Prof. Dr. Beat Steinmann (emeritiert)more information

Fakultäten » Medizinische Fakultät » Kinderspital Zürich: Medizinische Klinik » Stoffwechsel und Molekulare Pädiatrie, Abteilung für » Prof. Dr. Beat Steinmann (emeritiert)

Completed research projects

Project leader	Project title
Baumgartner	THE MOLECULAR BASIS AND FUNCTIONAL CHARACTERIZATION OF HUMAN 3-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY
Fowler	THE EFFECT OF COFACTORS AND VITAMINS ON HOMOCYSTEINE METABOLISM IN HEALTH AND DISEASE
Giunta Steinmann	MUTATION ANALYSIS IN VARIOUS TYPES OF THE EHLERS-DANLOS SYNDROME (EDS)
Steinmann	THE BRITTLE CORNEA SYNDROME : POSITIONAL CLONING AND MOLECULAR CHARACTERIZATION
	THE NEVO SYNDROME IS ALLELIC TO THE KYPHOSCOLIOTIC TYPE OF THE EHLERS-DANLOS SYDROME (EDS VIA)
	GALACTOKINASE DEFICIENCY, A CAUSE OF PRESENILE CATARACT IN HETEROZYGOTES?
	FANCONI-BICKEL SYNDROME: SECONDARY ENDOCRINOLOGICAL AND METABOLIC CHANGES