Metabolic and genetic disorders mimicking cerebral palsy

WS Hakami, KJ Hundallah, BM Tabarki - Neurosciences Journal, 2019 - nsj.org.sa
Cerebral palsy is a syndrome that encompasses a large group of childhood movement and
posture disorders that result from a lesion occurring in the developing brain. The clinical …

[PDF][PDF] The incidence and spectrum of central nervous system malformations in newborns over a decade (2001-2010) in the Central Region of Saudi Arabia

WS Hakami, MA Majeed-Saidan - Saudi Med J, 2011 - academia.edu
… The combined number of NTD and hydrocephalus in Mansouri’s study10 was 2.6/1000
LB, while in this study they represent 1/1000 LB. Rajab et al14 from the Sultanate of Oman …

< The> incidence and spectrum of central nervous system malformations in newborns over a decade [2001-2010] in the Central Region of Saudi Arabia

H Wejdan S, MS Muhammad A - 2011 - pesquisa.bvsalud.org
To study the incidence and spectrum of central nervous system [CNS] malformations
confirmed by computerized tomography [CT], or magnetic resonance imaging [MRI] in a Saudi …

Nutritional habits and weight status among Jazan university students: Eating patterns and healthy lifestyle assessment

…, AY Akour, TM Madkhly, HM Hakami… - … , and Public Health, 2016 - riviste.unimi.it
Objectives The purposes of this study were to assess the prevalence of underweight,
overweight, and obesity and to evaluate the nutritional habits, and related factors among the …

Bi-allelic variants in HCRT cause autosomal recessive narcolepsy

W Hakami, F Thabet, A Alhashem, A Alghamdi… - neurogenetics, 2024 - Springer
Narcolepsy with cataplexy is a complex disease with both genetic and environmental risk
factors. To gain further insight into the homozygous HCRT-related narcolepsy, we present a …

Lisdexamfetamine Therapy in Paroxysmal Non‐kinesigenic Dyskinesia Associated with the KCNMA1‐N999S Variant

S Keros, J Heim, W Hakami… - Movement Disorders …, 2022 - Wiley Online Library
Background KCNMA1‐linked channelopathy is a rare movement disorder first reported in
2005. Paroxysmal non‐kinesigenic dyskinesia (PNKD) in KCNMA1‐linked channelopathy is …

[HTML][HTML] Inherited metabolic causes of stroke in children: mechanisms, types, and management

B Tabarki, W Hakami, N Alkhuraish… - Frontiers in …, 2021 - frontiersin.org
… The use, distribution or reproduction in other forums is permitted, provided the original
author(s) and the copyright owner(s) are credited and that the original publication in this journal is …

The absence of mammillary body lesions for early differentiation of biotin-thiamine-responsive basal ganglia disease from Wernicke's encephalopathy

H Alsini, R Hommady, R Alsafh, Z Asmat, W Hakami… - 2023 - researchsquare.com
… absence of predisposing factors for Wernicke’s encephalopathy such as altered thiamine
intake … Wejdan Hakami: Analyzing or interpretation of the data and reviewing the manuscript. …

Hereditary Hyperekplexia in Saudi Arabia

…, K Hundallah, A Alghamdi, W Hakami, S AlShafi… - Pediatric Neurology, 2022 - Elsevier
Background Hyperekplexia is a rare disorder characterized by exaggerated startle responses
to unexpected sensory stimuli, recurrent apneas, and stiffness. Only few studies have been …

[HTML][HTML] Spinal cord involvement in pediatric-onset metabolic disorders with mendelian and mitochondrial inheritance

B Tabarki, W Hakami, N Alkhuraish… - Frontiers in …, 2021 - frontiersin.org
… The use, distribution or reproduction in other forums is permitted, provided the original
author(s) and the copyright owner(s) are credited and that the original publication in this journal is …