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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
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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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Premio Migliore poster SIMMESN 2024 - Ciampa M.
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Premio Migliore poster SIMMESN 2024 - Fecarotta S.
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Premio Migliore poster SIMMESN 2024 - Sallese M.
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1° premio Migliore comunicazione orale SIMMESN 2024 - Recupero S.
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2° premio Migliore comunicazione orale SIMMESN 2024 - Barbon E.
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3° premio Migliore comunicazione orale SIMMESN 2024 - Bergamin N.
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Premio Migliore poster SIMMESN 2023 Malvagia S.
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Premio Migliore poster SIMMESN 2023 Gragnaniello V.
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Premio Migliore poster SIMMESN 2023 Boenzi S.
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1° premio Migliore comunicazione orale SIMMESN 2023 Calbi V.
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2° premio Migliore comunicazione orale SIMMESN 2023 Messelodi D.
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3° premio Migliore comunicazione orale SIMMESN 2023 Pavan E.
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Massese M. - Migliore Poster congresso SIMMESN 2022
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Rinaldi M. - Migliore Poster congresso SIMMESN2022
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De Nicotlis F.: Migliore comunicazione orale congresso SIMMESN 2022
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Tonin R.: Migliore comuncazione orale congresso SIMMESN 2022
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Malattia di fabry e nuove varianti del gene gla: l'importanza degli studi funzionali
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Eterogeneita' clinica del deficit multiplo di acil-coa deidrogenasi (madd): esperienza di un centro regionale
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Deficit del recettore nicotinico neuronale a6 in un caso di parkinsonismo infantile
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Origine degli enzimi lisosomiali nel liquido cerebrospinale
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La malattia di fabry: correzione in vitro di errori di splicing e di mutazioni conformazionali
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Difficoltà nella diagnosi prenatale di mucopolisaccaridosi vii (mps vii)
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Test enzimatico per la diagnostica della vlcad in pazienti positivi allo screening neonatale: un metodo efficace per la valutazione del rischio
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Acidemia glutarica tipo 2: nuova mutazione sul gene etfdh in un soggetto identificato mediante screening metabolico allargato
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Miopatia reversibile da deficit di e3: effetto chaperone della riboflavina
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