Detalhe da pesquisa
1.
Characteristics and treatment of acute myeloid neoplasms with cutaneous involvement in infants up to 6 months of age: A retrospective study.
Pediatr Blood Cancer
; : e31006, 2024 Apr 14.
Artigo
Inglês
| MEDLINE | ID: mdl-38616361
2.
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
Am J Hematol
; 97(1): 18-29, 2022 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34677878
3.
Multiple neonicotinoids in children's cerebro-spinal fluid, plasma, and urine.
Environ Health
; 21(1): 10, 2022 01 11.
Artigo
Inglês
| MEDLINE | ID: mdl-35016674
4.
Genetic and functional insights into CDA-I prevalence and pathogenesis.
J Med Genet
; 58(3): 185-195, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-32518175
5.
PASTEC - a prospective, single-center, randomized, cross-over trial of pure physical versus physical plus attentional training in children with cancer.
Pediatr Hematol Oncol
; 39(4): 329-342, 2022 May.
Artigo
Inglês
| MEDLINE | ID: mdl-34752205
6.
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene.
Clin Genet
; 99(6): 780-788, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33586135
7.
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
Haematologica
; 106(11): 2960-2970, 2021 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33121234
8.
Spontaneous Partial Remission in a Child With B-Lineage Acute Lymphoblastic Leukemia and Chickenpox: A Role For Acyclovir?
J Pediatr Hematol Oncol
; 43(5): e711-e714, 2021 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33625075
9.
The landscape of pediatric Diamond-Blackfan anemia in Switzerland: genotype and phenotype characteristics.
Eur J Pediatr
; 180(12): 3581-3585, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-34110484
10.
Parental occupational exposure to pesticides and risk of childhood cancer in Switzerland: a census-based cohort study.
BMC Cancer
; 20(1): 819, 2020 Aug 28.
Artigo
Inglês
| MEDLINE | ID: mdl-32859175
11.
Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations.
Am J Hematol
; 95(1): 78-96, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31456233
12.
Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group.
Eur J Pediatr
; 179(4): 527-545, 2020 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-32020331
13.
[Iron deficiency with and without anemia in children: a brief update for caregivers]. / Carence en fer avec et sans anémie chez l'enfant : brève mise à jourpour le praticien.
Rev Med Suisse
; 15(638): 376-381, 2019 Feb 13.
Artigo
Francês
| MEDLINE | ID: mdl-30762998
14.
[Recent advances and future directions in CAR-T cell therapy in pediatric oncology]. / Progrès récents et orientations futures de la thérapie avec cellules CAR-T en oncologie pédiatrique.
Rev Med Suisse
; 15(N° 632-633): 85-91, 2019 Jan 09.
Artigo
Francês
| MEDLINE | ID: mdl-30629377
15.
A key role for Rac and Pak signaling in neutrophil extracellular traps (NETs) formation defines a new potential therapeutic target.
Am J Hematol
; 93(2): 269-276, 2018 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29124783
16.
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level.
Br J Haematol
; 198(1): e10-e14, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35417566
17.
Blood cells molecules and diseases in 2022: A fountain of youth.
Blood Cells Mol Dis
; 95: 102665, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35462122
18.
Opportunities and challenges in the immunological therapy of pediatric malignancy: a concise snapshot.
Eur J Pediatr
; 176(9): 1163-1172, 2017 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-28803259
19.
Aldehyde dehydrogenase activity plays a Key role in the aggressive phenotype of neuroblastoma.
BMC Cancer
; 16(1): 781, 2016 10 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27724856
20.
Cancer surveillance in children with Ollier Disease and Maffucci Syndrome.
Am J Med Genet A
; 185(4): 1338-1340, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33433055