Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Epidermolysis bullosa: novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy.
The Journal of investigative dermatology·2000
Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene.
The Journal of investigative dermatology·2000
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa.
The Journal of investigative dermatology·2000
Cutaneous gene therapy. Principles and prospects.
Dermatologic clinics·2000
A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.
American journal of ophthalmology·1999
Update on Current Care Guideline: Psoriasis (skin and joints).
Duodecim; laaketieteellinen aikakauskirja·2017
FOUR score in monitoring the level of consciousness of an intensive care patient: first experience of the use of the Finnish language version.
Duodecim; laaketieteellinen aikakauskirja·2017
Discussing a serious illness with a patient and family.
Duodecim; laaketieteellinen aikakauskirja·2017
Invasive treatment of superficial veins of the lower extremities.
Duodecim; laaketieteellinen aikakauskirja·2017
When should a drain be left in the abdominal cavity upon surgery?
Duodecim; laaketieteellinen aikakauskirja·2017
Diagnostics and current care of myasthenia gravis.
Duodecim; laaketieteellinen aikakauskirja·2017