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

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

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 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

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

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

Alcohol consumption of patients with essential tremorRAUTAKORPI, I; MARTTILA, R. J; RINNE, U. K et al.Acta neurologica scandinavica. 1983, Vol 68, Num 3, pp 177-179, issn 0001-6314Article

Essential familial myoclonusPRZUNTEK, H; MUHR, H.Journal of neurology. 1983, Vol 230, Num 3, pp 153-162, issn 0340-5354Article

Zur Frage der Erblichkeit der Vitiligo = Le problème de l'hérédité du vitiligo = The question of heredity in vitiligoSALAMON, T; HADZISELIMOVIC, R; HALEPOVIC, E et al.Hautarzt. 1989, Vol 40, Num 3, pp 141-145, issn 0017-8470Article

Hereditary angio-edema (HAE)BLOK, P. H. H. M; BAARSMA, E. A.Journal of laryngology and otology. 1984, Vol 98, Num 1, pp 59-63, issn 0022-2151Article

Muscle weakness in an adult with infantile X-linked hypogammaglobulinemiaMONTANARO, A; BARDANA, E. J. JR.Annals of allergy. 1984, Vol 52, Num 3, pp 153-154, issn 0003-4738Article

Alcoholism in essential tremorKOLLER, W. C.Neurology. 1983, Vol 33, Num 8, pp 1074-1076, issn 0028-3878Article

Histochemical study of rectal aminergic nerves in type I familial amyloid polyneuropathyIKEDA, S; OGUCHI, K; KOBAYASHI, S et al.Neurology. 1983, Vol 33, Num 8, pp 1055-1058, issn 0028-3878Article

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