Suchergebnisse - "Jamwal, Manu"

PubPharm (15)

1

Preclinical safety assessment of photoluminescent metal quantum clusters stabilized with autologous serum proteins for host specific theranostics

enthalten in: Nanotheranostics | 2023

von Sood, K. | Yadav, P. | Jamwal, M. | +2

2

Ultra-rare Hb Regina (HBB:c.289C>G) with coinherited β-thalassaemia trait : solving the puzzle for extreme erythrocytosis

enthalten in: Journal of clinical pathology | 2022

von Mallik, N. | Jamwal, M. | Sharma, R. | +6

3

Imatinib responsive erythrocytosis in a patient with FIP1L1::PDGFRA rearranged myeloid neoplasm with hypereosinophilia - Another manifestation of a stem cell neoplasm

enthalten in: Leukemia research | 2022

von Virk, H. | Rathore, S. | Anshu, A. | +4

4

A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1

enthalten in: Cancer genetics | 2022

von Mallik, N. | Singh, N. | Jamwal, M. | +5

5

Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap

enthalten in: Leukemia research | 2022

von Sreedharanunni, S. | Jamwal, M. | Balakrishnan, A. | +9

6

Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin-linked hemolytic anemia masquerading as congenital dyserythropoietic anemia

enthalten in: Pediatric blood & cancer | 2021

von Jamwal, M. | Aggarwal, A. | Sharma, P. | +6

7

Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity

enthalten in: The Journal of molecular diagnostics : JMD | 2020

von Jamwal, M. | Aggarwal, A. | Palodhi, A. | +6

8

Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing : First South Asian study

enthalten in: British journal of haematology | 2020

von Aggarwal, A. | Jamwal, M. | Sharma, P. | +4

CommentIn: Int J Lab Hematol. 2021 Oct;43(5):e242-e243. - PMID 33470548

9

Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia

enthalten in: Blood cells, molecules & diseases | 2020

von Jamwal, M. | Aggarwal, A. | Sharma, P. | +3

10

A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia : genetic analysis exemplifies ambiguity due to multiple Isoforms

enthalten in: British journal of haematology | 2019

von Jamwal, M. | Aggarwal, A. | Palodi, A. | +4