W. Muss

发表

Recurrent Keratoconus in a Patient with Leber Congenital Amaurosis

G. Grabner, J. Ruckhofer, J. Stoiber, 2000, Cornea.

Corneal lathing using the excimer laser and a computer-controlled positioning system.

G. Grabner, W. Husinsky, P. Homolka, 2000, Journal of refractive surgery.

Light and transmission electron microscopic studies following frontal sinus obliteration with ionomer cement in cats

S. Dazert, W. Muss, 2004, European Archives of Oto-Rhino-Laryngology.

Distribution of two VIP-related peptides, helospectin and pituitary adenylate cyclase activating peptide (PACAP), in the human upper respiratory system

F. Sundler, A. Arimura, O. Dietze, 1996, Regulatory Peptides.

A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency.

J. Uitto, A. Klausegger, B. Kofler, 2001, The American journal of pathology.

Routine, rapid, noninvasive diagnosis of viral skin exanthems

N. Bannert, H. Gelderblom, W. Muss, 2006, The British journal of dermatology.

Elemental Analysis in Electron Microscopy for Medical Diagnostics

W. Muss, E. Zellmann, L. Jonas, 2007, Microscopy and Microanalysis.

Evidence of mild founder LMOD3 mutations causing nemaline myopathy 10 in Germany and Austria

S. Rudnik-Schöneborn, W. Schmidt, B. Schoser, 2018, Neurology.

Autonomic and peptidergic innervation of human nasal mucosa.

A. Saria, G. Hacker, K. Albegger, 1993, Acta oto-laryngologica.

Ocular involvement in IgA–epidermolysis bullosa acquisita

D. Metze, G. Grabner, J. Ruckhofer, 1999, The British journal of dermatology.

Feline orthopoxvirus infection transmitted from cat to human.

H. Schaeppi, T. Hawranek, W. Muss, 2003, Journal of the American Academy of Dermatology.

Eurosol Versus Fetal Bovine Serum-containing Corneal Storage Medium

G. Grabner, J. Ruckhofer, W. Hitzl, 2001, Cornea.

Histopathology of Human Corneas After Amniotic Membrane and Limbal Stem Cell Transplantation for Severe Chemical Burn

G. Grabner, J. Ruckhofer, J. Stoiber, 2002, Cornea.

Acute keratoconus with perforation in a patient with Down’s syndrome

G. Grabner, J. Ruckhofer, J. Stoiber, 2003, The British journal of ophthalmology.

Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.

A. Klausegger, M. Laimer, J. Bauer, 2006, Archives of dermatology.

Pre-Embedding Immunocytochemistry in Transmission Electron Microscopy

W. Kummer, W. Muss, C. Hauser-kronberger, 1994 .

Deficiency of mitochondrial ATP synthase of nuclear genetic origin

E. Holme, J. Zeman, J. Houštěk, 2006, Neuromuscular Disorders.

A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.

O. Rittinger, W. Muss, E. Plöchl, 1997, Klinische Padiatrie.

EM as an important diagnostic tool in neuronal ceroid-lipofuscinosis (NCL, Batten's disease)

W. Muss, J. Thurner, R. Puttinger, 1992 .

Immunocytochemical localization of estrogen and progesterone receptors in human thyroid.

W. Thelmo, S. Money, B. Jaffe, 1989, Surgery.

Combined Cy3 / Nanogold Conjugates for ImmunocytoChemistry and in Situ Hybridization

J. Hainfeld, R. Powell, C. M. Halsey, 1999, Microscopy and Microanalysis.

Cerebral Localized Marginal Zone Lymphoma Presenting as Hypothalamic-Pituitary Region Disorder

G. Ladurner, E. Trinka, A. Kunz, 2011, Case Reports in Neurology.

Closure of a Large Chronic Wound through Transplantation of Gene-Corrected Epidermal Stem Cells.

G. Pellegrini, S. Bondanza, M. De Luca, 2017, The Journal of investigative dermatology.

Danon disease: Case report and detection of new mutation

H. Budka, H. Bernheimer, W. Pickl, 2009, Journal of Inherited Metabolic Disease.

Stereologic parameters of nuclear ultrastructure as markers of the steroid receptor status in breast cancer epithelium.

O. Dietze, G. Hacker, W. Muss, 1994, Pathology, research and practice.

Silver Acetate Autometallography: An Alternative Enhancement Technique for Immunogold-Silver Staining (IGSS) and Silver Amplification of Gold, Silver, Mercury and Zinc in Tissues

Gerhard W. Hacker, G. Bernatzky, G. Danscher, 1988 .

Gene symbol: Kind1. Disease: kindler syndrome.

A. Klausegger, J. Bauer, W. Muss, 2004, Human genetics.

An ex vivo RNA trans‐splicing strategy to correct human generalized severe epidermolysis bullosa simplex

J. Reichelt, T. Lettner, T. Kocher, 2018, The British journal of dermatology.

Functional correction of type VII collagen expression in dystrophic epidermolysis bullosa.

A. Klausegger, J. Bauer, W. Muss, 2011, The Journal of investigative dermatology.

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa

A. Klausegger, M. Laimer, J. Bauer, 2006, The British journal of dermatology.

[Autonomic and peptidergic innervation of the human larynx].

A. Saria, O. Dietze, G. Hacker, 1994, HNO.

The contemporary role of electron microscopy in the diagnosis of mitochondrial encephalomyopathies

K. Kyriacou, T. Kyriakides, W. Muss, 2003 .

Diaminobenzidine as a myelin stain in semithin plastic sections.

W. Muss, 2000, Biotechnic & Histochemistry.

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

A. Klausegger, J. Bauer, W. Muss, 2003, Journal of cutaneous pathology.