AAAAAA

   
Results: 1-15 |
Results: 15
Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester
Authors: Pihusch, R Buchholz, T Lohse, P Rubsamen, H Rogenhofer, N Hasbargen, U Hiller, E Thaler, CJ
Citation: R. Pihusch et al., Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester, AM J REPROD, 46(2), 2001, pp. 124-131
Phenotypic correction of lipid storage and growth arrest in Wolman diseasefibroblasts by gene transfer of lysosomal acid lipase
Authors: Tietge, UJF Sun, GS Czarnecki, S Yu, QC Lohse, P Du, H Grabowski, GA Glick, JM Rader, DJ
Citation: Ujf. Tietge et al., Phenotypic correction of lipid storage and growth arrest in Wolman diseasefibroblasts by gene transfer of lysosomal acid lipase, HUM GENE TH, 12(3), 2001, pp. 279-289
S680N substitution of the follicle-stimulating hormone receptor is a common polymorphism not associated with spontaneous human twinning
Authors: Hasbargen, U Thaler, CJ Ruebsamen, H Fuchshuber, S Lohse, P
Citation: U. Hasbargen et al., S680N substitution of the follicle-stimulating hormone receptor is a common polymorphism not associated with spontaneous human twinning, EUR J MED R, 6(7), 2001, pp. 315-316
Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: Mutations or polymorphisms?
Authors: Muller-Koch, Y Kopp, R Lohse, P Baretton, G Stoetzer, A Aust, D Daum, J Kerker, B Gross, M Dietmeier, W Holinksi-Feder, E
Citation: Y. Muller-koch et al., Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: Mutations or polymorphisms?, EUR J MED R, 6(11), 2001, pp. 473-482
Long-term administration of the HMG-CoA reductase inhibitor lovastatin in two patients with cholesteryl ester storage disease
Authors: Rassoul, F Richter, V Lohse, P Naumann, A Purschwitz, K Keller, E
Citation: F. Rassoul et al., Long-term administration of the HMG-CoA reductase inhibitor lovastatin in two patients with cholesteryl ester storage disease, INT J CL PH, 39(5), 2001, pp. 199-204
Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene
Authors: Fischereder, M Schneeberger, H Lohse, P Kramer, BK Schlondorff, D Land, W
Citation: M. Fischereder et al., Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene, AM J KIDNEY, 38(5), 2001, pp. 1061-1064
DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2
Authors: Holinski-Feder, E Muller-Koch, Y Friedl, W Moselein, G Keller, G Plaschke, J Ballhausen, W Gross, M Baldwin-Jedele, K Jungck, M Mangold, E Vogelsang, H Schackert, HK Lohse, P Murken, J Meitinger, T
Citation: E. Holinski-feder et al., DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2, J BIOCH BIO, 47(1-2), 2001, pp. 21-32
Case study - Familial Mediterranean fever
Authors: Ascherl, J Schmidbaur, W Wienbeck, M Lohse, P
Citation: J. Ascherl et al., Case study - Familial Mediterranean fever, INTERNIST, 42(8), 2001, pp. 1156-1160
Fluorescence-based detection of the CETP TaqIB polymorphism: False positives with the TaqMan-based exonuclease assay attributable to a previously unknown gene variant
Authors: Teupser, D Rupprecht, W Lohse, P Thiery, J
Citation: D. Teupser et al., Fluorescence-based detection of the CETP TaqIB polymorphism: False positives with the TaqMan-based exonuclease assay attributable to a previously unknown gene variant, CLIN CHEM, 47(5), 2001, pp. 852-857
The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C -> T mutation
Authors: Hasbargen, U Lohse, P Thaler, CJ
Citation: U. Hasbargen et al., The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C -> T mutation, HUM REPR, 15(12), 2000, pp. 2659-2662
Subclinical course of cholesteryl ester storage disease in an adult with hypercholesterolemia, accelerated atherosclerosis, and liver cancer
Authors: Elleder, M Chlumska, A Hyanek, J Poupetova, H Ledvinova, J Maas, S Lohse, P
Citation: M. Elleder et al., Subclinical course of cholesteryl ester storage disease in an adult with hypercholesterolemia, accelerated atherosclerosis, and liver cancer, J HEPATOL, 32(3), 2000, pp. 528-534
Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease
Authors: Lohse, P Maas, S Lohse, P Elleder, M Kirk, JM Besley, GTN Seidel, D
Citation: P. Lohse et al., Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease, J LIPID RES, 41(1), 2000, pp. 23-31
Porphyria cutanea tarda related to genetically linked iron overload in compound heterozygous anlage for 2 mutations in the hemochromatosis gene
Authors: Mangold, E Diepolder, H Lohse, P Pape, GR Ritter, MM
Citation: E. Mangold et al., Porphyria cutanea tarda related to genetically linked iron overload in compound heterozygous anlage for 2 mutations in the hemochromatosis gene, INTERNIST, 41(10), 2000, pp. 1103-1107
Central pulmonary embolism found in prothrombin dimorphism (hereditary thrombophilia)
Authors: Tischer, J Forstpointner, R Lohse, P Hiller, E
Citation: J. Tischer et al., Central pulmonary embolism found in prothrombin dimorphism (hereditary thrombophilia), INTERNIST, 41(1), 2000, pp. 61-65
Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease
Authors: Lohse, P Maas, S Lohse, P Sewell, AC van Diggelen, OP Seidel, D
Citation: P. Lohse et al., Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease, J LIPID RES, 40(2), 1999, pp. 221-228
Risultati: 1-15 |