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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

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

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

HEREDITARY PYROPOIKILOCYTOSIS AND ELLIPTOCYTOSIS: CLINICAL, LABORATORY, AND ULTRASTRUCTURAL FEATURES IN INFANTS AND CHILDRENPRCHAL JT; CASTLEBERRY RP; PARMLEY RT et al.1982; PEDIATRIC RESEARCH; ISSN 0031-3998; USA; DA. 1982; VOL. 16; NO 6; PP. 484-489; BIBL. 35 REF.Article

THE SPECTRIN MEMBRANE SKELETON OF NORMAL AND ABNORMAL HUMAN ERYTHROCYTES: A REVIEWGOODMAN SR; SHIFFER K.1983; AMERICAN JOURNAL OF PHYSIOLOGY. CELL PHYSIOLOGY; ISSN 0363-6143; USA; DA. 1983; VOL. 13; NO 2; PP. C121-C141; BIBL. 117 REF.Article

SPECTRIN BETA -CHAIN VARIANT ASSOCIATED WITH HEREDITARY ELLIPTOCYTOSISDHERMY D; LECOMTE MC; GARBARZ M et al.1982; J. CLIN. INVEST.; ISSN 0021-9738; USA; DA. 1982; VOL. 70; NO 4; PP. 707-715; BIBL. 39 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

HEREDITARY HEPATOSPLENOMEGALYCHENG DS; WILLIAMS HJ; KITAHARA M et al.1980; WEST. J. MED.; USA; DA. 1980; VOL. 132; NO 1; PP. 70-74; BIBL. 13 REF.Article

KLINISCHE DEMONSTRATIONEN = PRESENTATIONS CLINIQUESMARTI HR.1980; SCHWEIZ. MED. WOCHENSCHR.; ISSN 0036-7672; CHE; DA. 1980; VOL. 110; NO 49; PP. 1857-1863; BIBL. 34 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

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

SPECTRIN: STRUCTURE, FUNCTION, AND ABNORMALITIESKNOWLES W; MARCHESI SL; MARCHESI VT et al.1983; SEMINARS IN HEMATOLOGY; ISSN 0037-1963; USA; DA. 1983; VOL. 20; NO 3; PP. 159-174; BIBL. 69 REF.Article

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

PREVIOUSLY UNDESCRIBED SYNDROME OF CRANIOFACIAL, HAND ANOMALIES, AND SENSORINEURAL DEAFNESSSOMMER A; YOUNG WEE T; FRYE T et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 1; PP. 71-77; BIBL. 13 REF.Article

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

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