Elliptocytose héréditaire avec poïkilocytose transitoire de l'enfant = Hereditary elliptocytosis with transient poikilocytosis in childrenGRETILLAT, F; DELEPINE, N; DESBOIS, J. C et al.La Presse médicale (1983). 1983, Vol 12, Num 44, issn 0755-4982, 2823Article

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

Spectrin Tunis (α^1/78): 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

Grothendieck groups and tilting objectsREITEN, Idun; VAN DEN BERGH, Michel.Algebras and representation theory. 2001, Vol 4, Num 1, pp 1-23, issn 1386-923XArticle

Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin α-subunitLAWLER, J; PALEK, J; SHIH-CHUN LIU et al.Blood. 1983, Vol 62, Num 6, pp 1182-1189, issn 0006-4971Article

Hereditary continuous muscle fiber activityMCGUIRE, S. A; TOMASOVIC, J. J; ACKERMAN, N. JR et al.Archives of neurology (Chicago). 1984, Vol 41, Num 4, pp 395-396, issn 0003-9942Article

Identification of the hereditary pyropoikilocytosis carrier stateMENTZER, W. C; TURETSKY, T; MOHANDAS, N et al.Blood. 1984, Vol 63, Num 6, pp 1439-1446, issn 0006-4971Article

Familial acromegalyJONES, M. K; EVANS, P. J; JONES, I. R et al.Clinical endocrinology (Oxford. Print). 1984, Vol 20, Num 3, pp 355-358, issn 0300-0664Article

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

RED PULP OF THE SPLEEN IN HEREDITARY ELLIPTOCYTOSIS.SHNEIDMAN D; KIESSLING P; ONSTAD J et al.1977; VIRCHOWS ARCH., A; DTSCH.; DA. 1977; VOL. 372; NO 4; PP. 337-342; BIBL. 7 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

Disorders of red cell membraneXIULI AN; MOHANDAS, Narla.British journal of haematology. 2008, Vol 141, Num 3, pp 367-375, issn 0007-1048, 9 p.Conference Paper

L'elliptocytose héréditaire en Afrique de l'Ouest: fréquence et répartition des variants de la spectrine = Hereditary elliptocytosis in West Africa: frequency and repartition of spectrine variantsLECOMTE, M.-C; DHERMY, D; GAUTERO, H et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1988, Vol 306, Num 2, pp 43-46, issn 0764-4469Article

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosisLANE, P. A; SHEW, R. L; IAROCCI, T. A et al.The Journal of clinical investigation. 1987, Vol 79, Num 3, pp 989-996, issn 0021-9738Article

How I treat heterozygous hereditary antithrombin deficiency in pregnancyBRAMHAM, Kate; RETTER, Andrew; ROBINSON, Susan E et al.Thrombosis and haemostasis. 2013, Vol 110, Num 3, pp 550-559, issn 0340-6245, 10 p.Article

Mild elliptocytosis associated with the α34 Arg→Trp mutation in spectrin genova (α^I/74)PERROTTA, S; MIRAGLIA DEL GIUDICE, E; ALLOISIO, N et al.Blood. 1994, Vol 83, Num 11, pp 3346-3349, issn 0006-4971Article

Interactions of spectrin in hereditary elliptocytes containing truncated spectrin β-chainsEBER, S. W; MORRIS, S. A; SCHRÖTER, W et al.The Journal of clinical investigation. 1988, Vol 81, Num 2, pp 523-530, issn 0021-9738Article

Gerbich reactivity in 4.1(-) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiencySONDAG, D; ALLOISIO, N; BLANCHARD, D et al.British journal of haematology. 1987, Vol 65, Num 1, pp 43-50, issn 0007-1048Article

Abnormal electrophoretic mobility of spectrin tetramers in hereditary elliptocytosisDHERMY, D; GARBARZ, M; LECOMTE, M.-C et al.Human genetics. 1986, Vol 74, Num 4, pp 363-367, issn 0340-6717Article

Spα^I/65 Hereditary elliptocytosis in North AfricaALLOISIO, N; GUETARNI, D; MORCE, L et al.American journal of hematology. 1986, Vol 23, Num 2, pp 113-122, issn 0361-8609Article

Vers une définition moléculaire des maladies de la membrane érythrocytaire = Towards a molecular definition of diseases of the erythrocyte membraneBOIVIN, P.Actualités hématologiques. 1983, Vol 17, pp 26-35, issn 0567-8757Article

Double frameshift mutations in APC and MSH2 in the same individualSORAVIA, Claudio; DELOZIER, Celia D; DOBBIE, Zuzana et al.International journal of colorectal disease (Print). 2006, Vol 21, Num 1, pp 79-83, issn 0179-1958, 5 p.Article

Abnormal spectrin in hereditary elliptocytosisMARCHESI, S. L; KNOWLES, W. J; MORROW, J. S et al.Blood. 1986, Vol 67, Num 1, pp 141-151, issn 0006-4971Article

An inclusion principle for hereditary systemsOHTA, Y; SILJAK, D. D.Journal of mathematical analysis and applications. 1984, Vol 98, Num 2, pp 581-598, issn 0022-247XArticle