Video head impulse gain is impaired in myotonic dystrophy types 1 and 2
Fuente:
Wiley Open Access
Guardado en:
| Autores principales: | Zeljka Calic, Stojan Peric, Milorad Vujnic, Bogdan Bjelica, Ivo Bozovic, Vidosava Rakocevic‐Stojanovic, Andrew Bradshaw, James G. Colebatch, Miriam S. Welgampola |
|---|---|
| Formato: | Artículo Open Access |
| Publicado: |
Wiley
2024
|
| Materias: | |
| Acceso en línea: | |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
Transcranial Brain Parenchyma Sonographic Findings in Familial and Sporadic Amyotrophic Lateral Sclerosis
por: Ivo Bozovic, et al.
Publicado: (2025)
por: Ivo Bozovic, et al.
Publicado: (2025)
Reply to the Comment by Zhang et al
por: Bogdan Bjelica
Publicado: (2026)
por: Bogdan Bjelica
Publicado: (2026)
Clinical genetic approaches to the management of patients with myotonic dystrophy type 1 and their families
por: Katsuya Nakamura
Publicado: (2024)
por: Katsuya Nakamura
Publicado: (2024)
Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1
por: Federica Trucco, et al.
Publicado: (2024)
por: Federica Trucco, et al.
Publicado: (2024)
RNA mis‐splicing in children with congenital myotonic dystrophy is associated with physical function
por: Julia M. Hartman, et al.
Publicado: (2024)
por: Julia M. Hartman, et al.
Publicado: (2024)
Novel Mutations in Titin Exon 363 With Different Phenotypes Including a Founder Mutation in Eastern Europe
por: Veronica Sian, et al.
Publicado: (2025)
por: Veronica Sian, et al.
Publicado: (2025)
LMNA‐related muscular dystrophy presenting as an inflammatory myopathy
por: Alexandra Santana Almansa, et al.
Publicado: (2024)
por: Alexandra Santana Almansa, et al.
Publicado: (2024)
Outcomes of cerebrovascular disease in muscular dystrophies: A propensity‐matched nationwide analysis
por: Ali Al‐Salahat, et al.
Publicado: (2024)
por: Ali Al‐Salahat, et al.
Publicado: (2024)
Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy
por: Shruthi Mohan, et al.
Publicado: (2024)
por: Shruthi Mohan, et al.
Publicado: (2024)
Dystrophin isoform deficiency and upper‐limb and respiratory function in Duchenne muscular dystrophy
Publicado: (2025)
Publicado: (2025)
Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids
por: Marianela Schiava, et al.
Publicado: (2024)
por: Marianela Schiava, et al.
Publicado: (2024)
Access to novel therapies for Duchenne muscular dystrophy—Insights from expert treating physicians
por: Aravindhan Veerapandiyan, et al.
Publicado: (2024)
por: Aravindhan Veerapandiyan, et al.
Publicado: (2024)
Fetal development of the human amygdala
por: Damir Mulc, et al.
Publicado: (2024)
por: Damir Mulc, et al.
Publicado: (2024)
Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the Phenotype
por: Christopher J. Record, et al.
Publicado: (2024)
por: Christopher J. Record, et al.
Publicado: (2024)
Muscular dystrophy patients show low exercise‐induced blood flow in muscles with normal strength
por: Orna Gera, et al.
Publicado: (2024)
por: Orna Gera, et al.
Publicado: (2024)
Psychometric evaluation of the PROMIS parent proxy mobility item bank for use in Duchenne muscular dystrophy
por: Linda Pax Lowes, et al.
Publicado: (2024)
por: Linda Pax Lowes, et al.
Publicado: (2024)
Screening for brain‐related comorbidities in Duchenne muscular dystrophy: Construction, reliability, and validity of the BIND screener
por: Ruben Miranda, et al.
Publicado: (2026)
por: Ruben Miranda, et al.
Publicado: (2026)
Screening for brain‐related comorbidities in Duchenne muscular dystrophy: Construction, reliability, and validity of the BIND screener
Publicado: (2026)
Publicado: (2026)
Psychometric evaluation of a patient‐reported outcome measurement information system for use in Duchenne muscular dystrophy
Publicado: (2025)
Publicado: (2025)
Height, weight, and body mass index trajectories and their correlation with functional outcome assessments in boys with Duchenne muscular dystrophy
por: Marianela Schiava, et al.
Publicado: (2025)
por: Marianela Schiava, et al.
Publicado: (2025)
Making brain health routine in Duchenne muscular dystrophy: What the BIND screener adds—and what it is not designed to do
por: Yoshitsugu Aoki
Publicado: (2026)
por: Yoshitsugu Aoki
Publicado: (2026)
Compound Muscle Action Potential (CMAP) Amplitude Trajectories and Pattern in Adults with 5q‐Spinal Muscular Atrophy Receiving Nusinersen Therapy: A Multicenter, Binational Observational Study
por: Bogdan Bjelica, et al.
Publicado: (2025)
por: Bogdan Bjelica, et al.
Publicado: (2025)
Improved diagnostic performance of high‐sensitivity cardiac troponins in muscle dystrophies using comprehensive definition criteria for cardiac involvement: A longitudinal study on 35 patients
por: Mustafa Yildirim, et al.
Publicado: (2024)
por: Mustafa Yildirim, et al.
Publicado: (2024)
Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient‐reported outcome measures
por: Bram De Wel, et al.
Publicado: (2024)
por: Bram De Wel, et al.
Publicado: (2024)
Furthering Female Faculty: An American Neurological Association/Association of University Professors of Neurology Perspective
por: L. John Greenfield, et al.
Publicado: (2024)
por: L. John Greenfield, et al.
Publicado: (2024)
Measuring what really matters: Why developing patient‐reported outcome measures in Duchenne muscular dystrophy should involve patients and caregivers
por: Sebastian Friedrich, et al.
Publicado: (2024)
por: Sebastian Friedrich, et al.
Publicado: (2024)
The motor apparatus of head movements in the Oleander hawkmoth ( Daphnis nerii , Lepidoptera)
por: Agnish D. Prusty, et al.
Publicado: (2024)
por: Agnish D. Prusty, et al.
Publicado: (2024)
Cerebral visual impairment is permanent but not unchanging
por: Cathy Williams
Publicado: (2024)
por: Cathy Williams
Publicado: (2024)
Normal pressure hydrocephalus and cognitive impairment: The gait phenotype matters too
por: Eric Morel, et al.
Publicado: (2024)
por: Eric Morel, et al.
Publicado: (2024)
RNA Binding Protein Dysfunction Links Smoldering/Slowly Expanding Lesions to Neurodegeneration in Multiple Sclerosis
por: Miranda L. Messmer, et al.
Publicado: (2024)
por: Miranda L. Messmer, et al.
Publicado: (2024)
Cellular‐resolution gene expression mapping reveals organization in the head ganglia of the gastropod, Berghia stephanieae
por: M. Desmond Ramirez, et al.
Publicado: (2024)
por: M. Desmond Ramirez, et al.
Publicado: (2024)
Brain neurovascular coupling in amyotrophic lateral sclerosis: Correlations with disease progression and cognitive impairment
por: Francesca Trojsi, et al.
Publicado: (2024)
por: Francesca Trojsi, et al.
Publicado: (2024)
Risk factors of dementia in a cohort of individuals with mild cognitive impairment in the Italian Interceptor project
por: Claudia Carrarini, et al.
Publicado: (2025)
por: Claudia Carrarini, et al.
Publicado: (2025)
Beyond fixing: Reconsidering assumptions about child‐onset impairments
por: Peter Rosenbaum,
Publicado: (2024)
por: Peter Rosenbaum,
Publicado: (2024)
Assessing and enhancing visual responses in children with severe cerebral impairment
por: Richard Bowman
Publicado: (2025)
por: Richard Bowman
Publicado: (2025)
Natural history of cerebral visual impairment in children with cerebral palsy
Publicado: (2024)
Publicado: (2024)
Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry
por: Emilie Retailleau, et al.
Publicado: (2024)
por: Emilie Retailleau, et al.
Publicado: (2024)
Clinical variables contributing to the identification of biologically defined subgroups within cognitively unimpaired and mild cognitive impairment individuals
por: Sofia Marcolini, et al.
Publicado: (2024)
por: Sofia Marcolini, et al.
Publicado: (2024)
Identifying neurocognitive impairment risk in children with moyamoya: The role of routine neuroimaging
por: Lisa R. Sun
Publicado: (2025)
por: Lisa R. Sun
Publicado: (2025)
Psychosocial experiences of clinicians providing care for children with severe neurological impairment
por: Suzanne M. Nevin, et al.
Publicado: (2024)
por: Suzanne M. Nevin, et al.
Publicado: (2024)
Ejemplares similares
-
Transcranial Brain Parenchyma Sonographic Findings in Familial and Sporadic Amyotrophic Lateral Sclerosis
por: Ivo Bozovic, et al.
Publicado: (2025) -
Reply to the Comment by Zhang et al
por: Bogdan Bjelica
Publicado: (2026) -
Clinical genetic approaches to the management of patients with myotonic dystrophy type 1 and their families
por: Katsuya Nakamura
Publicado: (2024) -
Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1
por: Federica Trucco, et al.
Publicado: (2024) -
RNA mis‐splicing in children with congenital myotonic dystrophy is associated with physical function
por: Julia M. Hartman, et al.
Publicado: (2024)