Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Raja, Padidela"'
Autor:
Anuradha Khadilkar, Neha Kajale, Chirantap Oza, Rashmi Oke, Ketan Gondhalekar, Vivek Patwardhan, Vaman Khadilkar, Zulf Mughal, Raja Padidela
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Studies performed on Indian children to assess vitamin-D status have been on small sample sizes, limited to specific geographical locations and used non-standard methods to measure 25(OH)D3. This multicentre study assessed 25(OH)D3 concentra
Externí odkaz:
https://doaj.org/article/9a89ad2d64b74be9a3108d1ce8f22bb1
Publikováno v:
Clinical Case Reports, Vol 8, Iss 11, Pp 2181-2185 (2020)
Abstract Hypothyroidism and diabetes insipidus present in children with Aicardi Goutières Syndrome (AGS) often years after disease onset and frequently resolve spontaneously. Screening and regular reassessment for both conditions are recommended in
Externí odkaz:
https://doaj.org/article/2313d5318d694fc3aafffa1c4330fca1
Publikováno v:
Endocrine Connections, Vol 9, Iss 10, Pp 1051-1056 (2020)
X-linked hypophosphataemia (XLH) is caused by a pathogenic variant in the PHEX gene, which leads to elevated circulating FGF23. High FGF23 causes hypophosphataemia, reduced active vitamin D concentration and clinically manifests as rickets in childre
Externí odkaz:
https://doaj.org/article/7538396827af4132981a38d8e7074a20
Autor:
Raja Padidela, Robert Yates, Dan Benscoter, Gary McPhail, Elaine Chan, Jaya Nichani, M. Zulf Mughal, Charles Myer, Omendra Narayan, Claire Nissenbaum, Stuart Wilkinson, Shanggen Zhou, Howard M. Saal
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Perinatal and infantile hypophosphatasia (HPP) are associated with respiratory failure and respiratory complications. Effective management of such complications is of key clinical importance. In some infants with HPP, severe trach
Externí odkaz:
https://doaj.org/article/5cf80021bb684fdfafeb46428d8e18f5
Autor:
Raja Padidela, Ola Nilsson, Outi Makitie, Signe Beck-Nielsen, Gema Ariceta, Dirk Schnabel, Maria Luisa Brandi, Annemieke Boot, Elena Levtchenko, Michael Smyth, Ravi Jandhyala, Zulf Mughal
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background X-linked hypophosphataemia (XLH) is a rare, hereditary, progressive and lifelong phosphate wasting disorder characterised by pathological elevations in fibroblast growth factor (FGF) 23 concentration and activity; XLH has an incid
Externí odkaz:
https://doaj.org/article/d1eaabf96b4c4fabb33c9762c45a5fee
Autor:
Daphne Yau, Maria Salomon-Estebanez, Amish Chinoy, John Grainger, Ross J Craigie, Raja Padidela, Mars Skae, Mark J Dunne, Philip G Murray, Indraneel Banerjee
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)
Congenital hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy. To correct hypoglycaemia, high concentrations of dextrose are often required through a central venous catheter (CVC) with consequent risk of thrombosis. We des
Externí odkaz:
https://doaj.org/article/744d990cfc054927a853bbfd07b8635d
Autor:
Amish Chinoy, Raja Padidela
Publikováno v:
Indian Journal of Pediatrics. 90:574-581
Nutritional rickets, caused by vitamin D and/or calcium deficiency is by far the most common cause of rickets. In resource-limited settings, it is therefore not uncommon to treat rickets with vitamin D and calcium. If rickets fails to heal and/or if
Autor:
Vilius Floreskul, Fatema Z. Juma, Anjali B. Daniel, Imran Zamir, Andrew Rawdin, Matthew Stevenson, Zulf Mughal, Raja Padidela
Publikováno v:
Frontiers in Public Health, Vol 8 (2020)
Background: Literature on the cost of management of rickets and cost-effectiveness of vitamin D supplementation in preventing rickets is lacking.Methods: This study considered the cost-effectiveness of providing free vitamin D supplementation to preg
Externí odkaz:
https://doaj.org/article/4313ac1863134a33adc2b88c22e197d7
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Background Hypophosphatasia (HPP) is a rare, heterogeneous disease caused by low tissue-nonspecific alkaline phosphatase activity and associated with a range of signs and symptoms, including bone mineralization defects, respiratory problems,
Externí odkaz:
https://doaj.org/article/896b1344bd8f4dfa8894c75ee659dcfb
Autor:
Vivek G Patwardhan, Zulf M Mughal, Shashi A Chiplonkar, Ann R Webb, Richard Kift, Vaman V Khadilkar, Raja Padidela, Anuradha V Khadilkar
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 22, Iss 2, Pp 249-255 (2018)
Objectives: To investigate the duration of casual sunlight ultraviolet-B (UVB) exposure required to maintain optimal Vitamin D status (25-hydroxyvitamin-D [25(OH)D]) >50 nmol/L in urban Indian men, using polysulfone (PSU) dosimeters and a sunlight ex
Externí odkaz:
https://doaj.org/article/292d678571684a0e9782644612167829