RED CELL MEMBRANE SKELETAL DEFECTS IN HEREDITARY AND ACQUIRED HEMOLYTIC ANEMIASPALEK J; LUX SE.1983; SEMINARS IN HEMATOLOGY; ISSN 0037-1963; USA; DA. 1983; VOL. 20; NO 3; PP. 189-224; BIBL. 224 REF.Article

INHERITED DISORDERS OF THE RED CELL MEMBRANE SKELETONLUX SE; WOLFE LC.1980; PEDIATR. CLIN. N. AMER.; USA; DA. 1980; VOL. 27; NO 2; PP. 463-486; BIBL. 136 REF.Article

MEMBRANE PROTEIN PHOSPHORYLATION OF INTACT NORMAL AND HEREDITARY SPHEROCYTIC ERYTHROCYTESWOLFE LC; LUX SE.1978; J. BIOL. CHEM.; USA; DA. 1978; VOL. 253; NO 9; PP. 3336-3342; BIBL. 52 REF.Article

ISOLATION AND PARTIAL CHARACTERIZATION OF A HIGH MOLECULAR WEIGHT RED CELL MEMBRANE PROTEIN COMPLEX NORMALLY REMOVED BY THE SPLEEN.LUX SE; JOHN KM.1977; BLOOD; U.S.A.; DA. 1977; VOL. 50; NO 4; PP. 625-641; BIBL. 2 P.Article

NUTRITIONAL ANEMIAS OF CHILDHOODWOLFE LC; LUX SE IV.1979; PEDIATR. ANN.; USA; DA. 1979; VOL. 8; NO 7; PP. 38-52; (9 P.); BIBL. 3 REF.Article

DIMINISHED SPECTRIN EXTRACTION FROM ATP-DEPLETED HUMAN ERYTHROCYTES. EVIDENCE RELATING SPECTRIN TO CHANGES IN ERYTHROCYTE SHAPE AND DEFORMABILITY.LUX SE; JOHN KM; UKENA TE et al.1978; J. CLIN. INVEST.; U.S.A.; DA. 1978; VOL. 61; NO 3; PP. 815-827; BIBL. 2 P.Article

EXERCISE-INDUCED HEMOLYSIS IN XEROCYTOSIS: ERYTHROCYTE DEHYDRATION AND SHEAR SENSITIVITYPLATT OS; LUX SE; NATHAN DG et al.1981; J. CLIN. INVEST.; ISSN 0021-9738; USA; DA. 1981; VOL. 68; NO 3; PP. 631-638; BIBL. 38 REF.Article

COMPARISON OF THE PHOSPHORYLATION OF HUMAN ERYTHROCYTE SPECTRIN IN THE INTACT RED CELL AND IN VARIOUS CELL-FREE SYSTEMSHARRIS HW JR; LEVIN N; LUX SE et al.1980; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1980; VOL. 255; NO 23; PP. 11521-11525; BIBL. 31 REF.Article

STUDIES ON THE PROTEIN DEFECT IN TANGIER DISEASE. ISOLATION AND CHARACTERIZATION OF AN ABNORMAL HIGH DENSITY LIPOPROTEIN = RECHERCHES SUR LE DEFICIT PROTEIQUE DANS LA MALADIE DE TANGER. ISOLEMENT ET CARACTERISATION D'UNE LIPOPROTEINE DE DENSITE ANORMALEMENT ELEVEELUX SE; LEVY RI; GOTTO AM et al.1972; J. CLIN. INVEST.; U.S.A.; DA. 1972; VOL. 51; NO 10; PP. 2505-2519; BIBL. 63REF.Serial Issue

A GENETIC DEFECT IN THE BINDING OF PROTEIN 4.1 TO SPECTRIN IN KINDRED WITH HEREDITARY SPHEROCYTOSISWOLFE LC; JOHN KM; FALCONE JC et al.1982; NEW ENGLAND JOURNAL OF MEDICINE; ISSN 0028-4793; USA; DA. 1982; VOL. 307; NO 22; PP. 1367-1374; BIBL. 39 REF.Article

IMMUNOFLUORESCENCE STUDIES OF APOLIPOPROTEIN B IN INTESTINAL MUCOSA: ABSENCE IN ABETALIPOPROTEINEMIAGLICKMAN RM; GREEN PHR; LEES RS et al.1979; GASTROENTEROLOGY; USA; DA. 1979; VOL. 76; NO 2; PP. 288-292; BIBL. 30 REF.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

DIETARY AND DRUG TREATMENT OF PRIMARY HYPERLIPOPROTEINEMIA = TRAITEMENT DIETETIQUE ET MEDICAMENTEUX DE L'HYPERLIPOPROTEINEMIE PRIMITIVELEVY RI; FREDRICKSON DS; SHULMAN R et al.1972; ANN. INTERN. MED.; U.S.A.; DA. 1972; VOL. 77; NO 2; PP. 267-294; BIBL. 2 P. 1/2Serial Issue