| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A rare case report of hereditary hyperferritinemia cataract syndrome
|
Neofytou, Ariadni
|
|
|
10 |
1 |
p. 17-19
|
artikel
|
| 2 |
Cefiderocol for severe bloodstream infection by multidrug-resistant Klebsiella pneumoniae in a pediatric patient with acute myeloid leukemia
|
De Leonardis, Francesco
|
|
|
10 |
1 |
p. 57-58
|
artikel
|
| 3 |
Challenges faced in screening for thalassemia and other hemoglobinopathies in a North Indian population
|
Kumar, Manisha
|
|
|
10 |
1 |
p. 59-65
|
artikel
|
| 4 |
Corrigendum to “Peg-asparaginase associated toxicities in children with acute lymphoblastic leukemia: A single-center cross-sectional study” [J Pediatr Hematol Oncol 9 (1) (2024) 54–62 ISSN 2468-1245https://doi.org/10.1016/j.phoj.2024.03.001]
|
Awwad, Sameh
|
|
|
10 |
1 |
p. 41
|
artikel
|
| 5 |
Current management of pulmonary relapse in Ewing sarcoma: A report from the Pediatric Surgical Oncology Research Collaborative
|
Reiter, Audra J.
|
|
|
10 |
1 |
p. 20-23
|
artikel
|
| 6 |
Editorial Board Information
|
|
|
|
10 |
1 |
p. ii
|
artikel
|
| 7 |
Ewing sarcoma of the hands and feet: Outcome and prognostic factors of a rare subsite in a low-middle income country
|
Ganguly, Shuvadeep
|
|
|
10 |
1 |
p. 24-32
|
artikel
|
| 8 |
Global initiative for childhood cancer focused tumors in Indonesia: A single-center study
|
Indraswari, Braghmandita Widya
|
|
|
10 |
1 |
p. 1-8
|
artikel
|
| 9 |
Management outcomes of South African children diagnosed with neuroblastoma in adolescence
|
Jaques, Van Heerden
|
|
|
10 |
1 |
p. 9-16
|
artikel
|
| 10 |
Outcome and recurrence patterns of low-risk gonadal germ cell tumors in children and adolescents
|
Courtel, Tiphaine
|
|
|
10 |
1 |
p. 51-56
|
artikel
|
| 11 |
Pediatric mature B-cell non-hodgkin lymphoma in India: A retrospective multicenter pooled analysis of treatment approaches and outcomes
|
Roy Moulik, Nirmalya
|
|
|
10 |
1 |
p. 33-40
|
artikel
|
| 12 |
Prevalence of vitamin D deficiency in pediatric patients with sickle cell disease: A systematic review
|
de Souza Vilela, Thiago
|
|
|
10 |
1 |
p. 42-47
|
artikel
|
| 13 |
Thalassemia major due to compound heterozygous Codon 8/9 (+G) mutation with Dutch beta° thalassemia deletion
|
Shekhawat, Dolat Singh
|
|
|
10 |
1 |
p. 48-50
|
artikel
|
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