Detalhe da pesquisa
1.
The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review.
Am J Med Genet A
; 191(7): 1814-1825, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37053206
2.
Clinical features of generalized lipodystrophy in Turkey: A cohort analysis.
Diabetes Obes Metab
; 25(7): 1950-1963, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36946378
3.
Development of a mobile monitoring program for anxiety and depression in pregnancy and evaluation of 3-month results.
Ann Clin Psychiatry
; 35(4): 260-271, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37850996
4.
Responsiveness and Validity of Weight-Bearing Test for Measuring Loading Capacity in Patients With Triangular Fibrocartilage Complex Injury.
J Sport Rehabil
; 31(7): 876-884, 2022 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35461186
5.
Effectiveness of a supervised group exercise therapy based on the biopsychosocial model introduced simultaneously with anti-TNF therapy in anti-TNF-naive patients with active ankylosing spondylitis.
Turk J Med Sci
; 52(3): 667-676, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36326328
6.
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual Disability.
Cytogenet Genome Res
; 161(3-4): 153-159, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34229322
7.
Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience.
J Hum Genet
; 66(6): 585-596, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33288834
8.
Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey.
Am J Med Genet A
; 185(8): 2488-2495, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33987976
9.
Simple heteroaryl modifications in the 4,5-diarylisoxazol-3-carboxylic acid scaffold favorably modulates the activity as dual mPGES-1/5-LO inhibitors with in vivo efficacy.
Bioorg Chem
; 112: 104861, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826984
10.
A clinical scoring system for congenital contractural arachnodactyly.
Genet Med
; 22(1): 124-131, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31316167
11.
Reversal of deleterious effect of hypertension on the liver by inhibition of endoplasmic reticulum stress.
Mol Biol Rep
; 47(3): 2243-2252, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32072406
12.
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.
PLoS Genet
; 13(3): e1006683, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28346496
13.
Coronal craniosynostosis due to TCF12 mutations in patients from Turkey.
Am J Med Genet A
; 179(11): 2241-2245, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31353793
14.
Activation of Liver X Receptors by GW3965 Attenuated Deoxycorticosterone Acetate-Salt Hypertension-Induced Cardiac Functional and Structural Changes.
J Cardiovasc Pharmacol
; 74(2): 105-117, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31397742
15.
Antinociceptive Effect of Liposomal Bupivacaine Formulations After Intrathecal Administration in Rats
Turk J Med Sci
; 49(1): 429-434, 2019 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30761835
16.
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Hum Genet
; 137(6-7): 479-486, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29982980
17.
Renal complications of lipodystrophy: A closer look at the natural history of kidney disease.
Clin Endocrinol (Oxf)
; 89(1): 65-75, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29722904
18.
A novel AXIN2 gene mutation in sagittal synostosis.
Am J Med Genet A
; 176(9): 1976-1980, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30088857
19.
A new biopsychosocial and clinical questionnaire to assess juvenile idiopathic arthritis: JAB-Q.
Rheumatol Int
; 38(8): 1557-1564, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29869009
20.
Bone mineral density in patients with mucopolysaccharidosis type III.
J Bone Miner Metab
; 35(3): 338-343, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27193466