Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI
Por um escritor misterioso
Last updated 28 outubro 2024
Dr. Neelam Giri conducts clinical and laboratory research focused on the various diseases that are being studied as part of the DCEG Inherited Bone Marrow Failure Syndromes Program, including Fanconi's anemia, dyskeratosis congenita, Diamond-Blackfan anemia and Shwachman-Diamond syndrome.
Neelam GIRI, National Institutes of Health, MD, NIH
The Unique Role of Staff Clinicians in DCEG Research - NCI
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance
Cells, Free Full-Text
Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect
British Journal of Haematology
Dr. Neelam Giri, MD – Rockville, MD
PDF) Preemptive Bone Marrow Transplantation and Event-Free Survival in Fanconi Anemia
Neelam GIRI, National Institutes of Health, MD, NIH
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