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Molecular Genetics and Metabolism
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May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revision
A M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism
|
February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countries
R A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism
|
October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 cases
A MacDonald, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism
|
November 12, 2013
Dietary practices in pyridoxine non-responsive homocystinuria: a European survey
S Adam, M F Almeida, E Carbasius Weber, et al.
Orphanet Journal of Rare Diseases
|
January 27, 2018
International practices in the dietary management of fructose 1-6 biphosphatase deficiency
A Pinto, M Alfadhel, R Akroyd, et al.
Molecular Genetics and Metabolism
|
October 12, 2013
Dietary management of urea cycle disorders: European practice
S Adam, M F Almeida, M Assoun, et al.
Molecular Genetics and Metabolism Reports
|
March 10, 2017
Dietary practices in isovaleric acidemia: A European survey
A Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports
|
October 13, 2017
Dietary practices in propionic acidemia: A European survey
A Daly, A Pinto, S Evans, et al.
Molecular Genetics and Metabolism
|
April 12, 2015
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach
A Aguiar, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism Reports
|
February 2, 2019
Weaning practices in phenylketonuria vary between health professionals in Europe
A Pinto, S Adams, K Ahring, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 61) with videos related to
Sort By:
Page
of 7
Molecular Genetics and Metabolism
|
May 16, 2025
European guidelines on diagnosis and treatment of phenylketonuria: First revision
A M J van Wegberg, A MacDonald, K Ahring, et al.
Molecular Genetics and Metabolism
|
February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countries
R A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism
|
October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 cases
A MacDonald, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism
|
November 12, 2013
Dietary practices in pyridoxine non-responsive homocystinuria: a European survey
S Adam, M F Almeida, E Carbasius Weber, et al.
Orphanet Journal of Rare Diseases
|
January 27, 2018
International practices in the dietary management of fructose 1-6 biphosphatase deficiency
A Pinto, M Alfadhel, R Akroyd, et al.
Molecular Genetics and Metabolism
|
October 12, 2013
Dietary management of urea cycle disorders: European practice
S Adam, M F Almeida, M Assoun, et al.
Molecular Genetics and Metabolism Reports
|
March 10, 2017
Dietary practices in isovaleric acidemia: A European survey
A Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports
|
October 13, 2017
Dietary practices in propionic acidemia: A European survey
A Daly, A Pinto, S Evans, et al.
Molecular Genetics and Metabolism
|
April 12, 2015
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach
A Aguiar, K Ahring, M F Almeida, et al.
Molecular Genetics and Metabolism Reports
|
February 2, 2019
Weaning practices in phenylketonuria vary between health professionals in Europe
A Pinto, S Adams, K Ahring, et al.
Page
of 7