المؤلفون: halford, J, Brown, A, Clare, K, Ells, L, Ghosh, A, Giri, D, Hughes, C, Senniappan, S

وصف الملف: text

Relation: https://eprints.leedsbeckett.ac.uk/id/eprint/11090/1/InsightsFromTheActionTeensStudyASurveyOfAdolescentsLivingWithObesityTheirCaregiversAndHealthcareProfessionalsInTheUkPV-ELLS.pdf; halford, J and Brown, A and Clare, K and Ells, L and Ghosh, A and Giri, D and Hughes, C and Senniappan, S (2024) Insights from the ACTION Teens Study: a survey of adolescents living with obesity, their caregivers and healthcare professionals in the UK. BMJ Open, 14 (7). pp. 1-10. ISSN 2044-6055 DOI: https://doi.org/10.1136/bmjopen-2024-086391

الاتاحة: https://eprints.leedsbeckett.ac.uk/id/eprint/11090/
https://eprints.leedsbeckett.ac.uk/id/eprint/11090/1/InsightsFromTheActionTeensStudyASurveyOfAdolescentsLivingWithObesityTheirCaregiversAndHealthcareProfessionalsInTheUkPV-ELLS.pdf

المؤلفون: Dastamani, A, Yau, D, Gilbert, C, Morgan, K, De Coppi, P, Craigie, RJ, Bomanji, J, Biassoni, L, Sajjan, R, Flanagan, SE, Houghton, JAL, Senniappan, S, Didi, M, Dunne, MJ, Banerjee, I, Shah, P

المصدر: Journal of the Endocrine Society , 6 (6) pp. 1-7. (2022)

مصطلحات موضوعية: ABCC8 gene, focal lesion, hyperinsulinemic hypoglycemia

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/10179154/1/bvac033.pdf; https://discovery.ucl.ac.uk/id/eprint/10179154/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10179154/1/bvac033.pdf
https://discovery.ucl.ac.uk/id/eprint/10179154/

المؤلفون: Karuppanan Senniappan, S.

مصطلحات موضوعية: 618.92

URL الوصول: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.626703

المؤلفون: Shaikh, M. G., Lucas-Herald, A. K., Dastamani, A., Salomon Estebanez, M., Senniappan, S., Abid, N., Ahmad, S., Alexander, S., Avatapalle, B., Awan, N., Blair, H., Boyle, R., Chesover, A., Cochrane, B., Craigie, R., Cunjamalay, A., Dearman, S., De Coppi, P., Erlandson-Parry, K., Flanagan, S. E., Gilbert, C., Gilligan, N., Hall, C., Houghton, J., Kapoor, R., McDevitt, H., Mohamed, Z., Morgan, K., Nicholson, J., Nikiforovski, A., O'Shea, E., Shah, P., Wilson, K., Worth, C., Worthington, S., Banerjee, I.

مصطلحات موضوعية: Child, Infant, Humans, Preschool, Consensus, Congenital Hyperinsulinism/diagnosis/genetics/therapy, Pancreatectomy, United Kingdom, congenital hyperinsulinism, glucose, hypoglycaemia, patient organisation, standardised practice, treatment

Relation: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/38027197/; Shaikh MG, Lucas-Herald AK, Dastamani A, Salomon Estebanez M, Senniappan S, Abid N, et al. Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus. Front Endocrinol (Lausanne). 2023;14:1231043.; Frontiers in endocrinology; PMC10646160; https://hdl.handle.net/11287/623046

الاتاحة: https://hdl.handle.net/11287/623046
https://doi.org/10.3389/fendo.2023.1231043

المؤلفون: Yau D, Laver TW, Dastamani A, Senniappan S, Houghton JAL, Shaikh G, Cheetham T, Mushtaq T, Kapoor RR, Randell T, Ellard S, Shah P, Banerjee I, Flanagan SE

المصدر: PLoS ONE, 2020

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/263779; https://eprints.ncl.ac.uk/fulltext.aspx?url=263779/4328FA94-FBF5-4493-95F8-9A4F5983175F.pdf&pub_id=263779

الاتاحة: https://eprints.ncl.ac.uk/263779

المؤلفون: Banerjee, I, Senniappan, S, Laver, TW, Caswell, R, Zenker, M, Mohnike, K, Cheetham, T, Wakeling, MN, Ismail, D, Lennerz, B, Splitt, M, Berberoğlu, M, Empting, S, Wabitsch, M, Pötzsch, S, Shah, P, Siklar, Z, Verge, CF, Weedon, MN, Ellard, S, Hussain, K, Flanagan, SE

مصطلحات موضوعية: Chromosome 9p, Deletions, Hyperinsulinism, Hypoglycaemia

Relation: Vol. 4, article 149; 105636; http://hdl.handle.net/10871/122710; Wellcome Open Research

الاتاحة: http://hdl.handle.net/10871/122710
https://doi.org/10.12688/wellcomeopenres.15465.2

المؤلفون: Yau, D, Laver, TW, Dastamani, A, Senniappan, S, Houghton, JAL, Shaikh, G, Cheetham, T, Mushtaq, T, Kapoor, RR, Randell, T, Ellard, S, Shah, P, Banerjee, I, Flanagan, SE

Relation: Vol. 15, pp. e0228417 - e0228417; MR/M023265/1; http://hdl.handle.net/10871/40767; PLOS ONE

الاتاحة: http://hdl.handle.net/10871/40767
https://doi.org/10.1371/journal.pone.0228417

المؤلفون: Giri, D, Bockenhauer, D, Deshpande, C, Achermann, JC, Taylor, NF, Rumsby, G, Morgan, H, Senniappan, S, Ajzensztejn, M

المصدر: Hormone Research in Paediatrics (2020) (In press).

مصطلحات موضوعية: HSD3B2 deficiency · Bartter syndrome · Maternal isodisomy

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10100564/3/Achermann_giri%20et%20al%20revised.pdf; https://discovery.ucl.ac.uk/id/eprint/10100564/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10100564/3/Achermann_giri%20et%20al%20revised.pdf
https://discovery.ucl.ac.uk/id/eprint/10100564/

المؤلفون: Varughese, R, Bonomi, M, Butler, G, Candler, T, Cole, T, Dattani, M, Heger, S, Jayasena, C, Krone, N, Nordenstrom, A, Rohayem, J, Senniappan, S, Wood, C, Bryce, J, Ahmed, SF, Howard, SR

المصدر: SEXUAL DEVELOPMENT. 17:95-96

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:159459808

المؤلفون: Giri , D, Roncaroli, Federico, Sinha , A, Didi , M, Senniappan , S

المصدر: Giri , D , Roncaroli , F , Sinha , A , Didi , M & Senniappan , S 2017 , ' Silent Crooke's cell corticotroph adenoma of the pituitary gland presenting as delayed puberty ' , Endocrinology, diabetes & metabolism case reports . https://doi.org/10.1530/EDM-16-0153

الاتاحة: https://research.manchester.ac.uk/en/publications/ccd3a665-acbb-4b63-8ffa-cfa1a7c1c3be
https://doi.org/10.1530/EDM-16-0153

المؤلفون: Improda, N, Ponmani, C, Schoenmakers, N, Senniappan, S, Atterbury, A, Barnicoat, A, Chatterjee, K, Dattani, MT

المصدر: Hormone Research in Paediatrics , 88 (2) pp. 172-178. (2017)

مصطلحات موضوعية: 21-Hydroxylase, Thyroglobulin, Adrenal adenoma, Developmental delay

وصف الملف: text; image

Relation: https://discovery.ucl.ac.uk/id/eprint/1549842/11/Dattani_intrafamilial%20phenotypic.pdf; https://discovery.ucl.ac.uk/id/eprint/1549842/6/Figure%201.tif; https://discovery.ucl.ac.uk/id/eprint/1549842/1/Figure%202.tif; https://discovery.ucl.ac.uk/id/eprint/1549842/17/Dattani_Table%201.pdf; https://discovery.ucl.ac.uk/id/eprint/1549842/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/1549842/11/Dattani_intrafamilial%20phenotypic.pdf
https://discovery.ucl.ac.uk/id/eprint/1549842/6/Figure%201.tif
https://discovery.ucl.ac.uk/id/eprint/1549842/1/Figure%202.tif
https://discovery.ucl.ac.uk/id/eprint/1549842/17/Dattani_Table%201.pdf
https://discovery.ucl.ac.uk/id/eprint/1549842/

المؤلفون: Park, J, Titman, A, Lancaster, GA, Selvarajah, B, Collingwood, C, Powell, D, Das, U, Dharmaraj, P, Didi, M, Senniappan, S, Blair, J

مصطلحات موضوعية: R Medicine (General), R735 Medical education. Medical schools. Research

وصف الملف: text

Relation: https://eprints.keele.ac.uk/id/eprint/10970/1/Park,%20Titman,%20Lancaster%20et%20al%20FINAL%20LDSST%20paper%202022.pdf; https://eprints.keele.ac.uk/id/eprint/10970/7/Park,%20Titman,%20Lancaster%20et%20al%20FINAL%20LDSST%20paper%202022.docx; Park, J, Titman, A, Lancaster, GA orcid:0000-0002-6957-6177 , Selvarajah, B, Collingwood, C, Powell, D, Das, U, Dharmaraj, P, Didi, M, Senniappan, S and Blair, J (2022) Baseline and Peak Cortisol Response to the Low-Dose Short Synacthen Test Relates to Indication for Testing, Age, and Sex. Journal of the Endocrine Society, 6 (6). bvac043 - ?.

الاتاحة: https://eprints.keele.ac.uk/id/eprint/10970/
https://eprints.keele.ac.uk/id/eprint/10970/1/Park,%20Titman,%20Lancaster%20et%20al%20FINAL%20LDSST%20paper%202022.pdf
https://eprints.keele.ac.uk/id/eprint/10970/7/Park,%20Titman,%20Lancaster%20et%20al%20FINAL%20LDSST%20paper%202022.docx
https://academic.oup.com/jes/article-abstract/6/6/bvac043/6550852?redirectedFrom=fulltext
https://doi.org/10.1210/jendso/bvac043

المؤلفون: Arya, VB, Senniappan, S, Demirbilek, H, Alam, S, Flanagan, SE, Ellard, S, Hussain, K

مصطلحات موضوعية: Anthropometry, Base Sequence, Child, Congenital Hyperinsulinism, Diabetes Mellitus, Type 1, Enzyme-Linked Immunosorbent Assay, Exocrine Pancreatic Insufficiency, Humans, Hypoglycemia, Kaplan-Meier Estimate, London, Microsatellite Repeats, Molecular Sequence Data, Pancreas, Pancreatectomy, Pancreatic Elastase, Polymerase Chain Reaction, Potassium Channels, Inwardly Rectifying, Sequence Analysis, DNA, Sulfonylurea Receptors

Relation: http://www.ncbi.nlm.nih.gov/pubmed/24840042; http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098054; Vol. 9, No. 5, Article no. e98054; http://hdl.handle.net/10871/20434; PLoS One

الاتاحة: http://hdl.handle.net/10871/20434
https://doi.org/10.1371/journal.pone.0098054

المؤلفون: Arya, VB, Rahman, S, Senniappan, S, Flanagan, SE, Ellard, S, Hussain, K

المصدر: Diabet Med , 31 (3) e11-e15. (2014)

وصف الملف: application/pdf

Relation: https://discovery.ucl.ac.uk/id/eprint/1425047/1/dme12369.pdf; https://discovery.ucl.ac.uk/id/eprint/1425047/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/1425047/1/dme12369.pdf
https://discovery.ucl.ac.uk/id/eprint/1425047/

المؤلفون: Arya, V. B., Rahman, S., Senniappan, S., Flanagan, S. E., Ellard, S., Hussain, K.

المساهمون: Medical Council

المصدر: Diabetic Medicine ; volume 31, issue 3 ; ISSN 0742-3071 1464-5491

الاتاحة: http://dx.doi.org/10.1111/dme.12369
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fdme.12369
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dme.12369

المؤلفون: Shaikh Mg, Aftab S, Dastamani A, Pintus D, Giardini A, Shah P, Bath L, Swinburne C, Banerjee I, Chen Sc, Christov G, Yau D, Hunter L, Senniappan S

المصدر: Yearbook of Paediatric Endocrinology.

مصطلحات موضوعية: Hyperinsulinaemic hypoglycaemia, Pediatrics, medicine.medical_specialty, business.industry, Diazoxide, Medicine, Multi centre, business, medicine.disease, Pulmonary hypertension, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::aaed4644099ed605618ed4ae51bf5a15
https://doi.org/10.1530/ey.17.2.2

المؤلفون: Dimitri, P., Fernandez-Luque, L., Banerjee, I., Bergada, I., Calliari, L. E., Dahlgren, Jovanna, 1964, de Arriba, A., Lapatto, R., Reinehr, T., Senniappan, S., Thomas-Teinturier, C., Tsai, M. C., Zaini, A. A., Bagha, M., Koledova, E.

المصدر: Journal of Medical Internet Research. 23(5)

مصطلحات موضوعية: Clinical Medicine, Klinisk medicin, eHealth tools, pediatric growth disorders, referral and diagnosis, growth hormone therapy, adherence to treatment, workshop discussions, eHealth, pediatrics, growth failure, growth hormone, short children, health intervention, adolescents, care, deficiency, guidelines, management, adherence, transition, support, Health Care Sciences & Services, Medical Informatics

URL الوصول: https://gup.ub.gu.se/publication/306979

المؤلفون: Ghosh A, Schlecht H, Heptinstall LE, Bassett JK, Cartwright E, Bhaskar SS, Urquhart J, Broomfield A, Morris AAM, Jameson E, Schwahn BC, Walter JH, Douzgou S, Murphy H, Hendriksz C, Sharma R, Wilcox G, Crushell E, Monavari AA, Martin R, Doolan A, Senniappan S, Ramsden SC, Jones SA, Banka S

المصدر: Archives of Disease in Childhood, May 03, 2017

Relation: https://eprints.ncl.ac.uk/240352

الاتاحة: https://eprints.ncl.ac.uk/240352

المؤلفون: Giri, D, Vignola, ML, Gualtieri, A, Scagliotti, V, McNamara, P, Peak, M, Didi, M, Gaston-Massuet, C, Senniappan, S

مصطلحات موضوعية: Adult, Animals, Child, Preschool, Craniofacial Abnormalities, Female, HEK293 Cells, Hepatocyte Nuclear Factor 3-beta, Humans, Hyperinsulinism, Hypopituitarism, Male, Mice, Mutation, Pregnancy, Transcription Factors, Transfection

وصف الملف: 4315 - 4326

Relation: Hum Mol Genet; https://qmro.qmul.ac.uk/xmlui/handle/123456789/61680

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/61680
https://doi.org/10.1093/hmg/ddx318

المؤلفون: Arya, V.B., Guemes, M., Nessa, A., Alam, S., Shah, P., Gilbert, C., Senniappan, S., Flanagan, Sarah, Ellard, Sian, Hussain, K.

مصطلحات موضوعية: Wessex Classification Subject Headings::Oncology. Pathology.::Genetics

Relation: http://www.eje-online.org/cgi/pmidlookup?view=long&pmid=25201519; Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations. 2014, 171 (6):685-95 Eur. J. Endocrinol.; http://hdl.handle.net/11287/618202; European journal of endocrinology / European Federation of Endocrine Societies

الاتاحة: http://hdl.handle.net/11287/618202
https://doi.org/10.1530/EJE-14-0353