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Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence

Archives of disease in childhood, 2016-01, Vol.101 (1), p.96-100

2016

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The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients

The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.4942-4952

2013

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

The journal of clinical endocrinology and metabolism, 2015-06, Vol.100 (6), p.2158-2164

2015

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

The journal of clinical endocrinology and metabolism, 2014-12, Vol.99 (12), p.E2702-E2708

2014

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

Clinical endocrinology (Oxford), 2009-01, Vol.70 (1), p.96-103

2009

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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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Rest-Activity Disturbances in Children with Septo-Optic Dysplasia Characterized by Actigraphy and 24-Hour Plasma Melatonin Profiles

The journal of clinical endocrinology and metabolism, 2010-10, Vol.95 (10), p.E198-E203

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

Clinical endocrinology (Oxford), 2017-03, Vol.86 (3), p.410-418

2017

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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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Surgical treatment of children with hyperparathyroidism: Single centre experience

Journal of pediatric surgery, 2014-11, Vol.49 (11), p.1539-1543

2014

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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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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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An unusual case of an atypical eating disorder masquerading as a serious multi-systemic illness

Acta pædiatrica (Oslo), 2004-05, Vol.93 (5), p.714-716

2004

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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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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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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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A randomised study of two doses of biosynthetic human growth hormone on final height of pubertal children with growth hormone deficiency

Hormone research, 2008-01, Vol.70 (2), p.85-88

2008

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The Role of SOX2 in Hypogonadotropic Hypogonadism

Sexual development, 2008-01, Vol.2 (4-5), p.194-199

2008

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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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The measurement of growth hormone bioactivity in patient serum using an eluted stain assay

The journal of clinical endocrinology and metabolism, 1995-09, Vol.80 (9), p.2675-2683

1995

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Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

The New England journal of medicine, 2007-01, Vol.356 (3), p.237-247

2007

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Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence

The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients

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

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

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

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

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

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

Rest-Activity Disturbances in Children with Septo-Optic Dysplasia Characterized by Actigraphy and 24-Hour Plasma Melatonin Profiles

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

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

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

Surgical treatment of children with hyperparathyroidism: Single centre experience

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

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

An unusual case of an atypical eating disorder masquerading as a serious multi-systemic illness

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

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

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

A randomised study of two doses of biosynthetic human growth hormone on final height of pubertal children with growth hormone deficiency

The Role of SOX2 in Hypogonadotropic Hypogonadism

Novel insights into the aetiology and pathogenesis of hypopituitarism

The measurement of growth hormone bioactivity in patient serum using an eluted stain assay

Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

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