Detalhe da pesquisa
1.
Association of tumour necrosis factor-alpha -308 G/A polymorphism with primary open-angle glaucoma.
Clin Exp Ophthalmol
; 40(4): e156-62, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-21575121
2.
The role of human leucocyte antigens in children with hydatid disease: their association with clinical condition and prognosis.
Parasitol Res
; 106(4): 795-800, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20111876
3.
Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.
Turk J Pediatr
; 52(6): 576-81, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21428188
4.
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
J Clin Invest
; 112(3): 450-6, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12897212
5.
A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis.
Pediatr Infect Dis J
; 26(4): 366-8, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17414409
6.
A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.
Turk J Pediatr
; 48(4): 362-4, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17290574
7.
The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID).
Turk J Pediatr
; 47(3): 239-46, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16250308
8.
Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.
Am J Med Genet
; 108(4): 333-6, 2002 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11920841
9.
Trimethoprim-sulfamethoxazole induced prolonged hypoglycemia in an infant with MHC class II deficiency: diazoxide as a treatment option.
J Pediatr Endocrinol Metab
; 16(9): 1307-9, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14714756
10.
Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome.
Turk J Pediatr
; 44(4): 357-9, 2002.
Artigo
em Inglês
| MEDLINE | ID: mdl-12458817
11.
Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.
Turk J Pediatr
; 46(3): 204-7, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15503471
12.
Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.
Turk J Pediatr
; 46(3): 208-13, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15503472
13.
The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.
Turk J Pediatr
; 45(2): 95-8, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12921293
14.
The relationship between periodontal status and peripheral levels of neutrophils in two consanguineous siblings with severe congenital neutropenia: case reports.
Quintessence Int
; 34(3): 221-6, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12731605
15.
Immune function in children with classical phenylketonuria and tetrahydrobiopterin deficiencies.
Indian Pediatr
; 40(9): 822-33, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-14530542
16.
Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.
J Pediatr Hematol Oncol
; 29(5): 327-9, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17483712
17.
Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections.
J Clin Immunol
; 26(1): 1-6, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16418797
18.
Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.
J Pediatr
; 146(1): 137-40, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15644840
19.
Antibody response to a seven-valent pneumococcal conjugated vaccine in patients with ataxia-telangiectasia.
J Clin Immunol
; 24(4): 411-7, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15163897
20.
Malignant solid tumors associated with congenital immunodeficiency disorders.
Pediatr Hematol Oncol
; 21(5): 441-51, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15205088