Congenital deficiency of factor 13 in an Indian kindred

Adjuvant capecitabine in patients with triple-negative breast cancer after neoadjuvant chemotherapy.

ESMO open·2025

Clinical outcomes of early-stage triple-negative breast cancer after neoadjuvant chemotherapy according to HER2-low status☆.

ESMO open·2024

Human pregnane X receptor compromises the function of p53 and promotes malignant transformation.

Cell death discovery·2016

Placental involvement by non-Hodgkin lymphoma in a Crohn disease patient on long-term thiopurine therapy.

Internal medicine journal·2016

Isolated unilateral cerebellar hypoplasia. A case report.

The neuroradiology journal·2013

Two rare cases of Epstein-Barr virus-associated lymphoproliferative disorders in inflammatory bowel disease patients on thiopurines and other immunosuppressive medications.

Internal medicine journal·2013

Role of iron in the proliferation of the established human tumor cell lines U-937 and K-562: effects of suramin and a lipophilic iron chelator (PIH).

Scandinavian journal of haematology·1986

The efficacy and toxicity of VAD in the treatment of myeloma and related disorders.

Scandinavian journal of haematology·1986

RES phagocytosis in children with homozygous beta-thalassemia in relation to blood transfusion.

Scandinavian journal of haematology·1986

Two allotypes of factor IX present in haemophilia B.

Scandinavian journal of haematology·1986

Radioimmunoassay of erythropoietin in chronic uraemia or anephric patients.

Scandinavian journal of haematology·1986

Prognostic significance of a morphometric study of lymph node biopsies in chronic lymphocytic leukaemia.

Scandinavian journal of haematology·1986

The genome sequence of the Tufted Button, Acleris cristana (Denis & Schiffermüller, 1775).

Wellcome open research·2026

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations.

Journal of medical cases·2026

The genome sequence of Natterer's Bat, Myotis nattereri (Kuhl, 1817) (Chiroptera: Vespertilionidae).

Wellcome open research·2026

Genetic divergence between reservoir and pre-therapy plasma HIV-1 Env variants does not confer consistent compartment-specific differences in broadly neutralizing antibody sensitivity.

Journal of virology·2026

Diabetes related genetics and outcomes after total pancreatectomy with islet autotransplantation.

The Journal of clinical endocrinology and metabolism·2026

Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion·2026

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Congenital deficiency of factor 13 in an Indian kindred

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Adjuvant capecitabine in patients with triple-negative breast cancer after neoadjuvant chemotherapy.

Clinical outcomes of early-stage triple-negative breast cancer after neoadjuvant chemotherapy according to HER2-low status☆.

Human pregnane X receptor compromises the function of p53 and promotes malignant transformation.

Placental involvement by non-Hodgkin lymphoma in a Crohn disease patient on long-term thiopurine therapy.

Isolated unilateral cerebellar hypoplasia. A case report.

Two rare cases of Epstein-Barr virus-associated lymphoproliferative disorders in inflammatory bowel disease patients on thiopurines and other immunosuppressive medications.

Role of iron in the proliferation of the established human tumor cell lines U-937 and K-562: effects of suramin and a lipophilic iron chelator (PIH).

The efficacy and toxicity of VAD in the treatment of myeloma and related disorders.

RES phagocytosis in children with homozygous beta-thalassemia in relation to blood transfusion.

Two allotypes of factor IX present in haemophilia B.

Radioimmunoassay of erythropoietin in chronic uraemia or anephric patients.

Prognostic significance of a morphometric study of lymph node biopsies in chronic lymphocytic leukaemia.

The genome sequence of the Tufted Button, Acleris cristana (Denis & Schiffermüller, 1775).

CYP4F22-Related Autosomal Recessive Congenital Ichthyosis Associated With Hirschsprung Disease and Bartter-Like Renal Manifestations.

The genome sequence of Natterer's Bat, Myotis nattereri (Kuhl, 1817) (Chiroptera: Vespertilionidae).

Genetic divergence between reservoir and pre-therapy plasma HIV-1 Env variants does not confer consistent compartment-specific differences in broadly neutralizing antibody sensitivity.

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Congenital deficiency of factor 13 in an Indian kindred

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