about
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblastsGenetic deletion of the GATA1-regulated protein α-synuclein reduces oxidative stress and nitric oxide synthase levels in mature erythrocytesFulminant thrombotic microangiopathy in pediatrics: where diagnostic and therapeutic dilemmas meet.Generation of bivalent chromatin domains during cell fate decisionsStem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting.Aldehyde dehydrogenase activity plays a Key role in the aggressive phenotype of neuroblastoma.Flow cytometric assay for direct quantification of neutrophil extracellular traps in blood samples.miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F InductionChildhood extraordinary daytime urinary frequency-a case series and a systematic literature review.Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype.Progress in the congenital dyserythropoietic anemias: juicy but high-hanging fruits?Can smaller-scale comprehensive cancer centers provide outstanding care in abdominal and thoracic pediatric solid tumor surgery? Results of a 14-year retrospective single-center analysis.Opportunities and challenges in the immunological therapy of pediatric malignancy: a concise snapshot.Clinically-oriented proteomic investigation of sickle cell disease: Opportunities and challenges.Mathematical modeling of erythrocyte chimerism informs genetic intervention strategies for sickle cell disease.Isolated extraordinary daytime urinary frequency of childhood: a case series of 26 children in Switzerland.Frequency of congenital dyserythropoietic anemias in Europe.Breast-conserving surgery has equivalent effect as mastectomy on stage I breast cancer prognosis only when followed by radiotherapy.Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity.Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: clinical and radiographic delineation of a pleiotropic disorder.Decision-making in pediatrics: a practical algorithm to evaluate complementary and alternative medicine for children.Management of women with ductal carcinoma in situ of the breast: a population-based study.Burkholderia pseudomallei infection in chronic granulomatous diseaseHuman leucocyte antigen-identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft-versus-host disease and pre-existing viralExpression of the Neuroblastoma-Associated ALK-F1174L Activating Mutation During Embryogenesis Impairs the Differentiation of Neural Crest Progenitors in Sympathetic Ganglia[My child bleeds easily: clinical and paraclinical approach]A new case of spondyloenchondrodysplasia with immune dysregulation confirms the pleiotropic nature of the disorder: comment on "A syndrome of immunodeficiency, autoimmunity, and spondylometaphyseal dysplasia" by M.L. Kulkarni, K. Baskar, and P.M. Ku[Undifferentiated sarcoma of the liver: a rare tumor of childhood]Increased risk of acute myeloid leukaemia after treatment for breast cancerAge-dependent pathophysiology of acute chest syndrome in children with sickle cell diseaseRisk of cancer in patients with polycystic kidney diseaseDiagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group[Recent advances and future directions in CAR-T cell therapy in pediatric oncology][Iron deficiency with and without anemia in children: a brief update for caregivers]Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Raffaele Renella
@ast
Raffaele Renella
@en
Raffaele Renella
@es
Raffaele Renella
@nl
Raffaele Renella
@sl
type
label
Raffaele Renella
@ast
Raffaele Renella
@en
Raffaele Renella
@es
Raffaele Renella
@nl
Raffaele Renella
@sl
prefLabel
Raffaele Renella
@ast
Raffaele Renella
@en
Raffaele Renella
@es
Raffaele Renella
@nl
Raffaele Renella
@sl
P106
P21
P31
P496
0000-0002-5041-2308