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Burlina, A.
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1

P.28 Blood phenylalanine control in patients with phenylket..:

Pinto, A ; Ahring, K ; Almeida, MF...
Molecular Genetics and Metabolism.  141 (2024)  - p. 108394 , 2024
Link: https://doi.org/10.1016/..
 
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P.34 Impact of free amino acids, glycomacropeptide and slow..:

Tosi, M ; Montanari, C ; Fiori, L...
Molecular Genetics and Metabolism.  141 (2024)  - p. 108400 , 2024
Link: https://doi.org/10.1016/..
 
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3

Defining tetrahydrobiopterin responsiveness in phenylketonu..:

Evers, R.A.F. ; van Wegberg, A.M.J. ; Ahring, K....
Molecular Genetics and Metabolism.  132 (2021)  4 - p. 215-219 , 2021
Link: https://doi.org/10.1016/..
 
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4

Standardising clinical outcomes measures for adult clinical..:

Moreno-Martinez, D. ; Aguiar, P. ; Auray-Blais, C....
Molecular Genetics and Metabolism.  132 (2021)  4 - p. 234-243 , 2021
Link: https://doi.org/10.1016/..
 
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5

Heritable and non-heritable uncommon causes of stroke:

Bersano, A. ; Kraemer, M. ; Burlina, A....
Journal of Neurology.  268 (2020)  8 - p. 2780-2807 , 2020
Link: https://doi.org/10.1007/..
 
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6

Formulation and Clinical Evaluation of Sodium Benzoate Oral..:

Maines, E. ; Urru, S. A. M. ; Burri, E....
AAPS PharmSciTech.  21 (2020)  3 - p. , 2020
Link: https://doi.org/10.1208/..
 
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7

PKU dietary handbook to accompany PKU guidelines:

MacDonald, A. ; van Wegberg, A. M. J. ; Ahring, K....
Orphanet Journal of Rare Diseases.  15 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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8

Correction to: Heritable and non-heritable uncommon causes ..:

Bersano, A. ; Kraemer, M. ; Burlina, A....
Journal of Neurology.  268 (2020)  8 - p. 2808-2809 , 2020
Link: https://doi.org/10.1007/..
 
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9

Correction to: PKU dietary handbook to accompany PKU guidel..:

MacDonald, A. ; van Wegberg, A. M. J. ; Ahring, K....
Orphanet Journal of Rare Diseases.  15 (2020)  1 - p. , 2020
Link: https://doi.org/10.1186/..
 
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10

Monogenic cerebral small‐vessel diseases: diagnosis and the..:

Mancuso, M. ; Arnold, M. ; Bersano, A....
European Journal of Neurology.  27 (2020)  6 - p. 909-927 , 2020
Link: https://doi.org/10.1111/..
 
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11

Progressive electrocardiographic changes in parallel with c..:

Figliozzi, S ; Camporeale, A ; Pieroni, M...
European Heart Journal.  41 (2020)  Supplement_2 - p. , 2020
Link: https://doi.org/10.1093/..
 
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12

251Predictors of clinical evolution in prehypertrophic Fabr..:

Camporeale, A ; Pieroni, M ; Pieruzzi, F...
European Heart Journal - Cardiovascular Imaging.  20 (2019)  Supplement_2 - p. , 2019
Link: https://doi.org/10.1093/..
 
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13

The complete European guidelines on phenylketonuria: diagno..:

van Wegberg, A. M. J. ; MacDonald, A. ; Ahring, K....
Orphanet Journal of Rare Diseases.  12 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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14

Galactose‐1‐phosphate uridyltransferase deficiency: A liter..:

Viggiano, E. ; Marabotti, A. ; Politano, L..
Clinical Genetics.  93 (2017)  2 - p. 206-215 , 2017
Link: https://doi.org/10.1111/..
 
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15

Clinical, biochemical and molecular characterization of pro..:

Motta, M. ; Tatti, M. ; Furlan, F....
Clinical Genetics.  90 (2016)  3 - p. 220-229 , 2016
Link: https://doi.org/10.1111/..
 
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