Detalhe da pesquisa
1.
Variation of Diagnostic Approaches and Treatment Practices for Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome Among Pediatric Subspecialists.
J Pediatr
; 255: 65-71.e6, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328191
2.
Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes.
Am J Med Genet A
; 191(7): 1826-1835, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37067177
3.
Lymphoma in Partial DiGeorge Syndrome: Report of 2 Cases.
J Pediatr Hematol Oncol
; 44(3): e819-e822, 2022 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34966099
4.
Bone marrow necrosis in pediatric malignancies: 10-Year retrospective review and review of literature.
Pediatr Blood Cancer
; 68(3): e28806, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314722
5.
Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis.
Blood Cells Mol Dis
; 85: 102462, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32623341
6.
Female adolescent with recurrent anemia and thrombocytopenia: Questions.
Pediatr Nephrol
; 37(9): 2067-2068, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35275275
7.
Female adolescent with recurrent anemia and thrombocytopenia: Answers.
Pediatr Nephrol
; 37(9): 2069-2071, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35275276
8.
Infantile Pyknocytosis: End-Tidal CO, %Micro-R Measurements, Next-Generation Sequencing, and Transfusion Avoidance with Darbepoetin.
Biomed Hub
; 5(3): 227-234, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-34055814
9.
A Novel Variant in G6PD (c.1375C>G) Identified from a Hispanic Neonate with Extreme Hyperbilirubinemia and Low G6PD Enzymatic Activity.
Neonatology
; 117(4): 532-535, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32987391
10.
Leptomeningeal Enhancement Associated With Cerebral Venous Thrombosis.
JAMA Neurol
; 79(2): 195-196, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34870692
11.
Rare association of anophthalmia, complex congenital heart disease and pulmonary hypertension: case report. / Rara asociación de anoftalmía, malformación cardíaca compleja e hipertensión pulmonar: reporte de caso.
Medwave
; 16(9): e6568, 2016 Oct 07.
Artigo
em Espanhol, Inglês
| MEDLINE | ID: mdl-27813502