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DOES ATP DECREASE EXPONENTIALLY DURING RED CELL AGING. A COMMENTARYFEO C.1975; NOUV. REV. FR. HEMATOL.; FR.; DA. 1975; VOL. 15; NO 6; PP. 633-635; BIBL. 3 REF.Article

RANSFORMATION DISCOCYTE-ECHINOCYTE. ROLE DE LA FORMATION DE LYSOLECITHINE DANS LE PLASMAFEO C.1972; NORW. REV. FR. HEMATOL.; FR.; DA. 1972; VOL. 12; NO 4; PP. 455-463; BIBL. 16REF.Serial Issue

A QUANTITATIVE STUDY OF THE RED CELL SHAPE CHANGES PRODUCED BY ANIONIC AND CATIONIC DERIVATIVES OF PHENOTHIAZINE. = ETUDE QUANTITATIVE DES CHANGEMENTS DE FORME DES HEMATIES PRODUITS PAR LES DERIVES ANIONIQUES ET CATIONIQUES DE LA PHENOTHIAZINENARLA MOHANDAS; FEO C.1975; BLOOD CELLS; GERM.; DA. 1975; VOL. 1; NO 2; PP. 375-384; BIBL. 16 REF.; (RED CELL FORM DEFORMABILITY. XV. CONGR. INT. SOC. HEMATOL. PROC. SYMP.; JERUSALEM; 1974)Conference Paper

STUDY OF STEATOSIS INDUCED IN THE RAT BY OROTIC ACID = ETUDE DE LA STEATOSE INDUITE CHEZ LE RAT PAR L'ACIDE OROTIQUEFEO C; GARCON E.1973; BIOMEDICINE; FR.; DA. 1973; VOL. 19; NO 2; PP. 61-64; ABS. FR.; BIBL. 33REF.Serial Issue

ROLE OF ATP DEPLETION ON RED CELL SHAPE AND DEFORMABILITY.FEO C; MOHANDAS N.1977; BLOOD CELLS; GERM.; DA. 1977; VOL. 3; NO 1; PP. 153-161; BIBL. 8 REF.Article

CLARIFICATION OF ROLE OF ATP IN RED-CELL MORPHOLOGY AND FUNCTION.FEO C; MOHANDAS N.1977; NATURE; G.B.; DA. 1977; VOL. 265; NO 5590; PP. 166-168; BIBL. 8 REF.Article

Etude de la déformabilité érythrocytaire par visco-diffractométrie (ektacytomètre) au cours des anémies hémolytiques constitutionnelles = Analysis of redblood cell deformability in hereditary hemolytic anemiasHERRERA, A; FEO, C. J.Nouvelle revue française d'hématologie. 1984, Vol 26, Num 3, pp 169-177, issn 0029-4810Article

SEPARATE MECHANISMS OF DEFORMABILITY LOSS IN ATP-DEPLETED AND CA-LOADED ERYTHROCYTESCLARK MR; MOHANDAS N; FEO C et al.1981; J. CLIN. INVEST.; ISSN 0021-9738; USA; DA. 1981; VOL. 67; NO 2; PP. 531-539; BIBL. 34 REF.Article

THE EFFECT OF CELL HYDRATION ON THE DEFORMABILITY OF NORMAL AND SICKLE ERYTHROCYTESGULLEY ML; ROSS DW; FEO C et al.1982; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1982; VOL. 13; NO 4; PP. 283-291; BIBL. 26 REF.Article

MESURE DE LA DEFORMABILITE CELLULAIRE EN FONCTION DE LA PRESSION D'OXYGENE DANS LA DEPRANOCYTOSE. RESULTATS DONNES PAR UNE METHODE VISCO-DIFFRACTOMETRIQUE (EKTACYTOMETRE)FEO C; JONES E; BESSIS M et al.1981; C.R. SEANCES ACAD. SCI., SER. 3, SCI. VIE; ISSN 0249-6313; FRA; DA. 1981; VOL. 293; NO 1; PP. 57-62; ABS. ENG; BIBL. 7 REF.Article

ECHINOCYTIC SENSITIVITY AND DEFORMABILITY OF HUMAN NEWBORN RED CELLSCOULOMBEL L; TCHERNIA G; FEO C et al.1982; BIOL. NEONATE; ISSN 0006-3126; CHE; DA. 1982; VOL. 42; NO 5-6; PP. 284-290; BIBL. 17 REF.Article

Herpesvirus-like DNA sequences in non-AIDS Kaposi's sarcomaDE LELLIS, L; FABRIS, M; CASSAI, E et al.The Journal of infectious diseases. 1995, Vol 172, Num 6, pp 1605-1607, issn 0022-1899Article

SpαI/78: a mutation of the αI spectrin domain in a white kindred with HE and HPP phenotypesLECOMTE, M.-C; GARBARZ, M; SAHR, K. E et al.Blood. 1989, Vol 74, Num 3, pp 1126-1133, issn 0006-4971Article

Spectrin nice (β220/216): a shortened β-chain variant associated with an increase of the αI/74 fragment in a case of elliptocytosisPOTHIER, B; MORLE, L; BOIVIN, P et al.Blood. 1987, Vol 69, Num 6, pp 1759-1765, issn 0006-4971Article

Severe recessive poikilocytic anaemia with a new spectrin α chain variantLECOMTE, M. C; FEO, C; GAUTERO, H et al.British journal of haematology. 1990, Vol 74, Num 4, pp 497-507, issn 0007-1048, 11 p.Article

Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemiaPOTHIER, B; MORLE, L; FAVRE-GILLY, J et al.British journal of haematology. 1987, Vol 66, Num 3, pp 393-400, issn 0007-1048Article

Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemiaMORLE, L; POTHIER, B; BOIVIN, P et al.European journal of haematology. 1987, Vol 38, Num 5, pp 447-455, issn 0902-4441Article

Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family: transmission of the same molecular defect in spectrin through three generations with different clinical expressionLECOMTE, M. C; DHERMY, D; GARBARZ, M et al.Human genetics. 1987, Vol 77, Num 4, pp 329-334, issn 0340-6717Article

When CHIVA treatment could be video guided. CommentaryZAMBONI, P; MARCELLINO, M. G; FEO, C et al.Dermatologic surgery. 1995, Vol 21, Num 7, pp 621-626, issn 1076-0512Conference Paper

Abnormal rheological response of erythrocytes caused by nitroimidazoles and hyperthermiaRYBCZYNSKA, M; FEO, C; MARDEN, M et al.International journal of hyperthermia. 1993, Vol 9, Num 2, pp 313-323, issn 0265-6736Article

Hereditary pyropoikilocytosis and elliptocytosis in a white french family with the spectrin αI/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin αI domainGARBARZ, M; LECOMTE, M.-C; FORGET, B. G et al.Blood. 1990, Vol 75, Num 8, pp 1691-1698, issn 0006-4971, 8 p.Article

Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-associationTSE, W. T; LECOMTE, M.-C; COSTA, F. F et al.The Journal of clinical investigation. 1990, Vol 86, Num 3, pp 909-916, issn 0021-9738Article

Hemoglobin J guantanamo [α2β2 128 (H6) Ala→Asp] in association with hemoglobin C and α-thalassemia in a family from beninWAJCMAN, H; BAUDIN-CHICH, V; GALACTEROS, F et al.American journal of hematology. 1988, Vol 28, Num 3, pp 170-175, issn 0361-8609Article

Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrinDHERMY, D; FEO, C; GARBARZ, M et al.Prenatal diagnosis. 1987, Vol 7, Num 7, pp 471-483, issn 0197-3851Article

Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosisLECOMTE, M.-C; DHERMY, D; BOIVIN, P et al.Human genetics. 1985, Vol 71, Num 4, pp 351-357, issn 0340-6717Article

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