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LES DEFICITS CONGENITAUX EN FACTEURS DU COMPLEXE PROTHROMBINIQUE3. (FACTEURS II, V, VII, ET X)GERMAIN D; THOUVEREZ JP.1972; MED. INFANT.; FR.; DA. 1972; VOL. 79; NO 9; PP. 767-773 (7 P.)Serial Issue

LES ANOMALIES HEREDITAIRES DES ENZYMES DIGESTIVES1972; MED. CHIR. DIGEST.; FR.; DA. 1972; VOL. 1; NO 1; PP. 41-44; BIBL. 9REF.Serial Issue

ENZYME DEFICIENCY IN CHOLESTERYL ESTER STORAGE DISEASE = DEFICIENCE D'ENZYME DANS LA THESAURISMOSE DES ESTERS DU CHOLESTEROLSLOAN HR; FREDRICKSON DS.1972; J. CLIN. INVEST.; U.S.A.; DA. 1972; VOL. 51; NO 7; PP. 1923-1926; BIBL. 16REF.Serial Issue

LES TROUBLES CONGENITAUX DE LA THROMBOPLASTINO-FORMATION (EN DEHORS DE L'HEMOPHILIE)GERMAIN D; THOUVEREZ JP.1972; MED. INFANT.; FR.; DA. 1972; VOL. 79; NO 9; PP. 747-756 (6P.)Serial Issue

LES DEFICITS CONGENITAUX EN FACTEURS DU COMPLEXE PROTHROMBINIQUE (FACTEURS II, V, VII ET X)GERMAIN D; THOUVEREZ JP.1972; MED. INFANT.; FR.; DA. 1972; VOL. 79; NO 9; PP. 767-773Serial Issue

HEREDITARY DISORDERS OF BILIRUBIN METABOLISMGOLLAN JL; BILLING BH.1974; ACTA HEPATO-GASTROENTEROL; ALLEM.; DA. 1974; VOL. 21; NO 5; PP. 333-338; BIBL. 2P.Article

GENETIC DISEASES OF METABOLISMRAIVIO KO; SEEGMILLER JE.1972; ANNU. REV. BIOCHEM.; U.S.A.; DA. 1972; VOL. 41; PP. 543-576; BIBL. 7P.Serial Issue

KLINIK KINDLICHER IMMUNOPATHIEN = LES IMMUNOPATHIES INFANTILES. CLINIQUEBARANDUN S.1972; MED. WELT; DTSCH.; DA. 1972; NO 43; PP. 1533-1535Serial Issue

DETECTION AND PROPERTIES OF AN ACID ALPHA -GALACTOSIDASE (CERAMIDETRIHEXOSIDASE) IN NORMAL HUMAN URINERIETRA PJGM; TAGER JM; BORST P et al.1972; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1972; VOL. 279; NO 3; PP. 436-445; BIBL. 24REF.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

HYPERAMMONIEMIES PAR ENZYMOPATHIES GENOTYPIQUESCATHELINEAU L; POLONOVSKI C.1972; MED. CHIR. DIGEST.; FR.; DA. 1972; VOL. 1; NO 5; PP. 275-287; BIBL. 1P.1/2Serial Issue

ITTERI ERITROPATICI ED ENZIMOPENICI = ICTERES ERYTHROPATHIQUES ET ENZYMOPATHIQUESRASORE QUARTINO A.1972; PATHOLOGICA; ITAL.; DA. 1972; VOL. 64; NO 931-932; PP. 189-193; BIBL. 18REF.Serial Issue

LES ICTERES NON CHOLESTATIQUES, NON HEMOLYTIQUES (ICTERES PAR DEFICIT ENZYMATIQUE HEPATOCYTAIRE CONNU OU PROBABLE)DARNIS F; LEVY VG.1975; MED. INTERNE; FR.; DA. 1975; VOL. 10; NO 11; PP. 511-522 (10P.); BIBL. 1 P. 1/2Article

UTILIZATION OF LEUKOCYTES FOR THE STUDY OF INBORN ERRORS OF METABOLISM = UTILISATION DES LEUCOCYTES POUR L'ETUDE DES ERREURS INNEES DU METABOLISMEHSIA DYY.1972; ENZYME; SWITZ.; DA. 1972; VOL. 13; NO 1-3; PP. 161-168; BIBL. 2 P.Serial Issue

HOMOZYGOUS GLUTATHIONE-PEROXIDASE DEFICIENCY OF ERYTHROCYTES AND LEUKOCYTES = DEFICIT HOMOZYGOTE EN PEROXYDASE DU GLUTATHION DANS LES ERYTHROCYTES ET LES LEUCOCYTESNISHIMURA Y; CHIDA N; HAYASHI T et al.1972; TOHOKU J. EXPER. MED.; JAP.; DA. 1972; VOL. 108; NO 3; PP. 207-217; BIBL. 1P.1/2Serial Issue

CORNEAL DYSTROPHIES: A CLINICAL, PATHOLOGICAL, AND SURGICAL APPROACH = DYSTROPHIES CORNEENNES: APPROCHE CLINIQUE, PATHOLOGIQUE ET CHIRURGICALEMALBRAN ES.1972; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 74; NO 5; PP. 771-809; BIBL. 4 P. 1/2Serial Issue

BIOCHEMICAL AND METABOLIC BASIS OF FAMILIAL SPHINGOLIPIDOSES = LES BASES BIOCHIMIQUES ET METABOLIQUES DES SPHINGOLIPIDOSES FAMILIALESBRADY RO.1972; SEMINARS HEMATOL.; U.S.A.; DA. 1972; VOL. 9; NO 3; PP. 273-284; BIBL. 2P.Serial Issue

NEW INSIGHTS INTO THE CLASSIFICATION AND MECHANISMS OF HEREDITARY, CHRONIC, NON-HAEMOLYTIC HYPERBILIRUBINAEMIAS.BERTHELOT P; DHUMEAUX D.1978; ; GUT; G.B.; DA. 1978; VOL. 19; NO 6; PP. 474-480; BIBL. 2 P.Article

COEUR ET SURDITES GENETIQUESPERNOT C; HENRY M; DEBRUILLE C et al.1973; MED. INFANT.; FR.; DA. 1973; VOL. 80; NO 1; PP. 115-133; BIBL. 2P.1/2Serial Issue

LES TROUBLES CONGENITAUX DE LA THROMBOPLASTINOFORMATION (EN DEHORS DE L'HEMOPHILIE)GERMAIN D; THOUVEREZ JP.1972; MED. INFANT.; FR.; DA. 1972; VOL. 79; NO 9; PP. 747-756 (6 P.)Serial Issue

UEBERSICHT. MOLEKULARBIOLOGISCHE ERKENNTNISSE UEBER EINIGE GERINNUNGS-FAKTOREN = REVUE GENERALE. NOTIONS NOUVELLES DE BIOLOGIE MOLECULAIRE SUR QUELQUES FACTEURS DE COAGULATIONFIEDLER H.1972; FOLIA HAEMATOL.; ALLEM.; DA. 1972; VOL. 98; NO 2; PP. 121-139; ABS. ANGL. FR. RUSSE; BIBL. 6 P.Serial Issue

GAMMA -GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY. A CAUSE OF HEREDITARY HEMOLYTIC ANEMIA = DEFICIT EN GAMMA -GLUTAMYLCYSTEINE SYNTHETASE. UNE CAUSE D'ANEMIE HEMOLYTIQUE HEREDITAIREKONRAD PN; RICHARDS F II; VALENTINE WN et al.1972; NEW ENGL. J. MED.; U.S.A.; DA. 1972; VOL. 286; NO 11; PP. 557-561; BIBL. 25 REF.Serial Issue

LES ICTERES NON CHOLESTATIQUES, NON HEMOLYTIQUES ICTERES PAR DEFICIT ENZYMATIQUE HEPATOCYTAIRE, CONNU OU PROBABLEDARNIS F; LEVY VG.1975; PRESSE THERM. CLIMAT.; FR.; DA. 1975; VOL. 112; NO 4; PP. 180-188; BIBL. 37 REF.Article

LES MALADIES AMYLOIDES HEREDITAIRESLAGRUE G; VERNANT JP.1972; NOUV. PRESSE MED.; FR.; DA. 1972; VOL. 1; NO 38; PP. 2525-2528; BIBL. 12REF.Serial Issue

COAGULATION FACTOR VARIANTS = VARIANTES DES FACTEURS DE LA COAGULATIONBLOOM AL.1972; BRIT. J. HAEMATOL.; G.B.; DA. 1972; VOL. 23; NO 6; PP. 643-647; BIBL. 1P.Serial Issue

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