Chronic blood exchange transfusions in the management of pre-capillary pulmonary hypertension complicating sickle cell disease

M Turpin, C Chantalat-Auger, F Parent… - European …, 2018 - Eur Respiratory Soc
The long-term effects of chronic blood exchange transfusions (BETs) on pre-capillary
pulmonary hypertension complicating sickle cell disease (SCD) are unknown. 13 …

Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and …

C Préhu, S Pissard, M Al-Sheikh, C Le Niger… - …, 2005 - Taylor & Francis
We report two French Caucasian families suffering from dominant thalassemia-like
phenotypes due to hyper unstable hemoglobin (Hb) variants. In both cases, molecular …

VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis

A Lunati, A Petit, H Lapillonne… - American journal …, 2021 - pubmed.ncbi.nlm.nih.gov
VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of
dyserythropoiesis VPS4A mutation in syndromic congenital hemolytic anemia without obvious …

Ethical issues related to computerised family medical histories in sickle cell disease: Inforare

S Franrenet, N Duchange, F Galactéros… - Journal of medical …, 2010 - jme.bmj.com
The Inforare project aims to set up a system for the sharing of clinical and familial data, in
order to study how genes are related to the severity of sickle cell disease. While the …

Perinatal zidovudine prophylaxis in HIV type-1-infected pregnant women with thalassaemia carriage in Thailand

N Briand, S Pornprasert, N Ngo-Giang-Huong… - 2009 - journals.sagepub.com
Background To investigate a possible interaction between α-thalassaemia, β-thalassaemia
and haemoglobin-E trait and the haematological parameters of HIV type-1 (HIV-1)-infected …