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Inês Vaz Matos

ResearcherPublications, citations & collaboration network

Inês Vaz Matos is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 20 works, 116 citations, an h-index of 5 and an i10-index of 4.

20
Works
116
Citations
5
h-index
4
i10-index

How has Inês Vaz Matos's publication output changed over time?

ScholarIQpublication output · 2009–2025

Output grew0% over the shown period — from 1 works in 2009 to 1 in 2025.

1
2
1
1
2
1
1
1
20092010201320152017202220232025

What are the most-cited papers on Inês Vaz Matos?

ScholarIQmost cited works
Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency
Inês Vaz Matos, Esperanza Castejón, Silvia Meavilla, María del Mar O’Callaghan, Judit García‐Villoria, Anna López‐Sala, Antònia Ribes, Rafael Artuch, Ángeles García‐Cazorla
S42433034. 201341 Citations
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: genotype-phenotype correlation].
Catarina Mendes, Inês Vaz Matos, Luís Ribeiro, Maria João Oliveira, Helena Cardoso, Teresa Borges
PubMed. 201711 CitationsOPEN ACCESS
El papel de los cannabinoides en los trastornos del neurodesarrollo de niños y adolescentes
Francisca Freitas, Sofia Pimenta, Sara Soares, Diana Gonzaga, Inês Vaz Matos, C. Prior
Revista de Neurología. 202211 CitationsOPEN ACCESS
Hiperplasia Congénita da Suprarrenal por Deficiência de 21-Hidroxílase: Correlação Genótipo-Fenótipo
Catarina Mendes, Inês Vaz Matos, Luís Ribeiro, Maria João Oliveira, Helena Cardoso, Teresa Borges
Acta Médica Portuguesa. 20157 CitationsOPEN ACCESS

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Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency
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The interaction between DC and <i>Plasmodium berghei/chabaudi</i>‐infected erythrocytes in mice involves direct cell‐to‐cell contact, internalization and TLR
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[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: genotype-phenotype correlation].
Paper
El papel de los cannabinoides en los trastornos del neurodesarrollo de niños y adolescentes
Paper
Hiperplasia Congénita da Suprarrenal por Deficiência de 21-Hidroxílase: Correlação Genótipo-Fenótipo
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