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Breathe (Sheffield, England)
|
March 5, 2021
Response to: the adult multidisciplinary respiratory neuromuscular clinic
Tracey Willis, Mike Macfarlane, Derek Willis
Children (Basel, Switzerland)
|
May 28, 2022
Evaluating the Feasibility and Reliability of Remotely Delivering and Scoring the North Star Ambulatory Assessment in Ambulant Patients with Duchenne Muscular Dystrophy
Nicholas Emery, Kate Strachan, Richa Kulshrestha, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2022
PIEZO2-related distal arthrogryposis type 5: Longitudinal follow-up of a three-generation family broadens phenotypic spectrum, complications, and health surveillance recommendations for this patient group
Charlotte A Sherlaw-Sturrock, Tracey Willis, Nigel Kiely, et al.
Plos One
|
June 24, 2022
A pilot study of a single intermittent arm cycling exercise programme on people affected by Facioscapulohumeral dystrophy (FSHD)
Fraser Philp, Richa Kulshrestha, Nicholas Emery, et al.
Journal of Neurology
|
May 15, 2016
A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness
Tracey Willis, Carola Hedberg-Oldfors, Zoya Alhaswani, et al.
Neuromuscular Disorders : NMD
|
November 10, 2018
Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case
Richa Kulshrestha, Natalie Forrester, Thalia Antoniadi, et al.
Archives of Rehabilitation Research and Clinical Translation
|
January 3, 2022
Upper Limb Rehabilitation in Facioscapulohumeral Muscular Dystrophy: A Patients' Perspective
Alice Faux-Nightingale, Richa Kulshrestha, Nicholas Emery, et al.
Journal of Neuromuscular Diseases
|
February 19, 2026
Trunk control status in children with neuromuscular disorders and typically developing children: Is there a measurable difference?
Tania E Sakanaka, Penelope B Butler, Richa Kulshrestha, et al.
BMJ Supportive & Palliative Care
|
January 22, 2024
Myotonic dystrophy type 1: palliative care guidelines
Derek Willis, Tracey Willis, Claire Bassie, et al.
Pediatric Neurology
|
June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies
Emma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
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Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Breathe (Sheffield, England)
|
March 5, 2021
Response to: the adult multidisciplinary respiratory neuromuscular clinic
Tracey Willis, Mike Macfarlane, Derek Willis
Children (Basel, Switzerland)
|
May 28, 2022
Evaluating the Feasibility and Reliability of Remotely Delivering and Scoring the North Star Ambulatory Assessment in Ambulant Patients with Duchenne Muscular Dystrophy
Nicholas Emery, Kate Strachan, Richa Kulshrestha, et al.
American Journal of Medical Genetics. Part A
|
June 14, 2022
PIEZO2-related distal arthrogryposis type 5: Longitudinal follow-up of a three-generation family broadens phenotypic spectrum, complications, and health surveillance recommendations for this patient group
Charlotte A Sherlaw-Sturrock, Tracey Willis, Nigel Kiely, et al.
Plos One
|
June 24, 2022
A pilot study of a single intermittent arm cycling exercise programme on people affected by Facioscapulohumeral dystrophy (FSHD)
Fraser Philp, Richa Kulshrestha, Nicholas Emery, et al.
Journal of Neurology
|
May 15, 2016
A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness
Tracey Willis, Carola Hedberg-Oldfors, Zoya Alhaswani, et al.
Neuromuscular Disorders : NMD
|
November 10, 2018
Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case
Richa Kulshrestha, Natalie Forrester, Thalia Antoniadi, et al.
Archives of Rehabilitation Research and Clinical Translation
|
January 3, 2022
Upper Limb Rehabilitation in Facioscapulohumeral Muscular Dystrophy: A Patients' Perspective
Alice Faux-Nightingale, Richa Kulshrestha, Nicholas Emery, et al.
Journal of Neuromuscular Diseases
|
February 19, 2026
Trunk control status in children with neuromuscular disorders and typically developing children: Is there a measurable difference?
Tania E Sakanaka, Penelope B Butler, Richa Kulshrestha, et al.
BMJ Supportive & Palliative Care
|
January 22, 2024
Myotonic dystrophy type 1: palliative care guidelines
Derek Willis, Tracey Willis, Claire Bassie, et al.
Pediatric Neurology
|
June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies
Emma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
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of 4