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Phaeochromocytoma in multiple endocrine neoplasia type 2: RET codon‐specific penetrance and changes in management during the last four decades

Clinical endocrinology (Oxford), 2017-10, Vol.87 (4), p.320-326

2017

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Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotype

European journal of endocrinology, 2006-08, Vol.155 (2), p.229-236

2006

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2012 European Thyroid Association Guidelines for Genetic Testing and Its Clinical Consequences in Medullary Thyroid Cancer

European thyroid journal, 2013-01, Vol.1 (4), p.216-231

2013

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Long-Term Follow-Up and Treatment of Postoperative Permanent Hypoparathyroidism in Patients with Medullary Thyroid Carcinoma: Differences in Complete and Partial Disease

Hormone and metabolic research, 2016-12, Vol.48 (12), p.806-813

2016

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Are commonly recommended dosages for vitamin D supplementation too low? Vitamin D status and effects of supplementation on serum 25-hydroxyvitamin D levels--an observational study during clinical practice conditions

Osteoporosis international, 2011, Vol.22 (1), p.231-240

2011

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Rapid response to sorafenib in metastatic medullary thyroid carcinoma

Experimental and clinical endocrinology & diabetes, 2011-03, Vol.119 (3), p.151-155

2011

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The Role of the Extracellullar Calcium-Sensing Receptor in Health and Disease

Experimental and clinical endocrinology & diabetes, 2006-09, Vol.114 (8), p.397-405

2006

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Autoimmunthyreopathien in der Schwangerschaft

Geburtshilfe und Frauenheilkunde, 2005-08, Vol.65 (8), p.744-750

2005

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Diagnostik des Schilddrüsenkarzinoms

Onkologie (Heidelberg, Germany), 2005-01, Vol.11 (1), p.50-57

2005

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New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour

Experimental and clinical endocrinology & diabetes, 2010-08, Vol.118 (8), p.550-553

2010

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Early Malignant Progression of Hereditary Medullary Thyroid Cancer

The New England journal of medicine, 2003-10, Vol.349 (16), p.1517-1525

2003

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Neuroendocrine tumors : Classification, clinical presentation and imaging

Radiologe, 2019-11, Vol.59 (11), p.952-960

2019

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Somatostatin receptor imaging in persistent medullary thyroid carcinoma

Clinical endocrinology (Oxford), 1995-01, Vol.42 (1), p.31-37

1995

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Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT

Deutsche medizinische Wochenschrift (1946), 2011-09, Vol.136 (38), p.1889

2011

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Mutations of the ret protooncogene in German multiple endocrine neoplasia families : Relation between genotype and phenotype

The journal of clinical endocrinology and metabolism, 1996-05, Vol.81 (5), p.1780-1783

1996

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Multiple Endocrine Neoplasia Type 2: Clinical Features and Screening

Endocrinology and metabolism clinics of North America, 1994-03, Vol.23 (1), p.137-156

1994

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Schilddrüse 1995: Schilddrüsenerkrankungen in verschiedenen Lebensabschnitten. 12. Konferenz über die menschliche Schilddrüse. Henning-Symposium

K.-H. Usadel, B. Weinheimer / K.-H. Usadel, B. Weinheimer

2020

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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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Primary hyperparathyroidism—what the nephrologist should know—an update

Nephrology, dialysis, transplantation, 2007-03, Vol.22 (3), p.696-699

2007

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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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A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A

The journal of clinical endocrinology and metabolism, 1998-03, Vol.83 (3), p.770-774

1998

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Coincidence of Multiple Endocrine Neoplasia Types 1 and 2: Mutations in the RET Protooncogene and MEN1 Tumor Suppressor Gene in a Family Presenting with Recurrent Primary Hyperparathyroidism

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4063-4067

2005

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Change in the spectrum of RET mutations diagnosed between 1994 and 2006

Clinical laboratory (Heidelberg), 2007, Vol.53 (5-6), p.273

2007

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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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Sekundäre Osteoporose – praxisrelevante Besonderheiten bei der Diagnostik und Therapie

Deutsche medizinische Wochenschrift, 2012-02, Vol.137 (7), p.326-332

2012

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Phaeochromocytoma in multiple endocrine neoplasia type 2: RET codon‐specific penetrance and changes in management during the last four decades

Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotype

2012 European Thyroid Association Guidelines for Genetic Testing and Its Clinical Consequences in Medullary Thyroid Cancer

Long-Term Follow-Up and Treatment of Postoperative Permanent Hypoparathyroidism in Patients with Medullary Thyroid Carcinoma: Differences in Complete and Partial Disease

Are commonly recommended dosages for vitamin D supplementation too low? Vitamin D status and effects of supplementation on serum 25-hydroxyvitamin D levels--an observational study during clinical practice conditions

Rapid response to sorafenib in metastatic medullary thyroid carcinoma

The Role of the Extracellullar Calcium-Sensing Receptor in Health and Disease

Autoimmunthyreopathien in der Schwangerschaft

Diagnostik des Schilddrüsenkarzinoms

New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

Neuroendocrine tumors : Classification, clinical presentation and imaging

Somatostatin receptor imaging in persistent medullary thyroid carcinoma

Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT

Mutations of the ret protooncogene in German multiple endocrine neoplasia families : Relation between genotype and phenotype

Multiple Endocrine Neoplasia Type 2: Clinical Features and Screening

Schilddrüse 1995: Schilddrüsenerkrankungen in verschiedenen Lebensabschnitten. 12. Konferenz über die menschliche Schilddrüse. Henning-Symposium

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

Primary hyperparathyroidism—what the nephrologist should know—an update

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

A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A

Coincidence of Multiple Endocrine Neoplasia Types 1 and 2: Mutations in the RET Protooncogene and MEN1 Tumor Suppressor Gene in a Family Presenting with Recurrent Primary Hyperparathyroidism

Change in the spectrum of RET mutations diagnosed between 1994 and 2006

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

Sekundäre Osteoporose – praxisrelevante Besonderheiten bei der Diagnostik und Therapie

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