Detalhe da pesquisa
1.
MRI evaluation of right heart functions in children with mild cystic fibrosis.
Cardiol Young
; 33(10): 1828-1833, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36226672
2.
Clinical findings of patients with cystic fibrosis according to newborn screening results.
Pediatr Int
; 64(1): e14888, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34131975
3.
New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and Duodenum.
Pediatr Dev Pathol
; 24(3): 252-257, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33683986
4.
Assessment of Right Heart Functions in Children with Mild Cystic Fibrosis.
Klin Padiatr
; 233(5): 231-236, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33601431
5.
Post-intubation subglottic stenosis in children: Analysis of clinical features and risk factors.
Pediatr Int
; 62(3): 386-389, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883152
6.
Short-term azithromycin use is associated with QTc interval prolongation in children with cystic fibrosis.
Arch Pediatr
; 2024 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38637249
7.
Long-term outcomes of standardized training for caregivers of children with tracheostomies: The IStanbul PAediatric Tracheostomy (ISPAT) project.
Pediatr Pulmonol
; 59(2): 331-341, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37983721
8.
Comparison of clinical features of cystic fibrosis patients eligible but not on CFTR modulators to ineligible for CFTR modulators.
Pediatr Pulmonol
; 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38771207
9.
Clinical and Radiological Evaluation and Follow-Up of Patients with Noncardiac Plastic Bronchitis.
Turk Arch Pediatr
; 58(5): 515-518, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37670550
10.
A pediatric case of Takayasu's arteritis with anti-neutrophil cytoplasmic antibody-associated vasculitis triggered by COVID-19 infection.
North Clin Istanb
; 10(3): 393-397, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37435294
11.
Clinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry data.
Turk J Pediatr
; 65(2): 257-268, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37114691
12.
Patients with cystic fibrosis who could not receive the CFTR modulator treatment: What did they lose in 1 year?
Pediatr Pulmonol
; 58(9): 2505-2512, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37278544
13.
Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants.
Bone
; 155: 116293, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34902613
14.
Efficacy of standardized tracheostomy training with a simulation model for healthcare providers: A study by ISPAT team.
Pediatr Pulmonol
; 57(2): 418-426, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34821480
15.
The ISPAT project: Implementation of a standardized training program for caregivers of children with tracheostomy.
Pediatr Pulmonol
; 57(1): 176-184, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34562057
16.
The success of the Cystic Fibrosis Registry of Turkey for improvement of patient care.
Pediatr Pulmonol
; 57(5): 1245-1252, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35102722
17.
Effects of Long-Term Pamidronate Treatment on Bone Density and Fracture Rate in 65 Osteogenesis Imperfecta Patients.
Turk Arch Pediatr
; 56(5): 474-478, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35110117
18.
Effects of long-term azithromycin therapy on auditory functions in children with chronic respiratory diseases.
Int J Pediatr Otorhinolaryngol
; 147: 110808, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34186301
19.
Post-infectious bronchiolitis obliterans in children: Clinical and radiological evaluation and long-term results.
Heart Lung
; 50(5): 660-666, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34098236
20.
Balanced Double Aortic Arch Causing Persistent Respiratory Symptoms Mimicking Asthma in an Infant.
J Pediatr Intensive Care
; 10(2): 162-166, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33884220