日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta Thalassemia

腿部溃疡:E型β地中海贫血患者的病例报告及重型β地中海贫血文献综述

Mehta, Vikita; Kirubarajan, Abirami; Sabouhanian, Amir; Jayawardena, Sanasi M; Chandrakumaran, Priya; Thangavelu, Nila; Cader, Refai; Mettananda, Sachith; Bandara, Dayananda; Khan, Shawn; Weatherall, David J; Allen, Angela; Premawardhena, Anuja P; Olivieri, Nancy F

Discrepancies in self-reported financial conflicts of interest disclosures by physicians: a systematic review

医生自我报告的财务利益冲突披露存在差异:一项系统性综述

Tecimel, Osman; Bozkurt, İbrahim; Çepni, Şahin; Yaman, Fırat; Fırat, Ahmet; Öçgüder, Durmuş Ali; Taheri, Cameron; Kirubarajan, Abirami; Li, Xinglin; Lam, Andrew C L; Taheri, Sam; Olivieri, Nancy F

Single-center retrospective study of the effectiveness and toxicity of the oral iron chelating drugs deferiprone and deferasirox

一项单中心回顾性研究,旨在评估口服铁螯合药物地拉罗司和地拉罗司的疗效和毒性。

Olivieri, Nancy F; Sabouhanian, Amir; Gallie, Brenda L

Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.

在血红蛋白 E β-地中海贫血和 β-地中海贫血性状中,红细胞生成会抑制铁调素的产生

Jones Emma, Pasricha Sant-Rayn, Allen Angela, Evans Patricia, Fisher Chris A, Wray Katherine, Premawardhena Anuja, Bandara Dyananda, Perera Ashok, Webster Craig, Sturges Pamela, Olivieri Nancy F, St Pierre Timothy, Armitage Andrew E, Porter John B, Weatherall David J, Drakesmith Hal

Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia

地中海贫血患者的精氨酸代谢紊乱和心肺功能障碍

Morris, Claudia R; Kim, Hae-Young; Klings, Elizabeth S; Wood, John; Porter, John B; Trachtenberg, Felicia; Sweeters, Nancy; Olivieri, Nancy F; Kwiatkowski, Janet L; Virzi, Lisa; Hassell, Kathryn; Taher, Ali; Neufeld, Ellis J; Thompson, Alexis A; Larkin, Sandra; Suh, Jung H; Vichinsky, Elliott P; Kuypers, Frans A

Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension

西地那非治疗地中海贫血患者,这些患者经多普勒超声检查确定有肺动脉高压风险

Morris, Claudia R; Kim, Hae-Young; Wood, John; Porter, John B; Klings, Elizabeth S; Trachtenberg, Felicia L; Sweeters, Nancy; Olivieri, Nancy F; Kwiatkowski, Janet L; Virzi, Lisa; Singer, Sylvia T; Taher, Ali; Neufeld, Ellis J; Thompson, Alexis A; Sachdev, Vandana; Larkin, Sandra; Suh, Jung H; Kuypers, Frans A; Vichinsky, Elliott P

Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal Cohort

螯合疗法在北美和英国地中海贫血患者中的应用及铁负荷:来自地中海贫血纵向队列研究的报告

Kwiatkowski, Janet L; Kim, Hae-Young; Thompson, Alexis A; Quinn, Charles T; Mueller, Brigitta U; Odame, Isaac; Giardina, Patricia J; Vichinsky, Elliott P; Boudreaux, Jeanne M; Cohen, Alan R; Porter, John B; Coates, Thomas; Olivieri, Nancy F; Neufeld, Ellis J

Hemoglobin H-constant spring in North America: an alpha thalassemia with frequent complications

北美血红蛋白H恒定泉:一种并发症常见的α地中海贫血

Singer, Sylvia Titi; Kim, Hae-Young; Olivieri, Nancy F; Kwiatkowski, Janet L; Coates, Thomas D; Carson, Susan; Neufeld, Ellis; Cunningham, Melody J; Giardina, Patricia J; Mueller, Brigitta U; Quinn, Charles T; Fung, Ellen; Vichinsky, Elliott

Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions

接受输血的镰状细胞病患者和地中海贫血患者在铁过载管理方面存在差异

Fung, Ellen B; Harmatz, Paul R; Milet, Meredith; Balasa, Vinod; Ballas, Samir K; Casella, James F; Hilliard, Lee; Kutlar, Abdullah; McClain, Kenneth L; Olivieri, Nancy F; Porter, John B; Vichinsky, Elliott P

Age-related changes in adaptation to severe anemia in childhood in developing countries

发展中国家儿童时期对重度贫血适应性的年龄相关变化

O'Donnell, Angela; Premawardhena, A; Arambepola, M; Allen, S J; Peto, T E A; Fisher, C A; Rees, D C; Olivieri, Nancy F; Weatherall, D J