Detalhe da pesquisa
1.
Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes.
J Med Genet
; 60(8): 819-826, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36543534
2.
Increased risk for kidney sequelae surrogates in survivors of Wilms tumor.
Pediatr Nephrol
; 37(10): 2415-2426, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35118543
3.
Endoscopic septum division of tubular esophageal duplication in two children and systematic review.
Pediatr Surg Int
; 38(11): 1525-1531, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36048241
4.
Transient minimal hydronephrosis on contralateral kidney in infants with unilateral hydronephrosis: Is it an early sign of worsening of the affected kidney?
Turk J Med Sci
; 51(4): 2029-2035, 2021 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33896147
5.
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
Clin Genet
; 98(4): 390-395, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32666543
6.
Comparison of the efficacy of physical examination and radiological imaging in detecting sacroiliitis in patients with juvenile spondyloarthropathies.
Clin Exp Rheumatol
; 38(5): 1021-1028, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32167879
7.
Sinusoidal Obstruction Syndrome During Chemotherapy of Pediatric Cancers and its Successful Management With Defibrotide.
J Pediatr Hematol Oncol
; 39(7): e373-e376, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28859028
8.
Primary pericardial synovial sarcoma in an adolescent patient: magnetic resonance and diffusion-weighted imaging features.
J Pediatr Hematol Oncol
; 37(4): e230-3, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25647483
9.
Children With Type 1 Spinal Muscular Atrophy Are at Increased Risk for Nephrolithiasis.
Pediatr Neurol
; 150: 32-36, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37951159
10.
Magnetic resonance imaging based kidney volume assessment for risk stratification in pediatric autosomal dominant polycystic kidney disease.
Front Pediatr
; 12: 1357365, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38464892
11.
Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas.
Turk Arch Pediatr
; 58(4): 376-381, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37317574
12.
Comparison of color doppler US and CT portography in evaluating portal hypertension in children.
South Med J
; 105(1): 6-10, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22189660
13.
Focusing on Asthma and Chronic Obstructive Pulmonary Disease with COVID-19.
J Infect Dev Ctries
; 15(10): 1415-1425, 2021 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34780364
14.
Treatment of pediatric Burkitt lymphoma in Turkey.
J Pediatr Hematol Oncol
; 32(7): e279-84, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20736844
15.
Abdominal manifestations of polyarteritis nodosa demonstrated with CT.
Pediatr Radiol
; 40(5): 766-9, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20151119
16.
Urinary Ultrasound and Other Imaging for Ureteropelvic Junction Type Hydronephrosis (UPJHN).
Front Pediatr
; 8: 546, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33042907
17.
A novel combined treatment for plasminogen deficiency with lung involvement.
Pediatr Pulmonol
; 55(1): E1-E3, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31682330
18.
Bilateral Synchronous Testicular Germ Cell Tumors in Children: Case Report and Review of the Literature.
Urology
; 140: 155-158, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32199873
19.
Adrenal masses in children: Imaging, surgical treatment and outcome.
Asian J Surg
; 43(1): 207-212, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30962018
20.
Shwachman-Diamond syndrome with development of bone formation defects during prenatal life.
J Pediatr Gastroenterol Nutr
; 58(4): e38-40, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23254443