about
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyCorneal lathing using the excimer laser and a computer-controlled positioning system.Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.Cerebral localized marginal zone lymphoma presenting as hypothalamic-pituitary region disorder.Immunocytochemical localization of estrogen and progesterone receptors in human thyroid.Histopathology of human corneas after amniotic membrane and limbal stem cell transplantation for severe chemical burn.Acute keratoconus with perforation in a patient with Down's syndrome.Feline orthopoxvirus infection transmitted from cat to human.Functional correction of type VII collagen expression in dystrophic epidermolysis bullosa.Light and transmission electron microscopic studies following frontal sinus obliteration with ionomer cement in cats.A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.Danon disease: case report and detection of new mutation.An ex vivo RNA trans -splicing strategy to correct human generalized severe epidermolysis bullosa simplexAutonomic and Peptidergic Innervation of Human Nasal MucosaClosure of a Large Chronic Wound through Transplantation of Gene-Corrected Epidermal Stem Cells[Vascularization of the matrix of hyaline rib cartilage in the human: changes with increasing age][Rhabdomyosarcoma of the mouth. Clinical and electron microscopy findings]Home-made silicone rubber embedding moulds for electron microscopyElectron Microscopical Autometallography: Immunogold-Silver Staining (IGSS) and Heavy-Metal HistochemistryFatal arthrogryposis with respiratory insufficiency: a possible case of muscle phosphorylase b-kinase deficiencyStereologic parameters of nuclear ultrastructure as markers of the steroid receptor status in breast cancer epithelium[Autonomic and peptidergic innervation of the human larynx]Individual differences between nuclear parameters of normal and malignant breast epitheliumOcular involvement in IgA-epidermolysis bullosa acquisitaEurosol versus fetal bovine serum-containing corneal storage mediumDiaminobenzidine as a myelin stain in semithin plastic sectionsRecurrent keratoconus in a patient with Leber congenital amaurosisGene symbol: Kind1. Disease: kindler syndrome[Dental alterations in junctional epidermolysis bullosa--report of a patient with a mutation in the LAMB3-gene]Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosaRoutine, rapid, noninvasive diagnosis of viral skin exanthems
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description
researcher ORCID ID = 0000-0003-1536-9882
@en
name
Wolfgang Muss
@ast
Wolfgang Muss
@en
Wolfgang Muss
@es
Wolfgang Muss
@nl
type
label
Wolfgang Muss
@ast
Wolfgang Muss
@en
Wolfgang Muss
@es
Wolfgang Muss
@nl
prefLabel
Wolfgang Muss
@ast
Wolfgang Muss
@en
Wolfgang Muss
@es
Wolfgang Muss
@nl
P31
P496
0000-0003-1536-9882