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Search life-sciences literature (45,104,145 articles, preprints and more)

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Efficacy and Safety of Inhibitors of the Proximal Pathway of the Complement System in Paroxysmal Nocturnal Hemoglobinuria: A Meta-analysis of Randomized Controlled Trials.
Sobral MVS, Moulaz IR, Soares VG, Pirolla RDC, Bendaham LCAR, Faria HS, Peres CAP, Al-Sharif L, Bressa RC
Am J Ther, 22 Oct 2024
Cited by: 0 articles | PMID: 39432805
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Immunosuppressants in women with repeated implantation failure in assisted reproductive techniques: a systematic review and meta-analysis.
Santos ACFF, Zamora FV, Al-Sharif L, Sehgal K, Cavalcante DVS, Ferreira SH, da Silva PHCM
Rev Bras Ginecol Obstet, 46:e-rbgo70, 18 Sep 2024
Cited by: 0 articles | PMID: 39380592 | PMCID: PMC11460425
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Liver and cardiovascular outcomes in lean non-alcoholic fatty liver disease: an updated systematic review and meta-analysis of about 1 million individuals.
Souza M, Diaz I, Al-Sharif L
Hepatol Int, 18(5):1396-1415, 08 Aug 2024
Cited by: 0 articles | PMID: 39117942
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Outcomes of Single Anastomosis Sleeve Ileal (SASI) Bypass as an Alternative Procedure in Treating Obesity: An Updated Systematic Review and Meta-Analysis.
Ataya K, Patel N, Aljaafreh A, Melebari SS, Yang W, Guillen C, Bourji HE, Al-Sharif L, Global Obesity Collaborative
Obes Surg, 34(9):3285-3297, 26 Jul 2024
Cited by: 0 articles | PMID: 39060638
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Global epidemiology and implications of PNPLA3 I148M variant in MASLD: a systematic review and meta-analysis
Souza M, Al-Sharif L, Diaz I, Mantovani A, Villela-Nogueira CA
Research Square, 21 Mar 2024
Cited by: 0 articles | PPR: PPR825839
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The Expanding Role of ChatGPT (Chat-Generative Pre-Trained Transformer) in Neurosurgery: A Systematic Review of Literature and Conceptual Framework.
Roman A, Al-Sharif L, Al Gharyani M
Cureus, 15(8):e43502, 15 Aug 2023
Cited by: 7 articles | PMID: 37719492 | PMCID: PMC10500385
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Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3).
Khan AO, Shinwari J, Abu Dhaim N, Khalil D, Al Sharif L, Al Tassan N
Mol Vis, 17:971-976, 19 Apr 2011
Cited by: 12 articles | PMID: 21541264 | PMCID: PMC3084218
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Prolonged pursuit by optokinetic drum testing in asymptomatic female carriers of novel FRMD7 splice mutation c.1050 +5 G>A.
Khan AO, Shinwari J, Al-Sharif L, Khalil DS, Al Tassan N
Arch Ophthalmol, 129(7):936-940, 01 Jul 2011
Cited by: 5 articles | PMID: 21746984
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia.
Al Tassan N, Khalil D, Shinwari J, Al Sharif L, Bavi P, Abduljaleel Z, Abu Dhaim N, Magrashi A, Bobis S, Ahmed H, Alahmed S, Bohlega S
Hum Mutat, 33(2):351-354, 08 Dec 2011
Cited by: 24 articles | PMID: 22065524
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Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.
Khan AO, Shinwari J, Al Sharif L, Khalil D, Al-Gehedan S, Tassan NA
Mol Vis, 17:1997-2002, 20 Jul 2011
Cited by: 6 articles | PMID: 21850174 | PMCID: PMC3154136
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Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.
Bohlega SA, Shinwari JM, Al Sharif LJ, Khalil DS, Alkhairallah TS, Al Tassan NA
BMC Med Genet, 12:27, 16 Feb 2011
Cited by: 7 articles | PMID: 21324166 | PMCID: PMC3048493
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Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.
Khan AO, Shinwari J, Omar A, Al-Sharif L, Khalil DS, Alanazi M, Al-Amri A, Al Tassan N
Mol Vis, 17:218-224, 20 Jan 2011
Cited by: 8 articles | PMID: 21264235 | PMCID: PMC3025099
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Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus.
Khan AO, Khalil DS, Al-Sharif LJ, Al-Tassan NA
Ophthalmic Genet, 30(4):206-207, 01 Dec 2009
Cited by: 5 articles | PMID: 19852579
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Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles.
Khan AO, Khalil DS, Al Sharif LJ, Al-Ghadhfan FE, Al Tassan NA
Ophthalmology, 117(1):154-158, 05 Nov 2009
Cited by: 11 articles | PMID: 19896199
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Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.
Morales J, Al-Sharif L, Khalil DS, Shinwari JM, Bavi P, Al-Mahrouqi RA, Al-Rajhi A, Alkuraya FS, Meyer BF, Al Tassan N
Am J Hum Genet, 85(5):558-568, 01 Nov 2009
Cited by: 142 articles | PMID: 19836009 | PMCID: PMC2775842
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Bilateral synergistic convergence associated with homozygous ROB03 mutation (p.Pro771Leu).
Khan AO, Oystreck DT, Al-Tassan N, Al-Sharif L, Bosley TM
Ophthalmology, 115(12):2262-2265, 01 Dec 2008
Cited by: 17 articles | PMID: 19041479
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Analysis of lead levels in local Jordanian and imported sheep meat and organs using atomic absorption spectrometry.
Massadeh A, Al-Sharif L, Dalale'h R, Hassan M
Environ Monit Assess, 115(1-3):87-93, 28 Feb 2006
Cited by: 6 articles | PMID: 16508702
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