Maddalena Marinoni
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View article: Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient
Glucose-6-phosphate dehydrogenase deficiency induced hemolytic anemia and methemoglobinemia: a case report in a 7 -year-old female patient Open
View article: 311 | OUTCOMES OF PATIENTS WITH PRIMARY REFRACTORY AND EARLY RELAPSING LARGE B CELL LYMPHOMA ARE INFERIOR IN THE CD19 CAR T CELL THERAPY ERA
311 | OUTCOMES OF PATIENTS WITH PRIMARY REFRACTORY AND EARLY RELAPSING LARGE B CELL LYMPHOMA ARE INFERIOR IN THE CD19 CAR T CELL THERAPY ERA Open
View article: 309 | IMPACT OF AGE ON TREATMENT DECISIONS AND OUTCOMES IN RELAPSED/REFRACTORY LARGE B‐CELL LYMPHOMA
309 | IMPACT OF AGE ON TREATMENT DECISIONS AND OUTCOMES IN RELAPSED/REFRACTORY LARGE B‐CELL LYMPHOMA Open
View article: 328 | INTENTION‐TO‐TREATMENT ANALYSIS OF THIRD LINE CAR‐T FOR RELAPSE/REFRACTORY LARGE B CELL LYMPHOMA
328 | INTENTION‐TO‐TREATMENT ANALYSIS OF THIRD LINE CAR‐T FOR RELAPSE/REFRACTORY LARGE B CELL LYMPHOMA Open
View article: 454 | ASSOCIATION OF BRIDGING THERAPY WITH RESPONSE AND OUTCOMES IN PATIENTS WITH RELAPSED/REFRACTORY LARGE B CELL LYMPHOMA RECEIVING THIRD LINE CAR‐T
454 | ASSOCIATION OF BRIDGING THERAPY WITH RESPONSE AND OUTCOMES IN PATIENTS WITH RELAPSED/REFRACTORY LARGE B CELL LYMPHOMA RECEIVING THIRD LINE CAR‐T Open
View article: 735 | OUTCOMES IN DOUBLE‐EXPOSED CLASSICAL HODGKIN LYMPHOMA: IMPACT OF TREATMENT SEQUENCE AND SALVAGE STRATEGIES AFTER BRENTUXIMAB VEDOTIN AND CHECKPOINT INHIBITOR FAILURE
735 | OUTCOMES IN DOUBLE‐EXPOSED CLASSICAL HODGKIN LYMPHOMA: IMPACT OF TREATMENT SEQUENCE AND SALVAGE STRATEGIES AFTER BRENTUXIMAB VEDOTIN AND CHECKPOINT INHIBITOR FAILURE Open
View article: Pediatric Langerhans Cell Histiocytosis: Unifocal Localization in the Frontal Bone Presenting With Periorbital Swelling
Pediatric Langerhans Cell Histiocytosis: Unifocal Localization in the Frontal Bone Presenting With Periorbital Swelling Open
Background: Langerhans cell histiocytosis is a rare disease, the pathogenesis of which remains a subject of debate, with considerations of either a neoplastic origin or an inflammatory nature. It arises from the uncontrolled proliferation …
View article: Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era
Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era Open
View article: “CHildren with Inherited Platelet disorders Surveillance” (CHIPS) retrospective and prospective observational cohort study by Italian Association of Pediatric Hematology and Oncology (AIEOP)
“CHildren with Inherited Platelet disorders Surveillance” (CHIPS) retrospective and prospective observational cohort study by Italian Association of Pediatric Hematology and Oncology (AIEOP) Open
Background Inherited thrombocytopenias (ITs) are rare congenital bleeding disorders characterized by different clinical expression and variable prognosis. ITs are poorly known by clinicians and often misdiagnosed with most common forms of …
View article: Gliadin-reactive vitamin D-sensitive proinflammatory ILCPs are enriched in celiac patients
Gliadin-reactive vitamin D-sensitive proinflammatory ILCPs are enriched in celiac patients Open
View article: Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency Open
Common variable immunodeficiency (CVID) is the most frequent primary antibody deficiency whereby follicular helper T (Tfh) cells fail to establish productive responses with B cells in germinal centers. Here, we analyzed the frequency, phen…
View article: GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme
GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme Open
Not abstract available
View article: Association of Immune Thrombocytopenia and Coeliac Disease in Children (Retrospective Case Control Study)
Association of Immune Thrombocytopenia and Coeliac Disease in Children (Retrospective Case Control Study) Open
We think that screening for CD should be considered in children with ITP regardless of the presence of gastrointestinal symptoms. Furthermore, some patients may recover from ITP after starting a gluten-free diet.
View article: Association of Immune Thrombocytopenia and Inflammatory Bowel Disease in Children
Association of Immune Thrombocytopenia and Inflammatory Bowel Disease in Children Open
Background: The association between inflammatory bowel disease (IBD) and immune thrombocytopenia (ITP) is still uncertain. In this multicenter retrospective study, the coexistence of both diseases was investigated in children diagnosed fro…
View article: The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)
The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019) Open
Primary immunodeficiencies (PIDs) are heterogeneous disorders, characterized by variable clinical and immunological features. National PID registries offer useful insights on the epidemiology, diagnosis, and natural history of these disord…
View article: Children with cancer in the time of COVID‐19: An 8‐week report from the six pediatric onco‐hematology centers in Lombardia, Italy
Children with cancer in the time of COVID‐19: An 8‐week report from the six pediatric onco‐hematology centers in Lombardia, Italy Open
The authors declare that there is no conflict of interest.
View article: Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality Open
View article: Testing the Cow’s Milk-Related Symptom Score (CoMiSSTM) for the Response to a Cow’s Milk-Free Diet in Infants: A Prospective Study
Testing the Cow’s Milk-Related Symptom Score (CoMiSSTM) for the Response to a Cow’s Milk-Free Diet in Infants: A Prospective Study Open
The diagnosis of cow’s milk allergy (CMA) is particularly challenging in infants, especially with non-Immunoglobulin E (IgE)-mediated manifestations, and inaccurate diagnosis may lead to unnecessary dietary restrictions. The aim of this st…