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Page 1
Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation.
Bakkar AA, Alsaedi A, Kamal NM, Althobaiti E, Aboulkhair LA, Almalki AM, Alsalmi SA, Alharthi Q, Abosabie SA, Abosabie SA. Bakkar AA, et al. Among authors: abosabie sa. Clin Med Insights Endocrinol Diabetes. 2023 May 26;16:11795514231167059. doi: 10.1177/11795514231167059. eCollection 2023. Clin Med Insights Endocrinol Diabetes. 2023. PMID: 37255966 Free PMC article.
"Progressive myoclonic ataxia and developmental/epileptic encephalopathy associated with a novel homozygous mutation in TCN2 gene".
Oshi MAM, Alfaifi J, Alqahtani YAM, Aljabri MF, Kamal NM, Althopaity J, Althobaiti KA, Almalki AM, Abosabie SAS, Abosabie SA, Sherbiny HS, Almanjoomi SK, Abdallah EAA. Oshi MAM, et al. Among authors: abosabie sas, abosabie sa. Mol Genet Genomic Med. 2024 Jan;12(1):e2282. doi: 10.1002/mgg3.2282. Epub 2023 Oct 6. Mol Genet Genomic Med. 2024. PMID: 37800653 Free PMC article.
Renal angina index in critically ill children as an applicable and reliable tool in the prediction of severe acute kidney injury: Two tertiary centers' prospective observational study from the Middle East.
Soliman ASA, Al-Ghamdi HS, Abukhatwah MW, Kamal NM, Dabour SA, Elgendy SA, Alfaifi J, Abukhatwah OMW, Abosabie SAS, Abosabie SA, Oshi MAM, Althobaity J, Sakr Sherbiny H, Al-Juaid FA, Rahman EGA. Soliman ASA, et al. Among authors: abosabie sas, abosabie sa. Medicine (Baltimore). 2023 Dec 22;102(51):e36713. doi: 10.1097/MD.0000000000036713. Medicine (Baltimore). 2023. PMID: 38134055 Free PMC article.
Vertebral artery dissection aneurysm in a pediatric patient: A rare case with unusual clinical manifestations, diagnostic, and management challenges.
Oshi MAM, Aljabri MF, Alotaibi S, Alzahrani Y, Alfaifi J, Abosabie SAS, Abosabie SA, Algethami SS, Younes AE, Almanjoomi RK, Babkour B, Kamal NM. Oshi MAM, et al. Among authors: abosabie sas, abosabie sa. Medicine (Baltimore). 2023 Nov 24;102(47):e35906. doi: 10.1097/MD.0000000000035906. Medicine (Baltimore). 2023. PMID: 38013323 Free PMC article.
Unraveling Alström syndrome: Homozygous mutation c.2729C>G in ALMS1 gene across an extended family.
Abosabie SAS, Abosabie SA, Alfaifi J, Alqahtani YA, Shati AA, Alotaibi NA, Alghamdi OA, Alotaibi GN, Baabdullah AA, Kabrah LK, Kamal NM, Oshi MAM, Abdallah EAA. Abosabie SAS, et al. Among authors: abosabie sa. Mol Genet Genomic Med. 2024 Jan;12(1):e2314. doi: 10.1002/mgg3.2314. Epub 2023 Nov 8. Mol Genet Genomic Med. 2024. PMID: 37937857 Free PMC article. Review.
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