Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 88

1.

A multi-disciplinary, multimodal approach for the management of vascular anomalies.

Mazhar A, Moosa S, Abbas A, Mallick Y, Samad L.

Pak J Med Sci. 2020 Jan;36(1):S14-S19. doi: 10.12669/pjms.36.ICON-Suppl.1710.

2.

In vitro and in vivo characterization of a cranial window prosthesis for diagnostic and therapeutic cerebral ultrasound.

Prada F, Franzini A, Moosa S, Padilla F, Moore D, Solbiati L, DiMeco F, Legon W.

J Neurosurg. 2020 Jan 3:1-13. doi: 10.3171/2019.10.JNS191674. [Epub ahead of print]

PMID:
31899872
3.

A Case of Granulomatosis with Polyangiitis (Wegener's Granulomatosis) Presenting with Rapidly Progressive Glomerulonephritis.

Hasan MR, Sakibuzzaman M, Tabassum T, Moosa SA.

Cureus. 2019 Oct 12;11(10):e5896. doi: 10.7759/cureus.5896.

4.

Cavernous hemangioma of the conjunctiva.

Mukherjee B, Moosa S, Rajagopal R.

Indian J Ophthalmol. 2019 Dec;67(12):2061. doi: 10.4103/ijo.IJO_1783_18. No abstract available.

5.

Ultrasound Ablation in Neurosurgery: Current Clinical Applications and Future Perspectives.

Franzini A, Moosa S, Prada F, Elias WJ.

Neurosurgery. 2019 Nov 20. pii: nyz407. doi: 10.1093/neuros/nyz407. [Epub ahead of print]

PMID:
31745558
6.

Identifying the Neurogenetic Framework of Crohn's Disease Through Investigative Analysis of the Nucleotide-binding Oligomerization Domain-containing Protein 2 Gene Mutation.

Sakibuzzaman M, Moosa SA, Akhter M, Trisha IH, Talib KA.

Cureus. 2019 Sep 17;11(9):e5680. doi: 10.7759/cureus.5680. Review.

7.

The prevalence of burnout among registrars in the School of Clinical Medicine at the University of the Witwatersrand, Johannesburg, South Africa.

Zeijlemaker C, Moosa S.

S Afr Med J. 2019 Aug 28;109(9):668-672. doi: 10.7196/SAMJ.2019.v109i9.13667.

8.

Kampala Commitment 2019.

Moosa S.

Afr J Prim Health Care Fam Med. 2019 Sep 19;11(1):e1-e2. doi: 10.4102/phcfm.v11i1.2176.

9.

Collaboration with World Health Organization.

Moosa S.

Afr J Prim Health Care Fam Med. 2019 Sep 19;11(1):e1-e2. doi: 10.4102/phcfm.v11i1.2175.

10.

World Organisation of Family Doctors Africa is moving!

Moosa S.

Afr J Prim Health Care Fam Med. 2019 Sep 19;11(1):e1-e2. doi: 10.4102/phcfm.v11i1.2174.

11.

Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.

Moosa S, Yamamoto GL, Garbes L, Keupp K, Beleza-Meireles A, Moreno CA, Valadares ER, de Sousa SB, Maia S, Saraiva J, Honjo RS, Kim CA, Cabral de Menezes H, Lausch E, Lorini PV, Lamounier A Jr, Carniero TCB, Giunta C, Rohrbach M, Janner M, Semler O, Beleggia F, Li Y, Yigit G, Reintjes N, Altmüller J, Nürnberg P, Cavalcanti DP, Zabel B, Warman ML, Bertola DR, Wollnik B, Netzer C.

Am J Hum Genet. 2019 Oct 3;105(4):836-843. doi: 10.1016/j.ajhg.2019.08.008. Epub 2019 Sep 26.

PMID:
31564437
12.

Ablative brain surgery: an overview.

Franzini A, Moosa S, Servello D, Small I, DiMeco F, Xu Z, Elias WJ, Franzini A, Prada F.

Int J Hyperthermia. 2019 Oct;36(2):64-80. doi: 10.1080/02656736.2019.1616833.

13.

Gamma Knife Radiosurgery for Trigeminal Neuralgia Reduces Neurovascular Compression: A Case Report after 11 Years.

Moosa S, Wang TR, Mastorakos P, Sheehan JP, Elias WJ.

Stereotact Funct Neurosurg. 2019;97(3):202-206. doi: 10.1159/000501624. Epub 2019 Sep 5.

PMID:
31487732
14.

Deep brain stimulation of the posterior limb of the internal capsule in the treatment of central poststroke neuropathic pain of the lower limb: case series with long-term follow-up and literature review.

Franzini A, Messina G, Levi V, D'Ammando A, Cordella R, Moosa S, Prada F, Franzini A.

J Neurosurg. 2019 Aug 16:1-9. doi: 10.3171/2019.5.JNS19227. [Epub ahead of print]

PMID:
31419792
15.

The role of high-intensity focused ultrasound as a symptomatic treatment for Parkinson's disease.

Moosa S, Martínez-Fernández R, Elias WJ, Del Alamo M, Eisenberg HM, Fishman PS.

Mov Disord. 2019 Sep;34(9):1243-1251. doi: 10.1002/mds.27779. Epub 2019 Jul 10. Review.

PMID:
31291491
16.

Tumor to Cerebellar Peduncle T2-Weighted Imaging Intensity Ratio Fails to Predict Pituitary Adenoma Consistency.

Mastorakos P, Mehta GU, Chatrath A, Moosa S, Lopes MB, Payne SC, Jane JA Jr.

J Neurol Surg B Skull Base. 2019 Jun;80(3):252-257. doi: 10.1055/s-0038-1668516. Epub 2018 Aug 24.

PMID:
31143567
17.

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.

Lahrouchi N, George A, Ratbi I, Schneider R, Elalaoui SC, Moosa S, Bharti S, Sharma R, Abu-Asab M, Onojafe F, Adadi N, Lodder EM, Laarabi FZ, Lamsyah Y, Elorch H, Chebbar I, Postma AV, Lougaris V, Plebani A, Altmueller J, Kyrieleis H, Meiner V, McNeill H, Bharti K, Lyonnet S, Wollnik B, Henrion-Caude A, Berraho A, Hildebrandt F, Bezzina CR, Brooks BP, Sefiani A.

Nat Commun. 2019 Mar 12;10(1):1180. doi: 10.1038/s41467-019-08547-w.

18.

The neurosurgical treatment of craniofacial pain syndromes: current surgical indications and techniques.

Franzini A, Moosa S, D'Ammando A, Bono B, Scheitler-Ring K, Ferroli P, Messina G, Prada F, Franzini A.

Neurol Sci. 2019 May;40(Suppl 1):159-168. doi: 10.1007/s10072-019-03789-4. Review.

PMID:
30835002
19.

Ganglioglioma Arising from the Septum Pellucidum: Case Report and Review of the Literature.

Chatrath A, Mastorakos P, Mehta GU, Wildeman M, Moosa S, Jane JA Jr.

Pediatr Neurosurg. 2019;54(1):36-45. doi: 10.1159/000495043. Epub 2019 Jan 8. Review.

PMID:
30620941
20.

Exploring the sorting of patients in community health centres across Gauteng Province, South Africa.

Stott BA, Moosa S.

BMC Fam Pract. 2019 Jan 7;20(1):5. doi: 10.1186/s12875-018-0899-y.

21.

Get to know WONCA Africa.

Moosa S.

Afr J Prim Health Care Fam Med. 2018 Nov 29;10(1):e1-e2. doi: 10.4102/phcfm.v10i1.1984.

22.

Challenges and Solutions for Functional Neurosurgery in Developing Countries.

Fezeu F, Ramesh A, Melmer PD, Moosa S, Larson PS, Henderson F Jr.

Cureus. 2018 Sep 17;10(9):e3314. doi: 10.7759/cureus.3314. Review.

23.

Floating-Harbor Syndrome: Presentation of the First Romanian Patient with a SRCAP Mutation and Review of the Literature.

Budisteanu M, Bögershausen N, Papuc SM, Moosa S, Thoenes M, Riga D, Arghir A, Wollnik B.

Balkan J Med Genet. 2018 Oct 29;21(1):83-86. doi: 10.2478/bjmg-2018-0005. eCollection 2018 Jun.

24.

Emerging role of family medicine in South Africa.

Moosa S, Peersman W, Derese A, Kidd M, Pettigrew LM, Howe A, Martinez-Bianchi V, De Maeseneer J.

BMJ Glob Health. 2018 Sep 6;3(Suppl 3):e000736. doi: 10.1136/bmjgh-2018-000736. eCollection 2018. No abstract available.

25.

Deep brain stimulation for the treatment of drug addiction.

Wang TR, Moosa S, Dallapiazza RF, Elias WJ, Lynch WJ.

Neurosurg Focus. 2018 Aug;45(2):E11. doi: 10.3171/2018.5.FOCUS18163. Review.

26.

Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta.

Rodriguez Celin M, Moosa S, Fano V.

Ann Hum Genet. 2018 Nov;82(6):477-481. doi: 10.1111/ahg.12275. Epub 2018 Jul 24.

PMID:
30039845
27.

Rooibos tea extracts inhibit osteoclast formation and activity through the attenuation of NF-κB activity in RAW264.7 murine macrophages.

Moosa S, Kasonga AE, Deepak V, Marais S, Magoshi IB, Bester MJ, Kruger MC, Coetzee M.

Food Funct. 2018 Jun 20;9(6):3301-3312. doi: 10.1039/c7fo01497j.

PMID:
29790498
28.

Endoport-assisted surgical evacuation of a deep-seated cerebral abscess.

Moosa S, Ding D, Mastorakos P, Sheehan JP, Liu KC, Starke RM.

J Clin Neurosci. 2018 Jul;53:269-272. doi: 10.1016/j.jocn.2018.04.028. Epub 2018 Apr 30.

PMID:
29716807
29.

Thalamic Deep Brain Stimulation Salvages Failed Focused Ultrasound Thalamotomy for Essential Tremor: A Case Report.

Wang TR, Dallapiazza RF, Moosa S, Huss D, Shah BB, Elias WJ.

Stereotact Funct Neurosurg. 2018;96(1):60-64. doi: 10.1159/000486646. Epub 2018 Feb 12.

PMID:
29433124
30.

Transcranial magnetic resonance imaging-guided focused ultrasound thalamotomy for tremor: technical note.

Wang TR, Bond AE, Dallapiazza RF, Blanke A, Tilden D, Huerta TE, Moosa S, Prada FU, Elias WJ.

Neurosurg Focus. 2018 Feb;44(2):E3. doi: 10.3171/2017.10.FOCUS17609.

PMID:
29385914
31.

Review of cardiovascular magnetic resonance in human immunodeficiency virus-associated cardiovascular disease.

Sood V, Jermy S, Saad H, Samuels P, Moosa S, Ntusi N.

SA J Radiol. 2017 Nov 14;21(2):1248. doi: 10.4102/sajr.v21i2.1248. eCollection 2017. Review.

32.

Novel compound heterozygous mutations in TELO2 in a patient with severe expression of You-Hoover-Fong syndrome.

Moosa S, Altmüller J, Lyngbye T, Christensen R, Li Y, Nürnberg P, Yigit G, Vogel I, Wollnik B.

Mol Genet Genomic Med. 2017 Jul 28;5(5):580-584. doi: 10.1002/mgg3.287. eCollection 2017 Sep.

33.

Regulation mechanism of oxidative stress induced by high glucose through PI3K/Akt/Nrf2 pathway in juvenile blunt snout bream (Megalobrama amblycephala).

Pan W, Miao L, Lin Y, Huang X, Ge X, Moosa SL, Liu B, Ren M, Zhou Q, Liang H, Zhang W, Pan L.

Fish Shellfish Immunol. 2017 Nov;70:66-75. doi: 10.1016/j.fsi.2017.09.005. Epub 2017 Sep 4.

PMID:
28882793
34.

Metatarsal bony syndactyly in 2 fetuses with Smith-Lemli-Opitz syndrome: An under-recognized part of the clinical spectrum.

Moosa S, Loeys B, Altmüller J, Mortier G, Nürnberg P, Li Y, Wollnik B, Vogel I.

Clin Genet. 2017 Sep;92(3):342-343. doi: 10.1111/cge.12990. Epub 2017 Mar 30. No abstract available.

PMID:
28369852
35.

Stereotactic radiosurgery in the treatment of parasellar meningiomas: long-term volumetric evaluation.

Cohen-Inbar O, Tata A, Moosa S, Lee CC, Sheehan JP.

J Neurosurg. 2018 Feb;128(2):362-372. doi: 10.3171/2016.11.JNS161402. Epub 2017 Mar 24.

PMID:
28338439
36.

Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2.

Moosa S, Haagerup A, Gregersen PA, Petersen KK, Altmüller J, Thiele H, Nürnberg P, Cho TJ, Kim OH, Nishimura G, Wollnik B, Vogel I.

Am J Med Genet A. 2017 Apr;173(4):1102-1108. doi: 10.1002/ajmg.a.38116.

PMID:
28328135
37.

Volume-staged versus dose-staged stereotactic radiosurgery outcomes for large brain arteriovenous malformations: a systematic review.

Ilyas A, Chen CJ, Ding D, Taylor DG, Moosa S, Lee CC, Cohen-Inbar O, Sheehan JP.

J Neurosurg. 2018 Jan;128(1):154-164. doi: 10.3171/2016.9.JNS161571. Epub 2017 Jan 27.

PMID:
28128692
38.
39.

Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicism.

Moosa S, Böhrer-Rabel H, Altmüller J, Beleggia F, Nürnberg P, Li Y, Yigit G, Wollnik B.

Am J Med Genet A. 2017 Jan;173(1):264-267. doi: 10.1002/ajmg.a.37999. Epub 2016 Oct 18.

PMID:
27753196
40.

Insights of private general practitioners in group practice on the introduction of National Health Insurance in South Africa.

Moosa S, Luiz J, Carmichael T, Peersman W, Derese A.

Afr J Prim Health Care Fam Med. 2016 Jun 15;8(1):e1-6. doi: 10.4102/phcfm.v8i1.1025.

41.

A novel homozygous PAM16 mutation in a patient with a milder phenotype and longer survival.

Moosa S, Fano V, Obregon MG, Altmüller J, Thiele H, Nürnberg P, Nishimura G, Wollnik B.

Am J Med Genet A. 2016 Sep;170(9):2436-9. doi: 10.1002/ajmg.a.37823. Epub 2016 Jun 29. No abstract available.

PMID:
27354339
42.

Diagnosing cardiac disease during pregnancy: imaging modalities.

Ntusi NA, Samuels P, Moosa S, Mocumbi AO.

Cardiovasc J Afr. 2016 Mar-Apr;27(2):95-103. doi: 10.5830/CVJA-2016-022. Review.

43.

Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum.

Moosa S, Obregon MG, Altmüller J, Thiele H, Nürnberg P, Fano V, Wollnik B.

Am J Med Genet A. 2016 May;170A(5):1295-301. doi: 10.1002/ajmg.a.37570. Epub 2016 Jan 21.

PMID:
26792575
44.

A THANATOPHORIC DYSPLASIA TYPE I CASE WITH A FGFR3 P.R248C MUTATION AND SURVIVAL BEYOND THE NEONATAL PERIOD.

Sahin S, Ograg H, Aslan EA, Akcan AB, Turkmen MK, Moosa S, Elcioglu NH.

Genet Couns. 2016;27(4):513-517.

PMID:
30226972
45.

Altered FGF signalling in congenital craniofacial and skeletal disorders.

Moosa S, Wollnik B.

Semin Cell Dev Biol. 2016 May;53:115-25. doi: 10.1016/j.semcdb.2015.12.005. Epub 2015 Dec 11. Review.

PMID:
26686047
46.

Improving Brain Tumor Research in Resource-Limited Countries: A Review of the Literature Focusing on West Africa.

Ngulde SI, Fezeu F, Ramesh A, Moosa S, Purow B, Lopez B, Schiff D, Hussaini IM, Sandabe UK.

Cureus. 2015 Nov 3;7(11):e372. doi: 10.7759/cureus.372. Review.

47.

Commercial Honeybush (Cyclopia spp.) Tea Extract Inhibits Osteoclast Formation and Bone Resorption in RAW264.7 Murine Macrophages-An in vitro Study.

Visagie A, Kasonga A, Deepak V, Moosa S, Marais S, Kruger MC, Coetzee M.

Int J Environ Res Public Health. 2015 Oct 28;12(11):13779-93. doi: 10.3390/ijerph121113779.

48.

Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta.

Moosa S, Chung BH, Tung JY, Altmüller J, Thiele H, Nürnberg P, Netzer C, Nishimura G, Wollnik B.

Clin Genet. 2016 Apr;89(4):517-519. doi: 10.1111/cge.12678. Epub 2015 Oct 14. No abstract available.

PMID:
26467156
49.

Human resources for primary health care in sub-Saharan Africa: progress or stagnation?

Willcox ML, Peersman W, Daou P, Diakité C, Bajunirwe F, Mubangizi V, Mahmoud EH, Moosa S, Phaladze N, Nkomazana O, Khogali M, Diallo D, De Maeseneer J, Mant D.

Hum Resour Health. 2015 Sep 10;13:76. doi: 10.1186/s12960-015-0073-8.

50.

Infundibular dilations of the posterior communicating arteries: pathogenesis, anatomical variants, aneurysm formation, and subarachnoid hemorrhage.

Chen CJ, Moosa S, Ding D, Raper DM, Burke RM, Lee CC, Chivukula S, Wang TR, Starke RM, Crowley RW, Liu KC.

J Neurointerv Surg. 2016 Aug;8(8):791-5. doi: 10.1136/neurintsurg-2015-011827. Epub 2015 Jun 18. Review.

PMID:
26089400

Supplemental Content

Support Center