Morbus gaucher

Cll. Czitober, H., Grundig, E., and Schobel, B., Histochemische und biochemische Untersuchungen bei Morbus Gaucher. Klin. Wochenschr. 42, 1179-1184 (1964). [Pg.139]

Normal cerebrosides from brain are galactocerebrosides. An accumulation of glucocerebrosides has been found in Morbus Gaucher (Klenk 1940 Rennkamp 1942). [Pg.28]

Brante, G. Studies on the lipids in morbus Gaucher. I. Qualitative and quantitative determination of the hexose components in normal and Gaucher glycolipids. Acta Soc. Med. upsalien. 56, 125 (1951). [Pg.282]

CziTOBER, H., E. GrUNDIG, and B. Schobel Histochemische und biochemische Untersuchun-gen bei Morbus Gaucher. Klin. Wschr. 42, 1179 (1964). [Pg.283]

Fodisch, H. j. Morbus Gaucher mit splenopathischer Markhemmung beim Erwachsenen. II. Pathologisch-anatomischer Teil. Wien. Z. inn. Med. 43, 334 (1962). [Pg.283]

Landolt, R. F., H. U. Zollinger, and C. H. Eugster Uber die maligne, akut verlaufende Form des Morbus Gaucher. Helv. paediat. Acta 3, 319 (1948). [Pg.284]

Levine, S., and L. Solis-Cohen Gaucher s disease. Amer. J. Roentgenol. 50, 765 (1943). Lieb, H. Cerebrosidspeicherung bei Morbus Gaucher. Hoppe-Seylers Z. physiol. Chem. 140, 305 (1924). [Pg.284]

Pick, L. Zur pathologischen Anatomie des Morbus Gaucher. Med. Klin. 1922, 1408. [Pg.285]

SCHAIRER, E. Die Gehimveranderungen bei Morbus Gaucher des Sauglings. Virchows Arch, path. Anat. 315, 395 (1948). [Pg.286]

Weinschenk, C. tJber die Psychopathologie der juvenilen Form eines Morbus Gaucher (mit Falldemonstration). Med. Welt (Stuttg.) 1964, 140. [Pg.287]

Gerken, H. Heterozygotennachweis bei Morbus Gaucher. Mschr. Kinderheilk. 113,486 (1965). [Pg.524]

Rath, F. Akuter Morbus Gaucher bei einem Saugling. Mschr. Kinderheilk. 112, 355 (1964). [Pg.526]

Morbus Gaucher. Brady et al. (1965) and Brady (1966) showed, that accumulation of Glc-Cer in the reticuloendothelial system (Patrick, 1965), including plasma and erythrocytes (D. E. Vance et ah, 1969), in morbus Gaucher is caused by an attenuation of the activity of a glucocerebrosidase. Electron microscopic observations revealed that the stored Glc-Cer in cells showed a typical tubular appearance (Lee, 1968). In the spleen of one patient with Gaucher s disease a 20-fold increase of the normal ganglioside concentration was discovered (Kennaway and Woolf, 1968). [Pg.263]

It is interesting to note, that, in contrast to morbus Gaucher, where the Glc-Cer content is elevated in both plasma and red cells, in Fa-... [Pg.264]

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