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  1. Article

    HLA-haploidentical hematopoietic stem cells transplantation with regulatory and conventional T-cell adoptive immunotherapy in pediatric patients with very high-risk acute leukemia

    Allogeneic hematopoietic stem cell transplantation (HSCT) is still needed for many children with very high-risk acute leukemia. An HLA-haploidentical family donor is a suitable option for those without an HLA-...

    M. S. Massei, I. Capolsini, E. Mastrodicasa, K. Perruccio in Bone Marrow Transplantation (2023)

  2. No Access

    Article

    Impact of pretransplant minimal residual disease after cord blood transplantation for childhood acute lymphoblastic leukemia in remission: an Eurocord, PDWP–EBMT analysis

    To address the prognostic value of minimal residual disease (MRD) before unrelated cord blood transplantation (UCBT) in children with acute lymphoblastic leukemia (ALL), we analyzed 170 ALL children transplant...

    A Ruggeri, G Michel, J-H Dalle, M Caniglia, F Locatelli, A Campos in Leukemia (2012)

  3. Article

    Open Access

    P2.09 Increased Carotid Intima Media Thickness and Wave Reflection in Patients with Intracranial Aneurysms

    whether or not the presence of intracranial aneurysms (IAs) is associated with alterations in systemic arteries is not known.

    F. Santini, C. Morizzo, C. Martini, E. Malshi, M. Caniglia, M. Kozakova in Artery Research (2009)

  4. No Access

    Article

    Pre-transplant prognostic factors for patients with high-risk leukemia undergoing an unrelated cord blood transplantation

    From July 1995 to December 2001, 42 patients with leukemia aged 1–42 years underwent cord blood transplant (CBT) from unrelated, ⩽2 antigen HLA mismatched donors. In all, 26 patients were in ⩽2nd complete remi...

    A P Iori, R Cerretti, L De Felice, M Screnci, A Mengarelli in Bone Marrow Transplantation (2004)

  5. No Access

    Article

    Reciprocal bone marrow transplantation between brother and sister

    A child with AML underwent allogeneic BMT from an HLA-identical sister donor. Prompt and stable trilineage engraftment occurred and after few months he returned to a normal life. Eight years later a primary NH...

    I Rana, RM Pinto, M Caniglia, A Lombardi, G De Rossi in Bone Marrow Transplantation (2002)

  6. No Access

    Article

    Intravenous immune globulin in lysinuric protein intolerance

    In addition to systemic manifestations with skeletal, pulmonary, renal, and haematological signs, lysinuric protein intolerance (LPI), a membrane transport defect of cationic amino acids, is often complicated ...

    C. Dionisi-Vici, L. De Felice, M. El Hachem in Journal of Inherited Metabolic Disease (1998)

  7. Article

    TREATMENT OF ACUTE IDIOPATHIC THROMBOCYTOPENIC PURPURA (aITP) IN CHILDREN: A'RETROSPECTIVE EVALUATION OF 120 CASES 164

    C Baronci, A Petrone, C Miano, A Lombardi, M Caniglia, L A Russo in Pediatric Research (1997)

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    Article

    Early detection of IgA specific antibodies in HIV-1 infected children by peptide-ELISA and peptide time-resolved fluoro-immunoassay

    The presence of specific IgA antibodies in sera from 25 infants born to HIV-1 seropositive mothers was investigated by peptide-ELISA and peptide time-resolved fluoro-immunoassay (TR-FIA). The infants had been ...

    V. Lombardi, M. Caniglia, G. Scarlatti, M. Jansson in European Journal of Pediatrics (1993)

  9. No Access

    Article

    X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers

    While inherited X-linked (XL) isolated thrombocytopenia is a mild condition, the Wiskott-Aldrich syndrome (WAS) associates severe thrombocytopenia with an immunodeficiency component and has a poor prognosis. W...

    G. De Saint-Basile, N. Schlegel, M. Caniglia, F. Le Deist in Annals of Hematology (1991)