Suchergebnisse - "Jamwal, Manu"

PubPharm (74)

11

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

enthalten in: Indian journal of hematology and blood transfusion | 2023

von Sharma, R. | Jamwal, M. | Singh, N. | +8

12

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

enthalten in: Indian journal of hematology & blood transfusion | 2023

von Sharma, R. | Jamwal, M. | Singh, N. | +8

13

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

14

Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretation

enthalten in: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2023

von Sharma, R. | Jamwal, M. | Senee, H. | +6

15

A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother

enthalten in: International journal of laboratory hematology | 2022

von Sharma, R. | Jamwal, M. | Senee, H. | +5

16

High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor Growth

enthalten in: Biomacromolecules | 2022

von Mimansa | Jamwal, M. | Das, R. | +1

17

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

enthalten in: Annals of hematology | 2022

von Singh, N. | Jamwal, M. | Sharma, R. | +5

18

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

19

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

20

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

enthalten in: Annals of hematology | 2022

von Singh, N. | Jamwal, M. | Sharma, R. | +5