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Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.121-130

Dattani, Mehul T.

2005

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

Clinical endocrinology (Oxford), 2015-05, Vol.82 (5), p.728-738

2015

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Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

American journal of human genetics, 2005-05, Vol.76 (5), p.833-849

2005

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Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency

Clinical endocrinology (Oxford), 2012-03, Vol.76 (3), p.387-393

2012

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

Human molecular genetics, 2001, Vol.10 (1), p.39-45

2001

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

Nature genetics, 1998-06, Vol.19 (2), p.125-133

1998

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Molecular spectrum of TSH[beta] subunit gene defects in central hypothyroidism in the UK and Ireland

Clinical endocrinology (Oxford), 2017-03, Vol.86 (3), p.410

2017

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Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2005-08, Vol.90 (8), p.4762-4770

2005

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A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

The Journal of clinical investigation, 2003-10, Vol.112 (8), p.1192-1201

2003

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Is the Thyrotropin-Releasing Hormone Test Necessary in the Diagnosis of Central Hypothyroidism in Children

The journal of clinical endocrinology and metabolism, 2003-12, Vol.88 (12), p.5696-5703

2003

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

Clinical endocrinology (Oxford), 2005-07, Vol.63 (1), p.10-18

2005

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Blood pressure in children and adolescents with congenital adrenal hyperplasia (21-hydroxylase deficiency): a preliminary report

Clinical endocrinology (Oxford), 2003-05, Vol.58 (5), p.589-596

2003

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Use of growth hormone in children

Nature clinical practice. Endocrinology & metabolism, 2006-05, Vol.2 (5), p.260-268

2006

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Novel insights into the aetiology and pathogenesis of hypopituitarism

Hormone research, 2004-01, Vol.62 Suppl 3 (Suppl. 3), p.1-13

Dattani, Mehul T

2004

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Do centimetres matter? Self-reported versus estimated height measurements in parents

Acta Paediatrica, 2010-04, Vol.99 (4), p.569-574

2010

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The molecular basis for developmental disorders of the pituitary gland in man

Clinical genetics, 2000-05, Vol.57 (5), p.337-346

2000

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

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.223-231

2005

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An update on the biochemical diagnosis of congenital ACTH insufficiency

Clinical endocrinology (Oxford), 2005-03, Vol.62 (3), p.307-314

2005

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Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line

Journal of endocrinology, 2000-05, Vol.165 (2), p.313-320

2000

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GH deficiency might be associated with normal height in PROP1 deficiency

Clinical endocrinology (Oxford), 2002-08, Vol.57 (2), p.157-158

Dattani, Mehul T.

2002

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

Archives of disease in childhood, 1999-05, Vol.80 (5), p.443-447

1999

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DNA testing in patients with GH deficiency at the time of transition

Growth hormone & IGF research, 2003-08, Vol.13, p.S122-S129

Dattani, M.T.

2003

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Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene

Journal of Pediatric Endocrinology and Metabolism, 2003-12, Vol.16 (9), p.1207

Dattani, M T

2003

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Genetic evaluation supports differential diagnosis in adolescent patients with delayed puberty

Yearbook of Paediatric Endocrinology, 2022-09

2022

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Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?

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

Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency

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

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

Molecular spectrum of TSH[beta] subunit gene defects in central hypothyroidism in the UK and Ireland

Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency

A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

Is the Thyrotropin-Releasing Hormone Test Necessary in the Diagnosis of Central Hypothyroidism in Children

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

Blood pressure in children and adolescents with congenital adrenal hyperplasia (21-hydroxylase deficiency): a preliminary report

Use of growth hormone in children

Novel insights into the aetiology and pathogenesis of hypopituitarism

Do centimetres matter? Self-reported versus estimated height measurements in parents

The molecular basis for developmental disorders of the pituitary gland in man

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

An update on the biochemical diagnosis of congenital ACTH insufficiency

Loss-of-function mutations in the immunoglobulin superfamily member 1 gene ( IGSF1 ) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement

Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line

GH deficiency might be associated with normal height in PROP1 deficiency

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

DNA testing in patients with GH deficiency at the time of transition

Borjeson-Forssman-Lehmann syndrome: a novel pituitary phenotype due to mutation in a novel gene

Genetic evaluation supports differential diagnosis in adolescent patients with delayed puberty

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