Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Amish Chinoy"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::336234ca7c0c720908a7ea7062c5901e
https://doi.org/10.1007/s12098-023-04538-4
https://doi.org/10.1007/s12098-023-04538-4
Autor:
Amish Chinoy, Raja Padidela
Publikováno v:
Clinical Chemistry. 69:453-454
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93779eb9f6bea7ed74f5d18e26834d63
https://doi.org/10.1093/clinchem/hvad025
https://doi.org/10.1093/clinchem/hvad025
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3debc5f07f7590f0311d2ea6b77554af
https://doi.org/10.1530/endoabs.85.p77
https://doi.org/10.1530/endoabs.85.p77
Autor:
Amish Chinoy, Jacqueline Nicholson, Mars Skae, Fadil M. Hannan, Rajesh V. Thakker, M. Zulf Mughal, Raja Padidela
Publikováno v:
The Journal of Pediatrics. :113367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a21d5bee5b123afd634f848fd357678
https://doi.org/10.1016/j.jpeds.2023.02.013
https://doi.org/10.1016/j.jpeds.2023.02.013
Normal Mid-Gestation Fetal Ultrasonography Cannot Reliably Exclude Severe Perinatal Hypophosphatasia
Publikováno v:
Hormone Research in Paediatrics. 94:307-312
Introduction: Hypophosphatasia is a systemic bone disease characterized by inhibition of bone mineralization due to mutations in the ALPL gene that results in a deficiency of tissue nonspecific alkaline phosphatase. The perinatal form is the most sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a20aa79fd5bcb03668b123d8b7f29c43
https://doi.org/10.1159/000519209
https://doi.org/10.1159/000519209
Autor:
Amish, Chinoy, Grace R, Vassallo, Emma, Burkitt Wright, Judith, Eelloo, Siobhan, West, Eileen, Hupton, Paula, Galloway, Amy, Pilkington, Raja, Padidela, M Zulf, Mughal
Publikováno v:
Journal of musculoskeletalneuronal interactions. 22(1)
Neurofibromatosis type 1 (NF1) can affect multiple systems in the body. An under recognised phenotype is one of muscle weakness. Clinical studies using dynamometry and jumping mechanography have demonstrated that children with NF1 are more likely to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52eedc2189d7c7d513bc06199c391e2b
https://pubmed.ncbi.nlm.nih.gov/35234161
https://pubmed.ncbi.nlm.nih.gov/35234161
Autor:
Amish Chinoy, Raja Padidela, Ross J. Craigie, Maria Salomon-Estebanez, Mark J. Dunne, Philip Murray, John D. Grainger, Indraneel Banerjee, Daphne Yau, Mars Skae
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2019)
Endocrinology, Diabetes & Metabolism Case Reports
Yau, D, Salomon-Estebanez, M, Chinoy, A, Grainger, J, Craigie, R, Padidela, R, Skae, M, Dunne, M, Murray, P & Banerjee, I 2019, ' Central venous catheter-associated thrombosis in children with congenital hyperinsulinism ', Endocrinology, diabetes & metabolism case reports, vol. 2019, no. 1 . https://doi.org/10.1530/EDM-19-0032
Endocrinology, Diabetes & Metabolism Case Reports
Yau, D, Salomon-Estebanez, M, Chinoy, A, Grainger, J, Craigie, R, Padidela, R, Skae, M, Dunne, M, Murray, P & Banerjee, I 2019, ' Central venous catheter-associated thrombosis in children with congenital hyperinsulinism ', Endocrinology, diabetes & metabolism case reports, vol. 2019, no. 1 . https://doi.org/10.1530/EDM-19-0032
Summary 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2257963112db68d1c52815bcd7abc8dd
https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0032.xml
https://edm.bioscientifica.com/view/journals/edm/2019/1/EDM19-0032.xml
Publikováno v:
Acta Paediatrica (Oslo, Norway : 1992)
Chinoy, A, Mughal, M Z & Padidela, R 2020, ' Metabolic bone disease of prematurity—National survey of current neonatal and paediatric endocrine approaches ', ACTA PAEDIATRICA . https://doi.org/10.1111/apa.15654
Chinoy, A, Mughal, M Z & Padidela, R 2020, ' Metabolic bone disease of prematurity—National survey of current neonatal and paediatric endocrine approaches ', ACTA PAEDIATRICA . https://doi.org/10.1111/apa.15654
Aim This study aimed to identify current trends in the management of metabolic bone disease of prematurity (MBDP) in the United Kingdom. Methods A nationwide electronic survey was disseminated to all neonatal networks across the United Kingdom, as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a260f6fa61052d49f1fcdb76109858
https://pubmed.ncbi.nlm.nih.gov/33502022
https://pubmed.ncbi.nlm.nih.gov/33502022