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A THIRD COMMON ALLELE IN THE TRANSFERRIN SYSTEM, TFC3, DETECTED BY ISOELECTRIC FOCUSINGKUEHNL P; SPIELMANN W.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 2; PP. 193-198; BIBL. 15 REF.Article

IMPROVED COAGULATION FACTOR XIIIB (FXIIIB) PHENOTYPING AFTER NEURAMINIDASE TREATMENT OF PLASMA AND FIRST DESCRIPTION OF THE FXIIIB2 PHENOTYPEKRECKEL P; KUEHNL P.1982; BLUT; ISSN 0006-5242; DEU; DA. 1982; VOL. 45; NO 5; PP. 337-345; BIBL. 18 REF.Article

BLUTGRUPPENGUTACHTEN MIT NAHE VEWANDTEN EVENTUALVAETERN = EXPERTISES DE GROUPES SANGUINS AVEC PERES EVENTUELS PRESUMESSPIELMANN W; KUEHNL P.1980; WIEN. KLIN. WOCHENSCHR.; ISSN 0043-5325; AUT; DA. 1980; VOL. 92; NO 21; PP. 764-768; ABS. ENG; BIBL. 13 REF.Article

PIT: A NEW ALLELE IN THE ALPHA1-ANTITRYPSIN SYSTEMKUEHNL P; SPIELMANN W.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 2; PP. 221-223; BIBL. 11 REF.Article

HUMAN COAGULATION FACTOR XIIIA (FXIIIA) PHENOTYPING BY IMMUNOFIXATION AGAROSE GEL ELECTROPHORESIS (IAGE)KRECKEL P; KUEHNL P; SPIELMANN W et al.1982; BLUT; ISSN 0006-5242; DEU; DA. 1982; VOL. 44; NO 5; PP. 309-314; BIBL. 18 REF.Article

PEP A9, A NEW, UNSTABLE VARIANT IN THE PEPTIDASE A SYSTEMKUEHNL P; ANNEKEN K; SPIELMANN W et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 187-191; BIBL. 12 REF.Article

SCHLUSSWORT ZU H. RITTERS BRIEF AN DIE HERAUSGEBER = REPONSE A LA LETTRE A L'EDITEUR DE H. RITTERSKUEHNL P; NOWICKI L; SPIELMANN W et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 77-79Article

INVESTIGATIONS ON THE POLYMORPHISM OF GLYOXALASE I (EC 4.4.1.5) IN THE POPULATION OF HESSEN, GERMANY.KUEHNL P; SCHWABENLAND R; SPIELMANN W et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 99-106; BIBL. 19 REF.Article

UNTERSUCHUNGEN ZUM POLYMORPHISMUS DER GALAKTOSE-1-PHOSPHAT-URIDYLTRANSFERASE (EC : 2.7.7.12) MITTELS AGAROSEGELELEKTROPHORESE = RECHERCHES SUR LE POLYMORPHISME DE LA GALACTOSE-1-PHOSPHATE-URIDYLTRANSFERASE (EC : 2.7.7.12) PAR ELECTROPHORESE SUR GEL D'AGAROSEKUEHNL P; NOWICKI L; SPIELMANN W et al.1974; HUMANGENETIK; DTSCH.; DA. 1974; VOL. 24; NO 3; PP. 227-230; ABS. ANGL.; BIBL. 8REF.Article

A NEW PROCEDURE FOR THE DETERMINATION OF TRANSFERRINC (TFC) SUBTYPES BY ISOELECTRIC FOCUSING. EXISTENCE OF TWO ADDITIONAL ALLELES, TFC4 AND TFC5CONSTANS J; KUEHNL P; VIAU M et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 111-114; BIBL. 15 REF.Article

UNTERSUCHUNGEN ZUM GPT-SYSTEM UNTER BESONDERER BERUECKSICHTIGUNG DES STUMMEN ALLELS GPTO = RECHERCHES SUR LE SYSTEME GPT, CONCERNANT SPECIALEMENT LE GENE SILENCIEUX GPTOSPIELMANN W; KUEHNL P; REXRODT C et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 4; PP. 341-348; ABS. ANGL.; BIBL. 13REF.Serial Issue

Sklerodermie und HLA-Antigene = Scleroderma and HLA antigensHOLZMANN, H; SOLLBERG, S; SCHUÊTZ, K et al.Hautarzt. 1989, Vol 40, Num 3, pp 134-140, issn 0017-8470, 7 p.Article

Flow cytometric analysis of platelet membrane antigens during and after continuous-flow plateletpheresisGUTENSOHN, K; BARTSCH, N; KUEHNL, P et al.Transfusion (Philadelphia, PA). 1997, Vol 37, Num 8, pp 809-815, issn 0041-1132Article

Analyse der α1-antitrypsin-Defizenz durch DNA-Methoden = Evaluation of α1-antitrypsin deficiency by DNA-methodsWICK, U; KUÊHNL, P; ENGEL, W et al.Monatsschrift für Kinderheilkunde. 1990, Vol 138, Num 8, pp 438-442, issn 0026-9298, 5 p.Article

Biocompatibility of a new cell separator studied by flow cytometry : analyses of platelet antigens during apheresis and storageGUTENSOHN, K; ALISCH, A; CRESPEIGNE, N et al.Transfusion (Philadelphia, PA). 1999, Vol 39, Num 7, pp 742-747, issn 0041-1132Article

Linkage of HLA-DRβ specific restriction fragment length polymorphisms with Graves' diseaseBOEHM, B. O; SCHIFFERDECKER, E; KUEHNL, P et al.Acta endocrinologica (Oslo). 1988, Vol 119, Num 2, pp 251-256, issn 0001-5598Article

Flow cytometric analysis of coronary stent-induced alterations of platelet antigens in an in vitro modelGUTENSOHN, K; BEYTHIEN, C; BAU, J et al.Thrombosis research. 1997, Vol 86, Num 1, pp 49-56, issn 0049-3848Article

Extracorporeal plateletpheresis induces the interaction of activated platelets with white blood cellsGUTENSOHN, K; ALISCH, A; KRUEGER, W et al.Vox sanguinis (Basel. 1956). 2000, Vol 78, Num 2, pp 101-105, issn 0042-9007Article

Late-onset form of congenital adrenal hyperplasia in the HLA-B14;DR1 haplotype is caused by a duplication in the 21-OH MHC gene regionBOEHM, B. O; ROSAK, C; KUEHNL, P et al.Hormone and metabolic research. 1986, Vol 18, Num 11, pp 791-792, issn 0018-5043Article

Semi-automated flow cytometric analysis of CD34-expressing hematopoietic cells in peripheral blood progenitor cell apheresis productsGUTENSOHN, K; CARRERO, I; KRUEGER, W et al.Transfusion (Philadelphia, PA). 1999, Vol 39, Num 11-12, pp 1220-1226, issn 0041-1132Article

Identification of HLA-DR and -DQ alleles conferring susceptibility to pollen allergy and pollen associated food allergyBOEHNCKE, W.-H; LOELIGER, C; KUEHNL, P et al.Clinical and experimental allergy (Print). 1998, Vol 28, Num 4, pp 434-441, issn 0954-7894Article

TcR-alpha and TcR-beta dialellic RFLPs in insulin-dependent (Type I) caucasian diabetic patientsBOEHM, B. O; MANFRAS, B. J; ROSAK, C et al.Diabetes research. 1990, Vol 15, Num 2, pp 63-67, issn 0265-5985Article

The HLA-DR4-associated DQw8 allele is confined to HLA-DR3/DR4 heterozygous type I (insulin-dependent) diabeticsBOEHM, B. O; SCHIFFERDECKER, E; ROSAK, C et al.Tissue antigens. 1990, Vol 36, Num 2, pp 81-82, issn 0001-2815, 2 p.Article

Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene regionNOEHM, B. O; ROSAK, C; BOEHM, T. L. J et al.Molecular biology & medicine. 1986, Vol 3, Num 5, pp 437-448, issn 0735-1313Article

In vitro analyses of diamond-like carbon coated stents : Reduction of metal ion release, platelet activation, and thrombogenicityGUTENSOHN, K; BEYTHIEN, C; BAU, J et al.Thrombosis research. 2000, Vol 99, Num 6, pp 577-585, issn 0049-3848Article

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