Alikasifoglu M - Search Results

1

A novel variant in severe disease of DADA2: involving vasculitic and haematologic features.

Ayan G, Yagiz B, Cinar OE, Cagdas D, Ozbek DA, Tuncer A, Oguz KK, Ozen S, Alikasifoglu M, Karadag O. Ayan G, et al. Among authors: alikasifoglu m. Scand J Rheumatol. 2023 Jan;52(1):93-95. doi: 10.1080/03009742.2022.2095724. Epub 2022 Jul 19. Scand J Rheumatol. 2023. PMID: 35852217 No abstract available.

2

Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: importance of ACE polymorphism.

Ozen S, Alikasifoglu M, Saatci U, Bakkaloglu A, Besbas N, Kara N, Kocak H, Erbas B, Unsal I, Tuncbilek E. Ozen S, et al. Among authors: alikasifoglu m. Am J Kidney Dis. 1999 Jul;34(1):140-5. doi: 10.1016/s0272-6386(99)70120-4. Am J Kidney Dis. 1999. PMID: 10401028

3

Tumour necrosis factor alpha G-->A -238 and G-->A -308 polymorphisms in juvenile idiopathic arthritis.

Ozen S, Alikasifoglu M, Bakkaloglu A, Duzova A, Jarosova K, Nemcova D, Besbas N, Vencovsky J, Tuncbilek E. Ozen S, et al. Among authors: alikasifoglu m. Rheumatology (Oxford). 2002 Feb;41(2):223-7. doi: 10.1093/rheumatology/41.2.223. Rheumatology (Oxford). 2002. PMID: 11886974

4

Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Oguz KK, Haliloglu G, Temucin C, Gocmen R, Has AC, Doerschner K, Dolgun A, Alikasifoglu M. Oguz KK, et al. Among authors: alikasifoglu m. AJNR Am J Neuroradiol. 2013 Oct;34(10):1952-7. doi: 10.3174/ajnr.A3488. Epub 2013 Apr 18. AJNR Am J Neuroradiol. 2013. PMID: 23598833 Free PMC article.

5

Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome.

Utine GE, Akpınar B, Arslan U, Kiper PÖ, Volkan-Salancı B, Alanay Y, Aktaş D, Haliloğlu G, Oğuz KK, Boduroğlu K, Alikaşifoğlu M. Utine GE, et al. Among authors: alikasifoglu m. Am J Med Genet A. 2014 Jan;164A(1):99-105. doi: 10.1002/ajmg.a.36207. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259304

6

A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations.

Batu ED, Karadag O, Taskiran EZ, Kalyoncu U, Aksentijevich I, Alikasifoglu M, Özen S. Batu ED, et al. Among authors: alikasifoglu m. J Rheumatol. 2015 Aug;42(8):1532-4. doi: 10.3899/jrheum.150024. J Rheumatol. 2015. PMID: 26233953 No abstract available.

7

Systems-level analysis of genome wide association study results for a pilot juvenile idiopathic arthritis family study.

Aydın-Son Y, Batu ED, Demirkaya E, Bilginer Y, Kasapçopur Ö, Ünsal E, Alikaşifoglu M, Özen S. Aydın-Son Y, et al. Among authors: alikasifoglu m. Turk J Pediatr. 2015 Jul-Aug;57(4):324-33. Turk J Pediatr. 2015. PMID: 27186693

8

Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.

Ardicli D, Taskiran EZ, Kosukcu C, Temucin C, Oguz KK, Haliloglu G, Alikasifoglu M, Topaloglu H. Ardicli D, et al. Among authors: alikasifoglu m. Neuropediatrics. 2017 Dec;48(6):477-481. doi: 10.1055/s-0037-1604483. Epub 2017 Aug 11. Neuropediatrics. 2017. PMID: 28800659 No abstract available.

9

Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis.

Taşkıran EZ, Sönmez HE, Ayvaz DÇ, Koşukcu C, Batu ED, Esenboğa S, Topaloğlu R, Orhan D, Bilginer Y, Alikaşifoğlu M, Özen S, Tezcan İ. Taşkıran EZ, et al. Among authors: alikasifoglu m. Clin Immunol. 2018 Feb;187:92-94. doi: 10.1016/j.clim.2017.10.010. Epub 2017 Nov 7. Clin Immunol. 2018. PMID: 29107076 No abstract available.

10

Whole Exome Sequencing in Early-onset Systemic Lupus Erythematosus.

Batu ED, Koşukcu C, Taşkıran E, Sahin S, Akman S, Sözeri B, Ünsal E, Bilginer Y, Kasapcopur O, Alikaşifoğlu M, Ozen S. Batu ED, et al. Among authors: alikasifoglu m. J Rheumatol. 2018 Dec;45(12):1671-1679. doi: 10.3899/jrheum.171358. Epub 2018 Jul 15. J Rheumatol. 2018. PMID: 30008451

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