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Medullary thyroid cancer with ectopic Cushing's syndrome: A multicentre case series

Clinical endocrinology (Oxford), 2022-06, Vol.96 (6), p.847-856

2022

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Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma

Thyroid (New York, N.Y.), 2015-06, Vol.25 (6), p.567

2015

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Molecular genetics and phenomics of RET mutations: Impact on prognosis of MTC

Molecular and cellular endocrinology, 2010-06, Vol.322 (1), p.2-7

2010

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Genotype-phenotype correlation in multiple endocrine neoplasia type 2

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (suppl 1), p.69-75

2012

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Clinical relevance of RET variants G691S, L769L, S836S and S904S to sporadic medullary thyroid cancer

Clinical endocrinology (Oxford), 2012-05, Vol.76 (5), p.691-697

2012

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Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey

Clinical endocrinology (Oxford), 2011-12, Vol.75 (6), p.760-765

2011

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Age-related penetrance of endocrine tumours in multiple endocrine neoplasia type 1 (MEN1): a multicentre study of 258 gene carriers

Clinical endocrinology (Oxford), 2007-10, Vol.67 (4), p.613-622

2007

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Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia

PloS one, 2014-12, Vol.9 (12), p.e115178-e115178

2014

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Genotype-phenotype relationship in multiple endocrine neoplasia type 2. Implications for clinical management

Hormones (Athens, Greece), 2009-01, Vol.8 (1), p.23-28

2009

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Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidism

Clinical endocrinology (Oxford), 2011-07, Vol.75 (1), p.50-55

2011

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Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10

Human mutation, 2011-01, Vol.32 (1), p.51-58

2011

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Difference in development of medullary thyroid carcinoma among carriers of RET mutations in codons 790 and 791

Clinical endocrinology (Oxford), 2008-08, Vol.69 (2), p.259-263

2008

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CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum

European journal of endocrinology, 2011-09, Vol.165 (3), p.477

2011

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Novel Inactivating Mutations of the Calcium-Sensing Receptor: The Calcimimetic NPS R-568 Improves Signal Transduction of Mutant Receptors

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4797-4803

2008

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Schilddrüse und Schwangerschaft

Geburtshilfe und Frauenheilkunde, 2021-07, Vol.81 (7), p.745-748

Frank-Raue, Karin

2021

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Thyroid Cancer: Risk-Stratified Management and Individualized Therapy

Clinical cancer research, 2016-10, Vol.22 (20), p.5012-5021

2016

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Impact of modified radical neck dissection on biochemical cure in medullary thyroid carcinomas

Surgery, 2001-12, Vol.130 (6), p.1044-1049

2001

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Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation

Endocrine-related cancer, 2008-12, Vol.15 (4), p.1035-1041

2008

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Similar Stage-dependent Survival and Outcome in Sporadic and Hereditary Medullary Thyroid Carcinoma

The journal of clinical endocrinology and metabolism, 2021-09, Vol.106 (9), p.e3582-e3591

2021

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Long-Term Outcomes and Aggressiveness of Hereditary Medullary Thyroid Carcinoma: 40 Years of Experience at One Center

The journal of clinical endocrinology and metabolism, 2019-10, Vol.104 (10), p.4264-4272

2019

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Thyroid dysfunction in peri- and postmenopausal women—cumulative risks

Deutsches Ärzteblatt international, 2023-05, Vol.120 (18), p.311-316

2023

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Thyroid Dysfunction in Periand Postmenopausal Women-Cumulative Risks

Deutsches Ärzteblatt international, 2023-05, Vol.120 (18), p.311-316

2023

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Long-term outcome of “prophylactic therapy” for familial medullary thyroid cancer

Surgery, 2009-11, Vol.146 (5), p.906-912

2009

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Prophylactic Thyroidectomy in 75 Children and Adolescents with Hereditary Medullary Thyroid Carcinoma: German and Austrian Experience

World journal of surgery, 1998-07, Vol.22 (7), p.744-751

1998

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Proto-Oncogene Proteins C-Ret - Genetics
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Medullary thyroid cancer with ectopic Cushing's syndrome: A multicentre case series

Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma

Molecular genetics and phenomics of RET mutations: Impact on prognosis of MTC

Genotype-phenotype correlation in multiple endocrine neoplasia type 2

Clinical relevance of RET variants G691S, L769L, S836S and S904S to sporadic medullary thyroid cancer

Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey

Age-related penetrance of endocrine tumours in multiple endocrine neoplasia type 1 (MEN1): a multicentre study of 258 gene carriers

Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia

Genotype-phenotype relationship in multiple endocrine neoplasia type 2. Implications for clinical management

Inactivating calcium-sensing receptor mutations in patients with primary hyperparathyroidism

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10

Difference in development of medullary thyroid carcinoma among carriers of RET mutations in codons 790 and 791

Treatment of RET-Positive Advanced Medullary Thyroid Cancer with Multi-Tyrosine Kinase Inhibitors—A Retrospective Multi-Center Registry Analysis

CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum

Novel Inactivating Mutations of the Calcium-Sensing Receptor: The Calcimimetic NPS R-568 Improves Signal Transduction of Mutant Receptors

Schilddrüse und Schwangerschaft

Thyroid Cancer: Risk-Stratified Management and Individualized Therapy

Impact of modified radical neck dissection on biochemical cure in medullary thyroid carcinomas

Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation

Similar Stage-dependent Survival and Outcome in Sporadic and Hereditary Medullary Thyroid Carcinoma

Long-Term Outcomes and Aggressiveness of Hereditary Medullary Thyroid Carcinoma: 40 Years of Experience at One Center

Thyroid dysfunction in peri- and postmenopausal women—cumulative risks

Thyroid Dysfunction in Periand Postmenopausal Women-Cumulative Risks

Long-term outcome of “prophylactic therapy” for familial medullary thyroid cancer

Prophylactic Thyroidectomy in 75 Children and Adolescents with Hereditary Medullary Thyroid Carcinoma: German and Austrian Experience

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