Search Results - "Dhull, Rachita Singh"
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Bioavailable Vitamin D Levels in Children With First Episode Nephrotic Syndrome: A Longitudinal Study
Published in Indian pediatrics (01-10-2024)“…Objective To estimate the levels of serum bioavailable vitamin D in children presenting with first episode nephrotic syndrome (FENS) at diagnosis and after 4…”
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First episode of nephrotic syndrome with acute abdominal pain
Published in Clinical and experimental pediatrics (01-10-2020)“…Question: What are the likely causes of pain abdomen in Nephrotic syndrome? Finding: Severe hypovolemia leading to mesenteric ischemia, spontaneous bacterial…”
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Vitamin D-dependent rickets (VDDR) type 1: case series of two siblings with a CYP27B1 mutation and review of the literature
Published in Brazilian Journal of Nephrology (01-10-2020)“…Two siblings presented with clinical and biochemical features of rickets, initially suspected as hypophosphatemic rickets. There was no improvement initially,…”
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Oro-facial-digital syndrome Type 1: A case report
Published in Journal of the Indian Society of Pedodontics and Preventive Dentistry (01-04-2014)“…Oro-Facial Digital Syndrome (OFDS) is a generic term for group of apparently distinctive genetic diseases that affect the development of the oral cavity,…”
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Activin A: a marker of mineral bone disorder in children with chronic kidney disease?
Published in Pediatric nephrology (Berlin, West) (01-09-2024)“…Background Activin A has been shown to enhance osteoclast activity and its inhibition results in bone growth. The potential role of activin A as a marker of…”
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Nuclear Imaging in Pediatric Kidney Diseases
Published in Indian pediatrics (01-07-2018)“…Renal scintigraphy is a useful tool in diagnosis and management of various nephro-urological conditions. Tc-99m dimercaptosuccinic acid renal scintigraphy…”
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Infantile nephrotic syndrome secondary to cytomegalovirus infection in a 7-month-old girl: resolution with ganciclovir
Published in Paediatrics and international child health (01-05-2021)“…Infantile nephrotic syndrome is a rare disorder which is frequently caused by genetic defects. A 7-month-old girl presented with fever, loose stools and…”
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Frequent relapses in a child with nephrotic syndrome due to PLEVA
Published in Tropical doctor (01-10-2018)“…A seven-year-old boy with nephrotic syndrome presented with a frequent rash along with relapse of nephrotic syndrome. Clinical and histological features were…”
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Adenine Phosphoribosyltransferase Deficiency Due to Novel Mutation
Published in Kidney international reports (01-04-2019)Get full text
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Foreign Body in Root Canals of Two Adjacent Deciduous Molars: A Case Report
Published in International journal of clinical pediatric dentistry (01-01-2013)“…Children often tend to have the habit of inserting foreign objects in the oral cavity unknowingly for relief of dental pain. Sometimes, children do not reveal…”
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Infant oral health care: An invaluable clinical intervention
Published in Indian journal of dental sciences (01-01-2016)“…Dental assessments and evaluations for children during their 1st year of life have been recommended by the American Academy of Pediatric Dentistry and the…”
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Bilateral Mandibular Paramolars
Published in International journal of clinical pediatric dentistry (01-01-2014)“…Supernumerary tooth is a developmental anomaly and has been argued to arise from multiple etiologies. These teeth may remain embedded in the alveolar bone or…”
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Biological Restoration in Pediatric Dentistry: A Brief Insight
Published in International journal of clinical pediatric dentistry (01-09-2014)“…Dental caries is the most prevalent disease in humans, especially during early childhood. The restoration of such an extensive carious lesion should be done…”
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Infantile nephrotic syndrome secondary to cytomegalovirus infection in a 7-month-old girl: resolution with ganciclovir
Published in Paediatrics and International Child Health (03-04-2021)“…Infantile nephrotic syndrome is a rare disorder which is frequently caused by genetic defects. A 7-month-old girl presented with fever, loose stools and…”
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Adenine Phosphoribosyltransferase Deficiency Due to Novel Mutation
Published in Kidney international reports (01-04-2019)Get full text
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Oro-facial-digital syndrome type 1: a case report
Published in Journal of the Indian Society of Pedodontics and Preventive Dentistry (01-04-2014)“…Oro-Facial Digital Syndrome (OFDS) is a generic term for group of apparently distinctive genetic diseases that affect the development of the oral cavity,…”
Get more information
Journal Article