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Der Pathologe, ISSN 0172-8113, 11/2014, Volume 35, Issue S2, pp. 271 - 276
Globoside und ihre Isomere Isogloboside gehören zu neutralen Glykosphingolipiden, deren physiologische Funktion noch nicht geklärt ist. In der Pathogenese... 
Komplementaktivierung | Pathology | Thrombotic microangiopathy | Tubulusschaden | Tubular damage | Complement activation | Medicine & Public Health | Gb3 | α-Galaktosidase A | α-galactosidase A | Thrombotische Mikroangiopathie
Journal Article
Fortschritte der Neurologie · Psychiatrie, ISSN 0720-4299, 03/2013, Volume 81, Issue 3, pp. 138 - 144
Zusammenfassung Die Fabry-Krankheit ist eine X-chromosomal rezessiv vererbte lysosomale Speicherkrankheit, die durch das Fehlen oder das fehlerhafte Arbeiten... 
Kasuistik | Fabry's disease (FD) | Anderson-Fabry disease | α-galactosidase A deficiency
Journal Article
Der Schmerz, ISSN 0932-433X, 9/2012, Volume 26, Issue 5, pp. 609 - 619
Der M. Fabry ist eine X-chromosomal vererbte lysosomale Speicherkrankheit mit Mangel des Enzyms α-Galaktosidase A und Ablagerung des Glykosphingolipids... 
Globotriaosylceramide | M. Fabry | Psychotherapy | Fabry disease | Enzymersatztherapie | Globotriaosylceramid | Neuropathic pain | Pain Medicine | Medicine & Public Health | Enzyme replacement therapy | Neuropathische Schmerzen | α-Galaktosidase A | α-galactosidase A | Anesthesiology | Chiropractic Medicine | α-galactosidase A
Journal Article
Deutsche Medizinische Wochenschrift, ISSN 0012-0472, 10/2007, Volume 132, Issue 43, pp. 2271 - 2277
Journal Article
Nieren- und Hochdruckkrankheiten, ISSN 0300-5224, 07/2009, Volume 38, Issue 7, pp. 330 - 342
Journal Article
Internistische Praxis, ISSN 0020-9570, 09/2008, Volume 48, Issue 3, pp. 509 - 517
Journal Article
Klinische Pädiatrie, ISSN 0300-8630, 2006, Volume 218, Issue 1, pp. 38 - 40
Zusammenfassung Der Morbus Fabry ist eine angeborene Stoffwechselkrankheit, die durch das Fehlen des lysosomalen Enzyms α-Galaktosidase A bedingt ist. In der... 
Kasuistik | Fabry disease | Inherited metabolic disease | Gb3 | Enzyme replacement therapy | α-Galactosidase A
Journal Article
03/2010
Aspergillus parasiticus microbial type culture collection (MTCC)-2796, a new source of α-galactosidase is an efficient producer of enzyme in basic medium under... 
Aspergillus parasiticus | culture condition | α-galactosidase | submerged fermentation
Web Resource
Turkish Nephrology, Dialysis and Transplantation Journal, ISSN 1300-7718, 2018, Volume 27, Issue 3, pp. 324 - 326
Journal Article
Nieren- und Hochdruckkrankheiten, ISSN 0300-5224, 2001, Volume 30, Issue 6, pp. 261 - 266
Journal Article
Microbial Cell Factories, ISSN 1475-2859, 12/2019, Volume 18, Issue 1, pp. 1 - 17
Abstract Background α-Galactosidases are enzymes that act on galactosides present in many vegetables, mainly legumes and cereals, have growing importance with... 
Biochemical characterization | Production optimization | Raffinose family oligosaccharides | α-Galactosidase | Saccharomyces cerevisiae
Journal Article
The Journal of Nutrition, ISSN 0022-3166, 12/2014, Volume 144, Issue 12, pp. 1963 - 1969
Background: Disrupting the physical structure of pulses by blending them or by using a digestive supplement (α-galactosidase) to reduce intestinal discomfort... 
Nutrition and Disease | glucose | appetite | α-galactosidase | humans | Lentils
Journal Article
International Agricultural Engineering Journal, ISSN 0858-2114, 09/2017, Volume 26, Issue 3, pp. 184 - 192
Journal Article
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