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Items: 47

1.

Effect of Thermal Conductivity on Enhanced Evaporation of Water Droplets from Heated Graphene-PDMS Composite Surfaces.

Goel P, Dutta Choudhury M, Aqeel AB, Li X, Shao LH, Duan H.

Langmuir. 2019 May 28;35(21):6916-6921. doi: 10.1021/acs.langmuir.9b00799. Epub 2019 May 15.

PMID:
31058512
2.

The expression of SMN1, MART3, GLE1 and FUS genes in spinal muscular atrophy.

Alrafiah A, Alghanmi M, Almashhadi S, Aqeel A, Awaji A.

Folia Histochem Cytobiol. 2018;56(4):215-221. doi: 10.5603/FHC.a2018.0022. Epub 2018 Dec 19.

3.

Role of various factors affecting the photochemical treatment of N-nitrosamines related to CO2 capture.

Aqeel A, Lim HJ.

Environ Technol. 2018 Oct 19:1-10. doi: 10.1080/09593330.2018.1536172. [Epub ahead of print]

PMID:
30339495
4.

New magnetic phase of the chiral skyrmion material Cu2OSeO3.

Qian F, Bannenberg LJ, Wilhelm H, Chaboussant G, Debeer-Schmitt LM, Schmidt MP, Aqeel A, Palstra TTM, Brück E, Lefering AJE, Pappas C, Mostovoy M, Leonov AO.

Sci Adv. 2018 Sep 21;4(9):eaat7323. doi: 10.1126/sciadv.aat7323. eCollection 2018 Sep.

5.

Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).

Bramswig NC, Bertoli-Avella AM, Albrecht B, Al Aqeel AI, Alhashem A, Al-Sannaa N, Bah M, Bröhl K, Depienne C, Dorison N, Doummar D, Ehmke N, Elbendary HM, Gorokhova S, Héron D, Horn D, James K, Keren B, Kuechler A, Ismail S, Issa MY, Marey I, Mayer M, McEvoy-Venneri J, Megarbane A, Mignot C, Mohamed S, Nava C, Philip N, Ravix C, Rolfs A, Sadek AA, Segebrecht L, Stanley V, Trautman C, Valence S, Villard L, Wieland T, Engels H, Strom TM, Zaki MS, Gleeson JG, Lüdecke HJ, Bauer P, Wieczorek D.

Hum Genet. 2018 Sep;137(9):753-768. doi: 10.1007/s00439-018-1929-5. Epub 2018 Aug 23.

6.

Helimagnon Resonances in an Intrinsic Chiral Magnonic Crystal.

Weiler M, Aqeel A, Mostovoy M, Leonov A, Geprägs S, Gross R, Huebl H, Palstra TTM, Goennenwein STB.

Phys Rev Lett. 2017 Dec 8;119(23):237204. doi: 10.1103/PhysRevLett.119.237204. Epub 2017 Dec 6.

PMID:
29286698
7.

Expanded Newborn Screening Programme in Saudi Arabia: Are We Ready?

Al Aqeel AI.

J Paediatr Child Health. 2017 Dec;53(12):1242. doi: 10.1111/jpc.13747. No abstract available.

PMID:
29205653
8.

Epidemiological and clinical aspects of neonatal tetanus from a tertiary care hospital.

Aqeel AY, Arishi HM, Ageel HI, Arishi NH.

Int J Pediatr Adolesc Med. 2017 Jun;4(2):71-74. doi: 10.1016/j.ijpam.2016.10.001. Epub 2017 Jan 11.

9.

Reversible Vitamin B12 Deficiency Presenting with Acute Dementia, Paraparesis, and Normal Hemoglobin.

Almoallim H, Mehdawi FS, Cheikh MM, Al-Dhaheri F, Aqeel AM.

Case Rep Neurol Med. 2016;2016:4301769. doi: 10.1155/2016/4301769. Epub 2016 Dec 13.

10.

Simulation-based training for emergency medicine residents in sterile technique during central venous catheterization: impact on performance, policy, and outcomes.

Hoskote SS, Khouli H, Lanoix R, Rose K, Aqeel A, Clark M, Chalfin D, Shapiro J, Han Q.

Acad Emerg Med. 2015 Jan;22(1):81-7. doi: 10.1111/acem.12551. Epub 2014 Dec 31.

11.

Self-assembly of ferromagnetic organic-inorganic perovskite-like films.

Akhtar N, Polyakov AO, Aqeel A, Gordiichuk P, Blake GR, Baas J, Amenitsch H, Herrmann A, Rudolf P, Palstra TT.

Small. 2014 Dec 10;10(23):4912-9. doi: 10.1002/smll.201400259. Epub 2014 Jul 24.

PMID:
25059565
12.

Simulation-based training for nurses in sterile techniques during central vein catheterization.

Gerolemou L, Fidellaga A, Rose K, Cooper S, Venturanza M, Aqeel A, Han Q, Jones J, Shapiro J, Khouli H.

Am J Crit Care. 2014 Jan;23(1):40-8. doi: 10.4037/ajcc2014860.

13.

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Patrinos GP, Al Aama J, Al Aqeel A, Al-Mulla F, Borg J, Devereux A, Felice AE, Macrae F, Marafie MJ, Petersen MB, Qi M, Ramesar RS, Zlotogora J, Cotton RG.

Hum Mutat. 2011 Jan;32(1):2-9. doi: 10.1002/humu.21397.

14.

Performance of medical residents in sterile techniques during central vein catheterization: randomized trial of efficacy of simulation-based training.

Khouli H, Jahnes K, Shapiro J, Rose K, Mathew J, Gohil A, Han Q, Sotelo A, Jones J, Aqeel A, Eden E, Fried E.

Chest. 2011 Jan;139(1):80-7. doi: 10.1378/chest.10-0979. Epub 2010 Aug 12.

PMID:
20705795
15.

Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs).

Povey S, Al Aqeel AI, Cambon-Thomsen A, Dalgleish R, den Dunnen JT, Firth HV, Greenblatt MS, Barash CI, Parker M, Patrinos GP, Savige J, Sobrido MJ, Winship I, Cotton RG; Ethics Committee of the Human Genome Organization (HUGO).

Hum Mutat. 2010 Nov;31(11):1179-84. doi: 10.1002/humu.21339.

16.

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.

Cotton RG, Al Aqeel AI, Al-Mulla F, Carrera P, Claustres M, Ekong R, Hyland VJ, Macrae FA, Marafie MJ, Paalman MH, Patrinos GP, Qi M, Ramesar RS, Scott RJ, Sijmons RH, Sobrido MJ, Vihinen M; members of the Human Variome Project Data Collection from Clinics, Data Collection from Laboratories and Publication, Credit and Incentives Working Groups.

Genet Med. 2009 Dec;11(12):843-9. doi: 10.1097/GIM.0b013e3181c371c5.

PMID:
20010362
17.

Planning the human variome project: the Spain report.

Kaput J, Cotton RG, Hardman L, Watson M, Al Aqeel AI, Al-Aama JY, Al-Mulla F, Alonso S, Aretz S, Auerbach AD, Bapat B, Bernstein IT, Bhak J, Bleoo SL, Blöcker H, Brenner SE, Burn J, Bustamante M, Calzone R, Cambon-Thomsen A, Cargill M, Carrera P, Cavedon L, Cho YS, Chung YJ, Claustres M, Cutting G, Dalgleish R, den Dunnen JT, Díaz C, Dobrowolski S, dos Santos MR, Ekong R, Flanagan SB, Flicek P, Furukawa Y, Genuardi M, Ghang H, Golubenko MV, Greenblatt MS, Hamosh A, Hancock JM, Hardison R, Harrison TM, Hoffmann R, Horaitis R, Howard HJ, Barash CI, Izagirre N, Jung J, Kojima T, Laradi S, Lee YS, Lee JY, Gil-da-Silva-Lopes VL, Macrae FA, Maglott D, Marafie MJ, Marsh SG, Matsubara Y, Messiaen LM, Möslein G, Netea MG, Norton ML, Oefner PJ, Oetting WS, O'Leary JC, de Ramirez AM, Paalman MH, Parboosingh J, Patrinos GP, Perozzi G, Phillips IR, Povey S, Prasad S, Qi M, Quin DJ, Ramesar RS, Richards CS, Savige J, Scheible DG, Scott RJ, Seminara D, Shephard EA, Sijmons RH, Smith TD, Sobrido MJ, Tanaka T, Tavtigian SV, Taylor GR, Teague J, Töpel T, Ullman-Cullere M, Utsunomiya J, van Kranen HJ, Vihinen M, Webb E, Weber TK, Yeager M, Yeom YI, Yim SH, Yoo HS; Contributors to the Human Variome Project Planning Meeting.

Hum Mutat. 2009 Apr;30(4):496-510. doi: 10.1002/humu.20972.

18.

Variability in morphology and aggressiveness among North American vegetative compatibility groups of Colletotrichum coccodes.

Aqeel AM, Pasche JS, Gudmestad NC.

Phytopathology. 2008 Aug;98(8):901-9. doi: 10.1094/PHYTO-98-8-0901.

19.

Islamic ethical framework for research into and prevention of genetic diseases.

Al Aqeel AI.

Nat Genet. 2007 Nov;39(11):1293-8. Epub 2007 Oct 22. Review.

PMID:
17952074
20.

Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth.

Mosig RA, Dowling O, DiFeo A, Ramirez MC, Parker IC, Abe E, Diouri J, Aqeel AA, Wylie JD, Oblander SA, Madri J, Bianco P, Apte SS, Zaidi M, Doty SB, Majeska RJ, Schaffler MB, Martignetti JA.

Hum Mol Genet. 2007 May 1;16(9):1113-23. Epub 2007 Mar 30.

21.

Intact survival of an infant born at 22 weeks' gestation.

Aqeel A, Al-Alaiyan S.

Ann Saudi Med. 2000 May-July;20(3-4):336. No abstract available.

22.

Cryptophthalmos syndrome (Fraser syndrome) with cardiac findings in a Saudi newborn.

Aqeel A, Al-Alaiyan S.

Ann Saudi Med. 1999 Jul-Aug;19(4):357-8. No abstract available.

23.

Vertical transmission of fatal Rift Valley fever in a newborn.

Arishi HM, Aqeel AY, Al Hazmi MM.

Ann Trop Paediatr. 2006 Sep;26(3):251-3.

PMID:
16925964
24.

Differences in physician compliance with guideline on lipid profile determination within 24 h after acute myocardial infarction.

Al Aqeel A, Mojiminiyi OA, Al Dashti R, Al Ozairi ES.

Med Princ Pract. 2005 Jan-Feb;14(1):41-5.

25.

A novel molecular defect of the carnitine acylcarnitine translocase gene in a Saudi patient.

Al Aqeel AI, Rashid MS, Ruiter JP, Ijlst L, Wanders RJ.

Clin Genet. 2003 Aug;64(2):163-5. No abstract available.

PMID:
12859414
26.

Epidemic Rift Valley fever in Saudi Arabia: a clinical study of severe illness in humans.

Al-Hazmi M, Ayoola EA, Abdurahman M, Banzal S, Ashraf J, El-Bushra A, Hazmi A, Abdullah M, Abbo H, Elamin A, Al-Sammani el-T, Gadour M, Menon C, Hamza M, Rahim I, Hafez M, Jambavalikar M, Arishi H, Aqeel A.

Clin Infect Dis. 2003 Feb 1;36(3):245-52. Epub 2003 Jan 17.

PMID:
12539063
27.

Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.

Parvari R, Hershkovitz E, Grossman N, Gorodischer R, Loeys B, Zecic A, Mortier G, Gregory S, Sharony R, Kambouris M, Sakati N, Meyer BF, Al Aqeel AI, Al Humaidan AK, Al Zanhrani F, Al Swaid A, Al Othman J, Diaz GA, Weiner R, Khan KT, Gordon R, Gelb BD; HRD/Autosomal Recessive Kenny-Caffey Syndrome Consortium.

Nat Genet. 2002 Nov;32(3):448-52. Epub 2002 Oct 21.

PMID:
12389028
28.

The use of indomethacin for the prevention of intraventricular brain hemorrhage in high-risk neonates.

Al-Shawaf EM, Al-Alaiyan SA, Aqeel AY, Gamal MH.

Saudi Med J. 2000 Mar;21(3):274-7.

PMID:
11533797
29.

Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome.

Martignetti JA, Aqeel AA, Sewairi WA, Boumah CE, Kambouris M, Mayouf SA, Sheth KV, Eid WA, Dowling O, Harris J, Glucksman MJ, Bahabri S, Meyer BF, Desnick RJ.

Nat Genet. 2001 Jul;28(3):261-5.

PMID:
11431697
30.

Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family.

Al Aqeel A, Al Sewairi W, Edress B, Gorlin RJ, Desnick RJ, Martignetti JA.

Am J Med Genet. 2000 Jul 3;93(1):11-8.

PMID:
10861676
31.

The use of indomethacin for the prevention of intraventricular brain hemorrhage in high-risk neonates.

Al-Shawaf EM, Al-Alaiyan SA, Aqeel AY, Gamal MH.

Neurosciences (Riyadh). 2000 Apr;5(2):115-8.

PMID:
24276728
32.

Carnitine-acylcarnitine translocase deficiency is a treatable disease.

al Aqeel AI, Rashed MS, Wanders RJ.

J Inherit Metab Dis. 1999 May;22(3):271-5. No abstract available.

PMID:
10384385
33.

Unusual presentations of propionic acidemia.

Ozand PT, Rashed M, Gascon GG, Youssef NG, Harfi H, Rahbeeni Z, al Garawi S, al Aqeel A.

Brain Dev. 1994 Nov;16 Suppl:46-57.

PMID:
7726381
34.

A new patient with alpha-ketoglutaric aciduria and progressive extrapyramidal tract disease.

al Aqeel A, Rashed M, Ozand PT, Gascon GG, Rahbeeni Z, al Garawi S, al Odaib A, Brismar J.

Brain Dev. 1994 Nov;16 Suppl:33-7.

PMID:
7726379
35.

3-Methylglutaconic aciduria: ten new cases with a possible new phenotype.

al Aqeel A, Rashed M, Ozand PT, Brismar J, Gascon GG, al Odaib A, Dabbagh O.

Brain Dev. 1994 Nov;16 Suppl:23-32.

PMID:
7726378
36.

Experience of King Faisal Specialist Hospital and Research Center with Saudi organic acid disorders.

Rashed M, Ozand PT, al Aqeel A, Gascon GG.

Brain Dev. 1994 Nov;16 Suppl:1-6. Review.

PMID:
7726374
37.

Malonic aciduria.

Ozand PT, Nyhan WL, al Aqeel A, Christodoulou J.

Brain Dev. 1994 Nov;16 Suppl:7-11.

PMID:
7537025
38.

Response of 6-pyruvoyl-tetrahydropterin synthase deficiency to tetrahydrobiopterin.

al Aqeel A, Ozand PT, Gascon GG, Hughes H, Reynolds CT, Subramanyam SB.

J Child Neurol. 1992 Apr;7 Suppl:S26-30.

PMID:
1588012
39.

Saudi variant of multiple sulfatase deficiency.

al Aqeel A, Ozand PT, Brismar J, Gascon GG, Brismar G, Nester M, Sakati N.

J Child Neurol. 1992 Apr;7 Suppl:S12-21.

PMID:
1588009
40.

Biopterin-dependent hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase.

al Aqeel A, Ozand PT, Gascon G, Nester M, al Nasser M, Brismar J, Blau N, Hughes H, Subramanyan SB, Reynolds CT.

Neurology. 1991 May;41(5):730-7.

PMID:
2027491
41.

Prenatal detection of Canavan disease.

Ozand PT, Feryal RR, Gascon GG, Gleispach H, al Aqeel A, Cook JD, Nester MJ, al Odaib A, Leis HJ.

Lancet. 1991 Mar 23;337(8743):735-6. No abstract available.

PMID:
1672203
42.

Toxicological studies of the antimicrobial alkaloid juliflorine.

Aqeel A, Khursheed AK, Viqaruddin A.

Arzneimittelforschung. 1991 Feb;41(2):151-4.

PMID:
2043177
43.

3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi Arabia.

Ozand PT, al Aqeel A, Gascon G, Brismar J, Thomas E, Gleispach H.

J Inherit Metab Dis. 1991;14(2):174-88.

PMID:
1886403
44.

Maple syrup urine disease: findings on CT and MR scans of the brain in 10 infants.

Brismar J, Aqeel A, Brismar G, Coates R, Gascon G, Ozand P.

AJNR Am J Neuroradiol. 1990 Nov-Dec;11(6):1219-28.

PMID:
2124065
45.

Malignant hyperphenylalaninemia: CT and MR of the brain.

Brismar J, Aqeel A, Gascon G, Ozand P.

AJNR Am J Neuroradiol. 1990 Jan-Feb;11(1):135-8.

PMID:
2105595
46.

Prevalence of different types of lysosomal storage diseases in Saudi Arabia.

Ozand PT, Gascon G, al Aqeel A, Roberts G, Dhalla M, Subramanyam SB.

J Inherit Metab Dis. 1990;13(6):849-61.

PMID:
2079833
47.

Antimicrobial activity of julifloricine isolated from Prosopis juliflora.

Aqeel A, Khursheed AK, Viqaruddin A, Sabiha Q.

Arzneimittelforschung. 1989 Jun;39(6):652-5.

PMID:
2775330

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