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Treatment for vestibular schwannoma: Systematic review and single arm meta-analysis.
Am J Otolaryngol. 2022 Mar-Apr;43(2):103337. doi: 10.1016/j.amjoto.2021.103337. Epub 2021 Dec 20.
Am J Otolaryngol. 2022.
PMID: 34973662
Review.
Efficacy and resistance of different artemisinin-based combination therapies: a systematic review and network meta-analysis.
Mathenge PG, Low SK, Vuong NL, Mohamed MYF, Faraj HA, Alieldin GI, Al Khudari R, Yahia NA, Khan A, Diab OM, Mohamed YM, Zayan AH, Tawfik GM, Huy NT, Hirayama K.
Mathenge PG, et al. Among authors: al khudari r.
Parasitol Int. 2020 Feb;74:101919. doi: 10.1016/j.parint.2019.04.016. Epub 2019 Apr 20.
Parasitol Int. 2020.
PMID: 31015034
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Saphenous vein harvesting techniques for coronary artery bypass grafting: a systematic review and meta-analysis.
Vuong NL, Elfaituri MK, Eldoadoa M, Karimzadeh S, Mokhtar MA, Eid PS, Nam NH, Mostafa MR, Radwan I, Zaki MMM, Al Khudari R, Kassem M, Huy NT.
Vuong NL, et al. Among authors: al khudari r.
Coron Artery Dis. 2022 Mar 1;33(2):128-136. doi: 10.1097/MCA.0000000000001048.
Coron Artery Dis. 2022.
PMID: 34010184
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Familial Mediterranean fever and scleroderma: a rare case report from Syria.
Nahas L, Al Khudari R, Khalil B.
Nahas L, et al. Among authors: al khudari r.
Oxf Med Case Reports. 2023 Oct 23;2023(10):omad111. doi: 10.1093/omcr/omad111. eCollection 2023 Oct.
Oxf Med Case Reports. 2023.
PMID: 37881263
Free PMC article.
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Primary Stromal Breast Sarcoma with Concomitant Contralateral Carcinoma: A Rare Case from Syria.
Al Khudari R, Homsi M, Al Zohaily H, Saifo MS.
Al Khudari R, et al.
Case Rep Oncol Med. 2019 Sep 10;2019:6460847. doi: 10.1155/2019/6460847. eCollection 2019.
Case Rep Oncol Med. 2019.
PMID: 31583145
Free PMC article.
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First case of childhood Takayasu arteritis from Syria: a case report.
Alwattar W, Al Khudari R, Naameh J, Batha J, Almajzoub R, Khalil B.
Alwattar W, et al. Among authors: al khudari r.
J Med Case Rep. 2021 Sep 23;15(1):469. doi: 10.1186/s13256-021-03077-w.
J Med Case Rep. 2021.
PMID: 34551801
Free PMC article.
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Novel mutation in the RAB3GAP1 gene, the first diagnosed Warburg Micro syndrome case in Syria.
Tenawi S, Al Khudari R, Alasmar D.
Tenawi S, et al. Among authors: al khudari r.
Oxf Med Case Reports. 2020 May 23;2020(4):omaa031. doi: 10.1093/omcr/omaa031. eCollection 2020 Apr.
Oxf Med Case Reports. 2020.
PMID: 32477580
Free PMC article.
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Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report.
Al Khudari R, Batesh D, Habash R, Hamdn O.
Al Khudari R, et al.
J Med Case Rep. 2023 Nov 18;17(1):480. doi: 10.1186/s13256-023-04215-2.
J Med Case Rep. 2023.
PMID: 37978530
Free PMC article.
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