Suchergebnisse - "Bagla, Shruti"

PubPharm (25)

1

Defective monocyte plasticity and altered cAMP pathway characterize USB1-mutated poikiloderma with neutropenia Clericuzio type

enthalten in: British journal of haematology | 2024

von Parajuli, P. | Craig, D. | Gadgeel, M. | +7

CommentIn: Br J Haematol. 2024 Feb;204(2):395-396. - PMID 37932156

2

Exosomes in Epilepsy of Tuberous Sclerosis Complex : Carriers of Pro-Inflammatory MicroRNAs

enthalten in: Non-coding RNA | 2021

von Cukovic, D. | Bagla, S. | Ukasik, D. | +8

3

A novel finding in pediatric leiomyosarcoma : Expanding spectrum of FGFR rearrangements in childhood cancers

enthalten in: Pediatric blood & cancer | 2021

von Persaud, Y. | Bagla, S. | Shanti, C. | +3

4

Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin

enthalten in: Pediatric hematology and oncology | 2021

von Bagla, S. | Regling, K. | Wakeling, E. | +8

5

A novel finding in pediatric leiomyosarcoma : Expanding spectrum of FGFR rearrangements in childhood cancers

enthalten in: Pediatric Blood & Cancer | 2021

von Persaud, Y. | Bagla, S. | Shanti, C. | +3

6

CD14/16 monocyte profiling in juvenile myelomonocytic leukemia

enthalten in: Pediatric blood & cancer | 2020

von Gadgeel, M. | Bagla, S. | Buck, S. | +2

7

Clinical Diagnosis of Red Cell Membrane Disorders : Comparison of Osmotic Gradient Ektacytometry and Eosin Maleimide (EMA) Fluorescence Test for Red Cell Band 3 (AE1, SLC4A1) Content for Clinical Diagnosis

enthalten in: Frontiers in physiology | 2020

von Zaidi, A. | Buck, S. | Gadgeel, M. | +6

8

CD14/16 monocyte profiling in juvenile myelomonocytic leukemia

enthalten in: Pediatric Blood & Cancer | 2020

von Gadgeel, M. | Bagla, S. | Buck, S. | +2

9

TLR7 activation in epilepsy of tuberous sclerosis complex

enthalten in: Inflammation research : official journal of the European Histamine Research Society ... [et al. | 2019

von Dombkowski, A. | Cukovic, D. | Bagla, S. | +4

10

Compound heterozygosity in PKLR gene for a previously unrecognized intronic polymorphism and a rare missense mutation as a novel cause of severe pyruvate kinase deficiency

enthalten in: Haematologica | 2019

von Bagla, S. | Bhambhani, K. | Gadgeel, M. | +3