Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI
Descrição
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.
Telomere length in blood, buccal cells, and fibroblasts from patients with inherited bone marrow failure syndromes
Cells, Free Full-Text
Neelam GIRI, National Institutes of Health, MD, NIH
Diverse Applications of Nanomedicine
Neelam GIRI, National Institutes of Health, MD, NIH
PDF) Pathogenic germline IKZF1 variant alters hematopoietic gene expression profiles
Prognostic significance of pulmonary function tests in dyskeratosis congenita, a telomere biology disorder
The incidence and spectrum of congenital hand differences in patients with Fanconi anaemia: analysis of 48 patients - Grainne Bourke, Daniel Wilks, Sally Kinsey, Richard G. Feltbower, Neelam Giri, Blanche P. Alter, 2022
Dr. Edward Anders Kolb, MD, Wilmington, DE, Pediatric Hematologist-Oncologist
PDF) Preemptive Bone Marrow Transplantation and Event-Free Survival in Fanconi Anemia
Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders - The Journal of Pediatrics
Joel Walker Fund Fanconi Anemia Research Fund
Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect
Molecular Hematopoiesis
Dr. Neelam Giri, MD - Pediatrics Specialist in Rockville, MD
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por adulto (o preço varia de acordo com o tamanho do grupo)
