Marco Spada

University of Turin

Italy

Research Interests

Explore related searches

Professors in Italy

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (20)

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Collaborators (8)

Carlo Dionisi-Vici

Head of the Division

Ospedale Pediatrico Bambino Gesù

ITALY

View details

antonio amoroso

Full Professor medical genetics

University of Turin

ITALY

View details

Elvira Verduci

University of Milan

ITALY

View details

Margherita RUOPPOLO

University of Naples Federico II

ITALY

View details

Krishna Chatterjee

University of Cambridge

UNITED KINGDOM

View details

giancarlo parenti

Full Professor

Università degli Studi di Napoli Federico II

ITALY

View details

Erica L T van den Akker

NETHERLANDS

View details

Davide Tonduti

Assistant Professor

Università degli Studi di Torino

ITALY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Marco Spada

Research Interests

Explore related searches

Contact this professor

Articles (20)

Identification of Novel Mutations in Patients Affected by Gaucher Disease

Single Amino Acid Supplementation in Inherited Metabolic Disorders: An Evidence-Based Review of Interventions

Pediatric Post-Pump Chorea: Case Report and Implications for Differential Diagnosis

Long-Term Management of Patients with Mild Urea Cycle Disorders Identified through the Newborn Screening: An Expert Opinion for Clinical Practice

Towards needed improvements in inherited metabolic medicine in adulthood: The SIMMESN adult metabolic working group and MetabERN Joint Position Statement

Acid sphingomyelinase deficiency (ASMD): addressing knowledge gaps in unmet needs and patient journey in Italy—a Delphi consensus

An expert consensus on the recommendations for the use of biomarkers in Fabry disease

Effect of Migalastat on cArdiac InvOlvement in FabRry DiseAse: MAIORA study

Insulinoma in pediatric tuberous sclerosis complex: a case report

Long-term outcomes and health-related quality of life 20 years after pediatric liver transplantation

Long-Term Efficacy of T3 Analogue Triac in Children and Adults with MCT8 Deficiency: A Real-Life Retrospective Cohort Study

Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists.

Trabecular complexity as an early marker of cardiac involvement in Fabry disease

Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium.

Italian national consensus statement on management and pharmacological treatment of phenylketonuria

ECG-based score estimates the probability to detect Fabry Disease cardiac involvement

Genotype and residual enzyme activity in medium‐chain acyl‐CoA dehydrogenase ( MCAD ) deficiency: Are predictions possible?

Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study

The management of phenylketonuria in adult patients in Italy: a survey of six specialist metabolic centers

SLC25A19 deficiency and bilateral striatal necrosis with polyneuropathy: a new case and review of the literature

Collaborators (8)

Carlo Dionisi-Vici

antonio amoroso

Elvira Verduci

Margherita RUOPPOLO

Krishna Chatterjee

giancarlo parenti

Erica L T van den Akker

Davide Tonduti

Make your next move.