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Results: 1-18 |
Results: 18
PERICARDIAL-EFFUSION IN GLYCANOSIS CDG TYPE-I (MIM-212-065) - AN INFLAMMATORY ENDOPLASMIC-RETICULUM OVERLOAD RESPONSE
Authors: HEYNE K MAYATEPEK E WALTHER F WEIDINGER S PAHL HL
Citation: K. Heyne et al., PERICARDIAL-EFFUSION IN GLYCANOSIS CDG TYPE-I (MIM-212-065) - AN INFLAMMATORY ENDOPLASMIC-RETICULUM OVERLOAD RESPONSE, European journal of pediatrics, 157(2), 1998, pp. 168-169
ROLE OF STAPHYLOCOCCUS-AUREUS SURFACE-ASSOCIATED PROTEINS IN THE ATTACHMENT TO CULTURED HACAT KERATINOCYTES IN A NEW ADHESION ASSAY
Authors: MEMPEL M SCHMIDT T WEIDINGER S SCHNOPP C FOSTER T RING J ABECK D
Citation: M. Mempel et al., ROLE OF STAPHYLOCOCCUS-AUREUS SURFACE-ASSOCIATED PROTEINS IN THE ATTACHMENT TO CULTURED HACAT KERATINOCYTES IN A NEW ADHESION ASSAY, Journal of investigative dermatology, 111(3), 1998, pp. 452-456
APOLIPOPROTEIN-J DEFICIENCY IN TYPE-I AND TYPE-IV CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME (GLYCANOSIS CDG)
Authors: HEYNE K HENRY H MESSERLI B BACHMANN C STEPHANI U TISSOT JD WEIDINGER S
Citation: K. Heyne et al., APOLIPOPROTEIN-J DEFICIENCY IN TYPE-I AND TYPE-IV CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME (GLYCANOSIS CDG), European journal of pediatrics, 156(3), 1997, pp. 247-248
MICROHETEROGENEITY OF SERUM GLYCOPROTEINS AND THEIR LIVER PRECURSORS IN PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I -APPARENT DEFICIENCIES IN CLUSTERIN AND SERUM AMYLOID-P
Authors: HENRY H TISSOT JD MESSERLI B MARKERT M MUNTAU A SKLADAL D SPERL W JAEKEN J WEIDINGER S HEYNE K BACHMANN C
Citation: H. Henry et al., MICROHETEROGENEITY OF SERUM GLYCOPROTEINS AND THEIR LIVER PRECURSORS IN PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I -APPARENT DEFICIENCIES IN CLUSTERIN AND SERUM AMYLOID-P, The Journal of laboratory and clinical medicine, 129(4), 1997, pp. 412-421
ALPHA-1-ANTITRYPSIN DEFICIENCY (ALPHA-1-AD) - LIVER-DISEASE DEPENDINGON THE PHENOTYPE - A STUDY ON 50 PEDIATRIC-PATIENTS
Authors: LANG T MUHLBAUER M STROBELT M HARMS HK WEIDINGER S HADORN HB
Citation: T. Lang et al., ALPHA-1-ANTITRYPSIN DEFICIENCY (ALPHA-1-AD) - LIVER-DISEASE DEPENDINGON THE PHENOTYPE - A STUDY ON 50 PEDIATRIC-PATIENTS, Hepatology, 24(4), 1996, pp. 296-296
XANTHOMA CELLS IN THE CEREBROSPINAL-FLUID IN CARBOHYDRATE DEFICIENCY GLYCOPROTEIN SYNDROME TYPE-I (MIM-212-065)
Authors: HEYNE K WALTHER F WEIDINGER S
Citation: K. Heyne et al., XANTHOMA CELLS IN THE CEREBROSPINAL-FLUID IN CARBOHYDRATE DEFICIENCY GLYCOPROTEIN SYNDROME TYPE-I (MIM-212-065), Monatsschrift fur Kinderheilkunde, 144(1), 1996, pp. 75-75
DETECTION OF TYROSINASE-MESSENGER-RNA IN FINE-NEEDLE PUNCTURES FROM MALIGNANT-MELANOMA METASTASES BY REVERSE-TRANSCRIPTASE AND POLYMERASE CHAIN-REACTION
Authors: HOFMANN S REMY W BORELLI S VONREIS A WEIDINGER S
Citation: S. Hofmann et al., DETECTION OF TYROSINASE-MESSENGER-RNA IN FINE-NEEDLE PUNCTURES FROM MALIGNANT-MELANOMA METASTASES BY REVERSE-TRANSCRIPTASE AND POLYMERASE CHAIN-REACTION, Hautarzt, 47(3), 1996, pp. 197-199
THERAPEUTIC TRIAL IN 2 PATIENTS WITH GLYC ANOSIS CDG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME)
Authors: WALTHER F HEYNE K MARG W WEIDINGER S RADKE M KRUGER G KIENAST W TERPE R DRUCKLER E
Citation: F. Walther et al., THERAPEUTIC TRIAL IN 2 PATIENTS WITH GLYC ANOSIS CDG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME), Monatsschrift fur Kinderheilkunde, 143(1), 1995, pp. 50-54
ALLOTYPES OF ALPHA(1)-ANTITRYPSIN IN PATIENTS WITH CYSTIC-FIBROSIS, HOMOZYGOUS AND HETEROZYGOUS FOR DELTAF508
Authors: DORING G KROGHJOHANSEN H WEIDINGER S HOIBY N
Citation: G. Doring et al., ALLOTYPES OF ALPHA(1)-ANTITRYPSIN IN PATIENTS WITH CYSTIC-FIBROSIS, HOMOZYGOUS AND HETEROZYGOUS FOR DELTAF508, Pediatric pulmonology, 18(1), 1994, pp. 3-7
HIGH-DOSE INTRAVENOUS MELPHALAN IN A PATIENT WITH MULTIPLE-MYELOMA AND OLIGURIC RENAL-FAILURE
Authors: PECHERSTORFER M ZIMMERROTH I WEIDINGER S IRSIGLER K HALBMAYER WM ULRICH W FISCHER M BAUMGARTNER G
Citation: M. Pecherstorfer et al., HIGH-DOSE INTRAVENOUS MELPHALAN IN A PATIENT WITH MULTIPLE-MYELOMA AND OLIGURIC RENAL-FAILURE, The Clinical investigator, 72(7), 1994, pp. 522-525
HYPOTHYROIDISM PHENOCOPY IN GLYCANOSIS CDG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME)
Authors: HEYNE K MARG W WALTHER F STEPHANI U HERMANUSSEN M WEIDINGER S
Citation: K. Heyne et al., HYPOTHYROIDISM PHENOCOPY IN GLYCANOSIS CDG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME), European journal of pediatrics, 153(11), 1994, pp. 866-866
3 NEW BIOCHEMICAL MARKERS IN GLYCANOSIS C DG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME)
Authors: HEYNE K WEIDINGER S
Citation: K. Heyne et S. Weidinger, 3 NEW BIOCHEMICAL MARKERS IN GLYCANOSIS C DG (CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME), Monatsschrift fur Kinderheilkunde, 142(3), 1994, pp. 199-204
IDENTIFICATION AND DNA-SEQUENCE ANALYSIS OF 15 NEW ALPHA(1)-ANTITRYPSIN VARIANTS, INCLUDING 2 PI-ASTERISK-Q0 ALLELES AND ONE DEFICIENT PI-ASTERISK-M ALLELE
Authors: FABER JP POLLER W WEIDINGER S KIRCHGESSER M SCHWAAB R BIDLINGMAIER F OLEK K
Citation: Jp. Faber et al., IDENTIFICATION AND DNA-SEQUENCE ANALYSIS OF 15 NEW ALPHA(1)-ANTITRYPSIN VARIANTS, INCLUDING 2 PI-ASTERISK-Q0 ALLELES AND ONE DEFICIENT PI-ASTERISK-M ALLELE, American journal of human genetics, 55(6), 1994, pp. 1113-1121
NOMENCLATURE FOR HUMAN-COMPLEMENT FACTOR-B
Authors: KAZATCHKINE MD GESERICK G ABBAL M ALPER CA BERTRAMS J DUTOIT E HAUPTMANN G LOKKI ML MAUFF G NAKAMURA S SEGURADO OG SIEMENS I SUZUKI K WEIDINGER S
Citation: Md. Kazatchkine et al., NOMENCLATURE FOR HUMAN-COMPLEMENT FACTOR-B, European journal of immunogenetics, 20(4), 1993, pp. 307-309
A LEUCINE-TO-PROLINE SUBSTITUTION CAUSES A DEFECTIVE ALPHA(1)-ANTICHYMOTRYPSIN ALLELE ASSOCIATED WITH FAMILIAL OBSTRUCTIVE LUNG-DISEASE
Authors: POLLER W FABER JP WEIDINGER S TIEF K SCHOLZ S FISCHER M OLEK K KIRCHGESSER M HEIDTMANN HH
Citation: W. Poller et al., A LEUCINE-TO-PROLINE SUBSTITUTION CAUSES A DEFECTIVE ALPHA(1)-ANTICHYMOTRYPSIN ALLELE ASSOCIATED WITH FAMILIAL OBSTRUCTIVE LUNG-DISEASE, Genomics, 17(3), 1993, pp. 740-743
IMMUNOLOGICAL STANDARDIZATION - NOMENCLATURE FOR HUMAN-COMPLEMENT FACTOR-B (REPRINTED FROM BULL WHO, VOL 70, PG 541-543, 1992)
Authors: KAZATCHKINE MD GESERICK G ABBAL M ALPER CA BERTRAMS J DUTOIT E HAUPTMANN G LOKKI ML MAUFF G NAKAMURA S SEGURADO OG SIEMENS I SUZUKI K WEIDINGER S
Citation: Md. Kazatchkine et al., IMMUNOLOGICAL STANDARDIZATION - NOMENCLATURE FOR HUMAN-COMPLEMENT FACTOR-B (REPRINTED FROM BULL WHO, VOL 70, PG 541-543, 1992), Journal of immunological methods, 163(1), 1993, pp. 9-11
MOLECULAR-BASIS OF A DEFECTIVE ALPHA-1-ANTICHYMOTRYPSIN PHENOTYPE (BOCHUM-I) ASSOCIATED WITH FAMILIAL CHRONIC OBSTRUCTIVE LUNG-DISEASE
Authors: POLLER W FABER JP WEIDINGER S TIEF K SCHOLZ S OLEK K HEIDTMANN HH
Citation: W. Poller et al., MOLECULAR-BASIS OF A DEFECTIVE ALPHA-1-ANTICHYMOTRYPSIN PHENOTYPE (BOCHUM-I) ASSOCIATED WITH FAMILIAL CHRONIC OBSTRUCTIVE LUNG-DISEASE, The American review of respiratory disease, 147(4), 1993, pp. 677-677
PGD PORT-ELIZABETH - A NEW VARIANT FOUND IN SOUTH-AFRICA
Authors: SCHLAPHOFF T WEIDINGER S PETERSEN W MAY RM DUTOIT ED
Citation: T. Schlaphoff et al., PGD PORT-ELIZABETH - A NEW VARIANT FOUND IN SOUTH-AFRICA, Human genetics, 88(6), 1992, pp. 709-709
Risultati: 1-18 |