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Journal of Child Neurology
|
April 23, 2025
Childhood Dementia: The Collective Impact and the Urgent Need for Greater Awareness and Action
Kristina L Elvidge, Michelle A Farrar, John Christodoulou, et al.
Pediatric Neurology
|
February 22, 2025
Childhood Dementia: The Collective Impact and the Urgent Need for Greater Awareness and Action
Kristina L Elvidge, Michelle A Farrar, John Christodoulou, et al.
Journal of Paediatrics and Child Health
|
April 25, 2020
Neuronal ceroid lipofuscinosis type 2: an Australian case series
Alexandra M Johnson, Simone Mandelstam, Ian Andrews, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
March 25, 2023
Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imaging
Dhimas H Sakti, Elisa E Cornish, Clare L Fraser, et al.
Orphanet Journal of Rare Diseases
|
January 8, 2026
A timeline of symptom onset and disease progression in CLN3 disease
Ineka T Whiteman, Anthony L Cook, Erika F Augustine, et al.
Pediatric Neurology
|
October 8, 2023
Characterizing Common Phenotypes Across the Childhood Dementia Disorders: A Cross-sectional Study From Two Australian Centers
Jason V Djafar, Nicholas J Smith, Alexandra M Johnson, et al.
Molecular Genetics & Genomic Medicine
|
January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
Elizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
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Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Journal of Child Neurology
|
April 23, 2025
Childhood Dementia: The Collective Impact and the Urgent Need for Greater Awareness and Action
Kristina L Elvidge, Michelle A Farrar, John Christodoulou, et al.
Pediatric Neurology
|
February 22, 2025
Childhood Dementia: The Collective Impact and the Urgent Need for Greater Awareness and Action
Kristina L Elvidge, Michelle A Farrar, John Christodoulou, et al.
Journal of Paediatrics and Child Health
|
April 25, 2020
Neuronal ceroid lipofuscinosis type 2: an Australian case series
Alexandra M Johnson, Simone Mandelstam, Ian Andrews, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
March 25, 2023
Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imaging
Dhimas H Sakti, Elisa E Cornish, Clare L Fraser, et al.
Orphanet Journal of Rare Diseases
|
January 8, 2026
A timeline of symptom onset and disease progression in CLN3 disease
Ineka T Whiteman, Anthony L Cook, Erika F Augustine, et al.
Pediatric Neurology
|
October 8, 2023
Characterizing Common Phenotypes Across the Childhood Dementia Disorders: A Cross-sectional Study From Two Australian Centers
Jason V Djafar, Nicholas J Smith, Alexandra M Johnson, et al.
Molecular Genetics & Genomic Medicine
|
January 10, 2018
Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness
Elizabeth E Palmer, Deborah Schofield, Rupendra Shrestha, et al.
Page
of 2