Mohammed Aldosari
Mohammed Aldosari
Pediatric Neurologist, Cleveland Clinic Foundation
Verified email at ccf.org
Title
Cited by
Cited by
Year
Krabbe disease: neurophysiologic studies and MRI correlations
AM Husain, M Altuwaijri, M Aldosari
Neurology 63 (4), 617-620, 2004
652004
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay
MD Al-Sayed, H Al-Zaidan, AB Albakheet, H Hakami, R Kenana, ...
The American Journal of Human Genetics 93 (4), 721-726, 2013
572013
Neuronal ceroid lipofuscinosis caused by MFSD8 mutations: a common theme emerging
MA Aldahmesh, ZN Al-Hassnan, M Aldosari, FS Alkuraya
Neurogenetics 10 (4), 307-311, 2009
342009
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
B Al-Mubarak, M Abouelhoda, A Omar, H AlDhalaan, M Aldosari, ...
Scientific reports 7 (1), 1-14, 2017
272017
A novel X‐linked disorder with developmental delay and autistic features
N Kaya, D Colak, A Albakheet, M Al‐Owain, N Abu‐Dheim, B Al‐Younes, ...
Annals of neurology 71 (4), 498-508, 2012
272012
Brain-stem auditory and visual evoked potentials in children with Krabbe disease
M Aldosari, M Altuwaijri, AM Husain
Clinical neurophysiology 115 (7), 1653-1656, 2004
272004
Sensing technologies for autism spectrum disorder screening and intervention
JJ Cabibihan, H Javed, M Aldosari, TW Frazier, H Elbashir
Sensors 17 (1), 46, 2017
202017
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways
D Colak, H Al-Dhalaan, M Nester, AB AlBakheet, B Al-Younes, ...
Genomics 97 (1), 19-28, 2011
182011
Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations
OY Al‐Dirbashi, R Shaheen, M Al‐Sayed, M Al‐Dosari, N Makhseed, ...
American Journal of Medical Genetics Part A 149 (6), 1219-1223, 2009
122009
Delayed visual maturation associated with auditory neuropathy/dyssynchrony
M Aldosari, A Mabie, AM Husain
Journal of child neurology 18 (5), 358-361, 2003
112003
Social robots and wearable sensors for mitigating meltdowns in autism-A pilot test
JJ Cabibihan, R Chellali, CWC So, M Aldosari, O Connor, AY Alhaddad, ...
International Conference on Social Robotics, 103-114, 2018
72018
Prevalence and correlates of autism spectrum disorder in Qatar: a national study
F Alshaban, M Aldosari, H Al‐Shammari, S El‐Hag, I Ghazal, M Tolefat, ...
Journal of Child Psychology and Psychiatry 60 (12), 1254-1268, 2019
42019
Autism spectrum disorder in Qatar: Profiles and correlates of a large clinical sample
F Alshaban, M Aldosari, Z El Sayed, M Tolefat, S El Hag, H Al Shammari, ...
Autism & Developmental Language Impairments 2, 2396941517699215, 2017
42017
Culture as a driver for the design of social robots for autism spectrum disorder interventions in the middle east
H Javed, JJ Cabibihan, M Aldosari, A Al-Attiyah
International Conference on Social Robotics, 591-599, 2016
42016
Homozygosity analysis in subjects with autistic spectrum disorder
A Adi, B Tawil, M Aldosari, J Shinwari, M Nester, H Aldhalaan, ...
Molecular medicine reports 12 (2), 2307-2312, 2015
32015
Validation of the Arabic version of the Social Communication Questionnaire
M Aldosari, E Fombonne, H Aldhalaan, M Ouda, S Elhag, H Alshammari, ...
Autism 23 (7), 1655-1662, 2019
22019
Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management
MS Aldosari, SA Bohlega, MA Al-Jadid, MS El-Tamawy, MA Ramadan, ...
Neurosciences 12 (4), 279-281, 2007
22007
Intelligent Gaze-Based Screening System for Autism
AB Dris, A Alsalman, A Al-Wabil, M Aldosari
2019 2nd International Conference on Computer Applications & Information …, 2019
12019
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways
M Aldosary, AB Al-Bakheet, H Al-Dhalaan, R Almass, M Alsagob, ...
OMICS: A Journal of Integrative Biology 24 (3), 160-171, 2020
2020
Mutation screening and global gene expression analyses of Saudi Rett patients implicate mitochondrial dysfunction in the pathogenesis of Rett syndrome
D Colak, M Aldosary, A AlBakheet, OM Mustafa, R Almass, M Alsagob, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 306-307, 2019
2019
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