Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Maladie héréditaire")

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 70325

  • Page / 2813
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

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

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

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

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

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

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

Discovery of a novel Torque teno sus virus species: genetic characterization, epidemiological assessment and disease associationCORNELISSEN-KEIJSERS, Vivian; JIMENEZ-MELSIO, Alexandra; SONNEMANS, Denny et al.Journal of general virology. 2012, Vol 93, pp 2682-2691, issn 0022-1317, 10 p., 12Article

Genetics of neurodegenerative diseases: insights from high-throughput resequencingTSUJI, Shoji.Human molecular genetics (Print). 2010, Vol 19, Num 1, issn 0964-6906, R65-R70, NSArticle

Bone marrow replacement in the treatment of hemolytic disease in miceBERNSTEIN, S. E; DEVEAU, S. A.Experimental hematology. 1989, Vol 17, Num 10, pp 0004-1010, issn 0301-472X, 1007 p.Article

Autosomal dominant congenital cataract on chromosome 16MARNER, E.Clinical genetics. 1989, Vol 36, Num 5, issn 0009-9163, p. 326Conference Paper

Towards a complete resolution of the genetic architecture of diseaseSINGLETON, Andrew B; HARDY, John; TRAYNOR, Bryan J et al.Trends in genetics (Regular ed.). 2010, Vol 26, Num 10, pp 438-442, issn 0168-9525, 5 p.Article

Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donorsTEN KATE, L. P; TE MEERMAN, G. J; BUYS, C. H. C. M et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 148-149, issn 0148-7299, 2 p.Article

Benign familial hematuriaYOSHIKAWA, N; MATSUYAMA, S; IIJIMA, K et al.Archives of pathology & laboratory medicine (1976). 1988, Vol 112, Num 8, pp 794-797, issn 0363-0153Article

  • Page / 2813