Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management

…, YK Mousali, AT Yaghmour, AM Kurdi, SH Koussa… - Neurosciences …, 2007 - nsj.org.sa
Special Communication tendon jerks, resulting from hyperexcitability of the stretch reflex.” 1
Spasticity can produce impairment of active functions performed by the patient such as …

[HTML][HTML] A 20-year clinical and genetic neuromuscular cohort analysis in Lebanon: an international effort

…, D Hasbini, I Ghanem, S Koussa… - Journal of …, 2022 - content.iospress.com
Background: Clinical and molecular data on the occurrence and frequency of inherited
neuromuscular disorders (NMD) in the Lebanese population is scarce. Objective: This study aims …

Hypertransfusion: a successful method of treatment in thalassemia intermedia patients with spinal cord compression secondary to extramedullary hematopoiesis

A Chehal, E Aoun, S Koussa, H Skoury, S Koussa… - Spine, 2003 - journals.lww.com
Objective. This article reviews the literature and reports two cases of thalassemia intermedia
involving patients who presented with neurologic symptoms after acute spinal cord …

Mutations in TREM2 lead to pure early‐onset dementia without bone cysts

…, V Delague, A Bergougnoux, S Koussa… - Human …, 2008 - Wiley Online Library
A genome‐wide screen using 382 STR markers to localize and identify the gene implicated
in early‐onset dementia (EOD) without bone cysts in a Lebanese family with three affected …

[HTML][HTML] Linking multiple pathogenic pathways in Alzheimer's disease

RB Khalil, E Khoury, S Koussa - World journal of psychiatry, 2016 - ncbi.nlm.nih.gov
Alzheimer’s disease (AD) is a chronic neurodegenerative disorder presenting as progressive
cognitive decline with dementia that does not, to this day, benefit from any disease-…

An Arabic version of the mini-mental state examination for the Lebanese population: Reliability, validity, and normative data

…, A Wehbé, N Bassil, S Koussa… - Journal of …, 2019 - content.iospress.com
Background: The Mini-Mental State Examination (MMSE) has not been validated in the
Lebanese population and no normative data exist at the national level. Objective: To evaluate the …

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1

…, A Atkinson, K Bertaux, S Koussa… - Human molecular …, 2019 - academic.oup.com
Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases,
resembling Charcot–Marie–Tooth syndromes, but characterized by an exclusive involvement of …

[PDF][PDF] Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13. 1-13.3 in a large consanguineous Lebanese family …

…, S Tuffery, P Bouvagnet, E Chouery, S Koussa… - The American Journal of …, 2000 - cell.com
Autosomal recessive Charcot-Marie-Tooth disease (CMT) type 4 (CMT4) is a complex
group of demyelinating hereditary motor and sensory neuropathies presenting genetic …

[HTML][HTML] Prediction of the survival and functional ability of severe stroke patients after ICU therapeutic intervention

…, T Bazerbachi, Z Aoun-Bacha, G Khayat, S Koussa - BMC neurology, 2008 - Springer
Background This study evaluated the benefits and impact of ICU therapeutic interventions
on the survival and functional ability of severe cerebrovascular accident (CVA) patients. …

Acute paraplegia revealing an intraspinal neurenteric cyst in a child

…, J Maarrawi, R Hourani, P Jabbour, S Koussa… - Child's nervous …, 2001 - Springer
The authors report a case of intraspinal neurenteric cyst in a 22-month-old child, who presented
with acute paraplegia following a vesicourethrogram. Despite 8 days' delay in surgical …