S. Guth

发表

Very high prevalence of thyroid nodules detected by high frequency (13 MHz) ultrasound examination

J. Aberle, S. Guth, U. Theune, 2009, European journal of clinical investigation.

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation

Juliane Hoyer, Peter Nürnberg, André Reis, 2006, American journal of medical genetics. Part A.

The efficacy of forceful ankle and toe exercises to increase venous return: A comprehensive Doppler ultrasound study

E. Vettorazzi, C. Bamberger, S. Guth, 2018, Phlebology.

Conventional ultrasound for diagnosis of hepatic steatosis is better than believed

X. Cui, C. Dietrich, Z. Sparchez, 2021, Zeitschrift für Gastroenterologie.

A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males

A. Meindl, H. Hellebrand, W. Rascher, 2007, American journal of medical genetics. Part A.

Angiopoietin-like 3-derivative LNA043 for cartilage regeneration in osteoarthritis: a randomized phase 1 trial

J. Goldhahn, Yunyu Zhang, S. Brachat, 2022, Nature Medicine.

Managing Incidental Findings Reported by Medical, Sonography and Other Students Performing Educational Ultrasound Examinations.

C. Dietrich, H. Prosch, J. Abramowicz, 2021, Ultrasound in medicine & biology.

9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic.

A. Rauch, C. Zweier, U. Trautmann, 2005, European Journal of Medical Genetics.

Ultrasound Diagnosis of Hepatic Steatosis as a Surrogate for Atherosclerosis

E. Windler, S. Guth, C. Bamberger, 2016, Ultrasound International Open.

Stellenwert der Sonografie im Rahmen präventiver Untersuchungen im Vergleich zur Ganzkörper-MRT – eine retrospektive Untersuchung bei 833 Patienten

C. U. Herborn, S. Guth, A. Galach, 2012, Ultraschall in der Medizin.