STAT6 and STAT1 are essential antagonistic regulators of cell survival in classical Hodgkin lymphoma cell line
Baus, D, Nonnenmacher, F, Jankowski, S, Döring, C, Bräutigam, C, Frank, M, Hansmann, M-L, Pfitzner, E
Published in Leukemia (01.10.2009)
Published in Leukemia (01.10.2009)
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Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF
Assmann, B E, Robinson, R O, Surtees, R A H, Bräutigam, C, Heales, S J R, Wevers, R A, Zschocke, J, Hyland, K, Sharma, R, Hoffmann, G F
Published in Neurology (25.05.2004)
Published in Neurology (25.05.2004)
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Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies
Fiumara, A, Bräutigam, C, Hyland, K, Sharma, R, Lagae, L, Stoltenborg, B, Hoffmann, G F, Jaeken, J, Wevers, R A
Published in Neuropediatrics (01.08.2002)
Published in Neuropediatrics (01.08.2002)
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Journal Article
The influence of L‐dopa on methylation capacity in aromatic L‐amino acid decarboxylase deficiency: Biochemical findings in two patients
Bräutigam, C., Wevers, R. A., Hyland, K., Sharma, R. K., Knust, A., Hoffmann, G. F.
Published in Journal of inherited metabolic disease (01.06.2000)
Published in Journal of inherited metabolic disease (01.06.2000)
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Journal Article
Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency
Bräutigam, C, Hyland, K, Wevers, R, Sharma, R, Wagner, L, Stock, G-J, Heitmann, F, Hoffmann, G F
Published in Neuropediatrics (01.06.2002)
Published in Neuropediatrics (01.06.2002)
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Journal Article
A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)
Wevers, R. A., Rijk‐van Andel, J. F., Bräutigam, C., Geurtz, B., Heuvel, L. P. W. J., Steenbergen‐Spanjers, G. C. H., Smeitink, J. A. M., Hoffmann, G. F., Gabreëls, F. J. M.
Published in Journal of inherited metabolic disease (01.06.1999)
Published in Journal of inherited metabolic disease (01.06.1999)
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Journal Article
Conference Proceeding
Neurotransmitter metabolites in CSF: An external quality control scheme
Bräutigam, C., Weykamp, C., Hoffmann, G. F., Wevers, R. A.
Published in Journal of inherited metabolic disease (01.06.2002)
Published in Journal of inherited metabolic disease (01.06.2002)
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Journal Article
Biochemical and Molecular Genetic Characteristics of the Severe Form of Tyrosine Hydroxylase Deficiency
Brautigam, Christa, Steenbergen-Spanjers, Gerry C.H, Hoffmann, Georg F, Dionisi-Vici, Carlo, van den Heuvel, Lambert P.W.J, Smeitink, Jan A.M, Wevers, Ron A
Published in Clinical chemistry (Baltimore, Md.) (01.12.1999)
Published in Clinical chemistry (Baltimore, Md.) (01.12.1999)
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Tyrosine hydroxylase deficiency with severe clinical course: Clinical and biochemical investigations and optimization of therapy
Dionisi-Vici, Carlo, Hoffmann, Georg F, Leuzzi, Vincenzo, Hoffken, Helmut, Bräutigam, Christa, Rizzo, Cristiano, Steebergen-Spanjers, Gerry C.H, Smeitink, Jan A.M, Wevers, Ron A
Published in The Journal of pediatrics (01.04.2000)
Published in The Journal of pediatrics (01.04.2000)
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Detection of β‐ureidopropionase deficiency with HPLC–electrospray tandem mass spectrometry and confirmation of the defect at the enzyme level
Van Kuilenburg, A. B. P., Van Lenthe, H., Assmann, B., Göhlich‐Ratmann, G., Hoffmann, G. F., Bräutigam, C., Wevers, R. A., Van Gennip, A. H.
Published in Journal of inherited metabolic disease (01.11.2001)
Published in Journal of inherited metabolic disease (01.11.2001)
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Journal Article
Dihydropyridmidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?
Assmann, B., Hoffmann, G. F., Wagner, L., Bräutigam, C., Seyberth, H. W., Duran, M., Van Kuilenburg, A. B. P., Wevers, R., Van Gennip, A. H.
Published in Journal of inherited metabolic disease (01.09.1997)
Published in Journal of inherited metabolic disease (01.09.1997)
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Journal Article
Plasmalogen phospholipids in plasma lipoproteins of normolipidemic donors and patients with hypercholesterolemia treated by LDL apheresis
Bräutigam, Carola, Engelmann, Bernd, Reiss, Daniela, Reinhardt, Ulrike, Thiery, Joachim, Richter, Werner O., Brosche, Thorolf
Published in Atherosclerosis (05.01.1996)
Published in Atherosclerosis (05.01.1996)
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Journal Article
Pathobiochemical implications of hyperdopaminuria in patients with aromatic L‐amino acid decarboxylase deficiency
Abeling, N. G. G. M., Bräutigam, C., Hoffmann, G. F., Barth, P. G., Wevers, R. A., Jaeken, J., Fiumara, A., Knust, A., Gennip, A. H.
Published in Journal of inherited metabolic disease (01.06.2000)
Published in Journal of inherited metabolic disease (01.06.2000)
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Journal Article
Arachidonic acid of platelet phospholipids is decreased after extracorporeal removal of plasma low density lipoproteins in patients with familial hypercholesterolemia
Bräutigam, Robert, Bräutigam, Carola, Lorenz, Reinhard, Richter, Werner O, Engelmann, Bernd
Published in Atherosclerosis (01.05.1997)
Published in Atherosclerosis (01.05.1997)
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Journal Article
Fast transmission of alterations in plasma phosphatidylcholine/sphingomyelin ratio and lyso phosphatidylcholine levels into changes of red blood cell membrane phospholipid composition after low density lipoprotein apheresis
Kulschar, R, Engelmann, B, Bräutigam, C, Duhm, J, Thiery, J, Richter, W O
Published in European journal of clinical investigation (01.04.1995)
Published in European journal of clinical investigation (01.04.1995)
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