Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence von Murray, P G, Dattani, M T, Clayton, P E

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The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients von 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

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Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation von Gregory, L. C, Humayun, K. N, Turton, J. P. G, McCabe, M. J, Rhodes, S. J, Dattani, M. T

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SOX3 Deletion in Mouse and Human Is Associated With Persistence of the Craniopharyngeal Canal von 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

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Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency von Turton, J.P., Strom, M., Langham, S., Dattani, M.T., Le Tissier, P.

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The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism von 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.

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Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD) von 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.

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Do centimetres matter? Self-reported versus estimated height measurements in parents von Gozzi, T, Flück, CE, L'Allemand, D, Dattani, MT, Hindmarsh, PC, Mullis, PE

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Rest-Activity Disturbances in Children with Septo-Optic Dysplasia Characterized by Actigraphy and 24-Hour Plasma Melatonin Profiles von Webb, E. A, O'Reilly, M. A, Orgill, J, Dale, N, Salt, A, Gringras, P, Dattani, M. T

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Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland von 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.

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The molecular basis for developmental disorders of the pituitary gland in man von Dattani, Mt, Robinson, Ic

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Surgical treatment of children with hyperparathyroidism: Single centre experience von Alagaratnam, S, Brain, C, Spoudeas, H, Dattani, M.T, Hindmarsh, P, Allgrove, J, Van’t Hoff, W, Kurzawinski, T.R

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Failure of IGF-I and IGFBP-3 to diagnose growth hormone insufficiency von Mitchell, H, Dattani, M T, Nanduri, V, Hindmarsh, P C, Preece, M A, Brook, C G D

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Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia von 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

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Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line von Nuoffer, JM, Fluck, C, Deladoey, J, Eble, A, Dattani, MT, Mullis, PE

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An unusual case of an atypical eating disorder masquerading as a serious multi-systemic illness von MEHTA, A, VINER, R, CHRISTIE, D, NEWSON, T, DATTANI, M. T

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Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse von 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

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DNA testing in patients with GH deficiency at the time of transition von Dattani, M.T.

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A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction von Carvalho, L R, Woods, K S, Mendonca, B B, Marcal, N, Zamparini, AL, Stifani, S, Brickman, J M, Arnhold, IJP, Dattani, M T

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A Randomised Study of Two Doses of Biosynthetic Human Growth Hormone on Final Height of Pubertal Children with Growth Hormone Deficiency von Coelho, R., Brook, C.G.D., Preece, M.A., Stanhope, R.G., Dattani, M.T., Hindmarsh, P.C.

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