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Items: 10

1.

Building consensus for the development of child eye care services in South Darfur State of Sudan using the Delphi technique.

Alrasheed SH, Naidoo KS, Clarke-Farr PC, Binnawi KH.

Afr J Prim Health Care Fam Med. 2018 Oct 24;10(1):e1-e9. doi: 10.4102/phcfm.v10i1.1767.

2.
3.

Design and simulation of reflect-array metasurfaces in the visible regime.

Alrasheed S, Fabrizio ED.

Appl Opt. 2017 Apr 10;56(11):3213-3218. doi: 10.1364/AO.56.003213.

PMID:
28414383
4.

Detection of single amino acid mutation in human breast cancer by disordered plasmonic self-similar chain.

Coluccio ML, Gentile F, Das G, Nicastri A, Perri AM, Candeloro P, Perozziello G, Proietti Zaccaria R, Gongora JS, Alrasheed S, Fratalocchi A, Limongi T, Cuda G, Di Fabrizio E.

Sci Adv. 2015 Sep 4;1(8):e1500487. doi: 10.1126/sciadv.1500487. eCollection 2015 Sep.

5.

Perceptions, attitudes, and satisfaction concerning resident participation in health care among dermatology outpatients.

AlGhamdi KM, Almohanna HM, Alkeraye SS, Alsaif FM, Alrasheed SK.

J Cutan Med Surg. 2014 Jan-Feb;18(1):20-7.

PMID:
24377469
6.

Genetics of cholesterol efflux.

Iatan I, Palmyre A, Alrasheed S, Ruel I, Genest J.

Curr Atheroscler Rep. 2012 Jun;14(3):235-46. doi: 10.1007/s11883-012-0247-y. Review.

PMID:
22528521
7.

Genotype-phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures.

Bachmann-Gagescu R, Ishak GE, Dempsey JC, Adkins J, O'Day D, Phelps IG, Gunay-Aygun M, Kline AD, Szczaluba K, Martorell L, Alswaid A, Alrasheed S, Pai S, Izatt L, Ronan A, Parisi MA, Mefford H, Glass I, Doherty D.

J Med Genet. 2012 Feb;49(2):126-37. doi: 10.1136/jmedgenet-2011-100552.

PMID:
22241855
8.

Axial spondylometaphyseal dysplasia: additional reports.

Suzuki S, Kim OH, Makita Y, Saito T, Lim GY, Cho TJ, Al-Swaid A, Alrasheed S, Sadoon E, Miyazaki O, Nishina S, Superti-Furga A, Unger S, Fujieda K, Ikegawa S, Nishimura G.

Am J Med Genet A. 2011 Oct;155A(10):2521-8. doi: 10.1002/ajmg.a.34192. Epub 2011 Sep 9.

PMID:
21910225
9.

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis.

Salih MA, Abu-Amero KK, Alrasheed S, Alorainy IA, Liu L, McGrath JA, Van Maldergem L, Al-Faky YH, AlSuhaibani AH, Oystreck DT, Bosley TM.

BMC Med Genet. 2011 Feb 24;12:31. doi: 10.1186/1471-2350-12-31.

10.

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.

Christiansen HE, Schwarze U, Pyott SM, AlSwaid A, Al Balwi M, Alrasheed S, Pepin MG, Weis MA, Eyre DR, Byers PH.

Am J Hum Genet. 2010 Mar 12;86(3):389-98. doi: 10.1016/j.ajhg.2010.01.034. Epub 2010 Feb 25.

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