Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Stephanie Forté"'
Autor:
George Tomlinson, Ziad Solh, Jameel Abdulrehman, Kevin H M Kuo, Stephanie Forté, Lauren Bolster, Haowei (Linda) Sun, Pablo Bartolucci
Publikováno v:
BMJ Open, Vol 14, Iss 1 (2024)
Introduction Individuals with sickle cell disease (SCD) and central venous catheters (CVC) are at high risk for venous thromboembolism (VTE). Minimal data exist regarding the use of anticoagulation as thromboprophylaxis of VTE in this demographic, an
Externí odkaz:
https://doaj.org/article/fb2b638c3cef4f4c85597806c6a37ead
Publikováno v:
eJHaem, Vol 5, Iss 3, Pp 447-454 (2024)
Abstract A universal newborn screening program for sickle cell disease (uNS‐SCD) was implemented in the province of Québec (Qc) in November 2013, close in time to the recommendation of early initiation of hydroxyurea (HU) therapy for children. Thi
Externí odkaz:
https://doaj.org/article/487c5f2c3f5748cb93bc02655ccd3877
Autor:
Isabella Michelon, Maysa Vilbert, Isabella Silveira Pinheiro, Isabela Lino Costa, Cecilia Fernandes Lorea, Mathias Castonguay, Thai Hoa Tran, Stéphanie Forté
Publikováno v:
EClinicalMedicine, Vol 66, Iss , Pp 102330- (2023)
Summary: Background: Clinical manifestations and severity of SARS-CoV-2 infection in individuals with sickle cell disease (SCD) and sickle cell trait (SCT) are not well understood yet. Methods: We performed a systematic review and meta-analysis to as
Externí odkaz:
https://doaj.org/article/ceb1342190ef401d8d05305722ba59d0
Autor:
Isabella Ferreira Michelon, Isabella Silveira Pinheiro, Isabela Lino Costa, Maysa Vilbert, Cecilia Fernandes Lorea, Mathias Castonguay, Thai Hoa Tran, Stéphanie Forté
Publikováno v:
HemaSphere, Vol 7, p e9513186 (2023)
Externí odkaz:
https://doaj.org/article/cbe02a0323ce40a1a7298a39414edb41
Autor:
Stéphanie Forté, Olivia Sobczyk, Julien Poublanc, James Duffin, Gregory M. T. Hare, Joseph Arnold Fisher, David Mikulis, Kevin H. M. Kuo
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Background: Despite increased cerebral blood flow (CBF), cerebral infarcts occur in patients with sickle cell disease (SCD). This suggests increased CBF does not meet metabolic demand possibly due to compromised cerebral vasodilatory response. Hypoth
Externí odkaz:
https://doaj.org/article/bb7c254fe64c4caba2516b42041575b1
Autor:
Laurence Blain, Christian Watier, Xiaoduan Weng, Andre Masse, Marie-Josée Bédard, Nazila Bettache, Florence Weber, Michele Mahone, Stéphanie Forté, Vincent-Philippe Lavallée, Pierre-Olivier Gaudreau, Michael J. Newmarch, Denis Soulières
Publikováno v:
Diagnostics, Vol 13, Iss 11, p 1873 (2023)
It is believed that fetal hemoglobin (HbF) expression in adults is largely genetically regulated. The increased expression of HbF in pregnancy has been reported in a small number of articles. Different mechanisms have been proposed, but the descripti
Externí odkaz:
https://doaj.org/article/0cb420617487414cb8cf81d1c3a3a9e9
Autor:
Suella Martino, Rym Chouk Turki, Fouzia Zouiti, Romain Fort, Sadaf Pakdaman, Stéphanie Forté, Dehbia Menouche, David Calvet, Thomas Rupp, France Pirenne, Pablo Bartolucci
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 4, p 1256 (2023)
Background: Cerebral vasculopathy can induce chronic cerebral hypoperfusion leading to stroke in patients with sickle cell disease (SCD) and is treated by blood exchange transfusion (BET). However, no prospective clinical study has demonstrated the b
Externí odkaz:
https://doaj.org/article/dd1257832b7f4f63b9d48e3bd8796da1
Autor:
Maryline Couette, Stéphanie Forté, Damien Oudin Doglioni, Armand Mekontso-Dessap, David Calvet, Kevin H. M. Kuo, Pablo Bartolucci
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 4, p 1615 (2023)
This study sought to link neurocognitive profiles in sickle cell disease (SCD) patients with clinical characteristics. We conducted a prospective cohort study of adults with SCD who underwent comprehensive neuropsychological assessment at the UMGGR c
Externí odkaz:
https://doaj.org/article/e1896e85ccde47acab9edb7bc0619ef8
Autor:
Mathias Castonguay, Nawar Dakhallah, Justin Desroches, Marie-Laure Colaiacovo, Camille Jimenez-Cortes, Anne-Marie Claveau, Samuel Bérubé, Amer Yassine Hafsaoui, Amalia Souza, Pauline Tibout, Christophe Ah-Yan, Anne-Marie Vincent, Veronique Naessens, Josée Brossard, Sharon Abish, Raoul Santiago, Denis Soulières, Vincent Laroche, Yves Pastore, Thai Hoa Tran, Stéphanie Forté
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 24, p 7361 (2022)
Background: Patients with sickle cell disease (SCD) are considered at higher risk of severe COVID-19 infection. However, morbidity and mortality rates are variable among countries. To date, there are no published reports that document outcomes of SCD
Externí odkaz:
https://doaj.org/article/ee770be3e1964e45a0dd8d803066fd3d
Autor:
Igor Gomes Padilha, François Guilbert, Laurent Létourneau-Guillon, Stéphanie Forté, Kristoff Nelson, Manon Bélair, Jean Raymond, Denis Soulières
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 24, p 7463 (2022)
Magnetic resonance imaging (MRI) is used in patients with sickle cell disease (SCD) to detect silent cerebral infarcts. MR angiography (MRA) can identify arterial stenoses and intracranial aneurysms (ICANs) associated with SCD. In this study, we aime
Externí odkaz:
https://doaj.org/article/ce9b228b77c34ea39595f51b376570f5