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期刊名:Presse medicale

缩写:PRESSE MED

ISSN:0755-4982

e-ISSN:2213-0276

IF/分区:3.4/Q1

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共收录本刊相关文章索引3822
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Jean-Noël Trochu Jean-Noël Trochu
Background and objectives: Because of its severity, prevalence, and medical economic importance, heart failure is a chronic disease that is the subject of intense medical research. The aim of this article was to review th...
Galia Pollock,Olivier Negre,Jean-Antoine Ribeil Galia Pollock
Gene therapy is an innovative strategy that offers potential cure for patients with sickle cell disease, and no appropriate donor for transplant consideration. While we await long term data from these clinical trials, we remain optimistic t...
Daniel Y Chang,Zakary Wankier,Connie M Arthur et al. Daniel Y Chang et al.
RBC transfusion remains a cornerstone in the treatment of sickle cell disease (SCD). However, as with many interventions, transfusion of RBCs is not without risk. Allogeneic RBC exposure can result in the development of alloantibodies, whic...
Christophe Duvoux,Lorraine Blaise,Jean-Jacques Matimbo et al. Christophe Duvoux et al.
Liver involvement in SCD patients is frequent but often misdiagnosed or underestimated, except in case of advanced liver diseases. Because of so far poorly recognized forms of chronic SCD-related vascular injury that can silently evolved to...
Maryline Couette,Justine Roy,Damien Oudin Doglioni et al. Maryline Couette et al.
Neurovascular disease such as symptomatic stroke, silent brain infarcts and vascular cognitive impairment are common complications of sickle cell disease (SCD) that can have devastating consequences on quality of life, employment, and socia...
Marie-Sophie Meuleman,Lubka T Roumenina,Anne Grunenwald Marie-Sophie Meuleman
Sickle Cell Disease (SCD) is a hereditary blood disorder characterized by the presence of abnormal hemoglobin, leading to the formation of sickle-shaped red blood cells, causing vaso-occlusion. Inflammation is a key component of the pathoph...
Salma Al Kahf,Anne Roche,Audrey Baron et al. Salma Al Kahf et al.
Sickle cell disease (SCD) is a complex genetic disorder that has long challenged both patients and healthcare professionals. One of its chronic and debilitating complications is pulmonary hypertension (PH). SCD-associated PH is often post-c...