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Profil bibliographique

Z. Sawacha

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

239Publications signalées
2787Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Diabetic Foot Ulcer Assessment and ManagementBalance, Gait, and Falls PreventionMuscle activation and electromyography studiesLower Extremity Biomechanics and PathologiesParkinson's Disease Mechanisms and Treatments

Les publications récentes

Accès ouvert 2025 article OpenAlex

Low/High Multi‐Frequency Stimulation of the Subthalamic Nucleus Improves Verbal Fluency Maintaining Motor Control in Parkinson's Disease

Lucia Ricciardi, Francescopaolo Cucinotta, Elena Pegolo, Arturo Abundes‐Corona et autres

BACKGROUND: High frequency deep brain stimulation of the subthalamic nucleus (STN-DBS) is a well-established therapy for Parkinson's disease (PD) motor symptoms, however, its effect on non-motor symptoms is controversial. Low frequency DBS can improve cognition, but its effects on motor functions are …

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10 citations Movement Disorders
Accès ouvert 2025 article OpenAlex

Energetics of a Novel 3D-Printed Custom Ankle Foot Orthosis in a Population of Individuals with Foot Drop: A Pilot Study

Paolo Caravaggi, Giulia Rogati, Massimiliano Baleani, Roberta Fognani et autres

Passive Dynamic Ankle–Foot Orthoses (PD-AFOs) are medical devices prescribed to individuals with foot drop, a condition characterized by weakness of the ankle dorsiflexor muscles. PD-AFOs can store and release energy during the stance phase of the gait cycle, while supporting the foot …

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2 citations Applied Sciences
Accès ouvert 2025 article OpenAlex

Children With Fragile X Syndrome Display a Switch Towards Fast Fibres in Their Recruitment Strategy During Gait

Fabiola Spolaor, Federica Beghetti, W. Piatkowska, Annamaria Guiotto et autres

BACKGROUND: Fragile X Syndrome (FXS) is a genetic disorder caused by the lack of FMRP, a crucial protein for brain development and function. FMR1 mutations are categorized into premutation and full mutation (FXSFull), with somatic mosaicism (FXSMos) modulating the FXS phenotype. Recent …

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0 citations Journal of Intellectual Disability Research
Accès ouvert 2025 article OpenAlex

Neurobehavioral Outcomes Relate to Activation Ratio in Female Carriers of Fragile X Syndrome Full Mutation: Two Pediatric Case Studies

Elisa Di Giorgio, Silvia Benavides‐Varela, Annamaria Porru, Sara Caviola et autres

Fragile X syndrome (FXS) is a genetic neurodevelopmental disorder that causes a range of developmental problems including cognitive and behavioral impairment and learning disabilities. FXS is caused by full mutations (FM) of the FMR1 gene expansions to over 200 repeats, with hypermethylation …

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0 citations International Journal of Molecular Sciences
Accès ouvert 2025 article OpenAlex

Data imputation for gait analysis of children with Fragile X Syndrome

Federica Beghetti, Fabiola Spolaor, Damiano Varagnolo, Z. Sawacha

Missing values represent a critical challenge in gait analysis datasets, where due to the high variability across subjects, a large number of trials is needed to represent an individual gait pattern; however, this is rarely available in the context of pathological subjects. …

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0 citations IFAC-PapersOnLine

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