Namrata Singh

发表

Misdiagnosis of double heterozygous εGγ(Aγδβ)0-thalassemia/β++ thalassemia as homozygous β-thalassemia: A pitfall for molecular diagnostic laboratories.

A. Khadwal, R. Das, Prashant Sharma, 2019, Blood cells, molecules & diseases.

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

J. Ahluwalia, Anand Balakrishnan, P. Malhotra, 2021, Leukemia research.

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

P. Malhotra, R. Das, Nabhajit Mallik, 2021, Cancer genetics.

Comparison of overall efficacy and safety of oral versus subcutaneous methotrexate in severe psoriasis

S. Dogra, T. Narang, S. Handa, 2022, Dermatologic therapy.

Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis

R. Das, Prashant Sharma, M. Jamwal, 2022, Annals of Hematology.

Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis

A. Trehan, R. Das, Prashant Sharma, 2021, Indian Journal of Hematology and Blood Transfusion.

Eosinophilia characterized by a rare CCT6B mutation and responsive to tyrosine kinase inhibition: Case report and literature review

E. Wang, J. Baron, Abhay Singh, 2021, Leukemia research reports.

Disruption of pancreatic stellate cell myofibroblast phenotype promotes pancreatic tumor invasion

N. Gavara, M. Tatari, V. Rajeeve, 2022, Cell reports.

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

A. Trehan, D. Bansal, R. Das, 2022, Journal of Clinical Pathology.

Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect

J. Ahluwalia, A. Trehan, D. Bansal, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency

J. Ahluwalia, A. Trehan, D. Bansal, 2022, Indian Journal of Hematology and Blood Transfusion.

ETP all or mixed phenotype acute leukemia: Diagnostic dilemma in acute leukemia with simultaneous expression of thymic and myeloid markers

A. Dasgupta, Manisha V Ramani, Namrata Singh, 2023, Journal of Hematology and Allied Sciences.

Comparison of the efficacy and cost‐effectiveness of an immunologically targeted low‐dose rituximab protocol with the conventional rheumatoid arthritis protocol in severe pemphigus

N. Sachdeva, S. Handa, R. Mahajan, 2022, Clinical and experimental dermatology.

A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C > T Mutation (Chuvash Polycythemia)

D. Bansal, P. Malhotra, Anuradha Singh, 2023, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.