Detalhe da pesquisa
1.
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease.
Nat Immunol
; 23(1): 75-85, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34937930
2.
Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease.
Nat Immunol
; 22(2): 128-139, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33398182
3.
Hematopoietic Stem Cell Transplantation From Unrelated Donors in 2 Cases of Interleukin-10 Receptor Deficiency: Is Surgery Not a Requirement?
J Pediatr Hematol Oncol
; 41(1): 64-66, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29683948
4.
SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.
Am J Hum Genet
; 90(4): 689-92, 2012 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22444670
5.
Percutaneous endoscopic gastrostomy in children: Is early feeding safe?
J Pediatr Gastroenterol Nutr
; 57(5): 659-62, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23799454
6.
Extremely rare cause of congenital diarrhea: enteric anendocrinosis.
Pediatr Int
; 55(5): 661-3, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24134759
7.
The Ineffectiveness of Tacrolimus in an Infant With a Mutation in the IL-10 Receptor.
J Clin Gastroenterol
; 50(4): 352-3, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26828243
8.
HFE-Related Hereditary Hemochromatosis Is Not Invariably a Disease of Adulthood: Importance of Early Diagnosis and Phlebotomy in Childhood.
J Pediatr Gastroenterol Nutr
; 62(4): e35-7, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25000356
9.
The frequency of vitamin B12, iron, and folic acid deficiency in the neonatal period and infancy, and the relationship with maternal levels.
Turk Pediatri Ars
; 55(2): 139-148, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32684759
10.
Hearing evaluation with ABR in pediatric patients with celiac disease.
Turk J Gastroenterol
; 31(2): 163-166, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32141826
11.
Langerhans cell histiocytosis in IPEX syndrome: possible role for natural regulatory T cells?
Pediatr Allergy Immunol
; 25(6): 601-3, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24628744
12.
Intestinal dysfunction in APECED syndrome could mimic IPEX syndrome.
J Pediatr Gastroenterol Nutr
; 56(4): e27, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23287803
13.
Chromogranin-A staining reveals enteric anendocrinosis in unexplained congenital diarrhea.
J Pediatr Gastroenterol Nutr
; 57(4): e21, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24084374
14.
Pediatric Liver Transplantation: Our Experiences.
Eurasian J Med
; 48(3): 209-212, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28149148
15.
Total oxidant status, total antioxidant capacity and ischemia modified albumin levels in children with celiac disease.
Turk J Pediatr
; 57(5): 498-503, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27411418
16.
Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype.
Inflamm Bowel Dis
; 21(1): 40-7, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25479458
17.
A rare outcome of iron deficiency and pica: Rapunzel syndrome in a 5-year-old child iron deficiency and pica.
Turk J Gastroenterol
; 25(1): 100-2, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24918141
18.
A very rare cause of acute pancreatitis: Berardinelli-Seip congenital lipodystrophy.
Turk J Gastroenterol
; 25 Suppl 1: 216-9, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25910311
19.
The role of Bifidobacterium lactis B94 plus inulin in the treatment of acute infectious diarrhea in children.
Turk J Gastroenterol
; 25(6): 628-33, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25599772
20.
Bilateral congenital cataracts in an infant with Klinefelter syndrome.
Turk J Pediatr
; 56(5): 546-50, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-26022594