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Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs)

Gut, 2012-01, Vol.61 (1), p.6-32

2012

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Genetics of parathyroid tumours

Journal of internal medicine, 2016-12, Vol.280 (6), p.574-583

Thakker, R. V.

2016

Volltextzugriff (PDF)

Parafibromin – functional insights

Journal of internal medicine, 2009-07, Vol.266 (1), p.84-98

2009

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Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality

Acta biomaterialia, 2018-08, Vol.76, p.295-307

2018

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Genetic Contribution to Bone Metabolism, Calcium Excretion, and Vitamin D and Parathyroid Hormone Regulation

Journal of bone and mineral research, 2001-02, Vol.16 (2), p.371-378

2001

Volltextzugriff (PDF)

Genetics of neuroendocrine and carcinoid tumours

Endocrine-related cancer, 2003-12, Vol.10 (4), p.437-450

2003

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Guidelines for diagnosis and therapy of MEN type 1 and type 2

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5658-5671

2001

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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome

Journal of internal medicine, 2005-01, Vol.257 (1), p.18-26

2005

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Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone

Bone (New York, N.Y.), 2013-02, Vol.52 (2), p.689-698

2013

Volltextzugriff (PDF)

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours

Clinical endocrinology (Oxford), 2006-03, Vol.64 (3), p.299-306

2006

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UROMODULIN Mutations Cause Familial Juvenile Hyperuricemic Nephropathy

The journal of clinical endocrinology and metabolism, 2003-03, Vol.88 (3), p.1398-1401

2003

Volltextzugriff (PDF)

Phase II study of single agent capecitabine in the treatment of metastatic non-pancreatic neuroendocrine tumours

British journal of cancer, 2011-03, Vol.104 (7), p.1067-1070

2011

Volltextzugriff (PDF)

GATA3 haplo-insufficiency causes human HDR syndrome

Nature (London), 2000-07, Vol.406 (6794), p.419-422

2000

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Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal

Oncogene, 2007-02, Vol.26 (8), p.1213-1221

2007

Volltextzugriff (PDF)

Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1

American journal of human genetics, 1998-02, Vol.62 (2), p.232-244

1998

Volltextzugriff (PDF)

Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development

Bone (New York, N.Y.), 2012-09, Vol.51 (3), p.553-562

2012

Volltextzugriff (PDF)

A MEN1 pancreatic neuroendocrine tumour mouse model under temporal control

Endocrine Connections, 2017-05, Vol.6 (4), p.232-242

2017

Volltextzugriff (PDF)

Multiple endocrine neoplasia type 1

Endocrine-related cancer, 1999-12, Vol.6 (4), p.449-473

1999

Volltextzugriff (PDF)

Developments for funding clinical research in the UK

The Lancet (British edition), 2008-08, Vol.372 (9638), p.518-519

2008

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Intra-Renal and Subcellular Distribution of the Human Chloride Channel, CLC-5, Reveals a Pathophysiological Basis for Dent's Disease

Human molecular genetics, 1999-02, Vol.8 (2), p.247-257

1999

Volltextzugriff (PDF)

Multiple endocrine neoplasia--syndromes of the twentieth century

The journal of clinical endocrinology and metabolism, 1998-08, Vol.83 (8), p.2617-2620

Thakker, R V

1998

Volltextzugriff (PDF)

Animal models of pituitary neoplasia

Molecular and cellular endocrinology, 2016-02, Vol.421, p.68-81

2016

Volltextzugriff (PDF)

Multiple endocrine neoplasia type 1

Indian journal of endocrinology and metabolism, 2012-12, Vol.16 (Suppl 2), p.S272-S274

Thakker, R V

2012

Volltextzugriff (PDF)

Calcium-sensing receptor: Role in health and disease

Indian journal of endocrinology and metabolism, 2012-12, Vol.16 (Suppl 2), p.S213-S216

Thakker, R V

2012

Volltextzugriff (PDF)

miR-15a/miR-16-1 expression inversely correlates with cyclin D1 levels in Men1 pituitary NETs

Journal of endocrinology, 2019-01, Vol.240 (1), p.41-50

2019

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Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs)

Genetics of parathyroid tumours

Parafibromin – functional insights

Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality

Genetic Contribution to Bone Metabolism, Calcium Excretion, and Vitamin D and Parathyroid Hormone Regulation

Genetics of neuroendocrine and carcinoid tumours

Guidelines for diagnosis and therapy of MEN type 1 and type 2

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome

Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours

UROMODULIN Mutations Cause Familial Juvenile Hyperuricemic Nephropathy

Phase II study of single agent capecitabine in the treatment of metastatic non-pancreatic neuroendocrine tumours

GATA3 haplo-insufficiency causes human HDR syndrome

Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal

Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1

Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development

A MEN1 pancreatic neuroendocrine tumour mouse model under temporal control

Multiple endocrine neoplasia type 1

Developments for funding clinical research in the UK

Intra-Renal and Subcellular Distribution of the Human Chloride Channel, CLC-5, Reveals a Pathophysiological Basis for Dent's Disease

Multiple endocrine neoplasia--syndromes of the twentieth century

Animal models of pituitary neoplasia

Multiple endocrine neoplasia type 1

Calcium-sensing receptor: Role in health and disease

miR-15a/miR-16-1 expression inversely correlates with cyclin D1 levels in Men1 pituitary NETs

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