Markus M. Hess

Automatic Classification of Leukoplakia on Vocal Folds Using Color Texture Features

C. Münzenmayer, T. Wittenberg, M. Grobe, 2003 .

Differential Gene Expression Profiling of Vocal Fold Polyps and Reinke's Edema by Complementary DNA Microarray

G. Schade, Marshall E. Smith, S. Thibeault, 2006, The Annals of otology, rhinology, and laryngology.

OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)

K. Steel, M. Ptok, U. Zimmermann, 2015, Orphanet Journal of Rare Diseases.

Phenotypic variability of non-syndromic hearing loss in patients heterozygous for both c.35delG of GJB2 and the 342-kb deletion involving GJB6

H. Bolz, A. Gal, C. Kothe, 2004, Hearing Research.

Pulmonary function after total laryngectomy

R. Loddenkemper, W. Frank, Markus M. Hess, 1999, The Laryngoscope.

Impaired calmodulin binding of myosin‐7A causes autosomal dominant hearing loss (DFNA11)

H. Bolz, S. Bolz, A. Gal, 2004, Human mutation.

Laryngeal morphometry with a new laser ‘clip on’ device

G. Schade, R. Leuwer, B. Rassow, 2004, Lasers in surgery and medicine.