Alikaşifoğlu M - Search Results

1

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.

2

Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases.

Tezcan I, Tuncer M, Uçkan D, Cetin M, Alikaşifoğlu M, Ersoy F, Altay C. Tezcan I, et al. Among authors: alikasifoglu m. Pediatr Transplant. 1998 Aug;2(3):236-9. Pediatr Transplant. 1998. PMID: 10084749

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

Wilms tumor, AML and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemia.

Sari N, Akyuz C, Aktas D, Gumruk F, Orhan D, Alikasifoglu M, Aydin B, Alanay Y, Buyukpamukcu M. Sari N, et al. Among authors: alikasifoglu m. Pediatr Blood Cancer. 2009 Aug;53(2):208-10. doi: 10.1002/pbc.21966. Pediatr Blood Cancer. 2009. PMID: 19373780

5

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.

Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D. Alanay Y, et al. Among authors: alikasifoglu m. Am J Hum Genet. 2010 Apr 9;86(4):551-9. doi: 10.1016/j.ajhg.2010.02.022. Epub 2010 Apr 1. Am J Hum Genet. 2010. PMID: 20362275 Free PMC article.

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

HERC1 mutations in idiopathic intellectual disability.

Utine GE, Taşkıran EZ, Koşukcu C, Karaosmanoğlu B, Güleray N, Doğan ÖA, Kiper PÖ, Boduroğlu K, Alikaşifoğlu M. Utine GE, et al. Among authors: alikasifoglu m. Eur J Med Genet. 2017 May;60(5):279-283. doi: 10.1016/j.ejmg.2017.03.007. Epub 2017 Mar 18. Eur J Med Genet. 2017. PMID: 28323226

9

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.

10

Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome.

Taskiran EZ, Karaosmanoglu B, Koşukcu C, Doğan ÖA, Taylan-Şekeroğlu H, Şimşek-Kiper PÖ, Utine EG, Boduroğlu K, Alikaşifoğlu M. Taskiran EZ, et al. Among authors: alikasifoglu m. Am J Med Genet A. 2017 Dec;173(12):3143-3152. doi: 10.1002/ajmg.a.38495. Epub 2017 Oct 8. Am J Med Genet A. 2017. PMID: 28988429

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