MULTIPLE PITUITARY HORMONE DEFICIENCY CAUSED BY PIT-I MUTATION AND THE CHALLENGES OF MANAGEMENT IN A DEVELOPING COUNTRY

Por Ayoola, O.O, Oladejo, F.A, Dattani, M, Clayton, P.E
Publicado em 2008

Failure of IGF-I and IGFBP-3 to diagnose growth hormone insufficiency

Por Mitchell, H, Dattani, M, Nanduri, V, Hindmarsh, P, Preece, M, Brook, C
Publicado em 1999

Secondary nephrogenic diabetes insipidus as a complication of inherited renal diseases

Por Bockenhauer, D, van’t Hoff, W, Dattani, M., Lehnhardt, A, Subtirelu, M, Hildebrandt, F, Bichet, DG
Publicado em 2010

Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation

Por Gregory, L. C., Humayun, K. N., Turton, J. P. G., McCabe, M. J., Rhodes, S. J., Dattani, M. T.
Publicado no J Clin Endocrinol Metab (2015)

The proportion of tumour cells is an independent predictor for survival in colorectal cancer patients

Por West, N P, Dattani, M, McShane, P, Hutchins, G, Grabsch, J, Mueller, W, Treanor, D, Quirke, P, Grabsch, H
Publicado em 2010

Partial diazoxide responsiveness in a neonate with hyperinsulinism due to homozygous ABCC8 mutation

Por Kiff, Sarah, Babb, Carolyn, Guemes, Maria, Dastamani, Antonia, Gilbert, Clare, Flanagan, Sarah E, Ellard, Sian, Barton, John, Dattani, M, Shah, Pratik
Publicado no Endocrinol Diabetes Metab Case Rep (2019)

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

Por 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.
Publicado no Clin Endocrinol (Oxf) (2016)

The achiasmia spectrum: congenitally reduced chiasmal decussation

Por Sami, D A, Saunders, D, Thompson, D A, Russell-Eggitt, I M, Nischal, K K, Jeffery, G, Dattani, M, Clement, R A, Liassis, A, Taylor, D S
Publicado em 2005

Growth and hormone profiling in children with congenital melanocytic naevi

Por Waelchli, R., Williams, J., Cole, T., Dattani, M., Hindmarsh, P., Kennedy, H., Martinez, A., Khan, S., Semple, R.K., White, A., Sebire, N., Healy, E., Moore, G., Kinsler, V.A.
Publicado no Br J Dermatol (2015)

Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade.

Por Lindley, K J, Dunne, M J, Kane, C, Shepherd, R M, Squires, P E, James, R F, Johnson, P R, Eckhardt, S, Wakeling, E, Dattani, M, Milla, P J, Aynsley-Green, A
Publicado em 1996

Founder effect in the Horn of Africa for an insulin receptor mutation that may impair receptor recycling

Por Raffan, E., Soos, M. A., Rocha, N., Tuthill, A., Thomsen, A. R., Hyden, C. S., Gregory, J. W., Hindmarsh, P., Dattani, M., Cochran, E., Al Kaabi, J., Gorden, P., Barroso, I., Morling, N., O’Rahilly, S., Semple, R. K.
Publicado em 2011

The current landscape of European registries for rare endocrine conditions

Por Ali, S R, Bryce, J, Cools, M, Korbonits, M, Beun, J G, Taruscio, D, Danne, T, Dattani, M, Dekkers, O M, Linglart, A, Netchine, I, Nordenstrom, A, Patocs, A, Persani, L, Reisch, N, Smyth, A, Sumnik, Z, Visser, W E, Hiort, O, Pereira, A M, Ahmed, S F
Publicado no Eur J Endocrinol (2018)