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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Iria Roca

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Orphanet Journal of Rare Diseases|June 28, 2018

Carbohydrate status in patients with phenylketonuriaMaría L Couce, Paula Sánchez-Pintos, Isidro Vitoria, et al.

Medicine|October 3, 2019

Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in SpainMaría Luz Couce, Paula Sánchez-Pintos, Luís Aldámiz-Echevarría, et al.

Frontiers in Neuroscience|November 30, 2019

Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric PatientsAna Fernández-Marmiesse, Iria Roca, Felícitas Díaz-Flores, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Orphanet Journal of Rare Diseases|June 28, 2018

Carbohydrate status in patients with phenylketonuriaMaría L Couce, Paula Sánchez-Pintos, Isidro Vitoria, et al.

Medicine|October 3, 2019

Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in SpainMaría Luz Couce, Paula Sánchez-Pintos, Luís Aldámiz-Echevarría, et al.

Frontiers in Neuroscience|November 30, 2019

Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric PatientsAna Fernández-Marmiesse, Iria Roca, Felícitas Díaz-Flores, et al.

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