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Pasteurella multocida Septic Shock: Case Report and Literature Review.

Aljameely A, Wali G.

Case Rep Infect Dis. 2019 Nov 3;2019:1964161. doi: 10.1155/2019/1964161. eCollection 2019.


Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes.

Kumar KR, Davis RL, Tchan MC, Wali GM, Mahant N, Ng K, Kotschet K, Siow SF, Gu J, Walls Z, Kang C, Wali G, Levy S, Phua CS, Yiannikas C, Darveniza P, Chang FCF, Morales-Briceño H, Rowe DB, Drew A, Gayevskiy V, Cowley MJ, Minoche AE, Tisch S, Hayes M, Kummerfeld S, Fung VSC, Sue CM.

Parkinsonism Relat Disord. 2019 Dec;69:111-118. doi: 10.1016/j.parkreldis.2019.11.004. Epub 2019 Nov 7.


Assessment of Accuracy of an Artificial Intelligence Algorithm to Detect Melanoma in Images of Skin Lesions.

Phillips M, Marsden H, Jaffe W, Matin RN, Wali GN, Greenhalgh J, McGrath E, James R, Ladoyanni E, Bewley A, Argenziano G, Palamaras I.

JAMA Netw Open. 2019 Oct 2;2(10):e1913436. doi: 10.1001/jamanetworkopen.2019.13436. Erratum in: JAMA Netw Open. 2019 Nov 1;2(11):e1916430.


Efficacy of ceftazidime-avibactam in the treatment of infections due to Carbapenem-resistant Enterobacteriaceae.

Alraddadi BM, Saeedi M, Qutub M, Alshukairi A, Hassanien A, Wali G.

BMC Infect Dis. 2019 Sep 4;19(1):772. doi: 10.1186/s12879-019-4409-1.


Use of the Skin Cancer Quality of Life Impact Tool (SCQOLIT) - a feasibility study in non-melanoma skin cancer.

Wali GN, Gibbons E, Kelly L, Reed JR, Matin RN.

J Eur Acad Dermatol Venereol. 2019 Aug 16. doi: 10.1111/jdv.15887. [Epub ahead of print]


Genetic analysis of a family from India with Machado-Joseph disease.

Anjanappa RM, Jain S, Wali GM, Purushottam M.

Neurol India. 2019 Mar-Apr;67(2):582-588. doi: 10.4103/0028-3886.258030. No abstract available.


A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature Review.

Wali G, Wali GM, Sue CM, Kumar KR.

Neuropediatrics. 2019 Aug;50(4):248-252. doi: 10.1055/s-0039-1684052. Epub 2019 May 7.


A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia.

Giri S, Naiya T, Roy S, Das G, Wali GM, Das SK, Ray K, Ray J.

J Mol Neurosci. 2019 Jun;68(2):214-220. doi: 10.1007/s12031-019-01301-3. Epub 2019 Mar 25.


Implementation of an evidence-based practice to decrease surgical site infection after coronary artery bypass grafting.

Al Salmi H, Elmahrouk A, Arafat AA, Edrees A, Alshehri M, Wali G, Zabani I, Mahdi NA, Jamjoom A.

J Int Med Res. 2019 Aug;47(8):3491-3501. doi: 10.1177/0300060519836511. Epub 2019 Mar 21. No abstract available.


British Association of Dermatologists' guidelines for the management of Stevens-Johnson syndrome/toxic epidermal necrolysis in children and young people, 2018.

McPherson T, Exton LS, Biswas S, Creamer D, Dziewulski P, Newell L, Tabor KL, Wali GN, Walker G, Walker R, Walker S, Young AE, Mohd Mustapa MF, Murphy R.

Br J Dermatol. 2019 Jul;181(1):37-54. doi: 10.1111/bjd.17841. Epub 2019 Apr 25. No abstract available.


Establishing and developing a Teenage and Young Adult dermatology clinic with embedded specialist psychological support.

De Vere Hunt I, Chapman K, Wali G, Bullus S, Fisher R, Matin RN, McPherson T.

Clin Exp Dermatol. 2019 Dec;44(8):893-896. doi: 10.1111/ced.13950. Epub 2019 Mar 18.


Cutaneous hyperpigmentation and familial gastrointestinal stromal tumour associated with KIT mutation.

Wali GN, Halliday D, Dua J, Ieremia E, McPherson T, Matin RN.

Clin Exp Dermatol. 2019 Jun;44(4):418-421. doi: 10.1111/ced.13757. Epub 2018 Oct 2.


Expanding the spectrum of PEX16 mutations and novel insights into disease mechanisms.

Kumar KR, Wali G, Davis RL, Mallawaarachchi AC, Palmer EE, Gayevskiy V, Minoche AE, Veivers D, Dinger ME, Mackay-Sim A, Cowley MJ, Sue CM.

Mol Genet Metab Rep. 2018 Jul 20;16:46-51. doi: 10.1016/j.ymgmr.2018.07.003. eCollection 2018 Sep.


Patient-Derived Stem Cell Models in SPAST HSP: Disease Modelling and Drug Discovery.

Wali G, Sue CM, Mackay-Sim A.

Brain Sci. 2018 Jul 31;8(8). pii: E142. doi: 10.3390/brainsci8080142. Review.


Patient preferences for topical treatment of actinic keratoses: a discrete-choice experiment.

Kopasker D, Kwiatkowski A, Matin RN, Harwood CA, Ismail F, Lear JT, Thomson J, Hasan Z, Wali GN, Milligan A, Crawford L, Ahmed I, Duffy H, Proby CM, Allanson PF.

Br J Dermatol. 2019 Apr;180(4):902-909. doi: 10.1111/bjd.16801. Epub 2018 Jul 26.


Management of naevus sebaceous: a national survey of UK dermatologists and plastic surgeons.

Wali GN, Felton SJ, McPherson T.

Clin Exp Dermatol. 2018 Jul;43(5):589-591. doi: 10.1111/ced.13422. Epub 2018 Feb 20.


A Patient-Specific Stem Cell Model to Investigate the Neurological Phenotype Observed in Ataxia-Telangiectasia.

Stewart R, Wali G, Perry C, Lavin MF, Féron F, Mackay-Sim A, Sutharsan R.

Methods Mol Biol. 2017;1599:391-400. doi: 10.1007/978-1-4939-6955-5_28.


Risk Factors for Middle East Respiratory Syndrome Coronavirus Infection among Healthcare Personnel.

Alraddadi BM, Al-Salmi HS, Jacobs-Slifka K, Slayton RB, Estivariz CF, Geller AI, Al-Turkistani HH, Al-Rehily SS, Alserehi HA, Wali GY, Alshukairi AN, Azhar EI, Haynes L, Swerdlow DL, Jernigan JA, Madani TA.

Emerg Infect Dis. 2016 Nov;22(11):1915-1920. doi: 10.3201/eid2211.160920.


Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing.

Kumar KR, Wali GM, Kamate M, Wali G, Minoche AE, Puttick C, Pinese M, Gayevskiy V, Dinger ME, Roscioli T, Sue CM, Cowley MJ.

Neurogenetics. 2016 Oct;17(4):265-270. Epub 2016 Sep 28.


Two Indian Families with Quadrupedal Locomotion Resembling Uner Tan Syndrome: A Video Document.

Wali G.

Mov Disord Clin Pract. 2016 Jun 6;4(1):49-50. doi: 10.1002/mdc3.12380. eCollection 2017 Jan-Feb. No abstract available.


Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia.

Wali G, Sutharsan R, Fan Y, Stewart R, Tello Velasquez J, Sue CM, Crane DI, Mackay-Sim A.

Sci Rep. 2016 May 27;6:27004. doi: 10.1038/srep27004.


Antibody Response and Disease Severity in Healthcare Worker MERS Survivors.

Alshukairi AN, Khalid I, Ahmed WA, Dada AM, Bayumi DT, Malic LS, Althawadi S, Ignacio K, Alsalmi HS, Al-Abdely HM, Wali GY, Qushmaq IA, Alraddadi BM, Perlman S.

Emerg Infect Dis. 2016 Jun;22(6). doi: 10.3201/eid2206.160010.


Patient characteristics infected with Middle East respiratory syndrome coronavirus infection in a tertiary hospital.

Alraddadi B, Bawareth N, Omar H, Alsalmi H, Alshukairi A, Qushmaq I, Feteih M, Qutob M, Wali G, Khalid I.

Ann Thorac Med. 2016 Apr-Jun;11(2):128-31. doi: 10.4103/1817-1737.180027.


Impact of Middle East Respiratory Syndrome coronavirus (MERS-CoV) on pregnancy and perinatal outcome.

Alserehi H, Wali G, Alshukairi A, Alraddadi B.

BMC Infect Dis. 2016 Mar 2;16:105. doi: 10.1186/s12879-016-1437-y.


Four Simple Ward Based Initiatives to Reduce Unnecessary In-Hospital Patient Stay: A Quality Improvement Project.

Shabbir A, Wali G, Steuer A.

BMJ Qual Improv Rep. 2015 Jul 16;4(1). pii: u208974.w3661. doi: 10.1136/bmjquality.u208974.w3661. eCollection 2015.


A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations.

Abrahamsen G, Fan Y, Matigian N, Wali G, Bellette B, Sutharsan R, Raju J, Wood SA, Veivers D, Sue CM, Mackay-Sim A.

Dis Model Mech. 2015 Oct 1;8(10):1339. doi: 10.1242/dmm.023002. No abstract available.


Midterm functional outcome after operative management of midfoot injuries.

Latoo IA, Wani IH, Farooq M, Wali GR, Kamal Y, Gani NU.

Ortop Traumatol Rehabil. 2014 Nov-Dec;16(6):639-44. doi: 10.5604/15093492.1135124.


A rare but potentially fatal cause of diarrhoea and weight loss: enteropathy-associated T-cell lymphoma.

Wali GN, Tyrrell HE, Collins GP, Eagleton HJ.

BMJ Case Rep. 2015 Jan 7;2015. pii: bcr2014204125. doi: 10.1136/bcr-2014-204125.


Operative management of displaced acetabular fractures: an institutional experience with a midterm follow-up.

Bhat NA, Kangoo KA, Wani IH, Wali GR, Muzaffar N, Dar RA.

Ortop Traumatol Rehabil. 2014 May-Jun;16(3):245-52. doi: 10.5604/15093492.1112281.


Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia.

Fan Y, Wali G, Sutharsan R, Bellette B, Crane DI, Sue CM, Mackay-Sim A.

Biol Open. 2014 May 23;3(6):494-502. doi: 10.1242/bio.20147641.


Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India.

Kadakol GS, Kulkarni SS, Wali GM, Gai PB.

Neurol India. 2014 Mar-Apr;62(2):149-52. doi: 10.4103/0028-3886.132338.


Periprocedural stroke risk in patients undergoing catheter ablation for atrial fibrillation on uninterrupted warfarin.

Page SP, Herring N, Hunter RJ, Withycombe E, Lovell M, Wali G, Betts TR, Bashir Y, Dhinoja M, Earley MJ, Sporton SC, Rajappan K, Schilling RJ.

J Cardiovasc Electrophysiol. 2014 Jun;25(6):585-90. doi: 10.1111/jce.12411. Epub 2014 Apr 17.


Spinocerebellar ataxia type 7: Report of an Indian family.

Wali GM.

Ann Indian Acad Neurol. 2013 Oct;16(4):708-11. doi: 10.4103/0972-2327.120455.


A study on dentigerous cystic changes with radiographically normal impacted mandibular third molars.

Wali GG, Sridhar V, Shyla HN.

J Maxillofac Oral Surg. 2012 Dec;11(4):458-65. doi: 10.1007/s12663-011-0252-7. Epub 2011 Jul 6.


A case of erosive polyarthritis in a patient diagnosed with a suspicion of atypical mycobacteria.

Almoallim H, Alharbi L, Alshareef Z, Wali G.

Open Rheumatol J. 2013 Aug 28;7:64-6. doi: 10.2174/1874312901307010064. eCollection 2013.


Varix of the retromandibular vein within the parotid gland: case study.

Wali GN, Mawby TA, Sheerin F, Milford CA.

J Laryngol Otol. 2013 Aug;127(8):825-7. doi: 10.1017/S0022215113001369. Epub 2013 Jun 28.


A patient-derived olfactory stem cell disease model for ataxia-telangiectasia.

Stewart R, Kozlov S, Matigian N, Wali G, Gatei M, Sutharsan R, Bellette B, Wraith-Kijas A, Cochrane J, Coulthard M, Perry C, Sinclair K, Mackay-Sim A, Lavin MF.

Hum Mol Genet. 2013 Jun 15;22(12):2495-509. doi: 10.1093/hmg/ddt101. Epub 2013 Mar 7.


Successful use of antitumor necrosis factor-alpha biological therapy in managing human immunodeficiency virus-associated arthritis: three case studies from Saudi Arabia.

Almoallim H, Jali I, Wali G.

Joint Bone Spine. 2013 Jul;80(4):426-8. doi: 10.1016/j.jbspin.2013.01.002. Epub 2013 Mar 1.


A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations.

Abrahamsen G, Fan Y, Matigian N, Wali G, Bellette B, Sutharsan R, Raju J, Wood SA, Veivers D, Sue CM, Mackay-Sim A.

Dis Model Mech. 2013 Mar;6(2):489-502. doi: 10.1242/dmm.010884. Epub 2012 Dec 20. Erratum in: Dis Model Mech. 2015 Oct 1;8(10):1339.


Letter to the editor: response to "tension band wiring" a simplified approach for fracture reduction and intermittent stabilization by degala s and Gupta N.

Sridhar V, Wali GG.

J Maxillofac Oral Surg. 2011 Dec;10(4):367. doi: 10.1007/s12663-011-0254-5. Epub 2011 Jul 10. No abstract available.


PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.

Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H.

Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17.


Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.

Friedman J, Roze E, Abdenur JE, Chang R, Gasperini S, Saletti V, Wali GM, Eiroa H, Neville B, Felice A, Parascandalo R, Zafeiriou DI, Arrabal-Fernandez L, Dill P, Eichler FS, Echenne B, Gutierrez-Solana LG, Hoffmann GF, Hyland K, Kusmierska K, Tijssen MA, Lutz T, Mazzuca M, Penzien J, Poll-The BT, Sykut-Cegielska J, Szymanska K, Thöny B, Blau N.

Ann Neurol. 2012 Apr;71(4):520-30. doi: 10.1002/ana.22685.


Novel influenza A (H1N1) virus-induced hemophagocytosis: first case reported in Saudi Arabia.

Ur Rehman J, Wali G, Sayes NM, Maulawi A, Aslam M, Khalid I.

Ann Saudi Med. 2012 Jan-Feb;32(1):86-9.


Acute movement disorder with bilateral basal ganglia lesions in diabetic uremia.

Wali GM, Khanpet MS, Mali RV.

Ann Indian Acad Neurol. 2011 Jul;14(3):211-3. doi: 10.4103/0972-2327.85899.


Sepiapterin reductase deficiency: two Indian siblings with unusual clinical features.

Wali GM, Thony B, Blau N.

Mov Disord. 2010 May 15;25(7):954-5. doi: 10.1002/mds.23032. No abstract available.


Transverse myelitis as a presenting feature of late onset systemic lupus erythematosus.

Almoallim H, Bukhari M, Alwafi L, Wali G.

Ann Saudi Med. 2009 Mar-Apr;29(2):156-7. No abstract available.


Asymmetrical awake bruxism associated with multiple system atrophy.

Wali GM.

Mov Disord. 2004 Mar;19(3):352-5.


Parkinsonism associated with Addison's disease.

Wali GM.

Mov Disord. 2003 Mar;18(3):340-2.


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