Detalhe da pesquisa
1.
Are the current feeding volumes adequate for the growth of very preterm neonates?
Br J Nutr
; 130(8): 1338-1342, 2023 10 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36756759
2.
Gaucher Disease Type 2 Manifested as Hemophagocytic Lymphohistiocytosis in a Neonate in the COVID-19 Era.
J Pediatr Hematol Oncol
; 45(4): e506-e509, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36162002
3.
Cyanosis Due to Methemoglobinemia as the Presenting Sign of Glucose-6-Phosphate Dehydrogenase Deficiency in a Child: Diagnostic and Clinical Implications.
J Pediatr Hematol Oncol
; 43(8): e1140-e1144, 2021 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33031164
4.
Severe aplastic anaemia in children: Impact of histopathology profile and treatment on very long-term outcomes.
Acta Paediatr
; 110(4): 1308-1314, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32810910
5.
A Novel εγδß-Thalassemia Deletion Associated with Severe Anemia at Birth and a ß-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.
Hemoglobin
; 45(6): 351-354, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31829079
6.
Hematological manifestations of SARS-CoV-2 in children.
Pediatr Blood Cancer
; 67(12): e28745, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33009893
7.
National registry of hemoglobinopathies in Greece: updated demographics, current trends in affected births, and causes of mortality.
Ann Hematol
; 98(1): 55-66, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30196444
8.
Bone Marrow Failure in Fanconi Anemia: Clinical and Genetic Spectrum in a Cohort of 20 Pediatric Patients.
J Pediatr Hematol Oncol
; 41(8): 612-617, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31259830
9.
Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications.
Hemoglobin
; 42(5-6): 336-338, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30626242
10.
The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data.
Pediatr Blood Cancer
; 64(11)2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28509441
11.
Repetitive reddish discoloration of urine in a female adolescent following short-distance walking on a smooth road: Questions.
Pediatr Nephrol
; 32(12): 2253-2254, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28194571
12.
2017 Clinical trials update in new treatments of ß-thalassemia.
Am J Hematol
; 91(11): 1135-1145, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27502996
13.
A rare case report of simultaneous presentation of myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome in a child diagnosed with Kearns-Sayre syndrome.
Eur J Pediatr
; 172(4): 557-61, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22875312
14.
Hemorrhage of Upper Digestive and Respiratory Tracts in a Child with Glanzmann Thrombasthenia.
Maedica (Bucur)
; 18(2): 363-367, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37588843
15.
Unraveling the Immune Microenvironment in Classic Hodgkin Lymphoma: Prognostic and Therapeutic Implications.
Biology (Basel)
; 12(6)2023 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37372147
16.
Identification and Functional Analysis of Known and New Mutations in the Transcription Factor KLF1 Linked with ß-Thalassemia-like Phenotypes.
Biology (Basel)
; 12(4)2023 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37106711
17.
Unusual Manifestations of Kawasaki Disease in the COVID Era: A Case Series and Review of the Literature.
Cureus
; 15(12): e51104, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38274908
18.
The Diverse Genomic Landscape of Diamond-Blackfan Anemia: Two Novel Variants and a Mini-Review.
Children (Basel)
; 10(11)2023 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38002903
19.
Serum PCSK9 levels in infants with deviant birth weight: a biomarker of the lipoprotein metabolism.
J Matern Fetal Neonatal Med
; 36(1): 2188108, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36906794
20.
Gaucher disease and ß-thalassemia: A rare coinheritance.
Blood Cells Mol Dis
; 65: 35-37, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28458077