Detalhe da pesquisa
1.
Diffuse Large B-Cell Lymphoma, Epstein-Barr Virus -Positive Kappa Monotypic Plasma Cell Proliferation and Invasive Carcinoma, Developing in a Child With Defective Mismatch Repair.
Pediatr Dev Pathol
; 25(3): 339-344, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35227120
2.
A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation.
Metab Brain Dis
; 37(4): 1283-1287, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35254599
3.
Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants.
Neurol Sci
; 42(5): 2045-2057, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33443663
4.
Vitamin D receptor polymorphisms and bone health after kidney transplantation
Turk J Med Sci
; 51(2): 802-812, 2021 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33306336
5.
Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric Study.
J Clin Pediatr Dent
; 44(4): 262-267, 2020 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33167018
6.
Unusual Chromosomal Rearrangement Resulted in Interstitial Monosomy 9p: Case Report.
Cytogenet Genome Res
; 148(1): 19-24, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27166162
7.
A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.
Mol Vis
; 19: 196-202, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23378733
8.
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?
Eur J Pediatr
; 171(10): 1497-502, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22644991
9.
Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche.
J Pediatr Endocrinol Metab
; 24(11-12): 965-70, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22308849
10.
The association between telomere length and ischemic stroke risk and phenotype.
Sci Rep
; 11(1): 10967, 2021 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34040069
11.
Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia.
Ann Hematol
; 89(4): 359-64, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19798502
12.
A child with myelodysplastic syndrome with hypocellular fibrosis.
J Pediatr Hematol Oncol
; 32(8): 617-20, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20818271
13.
Effects of genomic imbalances on telomerase activity in gastric cancer: clues to telomerase regulation.
Oncol Res
; 17(10): 455-62, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19725225
14.
Psychometric liability to psychosis and childhood adversities are associated with shorter telomere length: A study on schizophrenia patients, unaffected siblings, and non-clinical controls.
J Psychiatr Res
; 111: 169-185, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30776705
15.
Expression of Survivin and Its Splice Variants in Pediatric Acute Lymphoblastic Leukemia.
Genet Test Mol Biomarkers
; 22(12): 680-685, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30489176
16.
Does telomere length affect blood pressure?
Adv Ther
; 24(2): 269-72, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17565916
17.
TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.
Turk J Pediatr
; 49(1): 61-8, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17479646
18.
ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants.
Turk J Pediatr
; 49(1): 69-74, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17479647
19.
Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.
Pediatr Endocrinol Rev
; 4(3): 210-7, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17551482
20.
Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment.
Turk J Haematol
; 34(2): 151-158, 2017 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28179212