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Home administration of bortezomib in multiple myeloma is cost-effective and is preferred by patients compared with hospital administration: results of a prospective single-center study

Annals of oncology, 2016-02, Vol.27 (2), p.314-318

2016

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Childhood acute lymphoblastic leukaemia and indicators of early immune stimulation: the Estelle study (SFCE)

British journal of cancer, 2015-03, Vol.112 (6), p.1017-1026

2015

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Upfront allogeneic stem-cell transplantation for patients with nonlocalized untreated peripheral T-cell lymphoma: an intention-to-treat analysis from a single center

Annals of oncology, 2015-02, Vol.26 (2), p.386-392

2015

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Impact of lenalidomide on immune functions in the setting of maintenance therapy for multiple myeloma

Leukemia, 2015-10, Vol.29 (10), p.2098-2100

2015

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Safety and efficacy of rituximab in steroid-refractory chronic GVHD

Bone marrow transplantation (Basingstoke), 2013-05, Vol.48 (5), p.734-736

2013

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Rituximab maintenance after autologous stem cell transplantation prolongs response duration in non-naive rituximab follicular lymphoma patients: a single institution experience

Annals of hematology, 2016-08, Vol.95 (8), p.1287-1293

2016

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Escalated lymphodepletion followed by donor lymphocyte infusion can induce a graft-versus-host response without overwhelming toxicity

Bone marrow transplantation (Basingstoke), 2012-08, Vol.47 (8), p.1112-1117

2012

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Features of EBV reactivation after reduced intensity conditioning unrelated umbilical cord blood transplantation

Bone marrow transplantation (Basingstoke), 2012-02, Vol.47 (2), p.251-257

2012

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Failure of bortezomib to cure acute antibody‐mediated rejection in a non‐compliant renal transplant patient

Pediatric transplantation, 2013-09, Vol.17 (6), p.E131-E136

2013

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Assessment of physiological demand in kitesurfing

European journal of applied physiology, 2009, Vol.105 (1), p.103-109

2009

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Mature B-cell lymphoblastic leukemia with MLL rearrangement: an uncommon and distinct subset of childhood acute leukemia

Leukemia, 2008-05, Vol.22 (5), p.1056-1059

2008

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Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness

Neurobiology of disease, 2002-07, Vol.10 (2), p.157-164

2002

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Prophylaxis with mycophenolate mofetil and CsA can decrease the incidence of severe acute GVHD after antithymocyte globulin-based reduced-intensity preparative regimen and allo-SCT from HLA-matched unrelated donors

Bone marrow transplantation (Basingstoke), 2010-04, Vol.45 (4), p.786-788

2010

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C/EBPbeta is over-expressed in gastric carcinogenesis and is associated with COX-2 expression

The Journal of pathology, 2006-12, Vol.210 (4), p.398-404

2006

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The place of neuropathy in the early diagnosis of Cockayne syndrome: Report on two siblings

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2017-04, Vol.24 (4), p.353-359

2017

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Factors predicting allogeneic PBSCs yield after G-CSF treatment in healthy donors

Bone marrow transplantation (Basingstoke), 2009-11, Vol.44 (9), p.613-615

2009

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GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

American journal of human genetics, 2005-12, Vol.77 (6), p.945-957

2005

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Influence of exogenic factors on age-related hearing impairment

HNO, 2009-10, Vol.57 (10), p.1023

2009

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Microsatellite and chromosome instability in squamous cell laryngeal carcinoma

International journal of oncology, 2001-08, Vol.19 (2), p.401

2001

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Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

American journal of human genetics, 2004-04, Vol.74 (4), p.770-776

2004

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Is ASCT with TBI superior to ASCT without TBI in mantle cell lymphoma patients?

Transplantation, 2012-08, Vol.94 (3), p.295-301

2012

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Analysis of candidate genes for genotypic diagnosis in the long QT syndrome

Journal of applied genetics, 2004, Vol.45 (3), p.375-381

2004

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Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment

International journal of molecular medicine, 2001-08, Vol.8 (2), p.189

2001

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Debrisoquine hydroxylase gene polymorphism in neurofibromatosis type 1

Anticancer research, 1997-11, Vol.17 (6D), p.4515

1997

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Classical and molecular cytogenetic methods in diagnosis of a rare translocation t(3;21)

International journal of molecular medicine, 1998-03, Vol.1 (3), p.569

1998

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Home administration of bortezomib in multiple myeloma is cost-effective and is preferred by patients compared with hospital administration: results of a prospective single-center study

Childhood acute lymphoblastic leukaemia and indicators of early immune stimulation: the Estelle study (SFCE)

Upfront allogeneic stem-cell transplantation for patients with nonlocalized untreated peripheral T-cell lymphoma: an intention-to-treat analysis from a single center

Impact of lenalidomide on immune functions in the setting of maintenance therapy for multiple myeloma

Safety and efficacy of rituximab in steroid-refractory chronic GVHD

Rituximab maintenance after autologous stem cell transplantation prolongs response duration in non-naive rituximab follicular lymphoma patients: a single institution experience

Escalated lymphodepletion followed by donor lymphocyte infusion can induce a graft-versus-host response without overwhelming toxicity

Features of EBV reactivation after reduced intensity conditioning unrelated umbilical cord blood transplantation

Failure of bortezomib to cure acute antibody‐mediated rejection in a non‐compliant renal transplant patient

Assessment of physiological demand in kitesurfing

Mature B-cell lymphoblastic leukemia with MLL rearrangement: an uncommon and distinct subset of childhood acute leukemia

Substitutions in the Conserved C2C Domain of Otoferlin Cause DFNB9, a Form of Nonsyndromic Autosomal Recessive Deafness

Prophylaxis with mycophenolate mofetil and CsA can decrease the incidence of severe acute GVHD after antithymocyte globulin-based reduced-intensity preparative regimen and allo-SCT from HLA-matched unrelated donors

C/EBPbeta is over-expressed in gastric carcinogenesis and is associated with COX-2 expression

The place of neuropathy in the early diagnosis of Cockayne syndrome: Report on two siblings

Factors predicting allogeneic PBSCs yield after G-CSF treatment in healthy donors

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Influence of exogenic factors on age-related hearing impairment

Microsatellite and chromosome instability in squamous cell laryngeal carcinoma

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Is ASCT with TBI superior to ASCT without TBI in mantle cell lymphoma patients?

Analysis of candidate genes for genotypic diagnosis in the long QT syndrome

Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment

Debrisoquine hydroxylase gene polymorphism in neurofibromatosis type 1

Classical and molecular cytogenetic methods in diagnosis of a rare translocation t(3;21)

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