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Fulminant Guillain-Barré Syndrome Post Hemorrhagic Stroke: Two Case Reports.
Neurol Int. 2021 May 6;13(2):190-194. doi: 10.3390/neurolint13020019.
Neurol Int. 2021.
PMID: 34066316
Free PMC article.
Novel MFN2 Missense Mutation Induces Hereditary Axonal Motor and Sensory Neuropathy in a Saudi Arabian Family.
Al-Harbi TM, Abdulmana SO, Bashir S, Dridi W.
Al-Harbi TM, et al. Among authors: abdulmana so.
J Clin Neuromuscul Dis. 2019 Sep;21(1):25-29. doi: 10.1097/CND.0000000000000244.
J Clin Neuromuscul Dis. 2019.
PMID: 31453851
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Clinical features and outcome of Guillain-Barre syndrome in Saudi Arabia: a multicenter, retrospective study.
Alanazy MH, Bakry SS, Alqahtani A, AlAkeel NS, Alazwary N, Osman AM, Mustafa RA, Al-Harbi TM, Abdulmana SO, Amper AC, Aldughaythir Y, Ali AS, Makkawi S, Maglan A, Alamoudi L, Alsulaiman F, Alabdali M, AlShareef AA, Abuzinadah AR, Bamaga AK.
Alanazy MH, et al. Among authors: abdulmana so.
BMC Neurol. 2021 Jul 12;21(1):275. doi: 10.1186/s12883-021-02314-5.
BMC Neurol. 2021.
PMID: 34253174
Free PMC article.
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Novel Homozygous Missense Mutation in CAPN3 Gene Detected in a Saudi Arabian Family With Limb-Girdle Muscular Dystrophy Type 2A.
Al-Harbi TM, Abdulmanaʼ SO, Dridi W.
Al-Harbi TM, et al. Among authors: abdulmana so.
J Clin Neuromuscul Dis. 2016 Dec;18(2):89-91. doi: 10.1097/CND.0000000000000129.
J Clin Neuromuscul Dis. 2016.
PMID: 27861222
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