Lista de obras - Elie Haddad - Dominio Público Uruguay

A child who was feverish for 2 years

artículo científico publicado en 1996

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

artículo científico publicado en 2013

Anaphylactic shock caused by immunoglobulin E sensitization after retreatment with the chimeric anti-interleukin-2 receptor monoclonal antibody basiliximab

artículo científico publicado en 2003

Brief report: correction of X-linked hyper-IgM syndrome by allogeneic bone marrow transplantation

scientific article published on 01 August 1995

CD133 expression is associated with poor outcome in neuroblastoma via chemoresistance mediated by the AKT pathway

artículo científico publicado en 2012

Chronic Active Gastritis in X-linked Lymphoproliferative Disease

scientific article published on 01 February 2008

Cord blood-derived and peripheral blood-derived cytokine-induced killer cells are sensitive to Fas-mediated apoptosis

artículo científico publicado en 2013

Cord-blood-derived mesenchymal stromal cells downmodulate CD4+ T-cell activation by inducing IL-10-producing Th1 cells

artículo científico publicado en 2013

Detection of donor‐derived Langerhans cells in MHC class II immunodeficient patients after allogeneic bone marrow transplantation ⬇️

artículo científico publicado el 1 de agosto de 1997

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: A retrospective survey of 31 patients

artículo científico publicado en 1999

Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohort

artículo científico publicado en 2010

Efficacy of cyclosporine A in the treatment of macrophage activation syndrome in juvenile arthritis: report of five cases

artículo científico publicado en 1996

Efficient BST2 antagonism by Vpu is critical for early HIV-1 dissemination in humanized mice

artículo científico publicado en 2013

Encrusted cystitis and pyelitis in children: an unusual condition with potentially severe consequences.

artículo científico publicado en 2004

Evolution and treatment of childhood chronic inflammatory polyneuropathy

scientific article published on 01 February 2007

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

article

Genetic and epigenetic modification of human primary NK cells for enhanced antitumor activity

scientific article published on 01 October 2020

Genotype analysis of tumor-initiating cells expressing CD133 in neuroblastoma

artículo científico publicado en 2012

Hepatic GVHD after HLA-haploidentical bone marrow transplantation in children with severe combined immunodeficiency: the effect of ursodeoxycholic acid

artículo científico publicado en 1997

How i treat primary haemophagocytic lymphohistiocytosis.

artículo científico publicado en 2018

Human interferon-alpha increases the cytotoxic effect of CD56(+) cord blood-derived cytokine-induced killer cells on human B-acute lymphoblastic leukemia cell lines

artículo científico publicado en 2012

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

artículo científico publicado en 2002

ICON: the early diagnosis of congenital immunodeficiencies

artículo científico

Impact of storage temperature and processing delays on cord blood quality: discrepancy between functional in vitro and in vivo assays

scientific article published on 15 April 2012

Implication of different effector mechanisms by cord blood-derived and peripheral blood-derived cytokine-induced killer cells to kill precursor B acute lymphoblastic leukemia cell lines

artículo científico publicado en 2014

Improved quality of life with home therapy with subcutaneous immunoglobulins for patients with secondary hypogammaglobulinaemia

artículo científico publicado en 2012

Inflammatory bowel disease and T cell lymphopenia in G6PC3 deficiency

artículo científico publicado en 2012

Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell–depleted bone marrow transplantationA retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society

artículo científico publicado en 1999

Invasive pulmonary infection due to Scedosporium apiospermum in two children with chronic granulomatous disease

artículo científico publicado en 1998

Limited sampling strategies for estimating intravenous and oral cyclosporine area under the curve in pediatric hematopoietic stem cell transplantation

artículo científico publicado en 2015

Molecular detection of t(8;21)/AML1-ETO in AML M1/M2: correlation with cytogenetics, morphology and immunophenotype

artículo científico publicado en 1996

Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort

artículo científico publicado en 2014

Noncoding regions are the main source of targetable tumor-specific antigens

scientific article published on 01 December 2018

Patient with X-linked phenotype of SCID, markedly skewed maternal X-inactivation, but normal common gamma chain (CD132) gene ORF sequence

artículo científico publicado en 2012

Pharmacoeconomic advantages of subcutaneous versus intravenous immunoglobulin treatment in a Canadian pediatric center

artículo científico publicado en 2012

Predictors of early inactive disease in a juvenile idiopathic arthritis cohort: results of a Canadian multicenter, prospective inception cohort study

artículo científico publicado en 2009

Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study

artículo científico publicado en 2013

Relationship between CD8+ T-cell phenotype and function, Epstein-Barr virus load, and clinical outcome in pediatric renal transplant recipients: a prospective study

artículo científico publicado en 2004

Renal granuloma and immunoglobulin M-complex glomerulonephritis: a case of common variable immunodeficiency?

artículo científico publicado en 2008

Role of Natural Killer Cells in Intravenous Immunoglobulin-Induced Graft-versus-Host Disease Inhibition in NOD/LtSz-scidIL2rg(-/-) (NSG) Mice.

artículo científico publicado en 2015

SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery

scientific article published on 28 August 2018

SCIg vs. IVIg: let’s give patients the choice!.

artículo científico publicado en 2014

Severe combined immunodeficiency (SCID) in Canadian children: a national surveillance study

artículo científico publicado en 2013

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

artículo científico publicado en 2003

Subcutaneous Immunoglobulin Replacement Therapy with Hizentra® is Safe and Effective in Children Less Than 5 Years of Age.

artículo científico publicado en 2015

Sudden blindness caused by anterior ischemic optic neuropathy in 5 children on continuous peritoneal dialysis

artículo científico publicado en 2003

Survey on retransplantation criteria for patients with severe combined immunodeficiency.

artículo científico

Targeted gene addition to human mesenchymal stromal cells as a cell-based plasma-soluble protein delivery platform.

artículo científico publicado en 2010

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

artículo científico publicado en 2024

The majority of myeloid‐antigen‐positive (My+) childhood B‐cell precursor acute lymphoblastic leukaemias express TEL‐AML1 fusion transcripts ⬇️

artículo científico publicado el 1 de octubre de 1997

Therapeutic efficacy of cord blood-derived mesenchymal stromal cells for the prevention of acute graft-versus-host disease in a xenogenic mouse model

scientific article published on 21 October 2011

Transplantation outcomes for severe combined immunodeficiency, 2000-2009.

artículo científico publicado en 2014

Treatment costs associated with hospital-based intravenous immunoglobulin therapy compared to home-based subcutaneous immunoglobulin therapy in a cohort of paediatric patients with primary immunodeficiency

artículo científico publicado en 2011

Varicella-zoster virus disease is more frequent after cord blood than after bone marrow transplantation

artículo científico publicado en 2008

Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans

artículo científico publicado en 2013

[Multiple talents of the chemokine receptor-CXCR4]

artículo científico publicado en 2007

Lista de obras de Elie Haddad

A child who was feverish for 2 years

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

Anaphylactic shock caused by immunoglobulin E sensitization after retreatment with the chimeric anti-interleukin-2 receptor monoclonal antibody basiliximab

Brief report: correction of X-linked hyper-IgM syndrome by allogeneic bone marrow transplantation

CD133 expression is associated with poor outcome in neuroblastoma via chemoresistance mediated by the AKT pathway

Chronic Active Gastritis in X-linked Lymphoproliferative Disease

Cord blood-derived and peripheral blood-derived cytokine-induced killer cells are sensitive to Fas-mediated apoptosis

Cord-blood-derived mesenchymal stromal cells downmodulate CD4+ T-cell activation by inducing IL-10-producing Th1 cells

Detection of donor‐derived Langerhans cells in MHC class II immunodeficient patients after allogeneic bone marrow transplantation ⬇️

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: A retrospective survey of 31 patients

Early outcomes and improvement of patients with juvenile idiopathic arthritis enrolled in a Canadian multicenter inception cohort

Efficacy of cyclosporine A in the treatment of macrophage activation syndrome in juvenile arthritis: report of five cases

Efficient BST2 antagonism by Vpu is critical for early HIV-1 dissemination in humanized mice

Encrusted cystitis and pyelitis in children: an unusual condition with potentially severe consequences.

Evolution and treatment of childhood chronic inflammatory polyneuropathy

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

Genetic and epigenetic modification of human primary NK cells for enhanced antitumor activity

Genotype analysis of tumor-initiating cells expressing CD133 in neuroblastoma

Hepatic GVHD after HLA-haploidentical bone marrow transplantation in children with severe combined immunodeficiency: the effect of ursodeoxycholic acid

How i treat primary haemophagocytic lymphohistiocytosis.

Human interferon-alpha increases the cytotoxic effect of CD56(+) cord blood-derived cytokine-induced killer cells on human B-acute lymphoblastic leukemia cell lines

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

ICON: the early diagnosis of congenital immunodeficiencies

Impact of storage temperature and processing delays on cord blood quality: discrepancy between functional in vitro and in vivo assays

Implication of different effector mechanisms by cord blood-derived and peripheral blood-derived cytokine-induced killer cells to kill precursor B acute lymphoblastic leukemia cell lines

Improved quality of life with home therapy with subcutaneous immunoglobulins for patients with secondary hypogammaglobulinaemia

Inflammatory bowel disease and T cell lymphopenia in G6PC3 deficiency

Influence of severe combined immunodeficiency phenotype on the outcome of HLA non-identical, T-cell–depleted bone marrow transplantationA retrospective European survey from the European Group for Bone Marrow Transplantation and the European Society

Invasive pulmonary infection due to Scedosporium apiospermum in two children with chronic granulomatous disease

Limited sampling strategies for estimating intravenous and oral cyclosporine area under the curve in pediatric hematopoietic stem cell transplantation

Molecular detection of t(8;21)/AML1-ETO in AML M1/M2: correlation with cytogenetics, morphology and immunophenotype

Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort

Noncoding regions are the main source of targetable tumor-specific antigens

Patient with X-linked phenotype of SCID, markedly skewed maternal X-inactivation, but normal common gamma chain (CD132) gene ORF sequence

Pharmacoeconomic advantages of subcutaneous versus intravenous immunoglobulin treatment in a Canadian pediatric center

Predictors of early inactive disease in a juvenile idiopathic arthritis cohort: results of a Canadian multicenter, prospective inception cohort study

Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study

Relationship between CD8+ T-cell phenotype and function, Epstein-Barr virus load, and clinical outcome in pediatric renal transplant recipients: a prospective study

Renal granuloma and immunoglobulin M-complex glomerulonephritis: a case of common variable immunodeficiency?

Role of Natural Killer Cells in Intravenous Immunoglobulin-Induced Graft-versus-Host Disease Inhibition in NOD/LtSz-scidIL2rg(-/-) (NSG) Mice.

SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery

SCIg vs. IVIg: let’s give patients the choice!.

Severe combined immunodeficiency (SCID) in Canadian children: a national surveillance study

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

Subcutaneous Immunoglobulin Replacement Therapy with Hizentra® is Safe and Effective in Children Less Than 5 Years of Age.

Sudden blindness caused by anterior ischemic optic neuropathy in 5 children on continuous peritoneal dialysis

Survey on retransplantation criteria for patients with severe combined immunodeficiency.

Targeted gene addition to human mesenchymal stromal cells as a cell-based plasma-soluble protein delivery platform.

The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

The majority of myeloid‐antigen‐positive (My+) childhood B‐cell precursor acute lymphoblastic leukaemias express TEL‐AML1 fusion transcripts ⬇️

Therapeutic efficacy of cord blood-derived mesenchymal stromal cells for the prevention of acute graft-versus-host disease in a xenogenic mouse model

Transplantation outcomes for severe combined immunodeficiency, 2000-2009.

Treatment costs associated with hospital-based intravenous immunoglobulin therapy compared to home-based subcutaneous immunoglobulin therapy in a cohort of paediatric patients with primary immunodeficiency

Varicella-zoster virus disease is more frequent after cord blood than after bone marrow transplantation

Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans

[Multiple talents of the chemokine receptor-CXCR4]