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Items: 11

1.

Spin Seebeck Effect from Antiferromagnetic Magnons and Critical Spin Fluctuations in Epitaxial FeF_{2} Films.

Li J, Shi Z, Ortiz VH, Aldosary M, Chen C, Aji V, Wei P, Shi J.

Phys Rev Lett. 2019 May 31;122(21):217204. doi: 10.1103/PhysRevLett.122.217204.

PMID:
31283322
2.

Highly Efficient Spin-Orbit Torque and Switching of Layered Ferromagnet Fe3GeTe2.

Alghamdi M, Lohmann M, Li J, Jothi PR, Shao Q, Aldosary M, Su T, Fokwa BPT, Shi J.

Nano Lett. 2019 Jul 10;19(7):4400-4405. doi: 10.1021/acs.nanolett.9b01043. Epub 2019 Jun 14.

PMID:
31177784
3.

Probing Magnetism in Insulating Cr2Ge2Te6 by Induced Anomalous Hall Effect in Pt.

Lohmann M, Su T, Niu B, Hou Y, Alghamdi M, Aldosary M, Xing W, Zhong J, Jia S, Han W, Wu R, Cui YT, Shi J.

Nano Lett. 2019 Apr 10;19(4):2397-2403. doi: 10.1021/acs.nanolett.8b05121. Epub 2019 Mar 11.

4.

Spin Hall-induced auto-oscillations in ultrathin YIG grown on Pt.

Evelt M, Safranski C, Aldosary M, Demidov VE, Barsukov I, Nosov AP, Rinkevich AB, Sobotkiewich K, Li X, Shi J, Krivorotov IN, Demokritov SO.

Sci Rep. 2018 Jan 19;8(1):1269. doi: 10.1038/s41598-018-19606-5.

5.

A Novel Homozygous Mutation in SPTBN2 Leads to Spinocerebellar Ataxia in a Consanguineous Family: Report of a New Infantile-Onset Case and Brief Review of the Literature.

Al-Muhaizea MA, AlMutairi F, Almass R, AlHarthi S, Aldosary MS, Alsagob M, AlOdaib A, Colak D, Kaya N.

Cerebellum. 2018 Jun;17(3):276-285. doi: 10.1007/s12311-017-0893-2. Review.

PMID:
29196973
6.

Molecular and clinical spectra of FBXL4 deficiency.

El-Hattab AW, Dai H, Almannai M, Wang J, Faqeih EA, Al Asmari A, Saleh MAM, Elamin MAO, Alfadhel M, Alkuraya FS, Hashem M, Aldosary MS, Almass R, Almutairi FB, Alsagob M, Al-Owain M, Al-Sharfa S, Al-Hassnan ZN, Rahbeeni Z, Al-Muhaizea MA, Makhseed N, Foskett GK, Stevenson DA, Gomez-Ospina N, Lee C, Boles RG, Schrier Vergano SA, Wortmann SB, Sperl W, Opladen T, Hoffmann GF, Hempel M, Prokisch H, Alhaddad B, Mayr JA, Chan W, Kaya N, Wong LC.

Hum Mutat. 2017 Dec;38(12):1649-1659. doi: 10.1002/humu.23341. Epub 2017 Oct 6. Review.

PMID:
28940506
7.

Hemophagocytic lymphohistiocytosis: A rare cause of recurrent encephalopathy.

Sulaiman RA, Shaheen MY, Al-Zaidan H, Al-Hassnan Z, Al-Sayed M, Rahbeeni Z, Bakshi NA, Kaya N, Aldosary M, Al-Owain M.

Intractable Rare Dis Res. 2016 Aug;5(3):227-30. doi: 10.5582/irdr.2016.01018.

8.

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability.

Kaya N, Alsagob M, D'Adamo MC, Al-Bakheet A, Hasan S, Muccioli M, Almutairi FB, Almass R, Aldosary M, Monies D, Mustafa OM, Alyounes B, Kenana R, Al-Zahrani J, Naim E, Binhumaid FS, Qari A, Almutairi F, Meyer B, Plageman TF, Pessia M, Colak D, Al-Owain M.

J Med Genet. 2016 Nov;53(11):786-792. doi: 10.1136/jmedgenet-2015-103637. Epub 2016 Aug 31.

PMID:
27582084
9.

Observation of magnon-mediated current drag in Pt/yttrium iron garnet/Pt(Ta) trilayers.

Li J, Xu Y, Aldosary M, Tang C, Lin Z, Zhang S, Lake R, Shi J.

Nat Commun. 2016 Mar 2;7:10858. doi: 10.1038/ncomms10858.

10.

Child homicide in Cairo from 2006 to 2010: characteristics and trends.

Alsaif D, Alsowayigh K, Alfaraidy M, Albayat M, Alshamsi G, Aldosary M, Madadin M, Afify M, Kharoshah M.

J Forensic Leg Med. 2013 Oct;20(7):929-32. doi: 10.1016/j.jflm.2013.08.003. Epub 2013 Aug 31.

PMID:
24112348
11.

Molecular characterization of Joubert syndrome in Saudi Arabia.

Alazami AM, Alshammari MJ, Salih MA, Alzahrani F, Hijazi H, Seidahmed MZ, Abu Safieh L, Aldosary M, Khan AO, Alkuraya FS.

Hum Mutat. 2012 Oct;33(10):1423-8. doi: 10.1002/humu.22134. Epub 2012 Jul 11.

PMID:
22693042

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