Jennifer C Hengeveld
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Explore the profile of Jennifer C Hengeveld including associated specialties, affiliations and a list of published articles.
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23
Citations
313
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Recent Articles
1.
Christidi F, Kleinerova J, Tan E, Delaney S, Tacheva A, Hengeveld J, et al.
Biology (Basel)
. 2024 Jul;
13(7).
PMID: 39056697
: While frontotemporal involvement is increasingly recognized in Amyotrophic lateral sclerosis (ALS), the degeneration of limbic networks remains poorly characterized, despite growing evidence of amnestic deficits, impaired emotional processing and...
2.
Tahedl M, Tan E, Kleinerova J, Delaney S, Hengeveld J, Doherty M, et al.
Neurology
. 2024 Jun;
103(2):e209623.
PMID: 38900989
Background And Objectives: Amyotrophic lateral sclerosis (ALS) is predominantly associated with motor cortex, corticospinal tract (CST), brainstem, and spinal cord degeneration, and cerebellar involvement is much less well characterized. However,...
3.
Kleinerova J, Tahedl M, Tan E, Delaney S, Hengeveld J, Doherty M, et al.
J Neurol
. 2024 Mar;
271(6):3239-3255.
PMID: 38438819
Background: Primary lateral sclerosis (PLS) is traditionally solely associated with progressive upper motor neuron dysfunction manifesting in limb spasticity, gait impairment, bulbar symptoms and pseudobulbar affect. Recent studies have described...
4.
Ryan M, Doherty M, Al Khleifat A, Costello E, Hengeveld J, Heverin M, et al.
Neurol Genet
. 2023 Dec;
10(1):e200112.
PMID: 38149039
Background And Objectives: A hexanucleotide repeat expansion in the noncoding region of the gene is the most common genetically identifiable cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia in...
5.
Tan E, Tahedl M, Lope J, Hengeveld J, Doherty M, McLaughlin R, et al.
J Neurol
. 2023 Sep;
271(1):431-445.
PMID: 37759084
Background: Primary lateral sclerosis (PLS) is traditionally regarded as a pure upper motor neuron disorder, but recent cases series have highlighted cognitive deficits in executive and language domains. Methods: A...
6.
Tahedl M, Tan E, Chipika R, Lope J, Hengeveld J, Doherty M, et al.
Brain Behav
. 2023 Sep;
13(11):e3250.
PMID: 37694825
Background: Language deficits are cardinal manifestations of some frontotemporal dementia (FTD) phenotypes and also increasingly recognized in sporadic and familial amyotrophic lateral sclerosis (ALS). They have considerable social and quality-of-life...
7.
Tahedl M, Tan E, Siah W, Hengeveld J, Doherty M, McLaughlin R, et al.
J Neurol Sci
. 2023 Jul;
451:120726.
PMID: 37421883
Introduction: Pseudobulbar affect (PBA) is a distressing symptom of a multitude of neurological conditions affecting patients with a rage of neuroinflammatory, neurovascular and neurodegenerative conditions. It manifests in disproportionate emotional...
8.
Tahedl M, Tan E, Chipika R, Hengeveld J, Vajda A, Doherty M, et al.
J Neurol
. 2023 Apr;
270(7):3511-3526.
PMID: 37022479
Background: Bulbar dysfunction is a cardinal feature of ALS with important quality of life and management implications. The objective of this study is the longitudinal evaluation of a large panel...
9.
Tahedl M, Tan E, Shing S, Chipika R, Siah W, Hengeveld J, et al.
Eur J Neurol
. 2023 Feb;
30(5):1232-1245.
PMID: 36739888
Background And Purpose: Primary lateral sclerosis (PLS) is a progressive upper motor neuron disorder associated with considerable clinical disability. Symptoms are typically exclusively linked to primary motor cortex degeneration and...
10.
McKenna M, Tahedl M, Lope J, Chipika R, Shing S, Doherty M, et al.
Brain Imaging Behav
. 2021 Dec;
16(3):1196-1207.
PMID: 34882275
Imaging studies of FTD typically present group-level statistics between large cohorts of genetically, molecularly or clinically stratified patients. Group-level statistics are indispensable to appraise unifying radiological traits and describe genotype-associated...