J. Riou

Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack

Nosocomial Meningococcemia in a Physician

The β-Thalassemias

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations

Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group

Inducible Nitric Oxide Synthase Mediates Prostaglandin H2 Synthase Nitration and Suppresses Eicosanoid Production

Nitric Oxide and Peroxynitrite in Health and Disease

Incidence of Chronic Thromboembolic Pulmonary Hypertension after Pulmonary Embolism

Clonal descent and microevolution of Neisseria meningitidis during 30 years of epidemic spread

CHRONIC THROMBOEMBOLIC PULMONARY HYPERTENSION

Is pulmonary embolism a common cause of chronic pulmonary hypertension? Limitations of the embolic hypothesis

Sickle-cell disease

Stroke recurrence in children with sickle cell disease treated with hydroxyurea following first clinical stroke

Abnormal hemoglobins with high oxygen affinity and erythrocytosis

2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association

Gut Microbiota in Health and Disease

Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set

Multilocus sequence typing: A portable approach to the identification of clones within populations of pathogenic microorganisms

Management of Massive and Submassive Pulmonary Embolism, Iliofemoral Deep Vein Thrombosis, and Chronic Thromboembolic Pulmonary Hypertension

Novel Diagnostic Algorithm for Identification of Mycobacteria Using Genus-Specific Amplification of the 16S-23S rRNA Gene Spacer and Restriction Endonucleases

Chronic Thromboembolic Pulmonary Hypertension

2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Health Care Settings

Developmental genetics of the human haemoglobins

New approaches to typing and identification of bacteria using the 16S-23S rDNA spacer region

An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age

Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes.

Neonatal screening for sickle cell disease in France

Characterization of serogroup ANeisseria meningitidisstrains by rRNA gene restriction patterns and PCR: Correlation with the results of serotyping, subtyping and multilocus enzyme electrophoresis

Hb Montfermeil [β 130(H8) Tyr→Cys]: suggests a key role for the interaction between helix A and H in oxygen affinity of the hemoglobin molecule

Hb Saint Nazaire (β103[G5]Phe→Ile): A new example of polycythemia due to a hemoglobin variant with increased oxygen affinity

Geographic distribution of 119 alleles of the alpha and beta globin genes detected in 432 French Caucasian carriers of haemoglobin variant.

Pulmonary thromboendarterectomy for chronic thromboembolic obstruction of the pulmonary artery in piglets

Hb Neuilly-Sur-Marne, a New Human Hemoglobin Variant with Ser-Asp-Leu Inserted between α86(F7) Leu and α87(F8) His: Characterization by High-Energy Collision-Induced Dissociation Liquid Secondary Ion Mass Spectrometry and Low Energy Collision-Induced Dissociation Tandem Mass Spectrometry in An Ion Trap Fitted with a Nanospray Ionization Source

Structural and functional studies of hemoglobin Poissy a₂β₂56 (D7) Gly → Arg and 86 (F2) Ala → Pro

Enzyme electrophoresis, sero- and subtyping, and outer membrane protein characterization of two Neisseria meningitidis strains involved in laboratory-acquired infections

Cation-exchange HPLC evaluated for presumptive identification of hemoglobin variants

Genetic regulation of ? gene expression: Study of the interaction of ?-thalassemia with heterocellular HPFH

Cation-exchange HPLC evaluated for presumptive identification of hemoglobin variants.