Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Egil, Støle"'
Autor:
Sverre Sandberg, Mette Christophersen Tollånes, Aasne K. Aarsand, Mira Mykletun, Egil Støle, Carl Baravelli, Jørild Haugen Villanger
Publikováno v:
Tidsskrift for Den norske legeforening. 134:831-835
Background Porphyria is an umbrella term for a group of largely hereditary diseases that are due to defective haem synthesis. The diseases have a varied and partly overlapping range of symptoms and presentations. The commonest forms of porphyria are
Autor:
Mira, Mykletun, Aasne Karine, Aarsand, Egil, Støle, Jørild Haugen, Villanger, Mette Christophersen, Tollånes, Carl, Baravelli, Sverre, Sandberg
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 134(8)
Porphyria is an umbrella term for a group of largely hereditary diseases that are due to defective haem synthesis. The diseases have a varied and partly overlapping range of symptoms and presentations. The commonest forms of porphyria are porphyria c
Autor:
Egil Støle, Aasne K. Aarsand, George H. Elder, Joanne T Marsden, Jean-Charles Deybach, Sverre Sandberg, Jørild Haugen Villanger, Jordi To-Figueras, Michael Norman Badminton
Publikováno v:
Clinical chemistry. 57(11)
BACKGROUND The porphyrias are a group of rare metabolic disorders whose diagnosis depends on identification of specific patterns of porphyrin precursor and porphyrin accumulation in urine, blood, and feces. Diagnostic tests for porphyria are performe