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Kate Williams

10PUBLICATIONS

7CO-AUTHORS

Major global burdens of diseaseCancer geneticsPodiatryNeurology and neuromuscular diseasesArts therapy

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Publications (10)

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|May 17, 2024

A qualitative study to explore the burden of disease in activated phosphoinositide 3-kinase delta syndrome (APDS).

Ian Hitchcock, Hanna Skrobanski, Elina Matter

|Oct 11, 2023

Symptoms and impacts of familial chylomicronemia syndrome: a qualitative study of the patient experience.

Kate Williams, Georgina Tickler, Pedro Valdivielso

|Mar 22, 2022

Symptoms and impacts of aromatic L-amino acid decarboxylase (AADC) deficiency among individuals with different levels of motor function.

Kate Williams, Hanna Skrobanski, Katharina Buesch

|Aug 22, 2021

Symptoms and impacts of ambulatory nonsense mutation Duchenne muscular dystrophy: a qualitative study and the development of a patient-centred conceptual model.

Kate Williams, Ian Davidson, Mark Rance

|Aug 10, 2021

A qualitative study on the impact of caring for an ambulatory individual with nonsense mutation Duchenne muscular dystrophy.

Kate Williams, Ian Davidson, Mark Rance

|Jul 14, 2021

The impact of caring for an individual with aromatic l-amino acid decarboxylase (AADC) deficiency: a qualitative study and the development of a conceptual model.

Hanna Skrobanski, Kate Williams, Christian Werner

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Frequent Collaborators

2 joint publications

Hanna Skrobanski

1 joint publications

Nizar Mahlaoui

1 joint publications

Daniel Aggio

1 joint publications

Peter Chen

1 joint publications

Katerina Anokhina

1 joint publications

Andrew J Lloyd

1 joint publications

Yan Wang

Frequent Collaborators

2 joint publications

Hanna Skrobanski

1 joint publications

Nizar Mahlaoui

1 joint publications

Daniel Aggio

1 joint publications

Peter Chen

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