Alex Pinto
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Explore the profile of Alex Pinto including associated specialties, affiliations and a list of published articles.
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73
Citations
569
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Recent Articles
11.
Pinto A, Daly A, Rocha J, Ashmore C, Evans S, Ilgaz F, et al.
Nutrients
. 2023 Dec;
15(23).
PMID: 38068761
In phenylketonuria (PKU), an important component of the UK dietary management system is a 50 mg phenylalanine (Phe)/1 g protein exchange system used to allocate the Phe/natural protein intakes according...
12.
Pinto A, Ilgaz F, Evans S, van Dam E, Rocha J, Karabulut E, et al.
Nutrients
. 2023 Aug;
15(16).
PMID: 37630696
In phenylketonuria (PKU), natural protein tolerance is defined as the maximum natural protein intake maintaining a blood phenylalanine (Phe) concentration within a target therapeutic range. Tolerance is affected by several...
13.
Pinto A, Daly A, Rocha J, Ashmore C, Evans S, Jackson R, et al.
Nutrients
. 2023 Jul;
15(13).
PMID: 37447372
In phenylketonuria (PKU), a previous intervention study assessing the patients ability to tolerate fruits and vegetables containing phenylalanine 76-100 mg/100 g without limit or measurement, found that an extra 50...
14.
Cassidy S, Evans S, Pinto A, Daly A, Ashmore C, Ford S, et al.
Nutrients
. 2023 May;
15(10).
PMID: 37242212
Background: A diagnosis of phenylketonuria (PKU) in an infant is a devastating and overwhelming event for their parents. Providing appropriate information and support is paramount, especially at the beginning of...
15.
Yilmaz O, Cochrane B, Wildgoose J, Pinto A, Evans S, Daly A, et al.
Orphanet J Rare Dis
. 2023 Jan;
18(1):16.
PMID: 36698214
Background: Phenylalanine-free infant formula is an essential source of safe protein in a phenylalanine restricted diet, but its efficacy is rarely studied. We report a multicentre, open, longitudinal, prospective intervention...
16.
Gama M, Adam S, Adams S, Allen H, Ashmore C, Bailey S, et al.
Nutrients
. 2022 Dec;
14(23).
PMID: 36501017
Introduction: There is little practical guidance about suitable food choices for higher natural protein tolerances in patients with phenylketonuria (PKU). This is particularly important to consider with the introduction of...
17.
Dillard L, Pinto A, Mueller K, Schubert C, Paulsen A, Merten N, et al.
J Aging Health
. 2022 Nov;
35(7-8):455-465.
PMID: 36412130
ObjectivesDetermine associations of hearing loss (HL) and hearing aid (HA) use with cognition, health-related quality of life (HRQoL), and depressive symptoms. Participants were from the Epidemiology of Hearing Loss Study...
18.
Yilmaz O, Pinto A, Daly A, Ashmore C, Evans S, Yabanci Ayhan N, et al.
Orphanet J Rare Dis
. 2022 Oct;
17(1):395.
PMID: 36303225
Background: In children with phenylketonuria (PKU), transitioning protein substitutes at the appropriate developmental age is essential to help with their long-term acceptance and ease of administration. We assessed the parental...
19.
Pinto A, Daly A, Rocha J, Ashmore C, Evans S, Jackson R, et al.
Nutrients
. 2022 Oct;
14(20).
PMID: 36296952
Fruits and vegetables containing phenylalanine ≤ 75 mg/100 g (except potatoes) have little impact on blood phenylalanine in phenylketonuria (PKU). In a randomized, controlled, crossover intervention trial, we examined the...
20.
Tims S, Marsaux C, Pinto A, Daly A, Karall D, Kuhn M, et al.
Mol Genet Metab
. 2022 Oct;
137(3):308-322.
PMID: 36274442
Propionic acidemia (PA) is an inherited metabolic disorder of propionate metabolism, where the gut microbiota may play a role in pathophysiology and therefore, represent a relevant therapeutic target. Little is...