Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("BENKMANN HG")

Publication Year[py]

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

Discipline (document) [di]

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

Results 1 to 25 of 38

  • Page / 2
Export

Selection :

  • and

ESTERASE-D POLYMORPHISM IN ASSAM BY CELLULOSE ACETATE ELECTROPHORESIS. = LE POLYMORPHISME DE L'ESTERASE-D EN ASSAM D'APRES L'ELECTROPHORESE SUR ACETATE DE CELLULOSEBENKMANN HG; GOEDDE HW.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 4; PP. 343-345; ABS. ALLEM.; BIBL. 7 REF.Article

FURTHER RESULTS ON THE POLYMORPHISM OF SOLUBLE GLUTAMIC-PYRUVIC TRANSAMINASE (GPT; EC: 2.6.1.2.) IN A POPULATION OF NORTHERN GERMANY = NOUVEAUX RESULTATS SUR LE POLYMORPHISME DE LA GLUTAMIC-PYRUVIC-TRANSAMINASE SOLUBLE (GPT; EC: 2.6.1.2) DANS UNE POPULATION DU NORD DE L'ALLEMAGNE)BENKMANN HG; GOEDDE HW.1972; HUM. HERED.; SWITZ.; DA. 1972; VOL. 22; NO 3; PP. 283-285; BIBL. 3REF.Serial Issue

ESTERASE D POLYMORPHISM: GENE FREQUENCIES AND FAMILY DATA = POLYMORPHISME DE L'ESTERASE D: FREQUENCE DES GENES ET DONNEES FAMILIALESBENKMANN HG; GEODDE HW.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 4; PP. 325-327; BIBL. 5REF.Article

ISOELECTRIC FOCUSING STUDIES OF HUMAN RED CELL PGM1 IN JAPANESE, WITH SPECIAL REFERENCE TO THE CHARACTERIZATION OF PGM17NISHIGAKI I; BENKMANN HG; GOEDDE HW et al.1982; HUM. HERED.; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 5; PP. 301-307; BIBL. 18 REF.Article

"THE DISTRIBUTION OF HUMAN GM-GLOBULIN AND INV-ALLOTYPES IN POPULATIONS OF EGYPT, SAUDI-ARABIA, AFGHANISTAN AND ECUADOR"HIRTH L; BENKMANN HG; GOEDDE HW et al.1982; Z. MORPHOL. ANTHROPOL.; ISSN 0044-314X; DEU; DA. 1982; VOL. 73; NO 1; PP. 107-108Article

POLYMORPHISM OF DELTA-AMINOLEVULINIC ACID DEHYDRATASE IN VARIOUS POPULATIONSBENKMANN HG; BOGDANSKI P; GOEDDE HW et al.1983; HUMAN HEREDITY; ISSN 0001-5652; CHE; DA. 1983; VOL. 33; NO 1; PP. 62-64; BIBL. 2 REF.Article

ULTRATHIN-LAYER ISOELECTROFOCUSING FOR RAPID DIAGNOSIS OF PROTEIN VARIANTSGOEDDE HW; BENKMANN HG; HIRTH L et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 4; PP. 434-436; BIBL. 7 REF.Article

THE DISTRIBUTION OF HUMAN GM-GLOBULIN AND INV-ALLOTYPES IN POPULATIONS OF EGYPT, SAUDI-ARABIA, AFGHANISTAN AND ECUADORHIRTH L; BENKMANN HG; GOEDDE HW et al.1979; Z. MORPHOL. ANTHROPOL.; DEU; DA. 1979; VOL. 70; NO 2; PP. 174-180; ABS. GER; BIBL. 15 REF.Article

THE USE OF SERUM CHOLINESTERASE IN SUCCINYLCHOLINE APNOEA.SCHOLLER KL; GOEDDE HW; BENKMANN HG et al.1977; CANAD. ANAESTHETISTS' SOC. J.; CANADA; DA. 1977; VOL. 24; NO 3; PP. 396-400; ABS. FR.; BIBL. 13 REF.Article

PHARMACOGENETICS OF CHOLINESTERASE: NEW VARIANTS AND SUXAMETHONIUM SENSITIVITYGOEDDE HW; AGARWAL DP; BENKMANN HG et al.1979; AERZTL. LAB.; DEU; DA. 1979; VOL. 25; NO 9; PP. 219-224; ABS. GER; BIBL. 33 REF.Article

GENETIC POLYMORPHISM OF THE THIRD COMPONENT OF COMPLEMENT (C3) AND LEVELS OF B1 C/B1 A-GLOBULIN IN SERA OF GERMAN AND SPANISH POPULATIONS = POLYMORPHISME GENETIQUE DE LA TROISIEME COMPOSANTE DU COMPLEMENT (C3) ET TAUX DE BETA 1C-BETA 1A-GLOBULINE DANS LE SERUM DE POPULATIONS ALLEMANDE ET ESPAGNOLESAGARWAL DP; BENKMANN HG; GOEDDE HW et al.1972; HUM. HERED.; SWITZ.; DA. 1972; VOL. 22; NO 4; PP. 356-361; BIBL. 16 REF.Serial Issue

HEREDITARY ATAXIA AND THE SIXTH CHROMOSOMEKOEPPEN AH; GOEDDE HW; HILLER C et al.1981; ARCH. NEUROL. (CHIC.); ISSN 0003-9942; USA; DA. 1981; VOL. 38; NO 3; PP. 158-164; BIBL. 30 REF.Article

GENETIC STUDIES IN ECUADOR. ACETYLATOR PHENOTYPES, RED CELL ENZYME AND SERUM PROTEIN POLYMORPHISMS OF SHUARA INDIANS.GOEDDE HW; BENKMANN HG; AGARWAL DP et al.1977; AMER. J. PHYS. ANTHROPOL.; U.S.A.; DA. 1977; VOL. 47; NO 3; PP. 419-425; BIBL. 1 P. 1/2Article

STUDIES ON THE POLYMORPHISM OF C3, TF AND BG IN DOWN'S SYNDROME AND OTHER DISEASES. = ETUDE DU POLYMORPHISME DE C3, TF ET BG DANS LE SYNDROME DE DOWN ET AUTRES MALADIESAGARWAL DP; SRIVASTAVA LM; BENKMANN HG et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 29; NO 1; PP. 23-28; ABS. ALLEM.; BIBL. 1 P.Article

BIOCHEMICAL, IMMUNOLOGICAL AND GENETIC STUDIES IN LEPROSY. II. GENETIC POLYMORPHISM OF C3 AND IMMUNOGLOBULIN PROFILE IN LEPROSY PATIENTS, HEALTHY FAMILY MEMBERS AND CONTROLSSRIVASTAVA LM; AGARWAL DP; BENKMANN HG et al.1975; TROPENMED. UND PARASITOL.; DTSCH.; DA. 1975; VOL. 26; NO 4; PP. 426-430; ABS. ALLEM.; BIBL. 29 REF.Article

AKTIVITAETSMESSUNGEN DER ALDOLASE-ISOENZYME IN ZWISLINGEN IM VERGLEICH MIT EINER STICHPROBE GESUNDER PERSONEN = MESURES D'ACTIVITE DES ISOENZYMES DE L'ALDOLASE CHEZ LES JUMEAUX PAR COMPARAISON AVEC DES ECHANTILLONS DE SUJETS SAINSGOEDDE HW; BENKMANN HG; HIRTH L et al.1974; Z. KLIN. CHEM. KLIN. BIOCHEM.; DTSCH.; DA. 1974; VOL. 12; NO 12; PP. 539-542; ABS. ANGL.; BIBL. 6REF.Article

GENETIC STUDIES IN EGYPT: RED CELL ENZYME AND PLASMA PROTEIN POLYMORPHISMSGOEDDE HW; BENKMANN HG; LAILA HUSSEIN et al.1980; Z. MORPHOL. ANTHROPOL.; ISSN 0044-314X; DEU; DA. 1980; VOL. 71; NO 3; PP. 329-335; ABS. GER; BIBL. 2 P.Article

FAMILY STUDIES ON THE THIRD COMPONENT OF COMPLEMENT (C3), ALPHA 1-ANTITRYPSIN AND PSEUDOCHOLINESTERASE POLYMORPHISM (LOCUS E1 AND E2) IN THE AREA OF MARBURG (GERMANY) = ETUDES FAMILIALES SUR LA TROISEME COMPOSANTE DU COMPLEMENT (C3), L'ALPHA 1-ANTITRYPSINE ET LE POLYMORPHISME DE LA PSEUDOCHOLINESTERASE (LOCUS E1 ET E2) DANS LA REGION DE MARBURG EN ALLEMAGNEGOEDDE HW; HIRTH L; BENKMANN HG et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 17; NO 1; PP. 85-87; BIBL. 12 REF.Serial Issue

PERFORIERENDE SIGMADIVERTIKULITIS BEI EINEIIGEN ZWILLIGEN = DIVERTICULITE PERFORANTE DU SIGMOIDE CHEZ DES JUMEAUX UNIVITALLINSPUSCH HH; BOERGER G; HIRTH L et al.1979; MUENCH. MED. WSCHR.; DEU; DA. 1979; VOL. 121; NO 28; PP. 947-948; BIBL. 13 REF.Article

QUANTITATIVE BESTIMMUNG UND PHAENOTYPISIERUNG DES CAERULOPLASMINS BEI MORBUS WILSON. = DETERMINATION QUANTITATIVE ET CARACTERISATION PHENOTYPIQUE DE LA CERULOPLASMINE AU COURS DE LA MALADIE DE WILSONGOEDDE HW; BENKMANN HG; LANGE J et al.1975; KLIN. WSCHR.; DTSCH.; DA. 1975; VOL. 53; NO 15; PP. 731-734; ABS. ANGL.; BIBL. 40 REF.Article

STUDIES ON THE POLYMORPHISMS OF PI, BF, GM SERUM LEVELS OF IMMUNOGLOBULINS AND COMPLEMENT COMPONENTS IN PATIENTS WITH DOWN'S SYNDROME AND OTHER DISEASESHIRTH L; AGARWAL DP; BENKMANN HG et al.1979; Z. MORPHOL. ANTHROPOL.; DEU; DA. 1979; VOL. 69; NO 3; PP. 316-323; ABS. GER; BIBL. 2 P.Article

SUCCINYLDICHOLIN - EMPFINDLICHKEIT ALS FOLGE GENETISCH BEDINGTER SERUMCHOLINESTERASEVARIANTEN. = SENSIBILITE A LA SUCCINYLDICHOLINE, CONSEQUENCE DE VARIANTS DE LA CHOLINESTERASE SERIQUE D'ORIGINE GENETIQUEGOEDDE HW; MUNSCH H; BENKMANN HG et al.1976; PRAKT. ANAESTH. WIEDERBELEB. INTENSIVTHERAP.; DTSCH.; DA. 1976; VOL. 11; NO 5; PP. 339-346; ABS. ANGL.; BIBL. 47 REF.Article

FURTHER INVESTIGATIONS ON THE INHERITED POLYMORPHISM OF THE THIRD COMPONENT OF COMPLEMENT (BETA 1C/BETA 1A-GLOBULIN) = NOUVELLES RECHERCHES SUR LE POLYMORPHISME HEREDITAIRE DE LA TROISIEME COMPOSANTE DU COMPLEMENT (BETA 1C/BETA 1A-GLOBULINE)GOEDDE HW; BENKMANN HG; AGARWAL DP et al.1972; HUM. HERED.; SWITZ.; DA. 1972; NO 5-6; PP. 488-495; BIBL. 19REF.Serial Issue

ACTIVITY OF CREATINE KINASE ISOENZYME MB IN SERUM AND RED CELL ACETYLCHOLINESTERASE VARIANTS IN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY.GOEDDE HW; BENKMANN HG; DAS PK et al.1977; KLIN. WSCHR.; DTSCH.; DA. 1977; VOL. 55; NO 5; PP. 215-217; ABS. ALLEM.; BIBL. 11 REF.Article

RED CELL ENZYME POLYMORPHISMS IN DIFFERENT POPULATIONS OF AFGHANISTAN.GOEDDE HW; BENKMANN HG; FLATZ G et al.1977; ANN. HUM. BIOL.; G.B.; DA. 1977; VOL. 4; NO 3; PP. 225-232; ABS. ALLEM. FR.; BIBL. 25 REF.Article

  • Page / 2