Alikaşifoğlu M - Search Results

1

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

2

Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects.

Boduroğlu K, Alikaşifoğlu M, Anar B, Tunçbilek E. Boduroğlu K, et al. Among authors: alikasifoglu m. J Child Neurol. 1999 Mar;14(3):159-61. doi: 10.1177/088307389901400305. J Child Neurol. 1999. PMID: 10190266 Clinical Trial.

3

Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.

Tunçbilek E, Alikasifoğlu M, Boduroğlu K, Aktas D, Anar B. Tunçbilek E, et al. Among authors: alikasifoglu m. Am J Med Genet. 1999 May 28;84(3):202-3. doi: 10.1002/(sici)1096-8628(19990528)84:3<202::aid-ajmg6>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10331591 No abstract available.

4

Results of the Turkish congenital malformation survey.

Tunçbilek E, Boduroğlu K, Alikaşifoğlu M. Tunçbilek E, et al. Among authors: alikasifoglu m. Turk J Pediatr. 1999 Jul-Sep;41(3):287-97. Turk J Pediatr. 1999. PMID: 10770088

5

Neural tube defects in Turkey: prevalence, distribution and risk factors.

Tunçbilek E, Boduroğlu K, Alikaşifoğlu M. Tunçbilek E, et al. Among authors: alikasifoglu m. Turk J Pediatr. 1999 Jul-Sep;41(3):299-305. Turk J Pediatr. 1999. PMID: 10770089

6

Screening for the fragile X syndrome among mentally retarded males by hair root analysis.

Tunçbilek E, Alikasifoğlu M, Aktas D, Duman F, Yanik H, Anar B, Oostra B, Willemsen R. Tunçbilek E, et al. Among authors: alikasifoglu m. Am J Med Genet. 2000 Nov 13;95(2):105-7. doi: 10.1002/1096-8628(20001113)95:2<105::aid-ajmg3>3.0.co;2-6. Am J Med Genet. 2000. PMID: 11078558

7

Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.

Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E. Boduroğlu K, et al. Among authors: alikasifoglu m. Turk J Pediatr. 2005 Oct-Dec;47(4):327-33. Turk J Pediatr. 2005. PMID: 16363341

8

Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogue.

Utine GE, Alikasifoglu A, Alikasifoglu M, Tuncbilek E. Utine GE, et al. Among authors: alikasifoglu a, alikasifoglu m. Eur J Med Genet. 2006 Jan-Feb;49(1):79-82. doi: 10.1016/j.ejmg.2005.04.020. Epub 2005 Jun 29. Eur J Med Genet. 2006. PMID: 16473313

9

Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.

Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E. Aktas D, et al. Among authors: alikasifoglu m. Eur J Med Genet. 2006 Mar-Apr;49(2):141-9. doi: 10.1016/j.ejmg.2005.05.012. Epub 2005 Jul 1. Eur J Med Genet. 2006. PMID: 16530711

10

A multidisciplinary approach to the management of individuals with fragile X syndrome.

Alanay Y, Unal F, Turanli G, Alikaşifoğlu M, Alehan D, Akyol U, Belgin E, Sener C, Aktaş D, Boduroğlu K, Utine E, Volkan-Salanci B, Ozusta S, Genç A, Başar F, Sevinç S, Tunçbilek E. Alanay Y, et al. Among authors: alikasifoglu m. J Intellect Disabil Res. 2007 Feb;51(Pt 2):151-61. doi: 10.1111/j.1365-2788.2006.00942.x. J Intellect Disabil Res. 2007. PMID: 17217479

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