Mineralocorticoid Deficiency and Treatment in Congenital Adrenal Hyperplasia

Por Padidela, Raja, Hindmarsh, Peter C.
Publicado em 2010

Echocardiography monitoring for diazoxide induced pericardial effusion

Por Avatapalle, Bindu, Banerjee, Indraneel, Malaiya, Nilima, Padidela, Raja
Publicado em 2012

Drug-induced hepatitis following use of octreotide for long-term treatment of congenital hyperinsulinism

Por Avatapalle, Bindu, Padidela, Raja, Randell, Tabitha, Banerjee, Indraneel
Publicado no BMJ Case Rep (2012)

Can network biology unravel the aetiology of congenital hyperinsulinism?

Por Stevens, Adam, Cosgrove, Karen E, Padidela, Raja, Skae, Mars S, Clayton, Peter E, Banerjee, Indraneel, Dunne, Mark J
Publicado em 2013

Randomized Control Trial Assessing Impact of Increased Sunlight Exposure versus Vitamin D Supplementation on Lipid Profile in Indian Vitamin D Deficient Men

Por Patwardhan, Vivek G., Mughal, Zulf M., Padidela, Raja, Chiplonkar, Shashi A., Khadilkar, Vaman V., Khadilkar, Anuradha V.
Publicado no Indian J Endocrinol Metab (2017)

The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight

Por Padidela, Raja, Bryan, Sinead M, Abu-Amero, Sayeda, Hudson-Davies, Rebecca E, Achermann, John C, Moore, Gudrun E, Hindmarsh, Peter C
Publicado em 2012

Interrelationship between serum 25-hydroxyvitamin D(3) concentration and lipid profiles in premenopausal Indian women

Por Patel, Pinal A., Patel, Prerna P., Mughal, Zulf, Padidela, Raja, Patel, Ashish D., Patwardhan, Vivek, Chiplonkar, Shashi A., Khadilkar, Vaman, Khadilkar, Anuradha
Publicado no Indian J Endocrinol Metab (2017)

Vineland adaptive behavior scales to identify neurodevelopmental problems in children with Congenital Hyperinsulinism (CHI)

Por Salomon-Estebanez, Maria, Mohamed, Zainab, Michaelidou, Maria, Collins, Hannah, Rigby, Lindsey, Skae, Mars, Padidela, Raja, Rust, Stewart, Dunne, Mark, Cosgrove, Karen, Banerjee, Indraneel, Nicholson, Jacqueline
Publicado no Orphanet J Rare Dis (2017)

Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism

Por Banerjee, Indraneel, Forsythe, Lynette, Skae, Mars, Avatapalle, Hima Bindu, Rigby, Lindsey, Bowden, Louise E., Craigie, Ross, Padidela, Raja, Ehtisham, Sarah, Patel, Leena, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado no Front Endocrinol (Lausanne) (2016)

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R)

Por Skae, Mars, Avatapalle, Hima Bindu, Banerjee, Indraneel, Rigby, Lindsey, Vail, Andy, Foster, Peter, Charalambous, Christiana, Bowden, Louise, Padidela, Raja, Patel, Leena, Ehtisham, Sarah, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2014

Atypical Forms of Congenital Hyperinsulinism in Infancy Are Associated With Mosaic Patterns of Immature Islet Cells

Por Han, Bing, Mohamed, Zainab, Estebanez, Maria Salomon, Craigie, Ross J., Newbould, Melanie, Cheesman, Edmund, Padidela, Raja, Skae, Mars, Johnson, Matthew, Flanagan, Sarah, Ellard, Sian, Cosgrove, Karen E., Banerjee, Indraneel, Dunne, Mark J.
Publicado no J Clin Endocrinol Metab (2017)

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

Por Avatapalle, Hima Bindu, Banerjee, Indraneel, Shah, Sajni, Pryce, Megan, Nicholson, Jacqueline, Rigby, Lindsey, Caine, Louise, Didi, Mohammed, Skae, Mars, Ehtisham, Sarah, Patel, Leena, Padidela, Raja, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado em 2013

Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease

Por Han, Bing, Newbould, Melanie, Batra, Gauri, Cheesman, Edmund, Craigie, Ross J., Mohamed, Zainab, Rigby, Lindsey, Padidela, Raja, Skae, Mars, Mironov, Aleksandr, Starborg, Tobias, Kadler, Karl E., Cosgrove, Karen E., Banerjee, Indraneel, Dunne, Mark J.
Publicado no Am J Clin Pathol (2016)

Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time

Por Salomon-Estebanez, Maria, Flanagan, Sarah E., Ellard, Sian, Rigby, Lindsey, Bowden, Louise, Mohamed, Zainab, Nicholson, Jacqueline, Skae, Mars, Hall, Caroline, Craigie, Ross, Padidela, Raja, Murphy, Nuala, Randell, Tabitha, Cosgrove, Karen E., Dunne, Mark J., Banerjee, Indraneel
Publicado no Orphanet J Rare Dis (2016)

Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia

Por Raivio, Taneli, Avbelj, Magdalena, McCabe, Mark J., Romero, Christopher J., Dwyer, Andrew A., Tommiska, Johanna, Sykiotis, Gerasimos P., Gregory, Louise C., Diaczok, Daniel, Tziaferi, Vaitsa, Elting, Mariet W., Padidela, Raja, Plummer, Lacey, Martin, Cecilia, Feng, Bihua, Zhang, Chengkang, Zhou, Qun-Yong, Chen, Huaibin, Mohammadi, Moosa, Quinton, Richard, Sidis, Yisrael, Radovick, Sally, Dattani, Mehul T., Pitteloud, Nelly
Publicado em 2012

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

Por Nicholas, Adeline K., Serra, Eva G., Cangul, Hakan, Alyaarubi, Saif, Ullah, Irfan, Schoenmakers, Erik, Deeb, Asma, Habeb, Abdelhadi M., Almaghamsi, Mohammad, Peters, Catherine, Nathwani, Nisha, Aycan, Zehra, Saglam, Halil, Bober, Ece, Dattani, Mehul, Shenoy, Savitha, Murray, Philip G., Babiker, Amir, Willemsen, Ruben, Thankamony, Ajay, Lyons, Greta, Irwin, Rachael, Padidela, Raja, Tharian, Kavitha, Davies, Justin H., Puthi, Vijith, Park, Soo-Mi, Massoud, Ahmed F., Gregory, John W., Albanese, Assunta, Pease-Gevers, Evelien, Martin, Howard, Brugger, Kim, Maher, Eamonn R., Chatterjee, V. Krishna K., Anderson, Carl A., Schoenmakers, Nadia
Publicado no J Clin Endocrinol Metab (2016)

Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

Por Schoenmakers, Erik, Agostini, Maura, Mitchell, Catherine, Schoenmakers, Nadia, Papp, Laura, Rajanayagam, Odelia, Padidela, Raja, Ceron-Gutierrez, Lourdes, Doffinger, Rainer, Prevosto, Claudia, Luan, Jian’an, Montano, Sergio, Lu, Jun, Castanet, Mireille, Clemons, Nick, Groeneveld, Matthijs, Castets, Perrine, Karbaschi, Mahsa, Aitken, Sri, Dixon, Adrian, Williams, Jane, Campi, Irene, Blount, Margaret, Burton, Hannah, Muntoni, Francesco, O’Donovan, Dominic, Dean, Andrew, Warren, Anne, Brierley, Charlotte, Baguley, David, Guicheney, Pascale, Fitzgerald, Rebecca, Coles, Alasdair, Gaston, Hill, Todd, Pamela, Holmgren, Arne, Khanna, Kum Kum, Cooke, Marcus, Semple, Robert, Halsall, David, Wareham, Nicholas, Schwabe, John, Grasso, Lucia, Beck-Peccoz, Paolo, Ogunko, Arthur, Dattani, Mehul, Gurnell, Mark, Chatterjee, Krishna
Publicado em 2010