A5107842148- Renal Diseases and Glomerulopathies
- Chronic Kidney Disease and Diabetes
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Spinal Cord Injury Research
- Mesenchymal stem cell research
- Systemic Lupus Erythematosus Research
- Acute Myeloid Leukemia Research
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Stroke Rehabilitation and Recovery
- Cerebral Palsy and Movement Disorders
- Pediatric Urology and Nephrology Studies
- Renal Transplantation Outcomes and Treatments
- Nerve injury and regeneration
- Renal and related cancers
- Muscle activation and electromyography studies
- Vasculitis and related conditions
- Systemic Sclerosis and Related Diseases
- Saffron Plant Research Studies
- Advances in Oncology and Radiotherapy
- Hydrogels: synthesis, properties, applications
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Research on Leishmaniasis Studies
- Urological Disorders and Treatments
- Medical Research and Treatments
- Neurological and metabolic disorders
Sawai ManSingh Medical College and Hospital
2025
All India Institute of Medical Sciences, Nagpur
2023
Program for Appropriate Technology in Health
2023
Royal Liverpool University Hospital
2020
University of Liverpool
2020
Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College
2010-2019
Arkana Laboratories
2019
Neurogen Brain & Spine Institute
2013-2018
All India Institute of Medical Sciences
2008-2015
DR. B.R.A. Institute Rotary Cancer Hospital
2013
Objective: The objective of this study was to formulate and optimize the validation Bacitracin Zinc Hydrogel using Sodium Alginate Carbopol-934 for wound healing. Aim: This primary aim improve a hydrogel with improved healing qualities by utilising carbopol-934 sodium alginate as gelling agents. assess physicochemical characteristics, medication release profile, efficacy, in addition verifying its performance topical therapy. objective: Objective : To Optimize Validation Using Materials...
A BSTRACT This case report highlights the unusual concurrent occurrence of disseminated histoplasmosis and pigment nephropathy in a 38-year-old immunocompetent male. The patient presented with 1-week history fever, abdominal pain, generalized body aches, vomiting, decreased urine output, which progressed to oliguric renal failure. Clinical laboratory findings revealed significant impairment, while imaging studies noted bilateral adrenal gland enlargement. biopsy showed acute tubular injury...
Detailed analysis of the clinical effects cell therapy for thoracolumbar spinal cord injury: an original study Alok Sharma,1 Nandini Gokulchandran,1 Hemangi Sane,2 Prerna Badhe,1 Pooja Kulkarni,2 Mamta Lohia,3 Anjana Nagrajan,3 Nancy Thomas3 1Department Medical Services and Clinical Research, 2Department Research Development, 3Department Neurorehabilitation, NeuroGen Brain Spine Institute, Surana Sethia Hospital Centre, Chembur, Mumbai, India Background: Cell is amongst most promising...
Cerebral palsy (CP) is one of the non-progressive neurological diseases caused by damage to brain tissue at birth, which leads physical, cognitive and perceptive symptoms. Even after lifelong medical therapeutic management there are residual deficits affect quality life patients their families. We examined a maximally rehabilitated, 20 year old male suffering from CP Mental Retardation (MR). He had diplegic gait Intelligence Quotient (IQ) score 44 with affected fine motor activities,...
Collapsing glomerulopathy (CG), once recognized as a distinct renal disease in HIV-positive patients, has since been described association with number of other conditions, including autoimmune diseases. Among the latter, CG reported Still’s disease. Extensive search literature revealed only three patients biopsy diagnosis presence clinical and serological evidence SLE (HIV-negative). This case report presents adult female HIV-negative who were detected having significant proteinuria...
AIM OF STUDY: Chronic lymphocytic leukemia (CLL) is the most common chronic lympho-proliferative disorder. This study was undertaken to know prevalence of ZAP-70 and CD 38 in treatment naive patients CLL seen at a tertiary care centre north India. MATERIALS AND METHODS: were tested by flow cytometry on peripheral blood samples. positive positivity defined as expression 20% 30% cells, respectively. Clinico-hematological profile its correlation with assessed consecutive 80 patients. RESULTS:...
Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder characterized by photosensitivity, cutaneous pigmentary changes, premature skin ageing and development of various internal malignancies at an early age as result defect in nucleotide excision repair following ultraviolet light exposure. Cutaneous angiosarcomas are aggressive neoplasms that rarely associated with XP. In this communication, we report the case 40-year-old male patient XP who developed angiosarcoma face discuss...
Primary focal segmental glomerulosclerosis (FSGS) has recently been divided into five subtypes by the Columbia classification. However, little is known about incidence of these in Indian population. In addition, there are very few studies evaluating clinico-pathologic features with morphometric parameters subtypes. This study was aimed at clinical, histopathological and various FSGS our referral center. Sixty-five (65) cases idiopathic FSGS, diagnosed over two years (2006-2007), were...
Frontal intraparenchymal "White epidermoid cyst": A rare occurrence Letters to the Editor from C5 D6 [Figures 234567].It was decided continue conservative treatment with ATT and steroids.On it, patient showed gradual improvement.Tubercular meningitis (TBM) is commonest chronic in India.Syringomyelia can rarely develop as an acute or complication of TBM.The incidence CNS TB related prevalence community, it still most common type infection developing countries, like India.The intracranial...
Nephrotic syndrome (NS) is a common renal disorder with significant tubulo-interstitial damage due to the combined effects of proteinuria and obstruction efferent blood flow. Peritubular capillary (PTC) loss has also been correlated interstitial fibrosis. This study included 30 pediatric cases idiopathic NS. Clinical details, including biochemical parameters, were recorded biopsy slides reviewed for histological features. PTCs highlighted using anti-CD34 antibody quantified help image...
Membranoproliferative glomerulonephritis (MPGN) is a rare cause of the nephrotic syndrome in adults and children. Though small focal crescents may be seen up to 10% cases MPGN, presence more than 50% (crescentic MPGN) rare. Very few crescentic transformation documented by subsequent renal biopsies, have been described literature. A young female patient underwent kidney biopsy for nephrotic-nephritic was diagnosed as idiopathic MPGN. She administered immunosuppressive therapy (steroids...
C1q nephropathy is a recently described clinico-pathologic entity with variable clinical presentation and pathology. Crescentic glomerulonephritis (GN) has been reported in only two patients the available literature. CD59 deficiency, along lack of CD55, responsible for paroxysmal nocturnal hemoglobinuria (PNH). Few cases isolated deficiency have PNH-like features. A middle-aged adult male presented rapidly progressive renal failure. Serological investigations were negative. biopsy revealed...
Dense deposit disease (DDD), previously known as membranoproliferative glomerulonephritis type 2, is an extremely rare affecting two to three people per million. The rarity of this makes it difficult for clinicians establish evidence-based clinical practices its management. Here, we report a case DDD who presented with features acute nephritic syndrome and did not respond most the treatment options available in literature.
Background: India is a vast country with four geographical zones. Zonal heterogeneity amongst prevalent adult glomerular diseases expected and has not been analysed in past studies.Methods: We conducted clinico-histological correlation of 290 kidney biopsies for (GD) at tertiary teaching hospital Eastern between January 2013 December 2015 compared our data biopsy from other zones to evaluate zonal variability (intra/inter) diseases.Results: Males dominated all clinical syndromes except...