Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("MALADIE HEREDITAIRE")

Filter

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Origin

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 105459

  • Page / 4219

Export

Selection :

  • and

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

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

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

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

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

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

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

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

GLI ERRORI CONGENITI DEL CICLO DELL'UREA = LES ERREURS CONGENITALES DU CYLE DE L'UREETANCREDI F; PIGNERO A.1972; BIOCHIM. APPL.; ITAL.; DA. 1972; VOL. 19; NO 1; PP. 1-28; ABS. ANGL.; BIBL. 1 P. 1/2Serial Issue

ROENTGEN FINDINGS IN MUCOLIPIDOSISIII. (PSEUDO-HURLER POLYDYSTROPHY = CONSTATATIONS RADIOLOGIQUES DANS LA MUCOLIPIDOSEIII. (PSEUDO-POLYDYSTROPHIE DE HURLER)MELHEM R; DORST JP; SCOTT CI JR et al.1973; RADIOLOGY,; U.S.A.; DA. 1973; VOL. 106; NO 1; PP. 153-160; BIBL. 15REF.Serial Issue

HYPERCONCAVITE (SCALLOPING) VERTEBRALE LOMBAIRE AU COURS DE LA MALADIE DE RECKLINGHAUSENDEBAENE A; ACQUAVIVA P; DUFOUR M et al.1973; J. RADIOL. ELECTROL. MED. NUCL.; FR.; DA. 1973; VOL. 54; NO 2; PP. 149-191; ABS. ANGL.; BIBL. 3REF.Serial Issue

SAISONALER PRURITUS ALS SYMPTOM DER ERYTHROPOETISCHEN PROTOPORPHYRINAEMISCHEN LICHTDERMATOSE. (EPL) = PRURIT SAISONNIER, SYMPTOME DE LA DERMATOSE ACTINIQUE ERYTHROPOIETIQUE PROTOPORPHYRINEMIQUEBURG G; PLEWIG G.1972; HAUTARZT; DTSCH.; DA. 1972; VOL. 23; NO 12; PP. 553-55; BIBL. 15REF.Serial Issue

REEVALUATION OF ROLE OF RECTAL BIOPSY IN DIAGNOSIS OF PEDIATRIC NEUROLOGIC DISORDERS = REEVALUATION DU ROLE DE LA BIOPSIE RECTALE DANS LE DIAGNOSTIC DES TROUBLES NEUROLOGIQUES EN PEDIATRIEMYERS GJ; HEDLEY WHYTE ET; FAGAN ME et al.1973; NEUROLOGY; U.S.A.; DA. 1973; VOL. 23; NO 1; PP. 27-34; BIBL. 33 REF.Serial Issue

WERNER'S SYNDROMEFLEISCHMAJER R; NEDWICH A.1973; AMER. J. MED.; U.S.A.; DA. 1973; VOL. 54; NO 1; PP. 111-118; BIBL. 17 REF.Serial Issue

THE OCULAR HISTOPATHOLOGY OF HOMOCYSTINURIA. A LIGHT AND ELECTRON MICROSCOPIC STUDYRAMSEY MS; YANOFF M; FINE BS et al.1972; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 74; NO 3; PP. 377-385; BIBL. 25 REF.Serial Issue

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

  • Page / 4219