A novel beta+-thalassemia mutation (codon 10 GCC --> GCA) and a rare transcriptional mutation (-28A --> G) in Indians

Acquired inhibitor to factor VIII: report of two unusual cases.

Haemophilia : the official journal of the World Federation of Hemophilia·2016

A successful twin pregnancy in a patient with HbE-β-thalassemia in western India.

Journal of postgraduate medicine·2015

Potentially toxic elements in lignite and its combustion residues from a power plant.

Environmental monitoring and assessment·2014

Male urethral diverticulum having multiple stones.

Annals of medical and health sciences research·2014

Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.

Clinical genetics·2013

Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal diagnosis from maternal plasma.

Journal of postgraduate medicine·2013

KPNA2-Mediated MYC Nuclear Import Enhances CAR-T Cell Memory and Potentiates Antitumor Efficacy.

Blood·2026

How I Identify and Diagnose Carriers of Hemophilia and Women and Girls with Hemophilia.

Blood·2026

The origins of rare glycosylphosphatidylinositol-deficient cells in normal and immune-mediated hematopoiesis.

Blood·2026

How I Treat Heavy Menstrual Bleeding in Patients with Bleeding Disorder of Unknown Cause.

Blood·2026

Choice of a different donor reduces relapse risk after second allogeneic SCT for MDS.

Blood·2026

A multicenter phase II study of glofitamab plus polatuzumab-R-CHP for patients with diffuse large B-cell lymphoma.

Blood·2026

The genetic landscape of myotonic dystrophy type 1: insights from nearly one million genomes.

Brain : a journal of neurology·2026

Cardiac phenotype in children with X-linked ichthyosis (STS-sEDD): findings from a prospective cohort.

European journal of pediatrics·2026

Preoperative diabetes status, circulating GDF15, and weight loss after sleeve gastrectomy.

Surgical endoscopy·2026

PNLDC1 deadenylase affects translational rate and cell proliferation in mESCs.

RNA (New York, N.Y.)·2026

Exploring potential association between bisphenol A exposure and spondyloarthritis: Integrative evidence from molecular analyses and NHANES.

Chemico-biological interactions·2026

From iPSC Disease Modeling to Epigenome Editing: Toward Therapeutic Reversal of Genomic Imprinting Disorders.

Neuroscience research·2026

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Acquired inhibitor to factor VIII: report of two unusual cases.

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Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.

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