S. Nesci

发表

Persistence of mixed chimerism in patients transplanted for the treatment of thalassemia.

M. Andreani, G. Lucarelli, M. Ripalti, 1996, Blood.

Identification of a new HLA-B*08 allele in a family of Iraqi origin.

S. Nesci, M. Valentini, O. Buffi, 2011, Tissue antigens.

Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia

C. Carcassi, F. Locatelli, G. Caocci, 2012, Human immunology.

Elevated interleukin-8 serum concentrations in beta-thalassemia and graft-versus-host disease.

A. Facchini, M. Ceska, G. Gasbarrini, 1993, Blood.

Unrelated Bone Marrow Transplantation for β‐Thalassemia Patients: The Experience of the Italian Bone Marrow Transplant Group

A. Pession, F. Locatelli, F. Fagioli, 2005, Annals of the New York Academy of Sciences.

Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation

M. Andreani, G. Lucarelli, E. Angelucci, 2000, Bone Marrow Transplantation.

The distribution of KIR-HLA functional blocks is different from north to south of Italy.

C. Carcassi, M. Martinetti, A. Amoroso, 2014, Tissue antigens.

Characterization of the novel HLA‐C*16:97 allele in an Italian bone marrow donor

S. Nesci, O. Buffi, A. Iliescu, 2016, HLA.

A new HLA allele, HLA-B*08:122, described in an unrelated donor of Caucasian origin.

S. Nesci, A. Bontadini, O. Buffi, 2014, Tissue antigens.

Characterization of a novel HLA-A*11 allele in a cord blood unit by sequence-based typing: HLA-A*1141.

S. Nesci, A. Bontadini, S. Manfroi, 2009, Tissue antigens.

Characterization of the novel allele HLA-Cw*0331 by sequence-based typing.

S. Nesci, G. Carella, A. Malagoli, 2007, Tissue antigens.

HLA-B*4904, a new allele identified in two unrelated individuals from the same Italian region.

S. Nesci, O. Buffi, A. Iliescu, 2006, Tissue antigens.

Increased serum concentrations of tumour necrosis factor in beta thalassaemia: effect of bone marrow transplantation.

E. Lalli, A. Facchini, G. Gasbarrini, 1992, Journal of clinical pathology.

The human leucocyte antigen‐G 14‐basepair polymorphism correlates with graft‐versus‐host disease in unrelated bone marrow transplantation for thalassaemia

C. Carcassi, F. Locatelli, M. Bernardo, 2007, British journal of haematology.

Distribution of killer cell immunoglobulin-like receptors genes in the Italian Caucasian population

C. Carcassi, M. Martinetti, R. Conte, 2006, Journal of Translational Medicine.

Coexistence of two functioning T-cell repertoires in healthy ex-thalassemics bearing a persistent mixed chimerism years after bone marrow transplantation.

J. Gorski, M. Battaglia, M. Andreani, 1999, Blood.

Mixed chimerism in thalassemic patients after bone marrow transplantation.

M. Andreani, G. Lucarelli, G. Graziosi, 1992, Bone marrow transplantation.

HLA compatibility for patients with thalassemia: implications for bone marrow transplantation.

G. Lucarelli, S. Nesci, M. Valentini, 1986, International journal of cell cloning.

An attempt to obtain a specific antiserum forin vitro immunological conditioning of bone marrow in acute non-lymphoblastic leukemia

G. Lucarelli, S. Nesci, A. Porcellini, 1981, La Ricerca in clinica e in laboratorio.

New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years.

M. Andreani, G. Lucarelli, D. Baronciani, 2004, Blood.

Recipient mHag-HA1 disparity and aGVHD in thalassemic-transplanted patients

M. Andreani, G. Lucarelli, S. Nesci, 2003, Bone Marrow Transplantation.

Bone marrow transplantation from alternative donors for thalassemia: HLA-phenotypically identical relative and HLA-nonidentical sibling or parent transplants

M. Andreani, G. Lucarelli, D. Baronciani, 2000, Bone Marrow Transplantation.

Marrow transplantation for patients with thalassemia: results in class 3 patients.

M. Andreani, G. Lucarelli, D. Baronciani, 1996, Blood.

Status of donor-recipient HLA class I ligands and not the KIR genotype is predictive for the outcome of unrelated hematopoietic stem cell transplantation in beta-thalassemia patients.

C. Carcassi, F. Locatelli, G. Caocci, 2007, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Influence of the conditioning regimens on the incidence of mixed chimerism in thalassemic transplanted patients.

M. Andreani, G. Lucarelli, M. Manna, 1993, Bone marrow transplantation.

Mixed Chimerism after Bone Marrow Transplantation in Thalassemia

M. Andreani, G. Lucarelli, M. Manna, 1998, Annals of the New York Academy of Sciences.

Serum amyloid A protein concentration in bone marrow transplantation for /B thalassaemia

G. Lucarelli, A. Facchini, S. Nesci, 2004 .

Serum amyloid A protein concentration in bone marrow transplantation for beta thalassaemia.

E. Lalli, A. Facchini, G. Gasbarrini, 1992, Journal of clinical pathology.

Use of DPB1 T‐cell epitope algorithm among italian transplant centers: A survey on behalf of Associazione Italiana di Immunogenetica e Biologia dei Trapianti

P. Chiusolo, C. Lombardo, M. Testi, 2021 .

An unusual DRB1*1503 haplotype without a detectable DRB5 locus in a black African family.

M. Andreani, G. Lucarelli, M. Manna, 1997, Tissue antigens.

patients aged less than 17 years A new approach for bone marrow transplantation in class 3 thalassemic

M. Andreani, E. Angelucci, P. Sodani, 2013 .

thalassemia aged younger than 17 years New approach for bone marrow transplantation in patients with class 3

M. Andreani, G. Lucarelli, D. Baronciani, 2013 .

Identification of a novel HLA-C*08 variant allele, C*08:31. Sequence analysis from exons 1 through 8.

S. Nesci, A. Bontadini, S. Manfroi, 2011, Tissue antigens.