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U Wendel

Showing results (11-20 of 186) with videos related to

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Monatsschrift Fur Kinderheilkunde|September 1, 1979
[Idiopathic osteolysis type Hajdu-Cheney in early childhood (author's transl)]U Wendel, H Kemperdick
Der Nervenarzt|February 1, 1976
[Letter: Significance of the medical check-up in a regional psychiatric hospital. Short communication]E Schulz, U Wendel
European Journal of Pediatrics|June 1, 1984
Betaine in the treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiencyU Wendel, H J Bremer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1986
[Type I glycogenosis: extending therapy with uncooked cornstarch]B Biggemann, R Hilgarth, U Wendel
Pediatric Neurology|September 1, 1993
Is demyelination a feature of maple syrup urine disease?K Müller, T Kahn, U Wendel
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1989
Analysis of maple syrup urine disease in cell culture: use of substratesP Schadewaldt, K Beck, U Wendel
Lancet (London, England)|September 3, 1983
HLA and Wolfram (DIDMOAD) syndromeJ Bertrams, U Wendel, S Koletzko
Journal of Inherited Metabolic Disease|February 21, 2007
Social outcome in adults with maple syrup urine disease (MSUD)E Simon, M Schwarz, U Wendel
Journal of Inherited Metabolic Disease|May 19, 1998
Pregnancy in a woman with maple syrup urine diseaseS Grünewald, F Hinrichs, U Wendel
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 15, 1993
Neonatal screening for maple syrup urine disease by an enzyme-mediated colorimetric methodU Wendel, J Gonzales, W Hummel
Pageof 19

Showing results (11-20 of 186) with videos related to

Sort By:
Pageof 19
Monatsschrift Fur Kinderheilkunde|September 1, 1979
[Idiopathic osteolysis type Hajdu-Cheney in early childhood (author's transl)]U Wendel, H Kemperdick
Der Nervenarzt|February 1, 1976
[Letter: Significance of the medical check-up in a regional psychiatric hospital. Short communication]E Schulz, U Wendel
European Journal of Pediatrics|June 1, 1984
Betaine in the treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiencyU Wendel, H J Bremer
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1986
[Type I glycogenosis: extending therapy with uncooked cornstarch]B Biggemann, R Hilgarth, U Wendel
Pediatric Neurology|September 1, 1993
Is demyelination a feature of maple syrup urine disease?K Müller, T Kahn, U Wendel
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 15, 1989
Analysis of maple syrup urine disease in cell culture: use of substratesP Schadewaldt, K Beck, U Wendel
Lancet (London, England)|September 3, 1983
HLA and Wolfram (DIDMOAD) syndromeJ Bertrams, U Wendel, S Koletzko
Journal of Inherited Metabolic Disease|February 21, 2007
Social outcome in adults with maple syrup urine disease (MSUD)E Simon, M Schwarz, U Wendel
Journal of Inherited Metabolic Disease|May 19, 1998
Pregnancy in a woman with maple syrup urine diseaseS Grünewald, F Hinrichs, U Wendel
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 15, 1993
Neonatal screening for maple syrup urine disease by an enzyme-mediated colorimetric methodU Wendel, J Gonzales, W Hummel
Pageof 19