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Members area
Home
The Society
About us
What are Inherited Metabolic Disorders
What is Neonatal Screening
Council members
Registration
Working groups
Honorary members
International societies
Neonatal Screening Laboratories
Diagnostic confirmation laboratories for ENS
Neonatal Screening Medical Facilities
Official Journal: JIM
Training
Master’s programmes
Schools and courses
Archive
Legislative acts
Council members minutes
Working group minutes
Technical report
Quality control reports
Publications
Guidelines
Scientific contributions
Speaker presentations
News
Updates
Job opportunities
Scholarships
Research calls
Press release
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National congresses
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Let’s read
External resources
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Home
The Society
About us
What are Inherited Metabolic Disorders
What is Neonatal Screening
Council members
Registration
Working groups
Honorary members
International societies
Neonatal Screening Laboratories
Diagnostic confirmation laboratories for ENS
Neonatal Screening Medical Facilities
Official Journal: JIM
Training
Master’s programmes
Schools and courses
Archive
Legislative acts
Council members minutes
Working group minutes
Technical report
Quality control reports
Publications
Guidelines
Scientific contributions
Speaker presentations
News
Updates
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Research calls
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Alterata funzione surrenalica in pazienti con glicogenosi tipo 1
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Terapia combinata di stimolazione enzimatica con miglustat e terapia enzimatica sostitutiva in pazienti affetti da malattia di pompe: un trial multicentrico italiano
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Sinergia tra terapia enzimatica sostitutiva con alfa-galattosidasi ricombinante e 1-deossigalattonojirimicina in sibroblasti di pazienti con malattia di fabry.
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L'estensione dello screening allargato alle immunodeficienze severe combinate nella regione toscana
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