The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
Joustra, S. D, Schoenmakers, N, Persani, L, Campi, I, Bonomi, M, Radetti, G, Beck-Peccoz, P, Zhu, H, Davis, T. M. E, Sun, Y, Corssmit, E. P, Appelman-Dijkstra, N. M, Heinen, C. A, Pereira, A. M, Varewijck, A. J, Janssen, J. A. M. J. L, Endert, E, Hennekam, R. C, Lombardi, M. P, Mannens, M. M. A. M, Bak, B, Bernard, D. J, Breuning, M. H, Chatterjee, K, Dattani, M. T, Oostdijk, W, Biermasz, N. R, Wit, J. M, van Trotsenburg, A. S. P
Published in The journal of clinical endocrinology and metabolism (01.12.2013)
Published in The journal of clinical endocrinology and metabolism (01.12.2013)
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Journal Article
SOX3 Deletion in Mouse and Human Is Associated With Persistence of the Craniopharyngeal Canal
Alatzoglou, K. S, Azriyanti, A, Rogers, N, Ryan, F, Curry, N, Noakes, C, Bignell, P, Hall, G. W, Littooij, A. S, Saunders, D, Thomas, P, Stewart, H, Dattani, M. T
Published in The journal of clinical endocrinology and metabolism (01.12.2014)
Published in The journal of clinical endocrinology and metabolism (01.12.2014)
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The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism
Gregory, L.C., Gaston-Massuet, C., Andoniadou, C.L., Carreno, G., Webb, E.A., Kelberman, D., McCabe, M.J., Panagiotakopoulos, L., Saldanha, J.W., Spoudeas, H.A., Torpiano, J., Rossi, M., Raine, J., Canham, N., Martinez-Barbera, J.P., Dattani, M.T.
Published in Clinical endocrinology (Oxford) (01.05.2015)
Published in Clinical endocrinology (Oxford) (01.05.2015)
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Journal Article
Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)
Kelberman, D., Turton, J. P. G., Woods, K. S., Mehta, A., Al-Khawari, M., Greening, J., Swift, P. G. F., Otonkoski, T., Rhodes, S. J., Dattani, M. T.
Published in Clinical endocrinology (Oxford) (01.01.2009)
Published in Clinical endocrinology (Oxford) (01.01.2009)
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Journal Article
Do centimetres matter? Self-reported versus estimated height measurements in parents
Gozzi, T, Flück, CE, L'Allemand, D, Dattani, MT, Hindmarsh, PC, Mullis, PE
Published in Acta Paediatrica (01.04.2010)
Published in Acta Paediatrica (01.04.2010)
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Journal Article
Rest-Activity Disturbances in Children with Septo-Optic Dysplasia Characterized by Actigraphy and 24-Hour Plasma Melatonin Profiles
Webb, E. A, O'Reilly, M. A, Orgill, J, Dale, N, Salt, A, Gringras, P, Dattani, M. T
Published in The journal of clinical endocrinology and metabolism (01.10.2010)
Published in The journal of clinical endocrinology and metabolism (01.10.2010)
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Journal Article
Failure of IGF-I and IGFBP-3 to diagnose growth hormone insufficiency
Mitchell, H, Dattani, M T, Nanduri, V, Hindmarsh, P C, Preece, M A, Brook, C G D
Published in Archives of disease in childhood (01.05.1999)
Published in Archives of disease in childhood (01.05.1999)
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Journal Article
Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland
Nicholas, A.K., Jaleel, S., Lyons, G., Schoenmakers, E., Dattani, M.T., Crowne, E., Bernhard, B., Kirk, J., Roche, E.F., Chatterjee, V.K., Schoenmakers, N.
Published in Clinical endocrinology (Oxford) (01.03.2017)
Published in Clinical endocrinology (Oxford) (01.03.2017)
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Journal Article
Surgical treatment of children with hyperparathyroidism: Single centre experience
Alagaratnam, S, Brain, C, Spoudeas, H, Dattani, M.T, Hindmarsh, P, Allgrove, J, Van’t Hoff, W, Kurzawinski, T.R
Published in Journal of pediatric surgery (01.11.2014)
Published in Journal of pediatric surgery (01.11.2014)
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Journal Article
An unusual case of an atypical eating disorder masquerading as a serious multi-systemic illness
MEHTA, A, VINER, R, CHRISTIE, D, NEWSON, T, DATTANI, M. T
Published in Acta pædiatrica (Oslo) (01.05.2004)
Published in Acta pædiatrica (Oslo) (01.05.2004)
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Journal Article
Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line
Nuoffer, JM, Fluck, C, Deladoey, J, Eble, A, Dattani, MT, Mullis, PE
Published in Journal of endocrinology (01.05.2000)
Published in Journal of endocrinology (01.05.2000)
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Journal Article
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia
THOMAS, Paul Q, DATTANI, Mehul T, STANHOPE, Richard, FORREST, Susan, ROBINSON, Iain C. A. F, BEDDINGTON, Rosa S. P, BRICKMAN, Joshua M, MCNAY, David, WARNE, Garry, ZACHARIN, Margaret, CAMERON, Fergus, HURST, Jane, WOODS, Katie, DUNGER, David
Published in Human molecular genetics (2001)
Published in Human molecular genetics (2001)
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Journal Article
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
Robinson, Iain C. A. F, Dattani, Mehul T, Martinez-Barbera, Juan-Pedro, Thomas, Paul Q, Brickman, Joshua M, Gupta, Raj, Mårtensson, Inga-Lill, Toresson, Håkan, Fox, Margaret, Wales, Jerry K. H, Hindmarsh, Peter C, Krauss, Stefan, Beddington, Rosa S. P
Published in Nature genetics (01.06.1998)
Published in Nature genetics (01.06.1998)
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