DISORDERS DUE TO ENZYME DEFECTS IN THE RED BLOOD CELL = DESORDRES PROVOQUES PAR DES DEFICITS ENZYMATIQUES DANS LES GLOBULES ROUGESBEUTLER E.1972; ADV. METABOL. DISORD.; U.S.A.; DA. 1972; VOL. 6; PP. 131-160; BIBL. 6P.Serial Issue

RED CELL ENZYME DEFICIENCIES AS A CAUSE OF HEMOLYTIC DISORDERS = LES DEFICIENCES DES ENZYMES ERYTHROCYTAIRES COMME CAUSE DE TROUBLES HEMOLYTIQUESVALENTINE WN.1972; ANNU. REV. MED.; U.S.A.; DA. 1972; VOL. 23; PP. 93-100; BIBL. 34REF.Serial Issue

THE GENETIC MUCOPOLYSACCHARIDOSES = LES MUCOPOLYSACCHARIDOSES GENETIQUESGROOVER RV; BURKE EC; GORDON H et al.1972; SEMINARS HEMATOL.,; U.S.A.; DA. 1972; VOL. 9; NO 4; PP. 371-402; BIBL. 5P.Serial Issue

THE HEREDITARY HEMOLYTIC ANAEMIAS. MEMBRANE AND ENZYME DEFECTS = LES ANEMIES HEMOLYTIQUES HEREDITAIRES: ANOMALIES DES MEMBRANES ET DES ENZYMESMILLER DR.1972; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1972; VOL. 19; NO 4; PP. 865-887; BIBL. 3 P. 1/2Serial Issue

COMPLETE DEFICIENCY OF LEUKOCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE WITH DEFECTIVE BACTERICIDAL ACTIVITY = DEFICIENCE COMPLETE DE G6PD LEUCOCYTAIRE AVEC ACTIVITE BACTERICIDE DEFECTUEUSE1972; J. CLINIC. INVEST.; U.S.A.; DA. 1972; VOL. 51; NO 4; PP. 769-778; BIBL. 1P.1/2Serial Issue

GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCYJAIN KK; CHOPRA PK.1972; INDIAN PEDIATR.; INDIA; DA. 1972; VOL. 9; NO 2; PP. 110-113; BIBL. 5REF.Serial Issue

LIVER DISEASE IN ADULTS WITH ALPHA₁-ANTITRYPSIN DEFICIENCY = LESIONS HEPATIQUES CHEZ LES ADULTES ATTEINTS DE DEFICIT EN ALPHA₁-ANTITRYPSINEBERG NO; ERIKSSON S.1972; NEW ENGL. J. MED.; U.S.A.; DA. 1972; VOL. 287; NO 25; PP. 1264-1267; BIBL. 16REF.Serial Issue

BASES MOLECULAIRES DES MALADIES ENZYMATIQUES GENETIQUESDREYFUS JC.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 559-571; ABS. ANGL.; BIBL. 1P.Serial Issue

LACTASE DEFICIENCY IN MEXICAN-AMERICAN MALES = CARENCE EN LACTASE CHEZ LES HOMMES MEXICAINS D'AMERIQUEDILL JE; LEVY M; WELLS RF et al.1972; AMER. J. CLIN. NUTRIT.; U.S.A.; DA. 1972; VOL. 25; NO 9; PP. 869-870; BIBL. 11 REF.Serial Issue

THE EFFECT OF COPPER ON THE ERYTHROCYTE HEXOSE MONOPHOSPHATE SHUNT PATHWAY = L'EFFET DU CUIVRE SUR LA VOIE DE L'HEXOSE MONOPHOSPHATE DU GLOBULE ROUGEMETZ EN; SAGONE AL JR.1972; J. LAB. CLIN. MED.; U.S.A.; DA. 1972; VOL. 80; NO 3; PP. 405-413; BIBL. 1P.1/2Serial Issue

DIAGNOSTICA ENZIMATICA DELLE GLICOLIPIDOSI = DIAGNOSTIC ENZYMATIQUE DES GLYCOLIPIDOSESZAMBOTTI V; DI DONATO S; RIMOLDI M et al.1972; QUAD. SCLAVO DIAGNOST. CLIN. LAB.; ITAL.; DA. 1972; VOL. 8; NO 1; PP. 183-198; ABS. ANGL.; BIBL. 13REF.Serial Issue

ASPECTS STOMATOLOGIQUES D'UNE HYPOPHOSPHATASIE A FORME BENIGNEAJACQUES JC.1973; ANN. ODONTO-STOMATOL.; FR.; DA. 1973; VOL. 30; NO 1; PP. 49-56; BIBL. 15 REF.Serial Issue

L'INSUFFISANCE DE LA GLUCOSE PHOSPHATE-6 DESHYDROGENASE, L'UNE DES FORMES DE L'ANEMIE HEMOLYTIQUE. (REVUE DE LA LITTERATURE)TSIRKINA AS.1973; LAB. DELO; S.S.S.R.; DA. 1973; NO 4; PP. 221-223; BIBL. 45REF.Serial Issue

METHODES DE THERAPIE METABOLIQUE DES MALADIES DU SYSTEME SANGUINIDEL'SON LI.1973; ZH. VSESOJUZ. KHIM. OBSHCHEST. D. I. MENDELEEVA; S.S.S.R.; DA. 1973; VOL. 18; NO 2; PP. 192-199; BIBL. 1 P.Serial Issue

DISORDERS OF LIPID METABOLISM = LES TROUBLES DU METABOLISME DES LIPIDESBRADY RO.1972; BIOCHEM. SOC. SYMP.; G.B.; DA. 1972; NO 35; PP. 113-127; BIBL. 1P.1/2; (CURR. TRENDS BIOCHEM. LIPIDS. PROC. INT. SYMP. LIPIDS; BANGALORE; 1971)Conference Paper

GLYCOGEN STORAGE DISEASESVAN HOOF F; HUE L; DE BARSY T et al.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 745-751; ABS. FR.; BIBL. 25REF.Serial Issue

THE ROLE OF LYSOSOMES IN THE PATHOGENY OF STORAGE DISEASESHERS HG.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 753-756; ABS. FR.; BIBL. 17REF.Serial Issue

METABOLIC ADAPTATION IN MUSCLE OF PHOSPHORYLASE DEFICIENCY (MCARDLE'S DISEASE). = ADAPTATION METABOLIQUE DU MUSCLE AU COURS DE LA CARENCE EN PHOSPHORYLASE (MALADIE DE MARDLE.NOLTE J; SCHOLLMEYER P.1973; KLIN. WSCHR.; DTSCH.; DA. 1973; VOL. 51; NO 5; PP. 250-251; ABS. ALLEM.; BIBL. 12REF.Serial Issue

GLYCOGEN STORAGE DISEASE, TYPE VIII = GLYCOGENOSE DE TYPE VIIILUDWIG M; WOLFSON S; RENNERT O et al.1972; ARCH. DIS. CHILDH.; G.B.; DA. 1972; VOL. 47; NO 255; PP. 830-833; BIBL. 10 REF.Serial Issue

STUDIES ON THE SUBSTRATE SPECIFICITY OF HEXOSAMINIDASE A AND B FROM LIVERWENGER DA; OKADA S; O'BRIEN JS et al.1972; ARCH. BIOCHEM. BIOPHYS.,; U.S.A.; DA. 1972; VOL. 153; NO 1; PP. 116-129; BIBL. 30REF.Serial Issue

INTOLERANCE AU FRUCTOSENORDMANN Y; SCHAPIRA F.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 741-744; ABS. ANGL.; BIBL. 21REF.Serial Issue

A SURVEY OF DIARRHOEAL DISEASE IN MALNOURISHED ABORIGINAL CHILDREN = COUP D'OEIL SUR UNE AFFECTION DIARRHEIQUE CHEZ DES ENFANTS ABORIGENES MALNUTRISWALKER AC; HARRY JG.1972; MED. J. AUSTRAL.; AUSTRAL.; DA. 1972; VOL. 59; NO 18; PP. 904-911; BIBL. 35REF.Serial Issue

DEFICIENCY OF ACID ALPHA GLUCOSIDASE IN THE URINE OF PATIENTS WITH POMPE'S DISEASE = DEFICIT EN ALPHA-GLUCOSIDASE ACIDE DANS LES URINES DES MALADES ATTEINTS D'UNE MALADIE DEPOMPESALAFSKY IS; NADLER HL.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 2; PP. 294-297; BIBL. 13REF.Serial Issue

UNUSUAL LATE NEUROLOGICAL SEQUELEA IN GALACTOSAEMIA = SEQUELLES NEUROLOGIQUES TARDIVES INHABITUELLES DANS LA GALACTOSEMIEJAN JE; WILSON RA.1973; DEVELOP. MED. CHILD NEUROL.; G.B.; DA. 1973; VOL. 15; NO 1; PP. 72-74; ABS. FR. ALLEM. ESP.; BIBL. 10REF.Serial Issue

LA GANGLIOSIDOSE A GM₁ (FORME INFANTILE) A PROPOS DE CINQ OBSERVATIONSLARBRE F; CHAZALETTE JP; GUIBAUD P et al.1973; LYON MED.,; FR.; DA. 1973; VOL. 229; NO 4; PP. 335-346; ABS. ANGL.; BIBL. 1P.Serial Issue