RandyMarcWindreichMD
Pediatric Hematology & Oncology • Pittsburgh, PAAssistant Professor, Pediatrics, University of Pittsburgh School of Medicine
Dr. Windreich is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
4401 Penn Avenue
Pittsburgh, PA 15224Phone+1 412-692-5055Fax+1 412-692-6752
Education & Training
UPMC Medical EducationFellowship, Pediatric Hematology/Oncology, 2008 - 2011
Inova Fairfax Medical Campus/Inova Children's HospitalResidency, Pediatrics, 2005 - 2008
Tel Aviv University SacklerClass of 2005
Certifications & Licensure
PA State Medical License 2008 - 2024
VA State Medical License 2005 - 2008- American Board of Pediatrics Pediatrics
- American Board of Pediatrics Pediatric Hematology-Oncology
Clinical Trials
- Pharmacokinetics-based Mycophenolate Mofetil Dosing for GVHD Prevention Start of enrollment: 2010 Jun 01
- Busulfan, Cyclophosphamide, and Melphalan or Busulfan and Fludarabine Phosphate Before Donor Hematopoietic Cell Transplant in Treating Younger Patients With Juvenile Myelomonocytic Leukemia Start of enrollment: 2013 Jun 24
- Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT Start of enrollment: 2014 Feb 04
Publications & Presentations
PubMed
- 1 citationsA mismatched syndrome: A five-year-old girl with very-high-risk leukemia and Lynch syndrome.Martha Stewart, Meghan McCormick, Randy M Windreich, Christine Munro, Julia Meade
Pediatric Blood & Cancer. 2023-11-01 - Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.Saskia B. Wortmann, Szymon Ziętkiewicz, Sergio Guerrero-Castillo, René G. Feichtinger, Matias Wagner
Genetics in Medicine. 2021-07-23 - 18 citationsNeutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.Saskia B. Wortmann, Szymon Ziętkiewicz, Sergio Guerrero-Castillo, René G. Feichtinger, Matias Wagner
Genetics in Medicine. 2021-06-17
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
