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DR. PAUL BRUCE BADER MD
MD
Hematology & Oncology Physician
NPI: 1740281450IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
143018(NY)
Education
OTHER
Class of 1993
Research & Publications (20)
Prognostic value of minimal residual disease quantification before allogeneic stem-cell transplantation in relapsed childhood acute lymphoblastic leukemia: the ALL-REZ BFM Study Group.
PMID 19064980·J Clin Oncol·2009
8-other
Monitoring of post-transplant remission of childhood malignancies: is there a standard?
PMID 18978741·Bone Marrow Transplant·2008
6-review
Children with myelodysplastic syndrome (MDS) and increasing mixed chimaerism after allogeneic stem cell transplantation have a poor outcome which can be improved by pre-emptive immunotherapy.
PMID 15725087·Br J Haematol·2005
3-trial
How and when should we monitor chimerism after allogeneic stem cell transplantation?
PMID 15502849·Bone Marrow Transplant·2005
6-review
Increasing mixed chimerism defines a high-risk group of childhood acute myelogenous leukemia patients after allogeneic stem cell transplantation where pre-emptive immunotherapy may be effective.
PMID 14990984·Bone Marrow Transplant·2004
3-trial
Increasing mixed chimerism is an important prognostic factor for unfavorable outcome in children with acute lymphoblastic leukemia after allogeneic stem-cell transplantation: possible role for pre-emptive immunotherapy?
PMID 15117992·J Clin Oncol·2004
4-observational
WT1 gene expression: useful marker for minimal residual disease in childhood myelodysplastic syndromes and juvenile myelo-monocytic leukemia?
PMID 15182334·Eur J Haematol·2004
8-other
Monitoring of donor cell chimerism for the detection of relapse and early immunotherapeutic intervention in acute lymphoblastic leukemias.
PMID 12611064·Ann Hematol·2002
8-other
Minimal residual disease (MRD) status prior to allogeneic stem cell transplantation is a powerful predictor for post-transplant outcome in children with ALL.
PMID 12200679·Leukemia·2002
8-other
Characterization of lineage-specific chimaerism in patients with acute leukaemia and myelodysplastic syndrome after allogeneic stem cell transplantation before and after relapse.
PMID 10792281·Br J Haematol·2000
8-other
Enrichment of cell subpopulations applying automated MACS technique: purity, recovery and applicability for PCR-based chimerism analysis.
PMID 19421174·Bone Marrow Transplant·2010
8-other
WT1 peptide-specific T cells generated from peripheral blood of healthy donors: possible implications for adoptive immunotherapy after allogeneic stem cell transplantation.
PMID 19357702·Leukemia·2009
8-other
PTCH1 duplication in a family with microcephaly and mild developmental delay.
PMID 18830227·Eur J Hum Genet·2009
8-other
Identification of critical regions for clinical features of distal 10q deletion syndrome.
PMID 19558528·Clin Genet·2009
5-case
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study.
PMID 19322206·Leukemia·2009
4-observational
Allogeneic transplantation for pediatric acute lymphoblastic leukemia: the emerging role of peritransplantation minimal residual disease/chimerism monitoring and novel chemotherapeutic, molecular, and immune approaches aimed at preventing relapse.
PMID 19147081·Biol Blood Marrow Transplant·2009
6-review
[Urinary diversions: which one one is right for which patient?].
PMID 19169659·Urologe A·2009
6-review
An algorithm for tailoring pharmacotherapy for smoking cessation: results from a Delphi panel of international experts.
PMID 18845621·Tob Control·2009
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9785 QUEENS BLVD
REGO PARK, NY 11374 - Phone
- (718) 261-9100
Quick Facts
- NPI
- 1740281450
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 33
- Publications
- 20
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