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European Journal of Pediatrics
|
May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?
E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Molecular Genetics and Metabolism
|
October 26, 2019
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria
Parith Wongkittichote, Gary Cunningham, Marshall L Summar, et al.
Molecular Genetics and Metabolism
|
May 15, 2001
Mutation analysis of the MCM gene in Israeli patients with mut(0) disease
I Berger, A Shaag, Y Anikster, et al.
European Journal of Pediatrics
|
September 15, 1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency
C Steen, E R Baumgartner, M Duran, et al.
Journal of Inherited Metabolic Disease
|
October 13, 2001
CblC/D defect combined with haemodynamically highly relevant VSD
M Tomaske, A Bosk, M K Heinemann, et al.
Journal of Inherited Metabolic Disease
|
May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promise
Bianca Dimitrov, Femke Molema, Monique Williams, et al.
Archives of General Psychiatry
|
November 1, 1984
Haloperidol. Plasma levels and prolactin response as predictors of clinical improvement in schizophrenia: chemical v radioreceptor plasma level assays
R C Smith, R Baumgartner, C H Misra, et al.
Biomed Research International
|
March 31, 2015
An open-label uncontrolled, multicenter study for the evaluation of the efficacy and safety of the dermal filler Princess VOLUME in the treatment of nasolabial folds
Daisy Kopera, Michael Palatin, Rolf Bartsch, et al.
BMC Veterinary Research
|
June 24, 2016
Erratum to: Long-term monitoring of opioid, sedative and anti-inflammatory drugs in horse hair using a selective and sensitive LC-MS/MS procedure
Milena M Madry, Barbara S Spycher, Jacqueline Kupper, et al.
Journal of Inherited Metabolic Disease
|
March 13, 2015
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines
Martina Huemer, Viktor Kožich, Piero Rinaldo, et al.
Page
of 77
Search research articles
Search
Showing results (521-530 of 770) with videos related to
Sort By:
Page
of 77
European Journal of Pediatrics
|
May 1, 1996
Atypical vitamin B12-unresponsive methylmalonic aciduria in sibship with severe progressive encephalomyelopathy: a new genetic disease?
E Mayatepek, G F Hoffmann, R Baumgartner, et al.
Molecular Genetics and Metabolism
|
October 26, 2019
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria
Parith Wongkittichote, Gary Cunningham, Marshall L Summar, et al.
Molecular Genetics and Metabolism
|
May 15, 2001
Mutation analysis of the MCM gene in Israeli patients with mut(0) disease
I Berger, A Shaag, Y Anikster, et al.
European Journal of Pediatrics
|
September 15, 1999
Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency
C Steen, E R Baumgartner, M Duran, et al.
Journal of Inherited Metabolic Disease
|
October 13, 2001
CblC/D defect combined with haemodynamically highly relevant VSD
M Tomaske, A Bosk, M K Heinemann, et al.
Journal of Inherited Metabolic Disease
|
May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promise
Bianca Dimitrov, Femke Molema, Monique Williams, et al.
Archives of General Psychiatry
|
November 1, 1984
Haloperidol. Plasma levels and prolactin response as predictors of clinical improvement in schizophrenia: chemical v radioreceptor plasma level assays
R C Smith, R Baumgartner, C H Misra, et al.
Biomed Research International
|
March 31, 2015
An open-label uncontrolled, multicenter study for the evaluation of the efficacy and safety of the dermal filler Princess VOLUME in the treatment of nasolabial folds
Daisy Kopera, Michael Palatin, Rolf Bartsch, et al.
BMC Veterinary Research
|
June 24, 2016
Erratum to: Long-term monitoring of opioid, sedative and anti-inflammatory drugs in horse hair using a selective and sensitive LC-MS/MS procedure
Milena M Madry, Barbara S Spycher, Jacqueline Kupper, et al.
Journal of Inherited Metabolic Disease
|
March 13, 2015
Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines
Martina Huemer, Viktor Kožich, Piero Rinaldo, et al.
Page
of 77