Results 111 to 120 of about 394 (137)
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Orbit, 2011
Lipoid proteinosis (LP) or Urbach-Wiethe disease is a recessively inherited disorder not usually seen by ophthalmologists. It is characterized by non-inflammatory, persistent papules on the skin and mucous membranes. The first clinical manifestation of LP is usually progressive hoarseness.
Miquel, Callizo +5 more
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Lipoid proteinosis (LP) or Urbach-Wiethe disease is a recessively inherited disorder not usually seen by ophthalmologists. It is characterized by non-inflammatory, persistent papules on the skin and mucous membranes. The first clinical manifestation of LP is usually progressive hoarseness.
Miquel, Callizo +5 more
openaire +4 more sources
Typical Radiological Findings of Lipoid Proteinosis of Urbach and Wiethe
The Neuroradiology Journal, 2009Lipoid proteinosis is a rare autosomal recessive dermatosis, which can be congenital or have onset in infancy. It is characterized by the progressive deposition of an amorphous hyaline substance with a glycoprotein constitution in the skin and mucous membranes and presents as papular lesions that can aggregate forming plaques with a yellowish ...
K G, Srinivasan +3 more
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XXIX Lipoid Proteinosis (Urbach-Wiethe)
Annals of Otology, Rhinology & Laryngology, 1964R F, DICKEY, S, DAVIS
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Ultrastructural aspects of the skin in lipoid proteinosis (Urbach-Wiethe disease)
Anais Brasileiros De Dermatologia, 2021Hiram Larangeira de Almeida +2 more
exaly
[Clinical symptoms, differential diagnosis and therapy of lipoid-proteinosis (Wiethe-Urbach)].
Monatsschrift fur Ohrenheilkunde und Laryngo-Rhinologie, 1971V, Vendég +6 more
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Lipoid proteinosis; reinvestigation of a case previously reported by Urbach and Wiethe in 1929.
Dermatologica, 2000I, KATZENELLENBOGEN, H, UNGAR
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