H. Gautero

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Superoxide Dismutase, Catatase, and Glutathione Peroxidase in Red Blood Cells from Patients with Malignant Diseases1

P. Boivin, C. Auclair, D. Dhermy, 2006 .

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes.

F. Galibert, B. Grandchamp, I. Devaux, 1989, Blood.

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.

F. Galibert, I. Devaux, C. Féo, 1990, Blood.

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

B. Forget, P. Gallagher, I. Devaux, 1996, British journal of haematology.

Spectrin self-association site: characterization and study of beta-spectrin mutations associated with hereditary elliptocytosis.

C. Craescu, G. Nicolas, M. Lecomte, 1998, The Biochemical journal.

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis.

C. Féo, P. Boivin, M. Lecomte, 1986, Blood.

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

C. Féo, P. Boivin, M. Lecomte, 1986 .

Superoxide dismutase, catalase, and glutathione peroxidase in red blood cells from patients with malignant diseases.

P. Boivin, C. Auclair, R. Gonzales, 1984, Cancer research.

Spectrin pTandil , a Novel Shortened P-Chain Variant Associated With Hereditary Elliptocytosis Is Due to a Deletional Frameshift Mutation in the f 3-Spectrin Gene

P. Boivin, M. Lecomte, C. Galand, 2003 .

Effects of salicylate-copper complex on the metabolic activation in phagocytizing granulocytes.

P. Boivin, C. Auclair, H. Gautero, 1980, Biochemical pharmacology.

Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin αI variants

P. Boivin, M. Lecomte, D. Dhermy, 1993, British journal of haematology.

Abnormal tryptic peptide from the spectrin α‐chain resulting from α‐ or β‐chain mutations: two genetically distinct forms of the Sp αI/74 variant

P. Boivin, M. Lecomte, D. Dhermy, 1990 .

Severe recessive poikilocytic anaemia with a new spectrin α chain variant

C. Féo, P. Boivin, M. Lecomte, 1990 .

Molecular Defect of Spectrin in the Family of a Child with Congenital Hemolytic Poikilocytic Anemia

F. Gretillat, A. Herrera, C. Féo, 1984, Pediatric Research.

Hereditary elliptocytosis with a spectrin molecular defect in a white patient.

P. Boivin, M. Lecomte, D. Dhermy, 1984, Acta haematologica.

Spectrin beta-chain variant associated with hereditary elliptocytosis.

J. Delaunay, C. Féo, P. Boivin, 1982, The Journal of clinical investigation.

Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene.

L. Feldman, P. Boivin, M. Lecomte, 1992, Blood.

Elliptocytosis‐associated spectrin Rouen (β220/218) has a truncated but still phosphorylatable β chain

P. Boivin, M. Lecomte, J. Vannier, 1992 .

elliptocytosis A new abnormal variant of spectrin in black patients with hereditary

C. Féo, P. Boivin, M. Lecomte, 2011 .

homozygous elliptocytosis Double inheritance of an alpha I/65 spectrin variant in a child with

C. Féo, P. Boivin, M. Lecomte, 2011 .

Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosis

P. Boivin, M. Lecomte, D. Dhermy, 1986, Human Genetics.

Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis

C. Féo, P. Boivin, M. Lecomte, 2004, Human Genetics.

Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin

C. Féo, F. Daffos, F. Forestier, 1987, Prenatal diagnosis.

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.

C. Féo, P. Boivin, M. Lecomte, 1985, Blood.

Spectrin f-Chain Variant Associated with Hereditary

J., C. Féo, M. Lecomte, 2022 .

Inhibition of Phospholipase D Activity by Fodrin

P. Marin, J. Mira, M. Lecomte, 1996, The Journal of Biological Chemistry.

Hereditary Pyropoikilocytosis and Elliptocytosis in a White French Family (Arg to His) at Position 22 of the Spectrin a1 Domain With the Spectrin Variant Related to a CGT to CAT Codon Change

F. Galibert, B. Forget, I. Devaux, 2016 .

domain codon change (Arg to His) at position 22 of the spectrin alpha I family with the spectrin alpha I/74 variant related to a CGT to CAT Hereditary pyropoikilocytosis and elliptocytosis in a white French

F. Galibert, I. Devaux, C. Féo, 2013 .

Impaired in vitro bactericidal power of polymorphonuclear leukocytes in patients with protein calorie malnutrition.

J. Belghiti, P. Boivin, H. Gautero, 1983, Surgery, gynecology & obstetrics.

Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family

C. Féo, P. Boivin, M. Lecomte, 1987, Human Genetics.

In vitro effect of benzodiazepines on polymorphonuclear leukocyte oxidative activity.

J. Belghiti, P. Boivin, H. Gautero, 1984, Anesthesiology.

Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 cases.

C. Féo, P. Boivin, M. Lecomte, 1986, Nouvelle revue francaise d'hematologie.

Heterogeneous phosphorylation of erythrocyte spectrin beta chain in intact cells.

M. Lecomte, D. Dhermy, H. Gautero, 1993, The Biochemical journal.

with HE and HPP phenotypes Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred

F. Galibert, B. Grandchamp, I. Devaux, 2011 .

Method of site-directed mutagenesis using long primer-unique site elimination and exonuclease III.

G. Nicolas, H. Gautero, S. Pedroni, 1997, BioTechniques.

Severe recessive poikilocytic anaemia with a new spectrin alpha chain variant.

C. Féo, P. Boivin, M. Lecomte, 1990, British journal of haematology.

Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variant.

P. Boivin, M. Lecomte, D. Dhermy, 1990, British journal of haematology.