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The role of sources of social support on depression and quality of life for university students

International journal of adolescence and youth, 2019-10, Vol.24 (4), p.484-496

2019

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Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue

Dysphagia, 2022-08, Vol.37 (4), p.715-723

2022

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Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4

European journal of neurology, 2018-03, Vol.25 (3), p.512-518

2018

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Cardiac pathology in spinal muscular atrophy: a systematic review

Orphanet journal of rare diseases, 2017-04, Vol.12 (1), p.67-67, Article 67

2017

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Digital health literacy and digital engagement for people with severe mental ill health across the course of the COVID-19 pandemic in England

BMC medical informatics and decision making, 2023-09, Vol.23 (1), p.193-193, Article 193

2023

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Uncovering key patterns in self-harm in adolescents: Sequence analysis using the Card Sort Task for Self-harm (CaTS)

Journal of affective disorders, 2016-12, Vol.206, p.161-168

2016

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Measuring the digital divide among people with severe mental ill health using the essential digital skills framework

Perspectives in Public Health, 2024-01, Vol.144 (1), p.21-30

2024

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Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

Journal of neuromuscular diseases, 2020-01, Vol.7 (3), p.323-330

2020

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Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatment

European journal of paediatric neurology, 2023-01, Vol.42, p.34-41

2023

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'Everybody just thinks I'm weird': a qualitative exploration of the psychosocial experiences of adolescents with Tourette syndrome

Child : care, health & development, 2013-11, Vol.39 (6), p.880-886

2013

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Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy

Neuromuscular disorders : NMD, 2019-04, Vol.29 (4), p.321-329

2019

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Experience of Self-Harm and Its Treatment in Looked-After Young People: An Interpretative Phenomenological Analysis

Archives of suicide research, 2018-07, Vol.22 (3), p.365-379

2018

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Illness Perceptions in Pediatric Spinal Muscular Atrophy: Agreement between Children and their Parents, and its Association with Quality of Life

Journal of developmental and physical disabilities, 2021-04, Vol.33 (2), p.297-310

2021

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Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy

Journal of neuromuscular diseases, 2019-01, Vol.6 (3), p.361-368

2019

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Psychosocial Screening in Sickle Cell Disease: Validation of the Psychosocial Assessment Tool

Journal of pediatric psychology, 2020-05, Vol.45 (4), p.423-433

2020

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The health and quality of life of Thalidomide survivors as they age - Evidence from a UK survey

PloS one, 2019-01, Vol.14 (1), p.e0210222-e0210222

2019

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Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3

Neurology, 2012-11, Vol.79 (20), p.2050

2012

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J -factors for self-interacting dark matter in 20 dwarf spheroidal galaxies

Physical review. D, 2018, Vol.98 (4), Article 043017

2018

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Help-seeking and psychological distress in university students: Findings from a cross-sectional online survey in the UK

European psychiatry, 2017-04, Vol.41 (S1), p.S184-S185

2017

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Caregiver Perspectives on Family Psychosocial Risks and Resiliencies in Pediatric Sickle Cell Disease: Informing the Adaptation of the Psychosocial Assessment Tool

Clinical practice in pediatric psychology, 2017-12, Vol.5 (4), p.330-341

2017

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Adult attachment, psychological distress and help-seeking in university students: Findings from a cross-sectional online survey in England

Mental health & prevention, 2019-03, Vol.13, p.7-13

2019

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‘Everybody just thinks I'm weird’: a qualitative exploration of the psychosocial experiences of adolescents with T ourette syndrome

Child : care, health & development, 2013-11, Vol.39 (6), p.880-886

2013

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Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid

Journal of neurology, neurosurgery and psychiatry, 2011-08, Vol.82 (8), p.850-852

2011

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G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.871-872

2012

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P3.14 Drug treatment in spinal muscular atrophy types 1, 2 and 3: An update of the systematic Cochrane review

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.686-686

2011

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The role of sources of social support on depression and quality of life for university students

Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue

Muscle strength and motor function throughout life in a cross‐sectional cohort of 180 patients with spinal muscular atrophy types 1c–4

Cardiac pathology in spinal muscular atrophy: a systematic review

Digital health literacy and digital engagement for people with severe mental ill health across the course of the COVID-19 pandemic in England

Uncovering key patterns in self-harm in adolescents: Sequence analysis using the Card Sort Task for Self-harm (CaTS)

Measuring the digital divide among people with severe mental ill health using the essential digital skills framework

Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatment

'Everybody just thinks I'm weird': a qualitative exploration of the psychosocial experiences of adolescents with Tourette syndrome

Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy

Experience of Self-Harm and Its Treatment in Looked-After Young People: An Interpretative Phenomenological Analysis

Illness Perceptions in Pediatric Spinal Muscular Atrophy: Agreement between Children and their Parents, and its Association with Quality of Life

Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy

Psychosocial Screening in Sickle Cell Disease: Validation of the Psychosocial Assessment Tool

The health and quality of life of Thalidomide survivors as they age - Evidence from a UK survey

Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3

J -factors for self-interacting dark matter in 20 dwarf spheroidal galaxies

Help-seeking and psychological distress in university students: Findings from a cross-sectional online survey in the UK

Caregiver Perspectives on Family Psychosocial Risks and Resiliencies in Pediatric Sickle Cell Disease: Informing the Adaptation of the Psychosocial Assessment Tool

Adult attachment, psychological distress and help-seeking in university students: Findings from a cross-sectional online survey in England

‘Everybody just thinks I'm weird’: a qualitative exploration of the psychosocial experiences of adolescents with T ourette syndrome

Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid

G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3

P3.14 Drug treatment in spinal muscular atrophy types 1, 2 and 3: An update of the systematic Cochrane review

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