Mac Keith Press

10/01/2025

Individualized telehealth home programme for children with during the pandemic

In this podcast, Rachel Oliveira discusses her paper 'Individualized telehealth home programme for children with cerebral palsy during the COVID-19 pandemi...

10/01/2025

This CanChild editorial suggests including people with lived experience of in all stages of research is essential for meaningful and impactful progress

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09/01/2025

We hope everyone is enjoying this week! Hoping to still see many of you there!

Have a read of the conference abstracts, which are freely available here:

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09/01/2025

Patient and public involvement in health services: Paying more than lip service

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08/01/2025

We're excited to announce 'Gait Problems in Cerebral Palsy: Identification, Patient Goals, and Surgical Treatment' is coming very soon in hardback, eBook, and an integrated online resource!

Find out more at https://buff.ly/4h0N74h

Gait Problems in Cerebral Palsy focuses on the surgical care and postoperative rehabilitation of children with cerebral palsy as they grow through early and late childhood, and adolescence. This product is available in different formats: Hardback with video access (via automatic download as part of....

08/01/2025

Come and find us by the catering stands (near room L3) at

Browse our selection of books, learn about our new and upcoming releases, and take a catalogue!

07/01/2025

How can medical professionals and people with lived experience of best work together to co-create an inclusive future?

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07/01/2025

Idiopathic scoliosis is a condition in which, for no known reason, there is an atypical three-dimensional curvature and rotation of the spine. Idiopathic scoliosis is the most common type of scoliosis.

Discover the Gillette Children's Healthcare Series book about this topic at

Find out more: https://www.mackeith.co.uk/book/idiopathic-scoliosis/ Idiopathic scoliosis is a condition in which, for no known reason, there is an atypical ...

06/01/2025

We are excited about this week and look forward to seeing many of you there!

Have a read of the conference abstracts, which are freely available here:

Click on the title to browse this issue

06/01/2025

The February issue of has now been published! 📕

Highlights include papers on genetic investigations in , infection-triggered encephalopathy syndrome, CO-OP for children with and more

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03/01/2025

New Release — Craniosynostosis!

Learn about this condition with guidance on early interventions and lifelong care for syndromic cases. This practical book combines medical insights with real-life family experiences

Get your copy here at

Craniosynostosis is a condition where the bones of an infant’s skull fuse together too early. In most cases, surgery in the first year of life will effectively correct it and the child can go on to expect a typical life. For a minority, craniosynostosis is part of a syndrome, which is a lifelong c...

03/01/2025

Craniosynostosis is a condition where the bones of an infant’s skull fuse together too early.

Discover the Gillette Children's Healthcare Series book about this topic at

Find out more: https://www.mackeith.co.uk/book/craniosynostosis/ Craniosynostosis is a condition where the bones of an infant’s skull fuse together too early...

02/01/2025

New books on have been published by Gillette Children's Healthcare Press and !

With detailed medical explanations, evidence-based best-practice treatments, and lived experience stories of spastic , , and

https://buff.ly/4i363QL

30/12/2024

A case series illustrates the utility of in identifying copy number variants missed by conventional methods of testing in

This case series demonstrates the utility of whole genome sequencing in identifying copy number variants missed by conventional methods of testing. Plain language summary: https://onlinelibrary.wiley...

27/12/2024

A large genotype-phenotype study of ADGRL1-associated highlights variants found in a range of epilepsy syndromes +

Aim To expand the phenotypic spectrum of ADGRL1 and explore the correlation between epilepsy and the ADGRL1 genotype. Method We performed whole-exome sequencing in a cohort of 115 families (includ...

24/12/2024

Based on a retrospective study of seizure features in infants with syndrome, the authors make recommendations for early diagnosis and referral pathway

This original article is commented by Comi on pages 13–14 of this issue.

23/12/2024

As we near the end of 2024, discover our editor-in-chief Prof. Bernard Dan’s personal 2024 highlights –

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23/12/2024

This qualitative study of the transition of people with to adult care identifies barriers and potential facilitators, and suggests how the process can be improved

We conducted qualitative, semi-structured interviews with young adults with cerebral palsy (CP) and/or their caregivers regarding pediatric rehabilitation-related care and the transition into adult c...