Long-term follow-up of patients with Herlitz-type junctional epidermolysis bullosa

Autor: Yuen, W. Y., Duipmans, J. C., Molenbuur, B., Herpertz, I., Mandema, J. M., Jonkman, M. F.

Publikováno v: BRITISH JOURNAL OF DERMATOLOGY, 167(2), 374-382. Wiley

Background Junctional epidermolysis bullosa, type Herlitz (JEB-H) is a rare, autosomal recessive disease caused by absence of the epidermal basement membrane adhesion protein laminin-332. It is characterized by extensive and devastating blistering of

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https://research.rug.nl/en/publications/5da47e75-68b1-4788-a242-9e7b5055b97f

Long-term follow-up of patients with Herlitz-type junctional epidermolysis bullosa.

Autor: Yuen WY; Department of Dermatology, Center for Blistering Diseases, University of Groningen, University Medical Center Groningen, Hanzeplein 1, 9700 RB Groningen, The Netherlands. w.y.yuen@umcg.nl, Duipmans JC, Molenbuur B, Herpertz I, Mandema JM, Jonkman MF

Publikováno v: The British journal of dermatology [Br J Dermatol] 2012 Aug; Vol. 167 (2), pp. 374-82. Date of Electronic Publication: 2012 Jul 05.

Fatal side-effects of continuous propofol infusion in children may be related to malignant hyperthermia.

Autor: Plötz FB, Waalkens HJ, Verkade HJ, Strengers JL, Knoester H, Mandema JM

Publikováno v: Anaesthesia and intensive care [Anaesth Intensive Care] 1996 Dec; Vol. 24 (6), pp. 724.

Short-limbed dwarfism, subluxation of the knees, hypogenitalism, and dysmorphic facies: a new syndrome?

Autor: Willems PJ, De Vries-Van der Weerd S, Los FJ, Mandema JM, Smit GP

Publikováno v: The Journal of clinical dysmorphology [J Clin Dysmorphol] 1984 Spring; Vol. 2 (1), pp. 19-21.