Detalhe da pesquisa
1.
DNAJC21-related thrombocytopenia in a young adult female.
Am J Med Genet C Semin Med Genet
; 193(2): 193-197, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37186482
2.
Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and ß-thalassemia Carriers.
J Pediatr Hematol Oncol
; 42(7): e698-e701, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31688629
3.
Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome.
Pediatr Hematol Oncol
; 36(6): 390-393, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31522592
4.
Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10-year observational follow-up with the effects on hematological parameters and growth.
Pediatr Blood Cancer
; 65(2)2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28895280
5.
Maternal serum alpha-fetoprotein levels are normal in Fanconi anemia: Can it be a lack of postnatal inhibition of AFP gene resulting in the elevation?
Pediatr Blood Cancer
; 64(4)2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27805304
6.
Fanconi Anemia: A Rarely Considered Cause of Macrocytosis During Childhood.
J Pediatr Hematol Oncol
; 39(7): 570-572, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28060124
7.
Harris Platelet Syndrome in Patients of Non-Indian Origin.
J Pediatr Hematol Oncol
; 38(8): e326-e328, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27299593
8.
Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.
Blood
; 132(12): 1349-1353, 2018 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30064976
9.
Oculoectodermal syndrome: report of a new case with a broad clinical spectrum.
Am J Med Genet A
; 164A(11): 2947-51, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25251940
10.
Leukopenia in familial Mediterranean fever: case series and literature review with special emphasis on pathogenesis.
Pediatr Hematol Oncol
; 31(2): 120-8, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23560861
11.
The search for new approaches to treating type 1 plasminogen deficiency.
Pediatr Blood Cancer
; 65(4)2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29271612
12.
Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenita.
Int Ophthalmol
; 32(6): 615-22, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22814958
13.
Dyskeratosis congenita and limbal stem cell deficiency.
Exp Eye Res
; 90(3): 472-3, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20036237
14.
It is all in the bag: collodion bag versus HistoGel cell block method.
J Am Soc Cytopathol
; 9(1): 20-25, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31422016
15.
Dyskeratosis congenita with corneal limbal insufficiency.
Pediatr Blood Cancer
; 53(1): 95-7, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19199342
16.
Accuracy of herpes simplex virus detection in liquid-based (SurePath) Papanicolaou tests: a comparison with polymerase chain reaction.
Diagn Cytopathol
; 36(2): 94-103, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18181191
17.
Use of serum iron status and hemoglobin A2 levels for discrimination between iron deficiency and thalassemia minor.
Pediatr Hematol Oncol
; 30(2): 113-5, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23327659
18.
Dysplasia and disorder of cell membrane entirety in iron-deficiency anemia.
Pediatr Hematol Oncol
; 25(6): 492-501, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18728968
19.
Detection of blaOXA-48 and clonal relationship in carbapenem resistant K. pneumoniae isolates at a tertiary care center in Western Turkey.
J Infect Public Health
; 11(5): 640-642, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29709574
20.
A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene.
Acta Haematol
; 118(4): 244-7, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-18097132