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Results 1 to 25 of 160

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FAMILIENUNTERSUCHUNGEN BEI HEREDITAERER ELLIPTOZYTOSE = EXPLORATION FAMILIALE L'ELLIPTOCYTOSE HEREDITAIREHEILMANN E; ERHART R; NEUMANN KH et al.1980; FOLIA HAEMATOL.; DDR; DA. 1980; VOL. 107; NO 3; PP. 385-390; ABS. ENG/FRE/RUS; BIBL. 24 REF.Article

ELLIPTOCYTOSE CONSTITUTIONNELLEGAUDELUS J; DANDINE M; NATHANSON M et al.1983; MEDECINE INFANTILE; ISSN 0025-6773; FRA; DA. 1983; VOL. 90; NO 2; PP. 193-200; BIBL. 41 REF.Article

ELLIPTOCYTOSE CONSTITUTIONNELLE AU SENEGAL. ETUDE DE 5 CAS, DONT L'UN A NECESSITE UNE SPLENECTOMIEDERRIEN JP; GAULTIER Y; LARTISIEN D et al.1978; BULL. SOC. MED. AFR. NOIRE LANGUE FR.; SEN; DA. 1978; VOL. 23; NO 3; PP. 276-281; BIBL. 32 REF.Article

HAEMOGLOBIN LEPORE BOSTON AND ELLIPTOCYTOSIS IN A FAMILY OF INDONESIAN-GERMAN ANCESTRY = HEMOGLOBINE LEPORE BOSTON ET ELLIPTOCYTOSE DANS UNE FAMILLE D'ORIGINE INDONESIENNE ET ALLEMANDEWENT LN; DE SONG WW; BOS SE et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 1; PP. 83-88; BIBL. 1 P.Article

A TECHNIQUE TO DETECT REDUCED MECHANICAL STABILITY OF RED CELL MEMBRANES: RELEVANCE TO ELLIPTOCYTIC DISORDERSMOHANDAS N; CLARK MR; HEALTH BP et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 59; NO 4; PP. 768-774; BIBL. 27 REF.Article

THE ROLE OF THE SPLEEN IN THE PATHOPHYSIOLOGY OF HEREDITARY SPHEROCYTOSIS AND HEREDITARY ELLIPTOCYTOSISLUSHER JM; BARNHART MI.1980; AM. J. PEDIATR. HEMATOL.-ONCOL.; USA; DA. 1980; VOL. 2; NO 1; PP. 31-39; BIBL. 43 REF.Article

DEFECTIVE SPECTRIN DIMER-DIMER ASSOCIATION IN A FAMILY WITH TRANSFUSION DEPENDENT HOMOZYGOUS HEREDITARY ELLIPTOCYTOSISEVANS JPM; BAINES AJ; HANN LM et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 54; NO 2; PP. 163-172; BIBL. 25 REF.Article

THE MODE OF INHERITANCE OF OVALOCYTOSIS/ELLIPTOCYTOSIS IN MALAYSIAN ORANG ASLI FAMILIESFIX AG; BAER AS; LIE INJO LE et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 3; PP. 250-253; BIBL. 22 REF.Article

PREMIERE OBSERVATION DE L'ABSENCE D'UNE PROTEINE DE LA MEMBRANE ERYTHROCYTAIRE (BANDE 41) DANS UN CAS D'ANEMIE ELLIPTOCYTAIRE FAMILIALEFEO CJ; FISCHER S; PIAU JP et al.1980; NOUV. REV. FR. HEMATOL.; ISSN 0029-4810; FRA; DA. 1980; VOL. 22; NO 4; PP. 315-325; ABS. ENG; BIBL. 12 REF.Article

SELECTIVE DEPRESSION OF BLOOD GROUP ANTIGENS ASSOCIATED WITH HEREDITARY OVALOCYTOSIS AMONG MELANESIANS.BOOTH PB; SERJEANTON S; WOODFIELD DG et al.1977; VOX SANG.; SUISSE; DA. 1977; VOL. 32; NO 2; PP. 99-110; BIBL. 14 REF.Article

FINE STRUCTURES OF THE SPLEEN IN HEREDITARY ELLIPTOCYTOSIS.MATSUMOTO N; ISHIHARA T; TAKAHASHI M et al.1976; ACTA PATHOL. JAP.; JAP.; DA. 1976; VOL. 26; NO 5; PP. 533-542; BIBL. 16 REF.Article

OSMOTIC RESISTANCE OF ABNORMAL RED CELLS EXPOSED TO LEAD IN VITRO = RESISTANCE OSMOTIQUE D'HEMATIES PATHOLOGIQUES EXPOSEES AU PLOMB, IN VITROQAZI QH; SUAT CHENG GO; SMITH WICK EM et al.1972; BRIT. J. HAEMATOL.; G.B.; DA. 1972; VOL. 23; NO 5; PP. 631-633; BIBL. 8 REF.Serial Issue

STUDIO DI UN CASO DI ELLISSOCITOSI EREDITARIA IN UNA BAMBINA MARCHIGIANA = ETUDE D'UN CAS D'ELLIPSOCYTOSE HEREDITAIRE CHEZ UNE ENFANT DES MARCHESBARTOLOTTA E; GIACOMOZZI E; BALDONI ME et al.1979; CLIN. PEDIATR.; ITA; DA. 1979; VOL. 60; NO 9; PP. 456-462; ABS. ENG; BIBL. 30 REF.Article

L'ELLIPTOCYTOSE CONSTITUTIONNELLE. A PROPOS D'UN CAS FAMILIAL. COMMENTAIRES SUR LA TRANSMISSION GENETIQUE ET LA LIAISON AVEC LE GROUPE RHESUSBENTEGEAT J; VERGER P; BOISSEAU M et al.1973; SEM. HOP., ANN. PEDIATR.; FR.; DA. 1973; VOL. 49; NO 4; PP. 317-328; ABS. ANGL. ESP. ALLEM.; BIBL. 1P.1/2Serial Issue

HEREDITARY ELLIPTOCYTOSIS WITH PROTEIN BAND 4.1 DEFICIENCY IN THE DOGSMITH JE; MOORE K; ARENS M et al.1983; BLOOD; ISSN 0006-4971; USA; DA. 1983; VOL. 61; NO 2; PP. 373-377; BIBL. 32 REF.Article

ELLIPTOCYTOSIS: LINKAGE STUDY IN A FAMILY = ELLIPTOCYTOSE: ETUDE DES LIAISONS DANS UNE FAMILLESERVILLE F; BENTEGEAT J; VERGER P et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 49-51; BIBL. 14REF.Article

INCREASED HEAT SENSITIVITY OF RED BLOOD CELLS IN HEREDITARY ELLIPTOCYTOSIS WITH ACQUIRED COBALAMIN (VITAMIN B12) DEFICIENCYSCHOOMAKER ER; BUTLER WM; DIEHL LF et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 59; NO 6; PP. 1213-1219; BIBL. 23 REF.Article

AUTO-IMMUNE HAEMOLYTIC ANAEMIA COMPLICATING INFECTIOUS MONONUCLEOSIS IN A PATIENT WITH HEREDITARY ELLIPTOCYTOSIS.HO YEN DO.1978; ACTA HAEMATOL.; SUISSE; DA. 1978; VOL. 59; NO 1; PP. 45-52; BIBL. 17 REF.Article

ON THE ORIENTATION OF THE RH:EL1 LINKAGE GROUP.COOK PJL; NOADES JE; NEWTON MS et al.1977; ANN. HUM. GENET.; G.B.; DA. 1977; VOL. 41; NO 2; PP. 157-162; BIBL. 10 REF.Article

Spectrin Oran (αII/21), a new spectrin variant concerning the αII domain and causing severe elliptocytosis in the homozygous stateALLOISIO, N; MORLE, L; POTHIER, B et al.Blood. 1988, Vol 71, Num 4, pp 1039-1047, issn 0006-4971Article

Spectrin Tunis (α1/78): a new αI variant that causes asymptomatic hereditary elliptocytosis in the heterozygous stateMORLE, L; ALLOISIO, N; DUCLUZEAU, M. T et al.Blood. 1988, Vol 71, Num 2, pp 508-511, issn 0006-4971Article

Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisCOETZER, T; LAWLER, J; PRCHAL, J. T et al.Blood. 1987, Vol 70, Num 3, pp 766-772, issn 0006-4971Article

GENETIC FACTORS AND MALARIA IN THE TEMUANBAER A; LIE INJO LE; WELCH QB et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 2; PP. 179-188; BIBL. 26 REF.Article

Mutant forms of spectrin α-subunits in hereditary elliptocytosisMARCHESI, S. L; LETSINGER, J. T; SPEICHER, D. W et al.The Journal of clinical investigation. 1987, Vol 80, Num 1, pp 191-198, issn 0021-9738Article

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in transALLOISIO, N; MORLE, L; DELAUNAY, J et al.The Journal of clinical investigation. 1991, Vol 87, Num 6, pp 2169-2177, issn 0021-9738Article

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