Alessandro P Burlina

9PUBLICATIONS
13CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthNeonatologyEpidemiological methodsMedical biochemistry - amino acids and metabolites
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Publications (9)

|Apr 16, 2025
Arginase 1 deficiency: a treatable form of spastic paraplegia.

Alessandro Burlina, Anna Ardissone, Roberta Battini

|Feb 21, 2025
Newborn Screening for Gaucher Disease: Parental Stress and Psychological Burden.

Chiara Cazzorla, Vincenza Gragnaniello, Giacomo Gaiga

|Dec 27, 2024
Newborn Screening for Acid Sphingomyelinase Deficiency: Prevalence and Genotypic Findings in Italy.

Vincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi

|Jan 22, 2024
Light and Shadows in Newborn Screening for Lysosomal Storage Disorders: Eight Years of Experience in Northeast Italy.

Vincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi

|Jun 27, 2023
Newborn Screening for Fabry Disease: Current Status of Knowledge.

Vincenza Gragnaniello, Alessandro P Burlina, Anna Commone

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