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Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data

PaperCitations, authors & open-access status

Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data is a paper indexed in PICO Portal from OpenAlex.

How many citations does Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data have?

PICO Portalcitation count

Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data has 127 citations in the OpenAlex counts PICO Portal stores.

When was Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data published?

PICO Portalyear

Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data has 2007 year in the PICO Portal index.

What is the open-access status of Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data?

PICO Portaloa status

Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data has bronze oa status in the PICO Portal index.

What is the DOI of Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data?

PICO Portaldoi

The DOI for Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data is on the source record.

What is the PMID of Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data?

PICO Portalpmid

The PMID for Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data is on the source record.

What is the OpenAlex record for Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data?

PICO Portalopenalex

The OpenAlex for Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data is on the source record.

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