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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

SYSTEME DE DEPISTAGE PRECOCE DES MALADIES A ERREUR METABOLIQUEBELANGER M; SAINT HILAIRE B; BELANGER L et al.1973; UN. MED. CANADA; CANADA; DA. 1973; VOL. 102; NO 2; PP. 294-302; ABS. ANGL.; BIBL. 1P.Serial Issue

THE INHERITED DISORDERS OF CONNECTIVE TISSUE. II. = TROUBLES HEREDITAIRES DU TISSU CONJONCTIF. IIBEIGHTON P.1972; BULL. RHEUMATIC DIS.; U.S.A.; DA. 1972; VOL. 23; NO 3; PP. 702-707; BIBL. 37REF.Serial Issue

INSULINSEKRETION UND GLUKOSETOLERANZ BEI TIEREXPERIMENTELLER HYPERTONIE. I. UNTERSUCHUNGEN BEIM GENETISCH BEDINGTEN SPONTANEN HYPERTONUS DER RATTE = LA SECRETION INSULINIQUE ET LA TOLERANCE AU GLUCOSE I.V. DANS L'HYPERTENSION EXPERIMENTALE. I. ETUDES DANS L'HYPERTENSION SPONTANEE D'ORIGINE GENETIQUE DU RATWAGNER H; WESSELS F; ZIERDEN E et al.1972; MED. WELT; DTSCH.; DA. 1972; NO 25; PP. 907-910Serial Issue

VARIABILITY OF ARTERIAL PRESSURE IN NORMOTENSIVE AND SPONTANEOUSLY HYPERTENSIVE RATS = VARIABILITE DE LA P ARTERIELLE CHEZ DES RATS PRESENTANT UNE TENSION ARTERIELLE NORMALE OU UNE HYPERTENSION SPONTANEEFROHLICH ED; PFEFFER MA; WEISS AK et al.1972; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1972; VOL. 140; NO 1; PP. 145-148; BIBL. 11REF.Serial Issue

DIAGNOSIS AND TREATMENT OF INHERITED BLEEDING DISORDERS = DIAGNOSTIC ET TRAITEMENT DES TROUBLES HEMORRAGIQUES HEREDITAIRESSTRAUSS HS.1972; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1972; VOL. 19; NO 4; PP. 1009-1028; BIBL. 2 P. 1/2Serial Issue

LATE INFANTILE METACHROMATIC LEUCODYSTROPHY. REPORT OF 2CASES AND REVIEW OF IN VIVO DIAGNOSTIC TESTS = LA LEUCODYSTROPHIE METACHROMATIQUE INFANTILE D'APPARITION TARDIVE. RAPPORT DE 2CAS ET REVUE DES TESTS DIAGNOSTIQUES IN VIVOTHUNOLD S.sdBEITR. PATHOL.; DTSCH.; DA. 197; VOL. 146; NO 4; PP. 322-331; BIBL. 1P.Serial Issue

A GUIDE TO SCREENING NEWBORN INFANTS FOR INBORN ERRORS OF METABOLISM = UN GUIDE POUR DEPISTER LES ERREURS CONGENITALES DU METABOLISME CHEZ LES NOUVEAU-NESBUIST NRM; JHAVERI BM.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 3; PP. 511-522; BIBL. 1P.Serial Issue

Place des maladies lysosomales dans les maladies métaboliques = Status of lysosomal diseases amongst metabolic diseasesSAUDUBRAY, J.-M.La Revue de médecine interne (Paris). 2006, Vol 27, issn 0248-8663, S11-S13, SUP1Article

SCREENING THE NEGRO POPULATION FOR INBORN ERRORS OF METABOLISM = RECHERCHE DANS LA POPULATION NOIRE DES ERREURS CONGENITALES DE METABOLISMECALVERT AF; SCOTT RB.1972; MED. ANN. DISTR. COLUMBIA; U.S.A.; DA. 1972; VOL. 41; NO 5; PP. 285-287; BIBL. 14 REF.Serial Issue

HEREDODEGENERATIVE DISEASES OF THE CHILDREN'S NERVOUS SYSTEM = MALADIES HEREDO-DEGENERATIVES DU SYSTEME NERVEUX DE L'ENFANT1971; IN: IIND PRAGUE INST. SYMP. CHILD NEUROL., PRAGUE, 1970; PRAHA; UNIV. KARLOVA; DA. 1971; PP. 11-42; BIBL. DISSEM.Conference Proceedings

SCREENING FOR METABOLIC DISORDERS ASSOCIATED WITH MENTAL RETARDATION = DETECTION DES DESORDRES METABOLIQUES ASSOCIES A UN RETARD MENTALHILL A; ZALESKI WA.1972; CLIN. BIOCHEM.; CANADA; DA. 1972; VOL. 5; NO 1; PP. 33-45; BIBL. 1 P. 1/2Serial Issue

A guide to the genetics of psychiatric diseaseHOUGH, Christopher J; URSANO, Robert J.Psychiatry (Washington, D.C.). 2006, Vol 69, Num 1, pp 1-20, issn 0033-2747, 20 p.Article

How many genetic disease ?BILLINGS, P.Lancet (British edition). 1991, Vol 338, Num 8782-3, pp 1603-1604, issn 0140-6736Article

Maladies démyélinisantes d'origine génétique : Maladies démyélinisantes du système nerveux central = Genetic demyelinating diseases : Central nervous system demyelinating diseasesLABAUGE, Pierre; BOESPFLUG-TANGUY, Odile.La Presse médicale (1983). 2010, Vol 39, Num 3, pp 363-370, issn 0755-4982, 8 p.Article

Maladies génétiques = Genetic diseasesMS. Médecine sciences. 2005, Vol 21, Num 11, issn 0767-0974, 111 p.Serial Issue

Le génie génétique et le dépistage des maladies = Genetic engineering and diseases screeningWILLIAMSON, R.Médecine et hygiène. 1983, Vol 41, Num 1540, pp 4112-4120, issn 0025-6749Article

Etudes médico-génétiques des populations de Turkménie. III: Pathologie héréditaire chez les turkmen-NochurliGINTER, E. K; TURAEVA, SH. M; REVAZOV, A. A et al.Genetika. 1983, Vol 19, Num 8, pp 1344-1352, issn 0016-6758Article

MENKES'S KINKY HAIR SYNDROME. AN INHERITED DEFECT IN COPPER ABSORPTION WITH WIDESPREAD EFFECTS = SYNDROME DES CHEVEUX CREPELES DE MENKES. UN DEFAUT HEREDITAIRE DE L'ABSORPTION DU CUIVRE A EFFETS MULTIPLESDANKS DM; CAMPBELL PE; STEVENS BJ et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 2; PP. 188-201; BIBL. 20 REF.Serial Issue

PALMAR DERMATOGLYPHS IN TUBEROUS SCLEROSIS = DERMATOGLYPHES PALMAIRES DANS LA SCLEROSE TUBEREUSE1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 443-447; BIBL. 14REF.Serial Issue

EPILEPSIE AVEC TROUBLES DU METABOLISME DU PHOSPHORE CHEZ LES ENFANTSOBINTSOVA SS.1972; TRUDY LENINGRAD. NAUCH.-ISSLEDOVAT. PSIKHONEVROL. INST. V.M. BEKHTEREVA; S.S.S.R.; DA. 1972; VOL. 61; PP. 92-95; BIBL. 6REF.Serial Issue

MULTIPHASISCHE TESTUNG ZUR ERKENNUNG VON GENETISCHEN STOERUNGEN DES AMINOSAEURE-UND KOHLENHYDRATSTOFFWECHSELS, EINE PILOTSTUDIE = TEST MULTIPHASIQUE POUR LE DIAGNOSTIC DES TROUBLES GENETIQUES DES METABOLISMES DES ACIDES AMINES ET DES GLUCIDES. ETUDE PILOTEURNER U; AHLBEHRENDT I; FRIEDEMANN H et al.1973; DTSCHE GESUNDH.-WES.; DTSCH.; DA. 1973; VOL. 28; NO 2; PP. 49-53; ABS. RUSSE ANGL.; BIBL. 23REF.Serial Issue

INCREASED PLASMA RENIN ACTIVITY IN THE SPONTANEOUSLY HYPERTENSIVE RAT = AUGMENTATION DE L'ACTIVITE RENINIQUE DU PLASMA CHEZ LE RAT ATTEINT D'HYPERTENSION SPONTANEEDE JONG W; LOVENBERG W; SJOERDSMA A et al.1972; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1972; VOL. 139; NO 4; PP. 1213-1216; BIBL. 17REF.Article

PHOTOSENSITIVITY IN PORPHYRIARUNGE WJ.1972; PHOTOPHYSIOLOGY; U.S.A.; DA. 1972; VOL. 7; PP. 149-162; BIBL. 2P.Serial Issue

EXPRESSIONI CLINICHE DELLA PROTOPORFIRIA ERITROPOIETICA NELL'INFANZIA = MANIFESTATIONS CLINIQUES DE LA PROTOPORPHYRIE ERYTHROPOIETIQUE DE L'ENFANTPISANI M; SANTOIANNI P.1972; G. ITAL. DERMATOL., MINERVA DERMATOL.; ITAL.; DA. 1972; VOL. 47-113; NO 9; PP. 370-375; ABS. ANGL.; BIBL. 27 REF.Serial Issue

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