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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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Understanding hypopituitarism

Paediatrics and child health, 2015-07, Vol.25 (7), p.295-301

2015

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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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Metastatic prostate cancer presenting as incidental pelvic lymphadenopathy – a report of three cases with literature review

Radiology case reports, 2022-06, Vol.17 (6), p.2247-2252

2022

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P03-32 Height outcome in late diagnosed growth hormone (GH) deficiency type II with GH-1 gene mutation (GH-R178H) affecting secretion and action: Use of higher than standard dose GH and pubertal suppression to optimise final height

Growth hormone & IGF research, 2012-10, Vol.22, p.S82-S83

2012

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Did cinacalcet help in the management of neonatal severe primary hyperparathyroidism secondary to a novel homozygous inactivating mutation of the calcium-sensing receptor?

Bone (New York, N.Y.), 2009-07, Vol.45, p.S91-S92

2009

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Understanding hypopituitarism

Paediatrics and child health, 2011-07, Vol.21 (7), p.289-294

2011

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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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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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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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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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A randomised study of the effect of two doses of biosynthetic human growth hormone on final height of children with familial short stature

Hormone research, 2008-01, Vol.70 (2), p.89-92

2008

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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 & metabolism : JPEM, 2003-12, Vol.16 (9), p.1207

Dattani, M T

2003

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Diagnosis of Growth Hormone Deficiency

Endocrine development, 2010, Vol.18, p.55-66

2010

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Septo-Optic Dysplasia and Related Malformations

Hypothalamic-Pituitary Development, 2001, Vol.4, p.77-93

2001

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Priming of hypoxia-inducible factor by neuronal nitric oxide synthase is essential for adaptive responses to severe anemia

Proceedings of the National Academy of Sciences - PNAS, 2011-10, Vol.108 (42), p.17544-17549

2011

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Reassessing the risk of hemodilutional anemia: Some new pieces to an old puzzle

Canadian journal of anesthesia, 2010-08, Vol.57 (8), p.779-791

2010

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Surgical treatment of children with hyperparathyroidism: Single centre experience

Understanding hypopituitarism

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

Metastatic prostate cancer presenting as incidental pelvic lymphadenopathy – a report of three cases with literature review

P03-32 Height outcome in late diagnosed growth hormone (GH) deficiency type II with GH-1 gene mutation (GH-R178H) affecting secretion and action: Use of higher than standard dose GH and pubertal suppression to optimise final height

Did cinacalcet help in the management of neonatal severe primary hyperparathyroidism secondary to a novel homozygous inactivating mutation of the calcium-sensing receptor?

Understanding hypopituitarism

The Role of SOX2 in Hypogonadotropic Hypogonadism

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

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

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

A randomised study of the effect of two doses of biosynthetic human growth hormone on final height of children with familial short stature

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

Diagnosis of Growth Hormone Deficiency

Septo-Optic Dysplasia and Related Malformations

Priming of hypoxia-inducible factor by neuronal nitric oxide synthase is essential for adaptive responses to severe anemia

Reassessing the risk of hemodilutional anemia: Some new pieces to an old puzzle

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