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Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis: immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays

European journal of endocrinology, 2012-03, Vol.166 (3), p.391

2012

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Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (3), p.949-954

2007

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Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1

Autoimmunity (Chur, Switzerland), 2017-05, Vol.50 (4), p.223-231

2017

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Phenotype-Genotype Correlations in a Series of Wolfram Syndrome Families

Diabetes care, 2004-08, Vol.27 (8), p.2003-2009

2004

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A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A

Journal of medical genetics, 2015-04, Vol.52 (4), p.269-274

2015

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Recurrences of Pituitary Adenomas or Second De Novo Tumors: Comparisons with First Tumors

World neurosurgery, 2018-11, Vol.119, p.e118-e124

2018

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Changes in Altitude Cause Unintended Insulin Delivery From Insulin Pumps: Mechanisms and implications

Diabetes care, 2011-09, Vol.34 (9), p.1932-1933

2011

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Low dose growth hormone treatment in infants and toddlers with Prader-Willi syndrome is comparable to higher dosage regimens

Growth hormone & IGF research, 2017-06, Vol.34, p.1-7

2017

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Non-invasive detection of microvascular changes in a paediatric and adolescent population with type 1 diabetes: a pilot cross-sectional study

BMC endocrine disorders, 2013-10, Vol.13 (1), p.41-41, Article 41

2013

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Population-based incidence of diabetes in Australian youth aged 10-18 yr: increase in type 1 diabetes but not type 2 diabetes

Pediatric diabetes, 2014-12, Vol.15 (8), p.585-590

2014

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Pituitary Autoimmunity in Patients with Sheehan’s Syndrome

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4137-4141

2002

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Normal Cortisol Response on Low-Dose Synacthen (1 μg) Test in Children with Prader Willi Syndrome

The journal of clinical endocrinology and metabolism, 2010-12, Vol.95 (12), p.E464-E467

2010

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A rare case of pituitary infarction leading to spontaneous tumour resolution and CSF-sella syndrome in an 11-year-old girl and a review of the paediatric literature

Journal of pediatric endocrinology & metabolism : JPEM, 2014-09, Vol.27 (9-10), p.939

2014

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Increased detection of cystic-fibrosis-related diabetes in Australia

Archives of disease in childhood, 2011-09, Vol.96 (9), p.823-826

2011

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Sudden death in growth hormone–treated children with Prader-Willi syndrome

The Journal of pediatrics, 2004-01, Vol.144 (1), p.129-131

2004

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Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysitis

Pituitary, 2014-02, Vol.17 (1), p.22-29

2014

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Pituitary autoantibodies in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

Acta bio-medica de l'Ateneo Parmense, 2007-04, Vol.78 Suppl 1, p.248

2007

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A Compound Heterozygote Case of Type II Aldosterone Synthase Deficiency

The journal of clinical endocrinology and metabolism, 2003-06, Vol.88 (6), p.2518-2526

2003

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Changes in Altitude Cause Unintended Insulin Delivery From Insulin Pumps

Diabetes care, 2011-09, Vol.34 (9), p.1932-1933

2011

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The A, B, C, D of hypercalcaemia in Down syndrome

BMJ case reports, 2009, Vol.2009 (mar02 1), p.bcr0620080232-bcr0620080232

2009

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Global inequalities in paediatric endocrine practice: statement of minimal acceptable care. Statement from the international societies for paediatric endocrinology

Hormone research, 2006-03, Vol.65 (3), p.111-113

2006

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Identification of the 49-kDa Autoantigen Associated with Lymphocytic Hypophysitis as α-Enolase

The journal of clinical endocrinology and metabolism, 2002-02, Vol.87 (2), p.752-757

2002

Volltextzugriff (PDF)

Cytosolic autoantigens in lymphocytic hypophysitis

The journal of clinical endocrinology and metabolism, 1998-02, Vol.83 (2), p.609-618

CROCK, P. A

1998

Volltextzugriff (PDF)

Response to low dose growth hormone treatment in infants and toddlers with Prader-Willi Syndrome

International journal of pediatric endocrinology, 2015-04, Vol.2015 (S1), p.O31-O31, Article O31

2015

Volltextzugriff (PDF)

Multiple pituitary hormone gradients from inferior petrosal sinus sampling in Cushing's disease

Acta endocrinologica (Copenhagen), 1988-09, Vol.119 (1), p.75

1988

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Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis: immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays

Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1

Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1

Phenotype-Genotype Correlations in a Series of Wolfram Syndrome Families

A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A

Recurrences of Pituitary Adenomas or Second De Novo Tumors: Comparisons with First Tumors

Changes in Altitude Cause Unintended Insulin Delivery From Insulin Pumps: Mechanisms and implications

Low dose growth hormone treatment in infants and toddlers with Prader-Willi syndrome is comparable to higher dosage regimens

Non-invasive detection of microvascular changes in a paediatric and adolescent population with type 1 diabetes: a pilot cross-sectional study

Population-based incidence of diabetes in Australian youth aged 10-18 yr: increase in type 1 diabetes but not type 2 diabetes

Pituitary Autoimmunity in Patients with Sheehan’s Syndrome

Normal Cortisol Response on Low-Dose Synacthen (1 μg) Test in Children with Prader Willi Syndrome

A rare case of pituitary infarction leading to spontaneous tumour resolution and CSF-sella syndrome in an 11-year-old girl and a review of the paediatric literature

Increased detection of cystic-fibrosis-related diabetes in Australia

Sudden death in growth hormone–treated children with Prader-Willi syndrome

Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysitis

Pituitary autoantibodies in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

A Compound Heterozygote Case of Type II Aldosterone Synthase Deficiency

Changes in Altitude Cause Unintended Insulin Delivery From Insulin Pumps

The A, B, C, D of hypercalcaemia in Down syndrome

Global inequalities in paediatric endocrine practice: statement of minimal acceptable care. Statement from the international societies for paediatric endocrinology

Identification of the 49-kDa Autoantigen Associated with Lymphocytic Hypophysitis as α-Enolase

Cytosolic autoantigens in lymphocytic hypophysitis

Response to low dose growth hormone treatment in infants and toddlers with Prader-Willi Syndrome

Multiple pituitary hormone gradients from inferior petrosal sinus sampling in Cushing's disease

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