• Publications
  • Influence
Occurrence of epidermolysis bullosa in Finland.
  • M. Kero
  • Medicine
  • Acta dermato-venereologica
  • 1984
Cases of epidermolysis bullosa (EB) were gathered from the hospital files of dermatological clinics and university pediatric clinics in Finland over a period of 10 years. 40 families were identified,Expand
  • 24
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Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria
Aspartylglucosaminuria (AGU) is a lysosomal storage disorder caused by deficiency of aspartylglucosaminidase (AGA). The main symptom is progressive mental retardation. A spectrum of differentExpand
  • 16
  • 1
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Live Heap Space Bounds for Real-Time Systems
TLDR
In this paper we propose an analysis of live heap space upper bounds for real-time systems based on an accurate prediction of task execution orders. Expand
  • 12
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Enzymes of collagen biosynthesis in skin and serum in dermatological diseases. I. Enzymes of the skin.
Immunoreactive prolyl hydroxylase protein, prolyl hydroxylase activity and galactosylhydroxylysyl glucosyltransferase activity were measured in skin biopsies from 54 patients with variousExpand
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Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance.
Epidermolysis bullosa with unusually severe clinical features was associated with progressive muscular dystrophy in two siblings. Light and electron microscopic examination revealed an intraepidermalExpand
  • 72
Deficiency of galactosylhydroxylysyl glucosyltransferase, an enzyme of collagen synthesis, in a family with dominant epidermolysis bullosa simplex.
Members of a family with dominant epidermolysis bullosa simplex were found to have a deficiency of galactosylhydroxylysyl glucosyltransferase (GGT), an enzyme catalyzing the glucosylation ofExpand
  • 51
Type VII collagen is expressed but anchoring fibrils are defective in dystrophic epidermolysis bullosa inversa
A patient with dystrophic epidermolysis bullosa inversa was studied using electron microscopy and indirect immunofluorescence using antibodies to matrix macromolecules of the dermo‐epidermal junctionExpand
  • 48
Pregnancy as a trigger of epidermolysis bullosa acquisita.
A 38-year-old woman developed epidermolysis bullosa acquisita (A-EBD) in connection with her third pregnancy. The activity of visible blistering disappeared at menopause. Direct immunofluorescenceExpand
  • 5
Epidermolysis bullosa in Finland. Clinical features, morphology and relation to collagen metabolism.
  • M. Kero
  • Medicine
  • Acta dermato-venereologica. Supplementum
  • 1984
The inheritance and occurrence of various subtypes of epidermolysis bullosa (EB), the clinical and ultrastructural features of the disease (I) and its connections with possible defects in collagenExpand
  • 33
Guinea pig maximization test open epicutaneous test and chamber test in induction of delayed contact hypersensitivity
A comparison was made between the guinea pig maximization test (GPMT), open epicutaneous rest (OET) and chamber test (CT), and the allergens were neomycin sulphate and propylene glycol (PG). TheExpand
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