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1.
Altered expression of apoptosis-related, circulating cell-free miRNAs in children with familial Mediterranean fever: a cross-sectional study.
Rheumatol Int
; 41(1): 103-111, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-32140884
2.
Twenty-Year Experience of a Single Referral Center on Pediatric Familial Mediterranean Fever: What Has Changed Over the Last Decade?
J Clin Rheumatol
; 27(1): 18-24, 2021 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31693653
3.
Unicentric Castleman Disease Mimicking an Autoinflammatory Disorder: A Diagnostic Challenge in a Pediatric Patient With Recurrent Fever.
J Pediatr Hematol Oncol
; 42(3): 204-207, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31335823
4.
Is Henoch-Schönlein purpura a susceptibility factor for functional gastrointestinal disorders in children?
Rheumatol Int
; 39(2): 317-322, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30101368
5.
Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey.
Rheumatology (Oxford)
; 59(1): 254-256, 2020 01 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31292637
6.
Utility of renal resistive index measurement in juvenile systemic lupus erythematosus: a cross-sectional single-center study.
Clin Rheumatol
; 42(10): 2849-2854, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37481634
7.
Utility of a targeted next-generation sequencing-based genetic screening panel in patients with periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome.
Arch Rheumatol
; 38(2): 299-306, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-37680524
8.
An unusual manifestation in a pediatric patient with MAFB mutation: Sacroiliitis in multicentric carpotarsal osteolysis syndrome.
Int J Rheum Dis
; 26(10): 2064-2068, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37088798
9.
Clinical presentation of children with Deficiency of Adenosine deaminase 2: A case series.
Eur J Med Genet
; 65(8): 104555, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35777620
10.
Serum vitamin B12 and D levels in children with Primary Raynaud Phenomenon: a retrospective cohort study.
Eur J Clin Nutr
; 76(11): 1615-1617, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35488070
11.
A Rare Autoinflammatory Disorder in a Pediatric Patient with Favorable Response to Etanercept: Sideroblastic Anemia with B Cell Immunodeficiency, Periodic Fevers, and Developmental Delay Syndrome.
Pediatr Allergy Immunol Pulmonol
; 35(3): 129-132, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-36121781
12.
Evaluation of subclinical ocular involvement in patients with deficiency of adenosine deaminase 2 (DADA2).
Clin Rheumatol
; 41(8): 2533-2540, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-35508675
13.
Monogenic lupus due to DNASE1L3 deficiency in a pediatric patient with urticarial rash, hypocomplementemia, pulmonary hemorrhage, and immune-complex glomerulonephritis.
Eur J Med Genet
; 64(9): 104262, 2021 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-34161863
14.
Differentiating children with familial Mediterranean fever from other recurrent fever syndromes: The utility of new Eurofever/PRINTO classification criteria.
Arch Rheumatol
; 36(4): 493-498, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35382375
15.
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey.
Mol Syndromol
; 12(2): 112-117, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-34012381
16.
Phenotypic variability in two patients with tumor necrosis factor receptor associated periodic fever syndrome emphasizes a rare manifestation: Immunoglobulin A nephropathy.
Eur J Med Genet
; 63(4): 103780, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-31586650
17.
Different Clinical Manifestations of Three Prime Repair Exonuclease 1 Mutation: A Case Series.
Ann Indian Acad Neurol
; 23(5): 699-703, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33623276
18.
Retrospective Analysis of the Factors Affecting Growth Parameters in Turkish Children With Systemic Lupus Erythematosus.
Arch Rheumatol
; 35(3): 357-365, 2020 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-33458659
19.
Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?
CEN Case Rep
; 9(4): 344-346, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32372346
20.
Pre-Pulseless Takayasu Arteritis in a Child Represented With Prolonged Fever of Unknown Origin and Successful Management With Concomitant Mycophenolate Mofetil and Infliximab.
Arch Rheumatol
; 35(2): 278-282, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32851379