Suchergebnisse - "Jamwal, Manu"

PubPharm (74)

21

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

22

Quintuply-fortified salt for the improvement of micronutrient status among women of reproductive age and preschool-aged children in Punjab, India : protocol for a randomized, controlled, community-based trial

enthalten in: BMC nutrition | 2022

von McDonald, C. | Brown, K. | Goh, Y. | +12

23

Quintuply-fortified salt for the improvement of micronutrient status among women of reproductive age and preschool-aged children in Punjab, India: protocol for a randomized, controlled, community-based trial

enthalten in: BMC nutrition | 2022

von McDonald, C. | Brown, K. | Goh, Y. | +12

24

Hemoglobin Andrew-Minneapolis-Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β-thalassemia trait : A diagnostic and management conundrum

enthalten in: International journal of laboratory hematology | 2022

von Khaire, N. | Jamwal, M. | Sharma, P. | +4

25

Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource-poor setting

enthalten in: Journal of cutaneous pathology | 2022

von Mahajan, R. | Manjunath, S. | Madakshira, M. | +7

26

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

27

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

28

Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource‐poor setting

enthalten in: Journal of Cutaneous Pathology | 2022

von Mahajan, R. | Manjunath, S. | Madakshira, M. | +7

29

Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait : A diagnostic and management conundrum

enthalten in: International Journal of Laboratory Hematology | 2022

von Khaire, N. | Jamwal, M. | Sharma, P. | +4

30

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