Publications by authors named "Raue F"

Diffusion models (DMs) have disrupted the image super-resolution (SR) field and further closed the gap between image quality and human perceptual preferences. They are easy to train and can produce very high-quality samples that exceed the realism of those produced by previous generative methods. Despite their promising results, they also come with new challenges that need further research: high computational demands, comparability, lack of explainability, color shifts, and more.

View Article and Find Full Text PDF
Article Synopsis
  • Early screening for elevated calcitonin levels and RET gene mutations in families with MEN2 significantly improves cure rates for hereditary medullary thyroid carcinoma (MTC) through prophylactic thyroidectomy.
  • A long-term study tracked 277 MEN2 patients post-thyroidectomy for an average of 14.4 years, revealing that 55.6% achieved long-term cures.
  • Factors influencing long-term success included younger age at surgery and lower tumor stage, indicating that timely intervention based on mutation risk is crucial for maintaining low calcitonin levels.
View Article and Find Full Text PDF

With the advent of Deep Learning (DL), Super-Resolution (SR) has also become a thriving research area. However, despite promising results, the field still faces challenges that require further research, e.g.

View Article and Find Full Text PDF

Background: Menopausal estrogen depletion increases the risk of cardiovascular disease and of osteoporosis. Both of these risks can be increased by thyroid dysfunction as well. This cumulation of risks will be presented.

View Article and Find Full Text PDF

Background: (rearranged during transfection) variants are the most prevalent oncogenic events in medullary thyroid cancer (MTC). In advanced disease, multi-tyrosine kinase inhibitors (MKIs) cabozantinib and vandetanib are the approved standard treatment irrespective of status. The actual outcome of patients with -positive MTC treated with MKIs is ill described.

View Article and Find Full Text PDF

Objective: Ectopic Cushing's syndrome (ECS) induced by medullary thyroid cancer (MTC) is rare, and data on clinical characteristics, treatment and outcome are limited.

Design: Retrospective cohort study in three German and one Swiss referral centres.

Patients: Eleven patients with MTC and occurrence of ECS and 22 matched MTC patients without ECS were included.

View Article and Find Full Text PDF

With the advent of generative adversarial networks, synthesizing images from text descriptions has recently become an active research area. It is a flexible and intuitive way for conditional image generation with significant progress in the last years regarding visual realism, diversity, and semantic alignment. However, the field still faces several challenges that require further research efforts such as enabling the generation of high-resolution images with multiple objects, and developing suitable and reliable evaluation metrics that correlate with human judgement.

View Article and Find Full Text PDF

Objectives: Procalcitonin (PCT) has been suggested as a tumor marker in patients with medullary thyroid carcinoma (MTC). Clinical application data in long term follow-up are missing.

Methods: 210 serum samples of 169 consecutive patients with MTC (92 sporadic, 77 hereditary, 158 postoperative follow-up, 11 preoperative) were collected between 2018 and 2020.

View Article and Find Full Text PDF

Context: Long-term data are scarce on large cohorts with sporadic (sMTC) and hereditary medullary thyroid carcinoma (hMTC).

Objectives: To compare long-term disease-specific survival (DSS) and outcomes between sMTC and hMTC groups.

Design: Retrospective analysis.

View Article and Find Full Text PDF

Introduction: The thyroid parafollicular hormone calcitonin (CT) shows particularly high blood levels in early childhood, a period of high bone turnover, which decrease with increasing age. Data about the physiological role of CT during infancy, childhood, and adolescence are contradictory or lacking.

Objective: We hypothesize that CT demonstrates age-related correlations with parameters of bone growth and turnover as well as with parameters of calcium homeostasis.

View Article and Find Full Text PDF

Management of patients with advanced medullary thyroid cancer (MTC) remains a therapeutic challenge. The multi-tyrosine kinase inhibitors (TKIs) vandetanib and cabozantinib have been approved for the treatment of progressive MTC based on prolonged progression-free survival (PFS) in phase 3 clinical trials. To evaluate clinical characteristics, treatment regimens, efficacy, and treatment emergent adverse events (TEAEs) of vandetanib and cabozantinib in MTC patients outside clinical trials at four German tertiary care centers.

View Article and Find Full Text PDF

Objective: In this retrospective cohort study, we describe the clinical presentation and workup of parathyroid carcinoma (PC) and determine its clinical prognostic parameters. Primary outcome was recurrence free survival.

Summary Background Data: PC is an orphan malignancy for which diagnostic workup and treatment is not established.

View Article and Find Full Text PDF

Medullary thyroid carcinoma (MTC) is a rare malignancy and compromises only 3 % of all thyroid carcinomas. MTC cells secret calcitonin, which serves as a sensitive tumor marker for screening and follow-up of MTC. Calcitonin screening in patients with nodular goiter allows for early diagnosis of MTC and surgical curative treatment.

View Article and Find Full Text PDF

Context: The clinical relevance of bone metastases (BM) in advanced medullary thyroid carcinoma (MTC) is poorly described.

Objective: The objectives of this work are to describe the prevalence of BM, frequency of skeletal related events (SREs), and impact of BM morphology and SREs on prognosis, and to assess the role of antiresorptive treatment (ART).

Design: A retrospective cohort study was conducted.

View Article and Find Full Text PDF

Context: Neuroendocrine tumors (NET) are a heterogeneous group of neoplasms found in all organs. They often present with characteristic clinical syndromes due to hormone hypersecretion.

Diagnostics: In addition to hormone diagnostics molecular-genetic work-up can play an important role.

View Article and Find Full Text PDF

Context: Recent data on long-term outcomes and aggressiveness of medullary thyroid carcinoma (MTC) are lacking for patients with multiple endocrine neoplasia type 2 (MEN2).

Objectives: To analyze the long-term outcomes in MEN2 and compare MTC aggressiveness in three defined RET mutation-risk categories: moderate risk (MOD), high risk (H), and highest risk (HST).

Design, Setting: Retrospective study of 263 operated patients with MEN2 from one German tertiary referral center from 1979 to 2017 comparing demographic, biochemical, genetic, and outcome parameters.

View Article and Find Full Text PDF

Introduction: Liver metastases from neuroendocrine tumors in multiple endocrine neoplasia syndrome are common (75%) and significantly impairs the prognosis. Characterisation of liver lesions in these patients is challenging, as liver metastases are difficult to differentiate from benign liver lesions such as haemangioma.

Methods: In this study we aimed to characterize the radiological findings of hepatic metastases in MEN patients.

View Article and Find Full Text PDF
Article Synopsis
  • - The study focuses on establishing age- and gender-dependent serum reference ranges for calcitonin (CT) in a pediatric population to improve diagnostics for conditions like multiple endocrine neoplasia type 2 (MEN 2) and medullary thyroid carcinoma (MTC).
  • - Researchers analyzed 6090 serum samples from 2639 children aged 1 month to 17.9 years, finding that boys had significantly higher CT levels, and observed a notable decline in CT from newborns to children aged 4 and 5.
  • - The findings conclude that this study provides the largest set of pediatric reference ranges for CT and confirms minimal impact of thyroid diseases on CT levels in children, aiding in better clinical monitoring for MEN
View Article and Find Full Text PDF

Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant hereditary cancer syndrome caused by missense gain-of-function mutations in the proto-oncogene on chromosome 10. Specific mutations can predispose toward a particular phenotype and clinical course, with strong genotype-phenotype correlations. MEN2 is highly penetrant in medullary thyroid carcinoma (MTC), and it can be associated with bilateral pheochromocytoma and primary hyperparathyroidism.

View Article and Find Full Text PDF

Medullary thyroid cancer (MTC) arises from parafollicular C cells of the thyroid gland and is characterized by a calcitonin secretion. Basal calcitonin correlates with the tumor mass and is used as highly sensitive and specific tumor marker for MTC. Based on former assays, unspecific calcitonin increase has frequently been seen in Hashimoto's thyroiditis, kidney insufficiency, proton pump inhibitors etc.

View Article and Find Full Text PDF

Context: Recent long-term outcomes and survival data are lacking for patients with multiple endocrine neoplasia type 2B (MEN2B).

Objectives: To analyze long-term MEN2B outcomes and define prognostic factors.

Design, Setting, And Participants: Retrospective comparative study of 75 patients with MEN2B from two German tertiary referral centers.

View Article and Find Full Text PDF

Multiple endocrine neoplasia type 1 and 2 are hereditary cancer syndromes. They are characterized by the occurrence of many benign and malignant tumor types, in MEN1 parathyroid tumors, pituitary tumors, and pancreas tumors, in MEN2 medullary thyroid carcinoma, pheochromocytoma, and parathyroid tumors. The autosomal dominant inherited tumor syndromes are caused by mutations in the MEN1 gene, a tumor suppressor gene, and mutations in the RET gene, an activated oncogene, in MEN2.

View Article and Find Full Text PDF

Background: The objective of this study is the validation and proof of clinical relevance of a novel electrochemiluminescence immunoassay (ECLIA) for the determination of serum calcitonin (CT) in patients with medullary thyroid carcinoma (MTC) and in different diseases of the thyroid and of calcium homeostasis.

Methods: This was a multicenter prospective study on basal serum CT concentrations performed in 9 US and European referral institutions. In addition, stimulated CT concentrations were measured in 50 healthy volunteers after intravenous calcium administration (2.

View Article and Find Full Text PDF