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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.
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.
Medicine (Baltimore). 2023 Nov 24;102(47):e35906. doi: 10.1097/MD.0000000000035906.
Medicine (Baltimore). 2023.
PMID: 38013323
Free PMC article.
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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.
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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"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.
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.
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First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report.
Kamal NM, Alzeky AM, Omair MR, Attar RA, Alotaibi AM, Safar A, Alosaimi NS, Abosabie SAS.
Kamal NM, et al. Among authors: abosabie sas.
Ital J Pediatr. 2022 Jun 23;48(1):107. doi: 10.1186/s13052-022-01301-x.
Ital J Pediatr. 2022.
PMID: 35739559
Free PMC article.
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Case Report: Dubin-Johnson Syndrome Presenting With Infantile Cholestasis: An Overlooked Diagnosis in an Extended Family.
Kamal NM, Saadah O, Alghamdi H, Algarni A, El-Shabrawi MHF, Sherief LM, Abosabie SAS.
Kamal NM, et al. Among authors: abosabie sas.
Front Pediatr. 2022 May 25;10:855210. doi: 10.3389/fped.2022.855210. eCollection 2022.
Front Pediatr. 2022.
PMID: 35692971
Free PMC article.
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