
Autor:
Tiago da Silva Lopes, Samir K. Ballas, Jamille Evelyn Rodrigues Souza Santana, Pedro de Melo-Carneiro, Lilian Becerra de Oliveira, Katia Nunes Sá, Larissa Conceição Dias Lopes, Wellington dos Santos Silva, Rita Lucena, Abrahão Fontes Baptista
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Chronic joint pain (CJP) is among the significant musculoskeletal comorbidities in sickle cell disease (SCD) individuals. However, many healthcare professionals have difficulties in understanding and evaluating it. In addition, most musculoskeletal e
Externí odkaz:
https://doaj.org/article/366cdece73e6478eaa828438e5e52c7d
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 386-388 (2021)
Externí odkaz:
https://doaj.org/article/73786a099cda4c11889bf3733bbd099e
Autor:
Salam Alkindi, Anwaar R Al-Ghadani, Samah R Al-Zeheimi, Said Y Alkindi, Naglaa Fawaz, Samir K Ballas, Anil V Pathare
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
Objective To assess the clinical and laboratory predictors of venous thromboembolism (VTE) in patients with sickle cell anaemia (SCA) and its relationship to morbidity and mortality. Methods This retrospective case–control study analysed data from
Externí odkaz:
https://doaj.org/article/95ea4dfd75d2493b9f26a8775569912b
Autor:
Clarisse Lopes de Castro Lobo, Emilia Matos do Nascimento, Leonardo José Carvalho de Jesus, Thiago Gotelip de Freitas, Jocemir Ronaldo Lugon, Samir K. Ballas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 40, Iss 1, Pp 37-42 (2018)
Objective: To determine the mortality rate of children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil. Methods: The number of deaths, the mortality rate and the causes of deaths in patients with sickle cell anemia who were
Externí odkaz:
https://doaj.org/article/5727228513504317b1a0d441912a8cec
Autor:
Samir K. Ballas
Publikováno v:
Annals of Hematology. 100:1133-1138
According to the Center of Disease Control and Prevention (CDC) database, the total number of deaths due to opioid overdose from 1999 through 2018 was 840,629. Given the alarming nature of these statistics, patients who requested prescription for opi
Publikováno v:
European Journal of Haematology. 105:237-246
Early diagnosis, treatment, and prevention of a vaso-occlusive crisis (VOC) are critical to the management of patients with sickle cell disease. It is essential to differentiate between VOC-associated pain and chronic pain, hyperalgesia, neuropathy,
Autor:
Samir Raniga, Bushra Al-Salami, Samir K. Ballas, Salam Alkindi, Ikhlas Al-Busaidi, Anil Pathare
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-6 (2020)
Scientific Reports
Scientific Reports
Acute chest syndrome (ACS) is a major complication of sickle cell anaemia (SCA) and a leading cause for hospital admissions and death. We aimed to study the spectrum of clinical and laboratory features of ACS and to assess the predisposing factors an
Autor:
Samir K. Ballas
Publikováno v:
Journal of Clinical Medicine Research
Autor:
Nathalie Lemonne, Keyne Charlot, Xavier Waltz, Samir K. Ballas, Yann Lamarre, Ketty Lee, Régine Hierso, Catherine Connes, Maryse Etienne-Julan, Marc Romana, Philippe Connes
Publikováno v:
Haematologica, Vol 100, Iss 10 (2015)
Externí odkaz:
https://doaj.org/article/c1e9e8f208964ec6bf095edd79c7edfc