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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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S Feriozzi

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AJNR. American Journal of Neuroradiology|October 21, 2017

Redefining the Pulvinar Sign in Fabry DiseaseS Cocozza, C Russo, A Pisani, et al.

Clinical Genetics|September 17, 2013

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of casesC Fallerini, L Dosa, R Tita, et al.

Molecular Genetics and Metabolism|March 1, 2021

Standardising clinical outcomes measures for adult clinical trials in Fabry disease: A global Delphi consensusD Moreno-Martinez, P Aguiar, C Auray-Blais, et al.

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Search research articles

Showing results (31-40 of 33) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 33 results.

AJNR. American Journal of Neuroradiology|October 21, 2017

Redefining the Pulvinar Sign in Fabry DiseaseS Cocozza, C Russo, A Pisani, et al.

Clinical Genetics|September 17, 2013

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of casesC Fallerini, L Dosa, R Tita, et al.

Molecular Genetics and Metabolism|March 1, 2021

Standardising clinical outcomes measures for adult clinical trials in Fabry disease: A global Delphi consensusD Moreno-Martinez, P Aguiar, C Auray-Blais, et al.

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