Alikasifoğlu M - Search Results

1

Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.

Utine GE, Aktas D, Boduroğlu K, Alikasifoğlu M, Tunçbilek E. Utine GE, et al. Among authors: alikasifoglu m. Genet Couns. 2007;18(2):171-7. Genet Couns. 2007. PMID: 17710869

2

Acute lymphoblastic leukemia associated with Klinefelter syndrome.

Gürgey A, Kara A, Tuncer M, Alikaşifoğlu M, Tunçbilek E. Gürgey A, et al. Among authors: alikasifoglu m. Pediatr Hematol Oncol. 1994 Mar-Apr;11(2):227-9. doi: 10.3109/08880019409141662. Pediatr Hematol Oncol. 1994. PMID: 8204450 No abstract available.

3

Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experience.

Altay C, Alikaşifoglu M, Kara A, Tunçbilek E, Ozbek N, Schroeder-Kurth TM. Altay C, et al. Among authors: alikasifoglu m. Clin Genet. 1997 May;51(5):296-302. doi: 10.1111/j.1399-0004.1997.tb02477.x. Clin Genet. 1997. PMID: 9212176

4

Angiotensin converting enzyme gene polymorphism and the risk and extent of ischemic heart disease among Turkish patients.

Tokgözoğlu SL, Alikaşifoğlu M, Atalar E, Tunçbilek E, Ovünç K, Aksöyek S, Kabakçi G, Anar B, Unsal I, Kes S. Tokgözoğlu SL, et al. Among authors: alikasifoglu m. Coron Artery Dis. 1997 Mar-Apr;8(3-4):137-41. doi: 10.1097/00019501-199703000-00003. Coron Artery Dis. 1997. PMID: 9237022

5

677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey.

Boduroglu K, Alikasifoglu M, Anar B, Tuncbilek E. Boduroglu K, et al. Among authors: alikasifoglu m. Arch Dis Child Fetal Neonatal Ed. 1998 May;78(3):F235. doi: 10.1136/fn.78.3.f234c. Arch Dis Child Fetal Neonatal Ed. 1998. PMID: 9713045 Free PMC article. No abstract available.

6

Ring chromosome 13 in an infant with multiple congenital anomalies and penoscrotal transposition.

Boduroglu K, Alikaşifoglu M, Tunçbilek E, Uludogan S. Boduroglu K, et al. Among authors: alikasifoglu m. Clin Dysmorphol. 1998 Oct;7(4):299-301. doi: 10.1097/00019605-199810000-00012. Clin Dysmorphol. 1998. PMID: 9823499 No abstract available.

7

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.

8

Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate.

Tokgözoğlu SL, Alikaşifoğlu M, Unsal, Atalar E, Aytemir K, Ozer N, Ovünç K, Usal O, Kes S, Tunçbilek E. Tokgözoğlu SL, et al. Among authors: alikasifoglu m. Heart. 1999 May;81(5):518-22. doi: 10.1136/hrt.81.5.518. Heart. 1999. PMID: 10212171 Free PMC article.

9

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.

10

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

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