JIM 2025; 2 (3): e996
DOI: 10.61012_20258_996

Ten-year experience of newborn screening for glutaric aciduria type 1 in northeast Italy: successes, challenges and unexpected findings

JIM 2025; 2 (3): e998
DOI: 10.61012_20258_998

Exploring neuropathic pain in Fabry Disease: a review of pathogenesis, diagnostic pitfalls and management starting from clinical cases

JIM 2025; 2 (3): e1001
DOI: 10.61012_20258_1001

Biogenic amines in phenylketonuria: a narrative review

JIM 2025; 2 (3): e1003
DOI: 10.61012_20258_1003

Potential applications of digital health technologies in adults with inherited metabolic disorders

JIM 2025; 2 (3): e1005
DOI: 10.61012_20258_1005

The effects of neonatal nutrition on 17-α-hydroxyprogesterone levels in classic congenital adrenal hyperplasia screening: a retrospective study

JIM 2025; 2 (3): e1007
DOI: 10.61012_20258_1007

Survey on dietetic expertise and clinical application of the ketogenic diet in Italy: what professional resources are available for inherited metabolic disorders?

JIM 2025; 2 (Suppl 1): e951
DOI: 10.61012_20257_951

Why re-think dietary treatment in PKU?

JIM 2025; 2 (Suppl 1): e956
DOI: 10.61012_20257_956

Diet in patients with phenylketonuria treated with pegvaliase: a narrative review on the state-of-the-art and challenges

JIM 2025; 2 (Suppl 1): e958
DOI: 10.61012_20256_958

Adult phenylketonuria: transition management and follow-up

JIM 2025; 2 (Suppl 1): e954
DOI: 10.61012_20257_954

Assessment of executive functions, adaptive skills, emotional and behavioral outcomes from pediatric age to adulthood in patients with PKU: a systematic review

JIM 2025; 2 (2): e924
DOI: 10.61012_20255_924

A diagnostic x-ray in a newborn with skeletal abnormalities: a rare case of mucolipidosis type 2

JIM 2025; 2 (2): e922
DOI: 10.61012_20255_922

Primary lipid myopathies: a narrative review