A. Mehta

发表

The Use of Somatropin (Recombinant Growth Hormone) in Children of Short Stature

P. Hindmarsh, A. Mehta, 2002, Paediatric drugs.

Congenital hypopituitarism: clinical, molecular and neuroradiological correlates

M. Dattani, P. Hindmarsh, W. K. Chong, 2009, Clinical endocrinology.

Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.

M. Dattani, P. Hindmarsh, P. Clayton, 2009, The Journal of clinical endocrinology and metabolism.

Developmental disorders of the hypothalamus and pituitary gland associated with congenital hypopituitarism.

M. Dattani, A. Mehta, 2008, Best practice & research. Clinical endocrinology & metabolism.

An update on the biochemical diagnosis of congenital ACTH insufficiency

M. Dattani, P. Hindmarsh, A. Mehta, 2005, Clinical endocrinology.

Phenotypic spectrum of patients with congenital disorders of the hypothalamo-pituitary axis.

A. Mehta, 2007 .

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism.

R. Lovell-Badge, M. Dattani, P. Thomas, 2005, American journal of human genetics.

Congenital Disorders of the Hypothalamo‐Pituitary‐Somatotrope Axis

M. Dattani, E. Gevers, A. Mehta, 2010 .

Role of gonadotropin-releasing hormone and human chorionic gonadotropin stimulation tests in differentiating patients with hypogonadotropic hypogonadism from those with constitutional delay of growth and puberty.

M. Dattani, P. Hindmarsh, A. Anazodo, 2009, The Journal of clinical endocrinology and metabolism.

Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.

M. Dattani, P. Clayton, J. Hamilton, 2005, The Journal of clinical endocrinology and metabolism.

The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model

T. Cole, M. Dattani, P. Hindmarsh, 2005, Clinical endocrinology.

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)

M. Dattani, J. Starzyk, A. Tiulpakov, 2005, Clinical endocrinology.

Is the thyrotropin-releasing hormone test necessary in the diagnosis of central hypothyroidism in children.

M. Dattani, P. Hindmarsh, C. Brain, 2003, The Journal of clinical endocrinology and metabolism.

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

M. Dattani, S. Rhodes, P. Swift, 2009, Clinical endocrinology.

Genetic screening in a large cohort of patients with congenital hypopituitarism; current knowledge and future directions

M. Dattani, M. McCabe, E. Webb, 2012 .

Congenital Disorders of the Hypothalamic‐Pituitary Axis

M. Dattani, A. Mehta, 2007 .