Peroxisomal disorders in manROSCHER, A. A; ROLINSKI, B.Cell biochemistry and function. 1992, Vol 10, Num 3, pp 201-207, issn 0263-6484Article

Unusual presentation of the righ side of ectopic testicular spleenBRASCH, J; ROSCHER, A. A.International surgery. 1987, Vol 72, Num 4, pp 233-234, issn 0020-8868Article

Simple high-performance liquid chromatographic method for the detection of phenylpropionylglycine in urine as a diagnostic tool in inherited medium-chain acyl-coenzyme A dehydrogenase deficiencyFLATH, B; ROLINSKI, B; ROSCHER, A. A et al.Journal of chromatography. B, Biomedical sciences and applications. 1997, Vol 694, Num 1, pp 227-232, issn 1387-2273Article

Analysis of the two common alpha-1-antitrypsin deficiency alleles PiMS and PiMZ as modifiers of Pseudomonas aeruginosa susceptibility in cystic fibrosisMEYER, P; BRAUN, A; ROSCHER, A. A et al.Clinical genetics. 2002, Vol 62, Num 4, pp 325-327, issn 0009-9163Article

Supervised machine learning techniques for the classification of metabolic disorders in newbornsBAUMGARTNER, C; BÖHM, C; BAUMGARTNER, D et al.Bioinformatics (Oxford. Print). 2004, Vol 20, Num 17, pp 2985-2996, issn 1367-4803, 12 p.Article

Varianten angeborener Stoffwech-selstörungen mit spätem Beginn, aber bedrohlichem Verlauf = Variants of inborn errors of metabolism with late onset but nevertheless life threatening coursePLÖCHL, E; PLÖCHL, W; WERMUTH, B et al.Klinische Pädiatrie. 2001, Vol 213, Num 5, pp 261-265, issn 0300-8630Article

Synthesis of kininogen and degradation of bradykinin by PC12 cellsDENDORFER, A; WELLHÖNER, P; BRAUN, A et al.British journal of pharmacology. 1997, Vol 122, Num 8, pp 1585-1592, issn 0007-1188Article

Determination of total homocysteine in human plasma by isocratic high-performance liquid chromatographyFEUSSNER, A; ROLINSKI, B; WEISS, N et al.European journal of clinical chemistry and clinical biochemistry. 1997, Vol 35, Num 9, pp 687-691, issn 0939-4974Conference Paper

Pharmacokinetics of orally administered zidovudine in HIV-infected children and adultsWINTERGERST, U; ROLINSKI, B; VOCKS-HAUCK, M et al.Infection. 1995, Vol 23, Num 6, pp 344-348, issn 0300-8126Article

Evaluation of saliva as a specimen for monitoring zidovudine therapy in HIV-infected patientsROLINSKI, B; WINTERGERST, U; MATUSCHKE, A et al.AIDS (London). 1991, Vol 5, Num 7, pp 885-888, issn 0269-9370, 4 p.Article

Lung function of school children with low levels of α₁-antitrypsin and tobacco smoke exposureVON EHRENSTEIN, O. S; VON MUTIUS, E; MAIER, E et al.The European respiratory journal. 2002, Vol 19, Num 6, pp 1099-1106, issn 0903-1936Article

Lack of absorption of didanosine after rectal administration in human immunodeficiency virus-infected patientsWINTERGERST, U; ROLINSKI, B; SÖLDER, B et al.Antimicrobial agents and chemotherapy. 1999, Vol 43, Num 3, pp 699-701, issn 0066-4804Article

Identification and occurrence of mRNAs for components of the kallikrein-kinin system in human skin and in skin diseasesSCHREMMER-DANNINGER, E; HERMANN, A; FINK, E et al.Immunopharmacology (New York). 1999, Vol 43, Num 2-3, pp 287-291, issn 0162-3109Conference Paper

Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy geneHOLZINGER, A; MAIER, E; STÖCKLER-IPSIROGLU, S et al.Clinical genetics. 1998, Vol 53, Num 6, pp 482-487, issn 0009-9163Article

Solubilization and characterization of B₂ bradykinin receptors from cultured human fibroblastsFAUSSNER, A; HEINZ-ERIAN, P; KLIER, C et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 15, pp 9442-9446, issn 0021-9258, 5 p.Article

Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis. A complementation study involving cell lines from 19 patientsROSCHER, A. A; HOEFLER, S; HOEFLER, G et al.Pediatric research. 1989, Vol 26, Num 1, pp 67-72, issn 0031-3998, 6 p.Article

Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycleRÖSCHINGER, W; MUNTAU, A. C; DURAN, M et al.Clinica chimica acta. 2000, Vol 298, Num 1-2, pp 55-68, issn 0009-8981Article

Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy : A third biochemical variant of 2-hydroxyglutaric aciduria?MUNTAU, A. C; RÖSCHINGER, W; MERKENSCHLAGER, A et al.Neuropediatrics. 2000, Vol 31, Num 3, pp 137-140, issn 0174-304XArticle

Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduriaRANDAK, C; RÖSCHINGER, W; ROLINSKI, B et al.Journal of inherited metabolic disease. 2000, Vol 23, Num 5, pp 520-522, issn 0141-8955Article

Clinical and genetic aspects of X-linked adrenoleukodystrophyGÄRTNER, J; BRAUN, A; HOLZINGER, A et al.Neuropediatrics. 1998, Vol 29, Num 1, pp 3-13, issn 0174-304XArticle

A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor geneBRAUN, A; MAIER, E; KAMMERER, S et al.Human genetics. 1996, Vol 97, Num 5, pp 688-689, issn 0340-6717Article

Prenatal diagnosis in combined antithrombin and factor V gene mutationLANE, D. A; AUBERGER, K; IRELAND, H et al.British journal of haematology. 1996, Vol 94, Num 4, pp 753-755, issn 0007-1048Article

Population study of a sequence polymorphism in intron 2 of the human β-globin geneBRAUN, A; AMBACH, H; BICHLMAIER, R et al.Human genetics. 1995, Vol 95, Num 3, issn 0340-6717, p. 352Article

Autoradiographic localization and characterization of bradykinin receptors in human skinSCHREMMER-DANNINGER, E; HEINZ-ERIAN, P; TÖPFER-PETERSEN, E et al.European journal of pharmacology. 1995, Vol 283, Num 1-3, pp 207-216, issn 0014-2999Article

Anti-idiotypic antibodies bearing the internal image of a bradykinin epitope : production, characterization, and interaction with the kinin receptorHAASEMANN, M; BUSCHKO, J; FAUSSNER, A et al.The Journal of immunology (1950). 1991, Vol 147, Num 11, pp 3882-3892, issn 0022-1767Article