The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

R Rosa, Marie‐Odette Préhu, Yves Beuzard, +1

Journal of Clinical Investigation

Iron DeficiencyRedox BiologyOxidative StressAnemiaLaboratory Hematology +15

The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites

EF Jr Roth, MC Calvin, Isabelle Max‐Audit, +2

Blood

Diphosphoglycerate mutase and 2,3-diphosphoglycerate phosphatase activities of red cells: Comparative electrophoretic study

R Rosa, Josette Gaillardon, J. Rosa

Biochemical and Biophysical Research Communications

BiochemistryBioelectrochemistryNatural SciencesPhysiologyBioanalysis +10

A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemia

R Rosa, C George, M Fardeau, +3

Blood

Evidence for three enzymatic activities in one electrophoretic band of 3-phosphoglycerate mutase from red cells

R Rosa, Isabelle Max Audit, Jean Rosa

Biochimie

Cellular EnzymologyBiochemistryBioenergeticsElectrophoretic BandBioanalysis +9

Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequence.

V. Joulin, Jean Péduzzi, Paul‐Henri Roméo, +6

The EMBO Journal

MedicineGeneticsMolecular GeneticsMolecular CloningGene Expression +2

IgM monoclonal antibody against terminal moiety of GM2, GalNAc-GD1a and GalNAc-GM1b from a pure motor chronic demyelinating polyneuropathy patient: effects on neurotransmitter release

Nicolau Ortiz, R Rosa, Eduard Gallardo, +4

Journal of Neuroimmunology

Igm Monoclonal AntibodyPure MotorAmyotrophic Lateral SclerosisAutoimmune DiseaseNeurological Disorder +10

Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes: PGK Creteil and PGK Amiens

Martine Cohen‐Solal, C Valentin, François Plassa, +4

Blood

Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency

Valérie Lemarchandel, V. Joulin, C Valentin, +4

Blood

Nuerological finding in triosephosphate isomerase deficiency

Bwee Tien Poll‐The, Jean Aicardi, Robert Girot, +1

Annals of Neurology