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Results: 1-20 |
Results: 20
Gastro-intestinal tolerance following oral administration of spray-dried diclofenac-loaded nanocapsules and nanospheres
Authors: Guterres, SS Muller, CR Michalowski, CB Pohlmann, AR Dalla Costa, T
Citation: Ss. Guterres et al., Gastro-intestinal tolerance following oral administration of spray-dried diclofenac-loaded nanocapsules and nanospheres, STP PHARM S, 11(3), 2001, pp. 229-233
Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes
Authors: Schneider, C Wessig, C Muller, CR Brechtelsbauer, D Grimm, T
Citation: C. Schneider et al., Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes, NEUROMUSC D, 11(5), 2001, pp. 485-488
Quality control in mutation analysis: the European Molecular Genetics Quality Network (EMQN)
Authors: Muller, CR
Citation: Cr. Muller, Quality control in mutation analysis: the European Molecular Genetics Quality Network (EMQN), EUR J PED, 160(8), 2001, pp. 464-467
Evaluation of DHPLC in the analysis of hemophilia A
Authors: Oldenburg, J Ivaskevicius, V Rost, S Fregin, A White, K Holinski-Feder, E Muller, CR Weber, BHF
Citation: J. Oldenburg et al., Evaluation of DHPLC in the analysis of hemophilia A, J BIOCH BIO, 47(1-2), 2001, pp. 39-51
Spray-dried diclofenac-loaded poly(epsilon-caprolactone) nanocapsules and nanospheres. Preparation and physicochemical characterization
Authors: Muller, CR Schaffazick, SR Pohlmann, AR Freitas, LD da Silveira, NP Costa, TD Guterres, SS
Citation: Cr. Muller et al., Spray-dried diclofenac-loaded poly(epsilon-caprolactone) nanocapsules and nanospheres. Preparation and physicochemical characterization, PHARMAZIE, 56(11), 2001, pp. 864-867
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data
Authors: Ivaskevicius, V Jurgutis, R Rost, S Muller, A Schmitt, C Wulff, K Herrmann, FH Muller, CR Schwaab, R Oldenburg, J
Citation: V. Ivaskevicius et al., Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data, BR J HAEM, 112(4), 2001, pp. 1062-1070
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)
Authors: Schneider, C Grimm, T Kress, W Sommer, C Muller, CR
Citation: C. Schneider et al., Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM), NEUROMUSC D, 10(7), 2000, pp. 481-483
Preparation and characterization of spray-dried polymeric nanocapsules
Authors: Muller, CR Bassani, VL Pohlmann, AR Michalowski, CB Petrovick, PR Guterres, SS
Citation: Cr. Muller et al., Preparation and characterization of spray-dried polymeric nanocapsules, DRUG DEV IN, 26(3), 2000, pp. 343-347
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex
Authors: Oldenburg, J von Brederlow, B Fregin, A Rost, S Wolz, W Eberl, W Eber, S Lenz, E Schwabb, R Brackmann, HH Effenberger, W Harbrecht, U Schurgers, LJ Vermeer, C Muller, CR
Citation: J. Oldenburg et al., Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex, THROMB HAEM, 84(6), 2000, pp. 937-941
Spectral karyotyping of the human colon cancer cell lines SW480 and SW620
Authors: Melcher, R Steinlein, C Feichtinger, W Muller, CR Menzel, T Luhrs, H Scheppach, W Schmid, M
Citation: R. Melcher et al., Spectral karyotyping of the human colon cancer cell lines SW480 and SW620, CYTOG C GEN, 88(1-2), 2000, pp. 145-152
Comperative spectral karyotyping of two cell lines derived from a primary colorectal tumor and a metastatic site of the same patient
Authors: Melcher, R Steinlein, C Schmid, M Menzel, T Luhrs, H Scheppach, W Muller, CR
Citation: R. Melcher et al., Comperative spectral karyotyping of two cell lines derived from a primary colorectal tumor and a metastatic site of the same patient, ZBL CHIR, 125, 2000, pp. 21-22
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism
Authors: Oldenburg, J Rost, S El-Maarri, O Leuer, M Olek, K Muller, CR Schwaab, R
Citation: J. Oldenburg et al., De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism, BLOOD, 96(8), 2000, pp. 2805-2806
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism
Authors: Oldenburg, J Rost, S El-Maarri, O Leuer, M Olek, K Muller, CR Schwaab, R
Citation: J. Oldenburg et al., De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism, BLOOD, 96(8), 2000, pp. 2905-2906
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy
Authors: Nowak, KJ Wattanasirichaigoon, D Goebel, HH Wilce, M Pelin, K Donner, K Jacob, RL Hubner, C Oexle, K Anderson, JR Verity, CM North, KN Iannaccone, ST Muller, CR Nurnberg, P Muntoni, F Sewry, C Hughes, I Sutphen, R Lacson, AG Swoboda, KJ Vigneron, J Wallgren-Pettersson, C Beggs, AH Laing, NG
Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212
Allelic heterogeneity of alkaptonuria in Central Europe
Authors: Muller, CR Fregin, A Srsen, S Srsnova, K Halliger-Keller, B Felbor, U Seemanova, E Kress, W
Citation: Cr. Muller et al., Allelic heterogeneity of alkaptonuria in Central Europe, EUR J HUM G, 7(6), 1999, pp. 645-651
The genetic defect of the alkaptonuric mouse (aku)
Authors: Kress, W Schmidt, SR Halliger-Keller, B Montagutelli, X Muller, CR
Citation: W. Kress et al., The genetic defect of the alkaptonuric mouse (aku), MAMM GENOME, 10(1), 1999, pp. 68-70
Distribution of emerin during the cell cycle
Authors: Dabauvalle, MC Muller, E Ewald, A Kress, W Krohne, G Muller, CR
Citation: Mc. Dabauvalle et al., Distribution of emerin during the cell cycle, EUR J CELL, 78(10), 1999, pp. 749-756
Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions
Authors: Simoni, M Bakker, E Eurlings, MCM Matthijs, G Moro, E Muller, CR Vogt, PH
Citation: M. Simoni et al., Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions, INT J ANDR, 22(5), 1999, pp. 292-299
Diagnostic approach to muscular dystrophies - recent developments and casereports
Authors: Weilbach, FX Kress, W Strassburg, HM Muller, CR Gold, R
Citation: Fx. Weilbach et al., Diagnostic approach to muscular dystrophies - recent developments and casereports, NERVENARZT, 70(2), 1999, pp. 89-100
Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene
Authors: Felbor, U Mutsch, Y Grehn, F Muller, CR Kress, W
Citation: U. Felbor et al., Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene, BR J OPHTH, 83(6), 1999, pp. 680-683
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