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B Lüdecke

Showing results (1-10 of 9) with videos related to

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Human Genetics|June 1, 1995
Frequent sequence variant in the human tyrosine hydroxylase geneB Lüdecke, K Bartholomé
Methods of Information in Medicine. Supplement|January 1, 1972
[A mineral balance evaluation system]E Wolters, B Lüdecke
Advances in Pharmacology (San Diego, Calif.)|November 5, 1997
Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystoniaK Bartholomé, B Lüdecke
Neuroradiology|March 1, 1971
Technique and value of gas and Pantopaque cisternography in the diagnosis of cerebello-pontine angle tumoursS Wende, B Lüdecke
Human Genetics|January 1, 1995
A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndromeB Lüdecke, B Dworniczak, K Bartholomé
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 12, 2007
Clinical tumor growth and comparison with proliferation markers in non-functioning (inactive) pituitary adenomasW Saeger, B Lüdecke, D K Lüdecke
Human Genetics|March 1, 1993
Sequence variant of the human cathepsin G geneB Lüdecke, W Poller, K Olek, et al.
Human Molecular Genetics|July 1, 1995
Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase geneP M Knappskog, T Flatmark, J Mallet, et al.
Human Molecular Genetics|July 1, 1996
Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase geneB Lüdecke, P M Knappskog, P T Clayton, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genetics|June 1, 1995
Frequent sequence variant in the human tyrosine hydroxylase geneB Lüdecke, K Bartholomé
Methods of Information in Medicine. Supplement|January 1, 1972
[A mineral balance evaluation system]E Wolters, B Lüdecke
Advances in Pharmacology (San Diego, Calif.)|November 5, 1997
Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystoniaK Bartholomé, B Lüdecke
Neuroradiology|March 1, 1971
Technique and value of gas and Pantopaque cisternography in the diagnosis of cerebello-pontine angle tumoursS Wende, B Lüdecke
Human Genetics|January 1, 1995
A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndromeB Lüdecke, B Dworniczak, K Bartholomé
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 12, 2007
Clinical tumor growth and comparison with proliferation markers in non-functioning (inactive) pituitary adenomasW Saeger, B Lüdecke, D K Lüdecke
Human Genetics|March 1, 1993
Sequence variant of the human cathepsin G geneB Lüdecke, W Poller, K Olek, et al.
Human Molecular Genetics|July 1, 1995
Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase geneP M Knappskog, T Flatmark, J Mallet, et al.
Human Molecular Genetics|July 1, 1996
Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase geneB Lüdecke, P M Knappskog, P T Clayton, et al.
Pageof 1