• A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34
• A Meta-Analysis of the Effect of Sodium Glucose Cotransporter-2 Inhibitors on Metabolic Parameters in Patients With Polycystic Ovary Syndrome
• A novel vaginal drug delivery system: anti-HIV bioadhesive film containing abacavir
• A Recurrent Biallelic Pathogenic Variant in TBXAS1 Gene Causing Ghosal Hematodiaphyseal Dysplasia
• Alpha thalassemia/mental retardation syndrome X-linked gene product ATRX is required for proper replication restart and cellular resistance to replication stress
• Antibacterial and antiviral high-performance nanosystems to mitigate new SARS-CoV-2 variants of concern
• Assessment of insulin resistance and metabolic syndrome in drug naive patients of bipolar disorder
• Behavior profile of children with nephrotic syndrome
• Blocking COX unlocks response in GHDD
• Case report: Ghosal hematodiaphyseal dysplasia-A rare cause of skeletal dysplasia and cytopenia
• Castleman's disease--a rare disease with varying presentation
• Chronic steroid-response pancytopenia and increased bone density due to thromboxane synthase deficiency
• Clinico-radiological profile and outcome of dengue patients with central nervous system manifestations: A case series in an Eastern India tertiary care hospital
• Coexisting intracranial tumors with pituitary adenomas: genetic association or coincidence?
• Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India
• Diaphyseal dysplasia associated with anemia
• Early manifestation of Ghosal-type hemato-diaphyseal dysplasia
• Emotional content of dreams in obstructive sleep apnea hypopnea syndrome patients and sleepy snorers attending a sleep-disordered breathing clinic
• Even very low dose hydrocortisone might precipitate psychosis in Sheehan's syndrome: A need for caution
• Facial diplegia with hyperreflexia: a rare variant of Guillain-Barré syndrome
• Fatal leptomeningeal melanoma in neurocutaneous melanosis
• From cells to atoms: Cryo-EM as an essential tool to investigate pathogen biology, host-pathogen interaction, and drug discovery
• Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disorders
• Ghosal haemato-diaphyseal dysplasia: a new disorder
• Ghosal haematodiaphyseal dysplasia: a new case
• Ghosal hematodiaphyseal dysplasia and response to corticosteroid therapy
• Ghosal hematodiaphyseal dysplasia with autoimmune anemia in two adult siblings
• Ghosal hematodiaphyseal dysplasia with myelofibrosis
• Ghosal hematodiaphyseal dysplasia-a concise review including an illustrative patient
• Ghosal Hematodiaphyseal Dysplasia: A Case Report
• Ghosal hematodiaphyseal dysplasia: a rare cause of a myelophthisic anemia
• Ghosal Syndrome--Ten Years Follow-up
• Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease
• Ghosal Type Hematodiaphyseal Dysplasia
• Glucagon-like peptide-1 receptor agonists favorably address all components of metabolic syndrome
• Heritable sclerosing bone disorders: presentation and new molecular mechanisms
• Hoogsteen base-pairing revisited: resolving a role in normal biological processes and human diseases
• Identification of residues/sequences in the human riboflavin transporter-2 that is important for function and cell biology
• Invasive sphenocavernous aspergilloma complicating an operated case of acromegaly
• Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasia
• Management issues in a complex case of basilar invagination associated with a large fourth ventricular dermoid and Klippel-Feil syndrome
• Mechanisms and Regulation of DNA-Protein Crosslink Repair During DNA Replication by SPRTN Protease
• Melnick- needles osteodysplasty presenting with quadriparesis
• Multiple intracranial de-novo chloromas presenting with Garcin's syndrome
• Nephrotic syndrome in children; a survey of 45 cases
• Neurocutaneous spectrum of multiple endocrine neoplasia-1
• New answers to the old RIDDLE: RNF168 and the DNA damage response pathway
• Nonsteroidal anti-inflammatory drugs as a targeted therapy for bone marrow failure in Ghosal hematodiaphyseal dysplasia
• Novel compound heterozygous variants of TBXAS1 presenting with Ghosal hematodiaphyseal dysplasia treated with steroids
• Novel TBXAS1 variants in two Indian children with Ghosal hematodiaphyseal dysplasia: A concise report
• Observations on prednisolone treated cases of nephrotic syndrome; a preliminary report
• Papillon-Lefevre syndrome-like presentation in chronic arsenicosis: A rare mimicry
• Rheumatological manifestations in diabetes mellitus
• Rosette-Forming Glioneuronal Tumor in Opticochiasmatic Region-Novel Entity in New Location
• Screen time and metabolic syndrome among expatriate adolescents in the United Arab Emirates
• Steroid-responsive anemia in patients of Ghosal hematodiaphyseal dysplasia: simple to diagnose and easy to treat
• Structure of Human TMPRSS2 in Complex with SARS-CoV-2 Spike Glycoprotein and Implications for Potential Therapeutics
• Tackling COVID-19 Using Antiviral Nanocoating's-Recent Progress and Future Challenges
• The annealing helicase HARP protects stalled replication forks
• Three-dimensional insights into human enveloped viruses in vitro and in situ
• Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)