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NOAH BOWN DO
DO
Internal Medicine Physician
NPI: 1235768813IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
58.031293(OH)34.015431(OH)100994-875(WI)
Education
OTHER
Class of 2020
Research & Publications (20)
A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups.
PMID 18838613·Blood·2009
8-other
Post cardiac transplantation lymphoproliferative disorder presenting as t(8;14) Burkitt leukaemia/lymphoma treated with low intensity chemotherapy and rituximab.
PMID 19459198·Pediatr Blood Cancer·2009
5-case
FIP1L1-PDGFRA positive chronic eosinophilic leukaemia and associated central nervous system involvement.
PMID 18256119·J Clin Pathol·2008
5-case
Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemia.
PMID 18701506·Cancer Res·2008
8-other
Long-term immune reconstitution after anti-CD52-treated or anti-CD34-treated hematopoietic stem cell transplantation for severe T-lymphocyte immunodeficiency.
PMID 18086494·J Allergy Clin Immunol·2008
8-other
Ploidy and karyotype complexity are powerful prognostic indicators in the Ewing's sarcoma family of tumors: a study by the United Kingdom Cancer Cytogenetics and the Children's Cancer and Leukaemia Group.
PMID 18064647·Genes Chromosomes Cancer·2008
8-other
Donor lymphocyte infusions for post-transplant relapse of refractory anemia with excess blasts and monosomy 7.
PMID 17253642·Pediatr Blood Cancer·2008
5-case
High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
PMID 17213021·Cancer Genet Cytogenet·2007
4-observational
Quantitative assessment of mixed chimerism in allogeneic stem cell transplant patients: a comparison of molecular genetic and cytogenetic approaches.
PMID 17551410·J Pediatr Hematol Oncol·2007
8-other
Population-based demographic study of karyotypes in 1709 patients with adult acute myeloid leukemia.
PMID 16424877·Leukemia·2006
8-other
Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.
PMID 16149064·Genes Chromosomes Cancer·2006
8-other
Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations.
PMID 16239911·Leukemia·2005
8-other
Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma.
PMID 15800319·J Clin Oncol·2005
8-other
Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.
PMID 15833833·Cancer Res·2005
8-other
No correlation between trisomy 13 and FLT3 duplication in acute myeloid leukemia.
PMID 15588866·Cancer Genet Cytogenet·2005
8-other
Quality assessment of genetic markers used for therapy stratification.
PMID 12775732·J Clin Oncol·2003
4-observational
Abnormal constitutional karyotypes in patients with neuroblastoma: a report of four new cases and review of 47 others in the literature.
PMID 14623457·Cancer Genet Cytogenet·2003
6-review
Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions.
PMID 12750153·Blood·2003
3-trial
Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors.
PMID 12112532·Genes Chromosomes Cancer·2002
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
- W180N8000 TOWN HALL RD
MENOMONEE FALLS, WI 53051 - Phone
- (262) 255-2500
Quick Facts
- NPI
- 1235768813
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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