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Roser Pons

5PUBLICATIONS

44CO-AUTHORS

Neurology and neuromuscular diseasesEcohydrologyTesting, assessment and psychometricsChild and adolescent developmentDisease surveillance

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Publications (5)

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|Jan 19, 2026

International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen

|Jul 01, 2025

Early Levodopa Therapy in Tyrosine Hydroxylase Deficiency.

Claudio M de Gusmao, Roser Pons, Ganeshwaran H Mochida

|May 14, 2025

Development and Preliminary Validation of a Parkinsonism-Dystonia Scale for Infants and Young Children.

Roser Pons, Toni S Pearson, Belen Perez-Dueñas

|Mar 15, 2025

Patients with Allan-Herndon-Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment.

Nina-Maria Wilpert, Angela L Hewitt, Roser Pons

|Mar 19, 2024

The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency.

Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella

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Frequent Collaborators

2 joint publications

Manju Ann Kurian

2 joint publications

Thomas Opladen

2 joint publications

Sabine Jung-Klawitter

1 joint publications

Natalia Alexandra Julia-Palacios

1 joint publications

Oya Kuseyri Hübschmann

1 joint publications

Mireia Olivella

1 joint publications

Gabriella Horvath

1 joint publications

Cheuk-Wing Fung

1 joint publications

Elisenda Cortès-Saladelafont

1 joint publications

Juan Darío Ortigoza-Escobar

Frequent Collaborators

2 joint publications

Manju Ann Kurian

2 joint publications

Thomas Opladen

2 joint publications

Sabine Jung-Klawitter

1 joint publications

Natalia Alexandra Julia-Palacios

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