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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

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

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

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

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

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

HEREDITAERER NYSTAGMUS = NYSTAGMUS HEREDITAIRELISCH K.1980; KLIN. MONATSBL. AUGENHEILKD.; ISSN 0023-2165; DEU; DA. 1980; VOL. 177; NO 6; PP. 839-844; ABS. ENG; BIBL. 11 REF.Article

MOLECULAR DISEASES. WITH PARTICULAR REFERENCE TO THE HEMOGLOBINOPATHIES.YAMAMURA Y.1977; JAP. J. MED.; JAP.; DA. 1977; VOL. 16; NO 2; PP. 135-138Article

FAMILIAL SPASTIC PARAPLEGIA WITH KALLMANN'S SYNDROMETUCK RR; O'NEILL BP; GHARIB H et al.1983; JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1983; VOL. 46; NO 7; PP. 671-674; BIBL. 36 REF.Article

HEREDITARY DEAFNESS AND SENSORY RADICULAR NEUROPATHY.FITZPATRICK DB; HOOPER RE; SEIFE B et al.1976; ARCH. OTOLARYNGOL.; U.S.A.; DA. 1976; VOL. 102; NO 9; PP. 552-557; BIBL. 10 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

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

Association studies of erythoid α-spectrin at the tetramerization siteLAM, Vinh Q; ANTONIOU, Chloe; ROLIUS, Ramunas et al.British journal of haematology. 2009, Vol 147, Num 3, pp 392-395, issn 0007-1048, 4 p.Article

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

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

HEREDITARY DISORDERS OF RED CELL ENZYMES IN THE EMBDEN-MEYERHOF PATHWAYMIWA S.1983; AMERICAN JOURNAL OF HEMATOLOGY; ISSN 0361-8609; USA; DA. 1983; VOL. 14; NO 4; PP. 381-391; BIBL. 53 REF.Article

PHOSPHORYLATION OF CYTOCHROME-P-450-DEPENDENT MONOOXYGENASE COMPONENTS = PHOSPHORYLATION DE COMPOSANTS DE LA MONOOXYGENASE CYTOCHROME P-450 DEPENDANTEPYERIN W; WOLF CR; KINZEL V et al.1983; CARCINOGENESIS (LONDON); ISSN 0143-3334; GBR; DA. 1983; VOL. 4; NO 5; PP. 573-576; ABS. ENG; BIBL. 18 REF.; GRAPH, FIGArticle

BETA -THALASSEMIA-. SELECTED PSEUDOGENESSTEINBERG MH; ADAMS JG III.1982; MED. HYPOTHESES; ISSN 0306-9877; GBR; DA. 1982; VOL. 9; NO 6; PP. 599-604; BIBL. 38 REF.Article

CELLULAR HETEROGENEITY IN THE LATE-ONSET FORM OF HEREDITARY MELANOMAS IN THE XIPHOPHORUS FISH HYBRIDSOZATO K; WAKAMATSU Y.1981; DEV. GROWTH DIFFER.; ISSN 0012-1592; JPN; DA. 1981; VOL. 23; NO 3; PP. 273-285; BIBL. 29 REF.Article