Julia Maetzke
University of Ulm
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Publication
Featured researches published by Julia Maetzke.
Allergy | 2005
Julia Maetzke; Ralf Hinrichs; Lars Alexander Schneider; Karin Scharffetter-Kochanek
(a) lactose is obtained from whey by ultrafiltration; (b) lactose is hydrolyzed to galactose and glucose by immobilized lactase; (c) glucose is separated from the galactose by chromatographic separation; (d) the galactose stream is isomerized to tagatose by adding calcium hydroxide in a process that increases the pH to pH 12 for a prolonged period; (e) the tagatose stream is demineralized using ion exchangers; (f) the tagatose stream is purified by chromatographic separation; (g) the tagatose solution is decolorized using an active carbon filter; (h) tagatose is crystallized; (i) the tagatose is dried by fluid-bed drying.
Allergy | 2005
Julia Maetzke; Sperfeld Ad; Karin Scharffetter-Kochanek; Sunderkötter C
References 1. Kasper L, Sladek K, Duplaga M, Bochenek G, Liebhart J, Gladysz U, et al. Prevalence of asthma with aspirin hypersensitivity in the adult population of Poland. Allergy 2003;58:1064–1066. 2. Vally H, Taylor ML, Thompson PJ. The prevalence of aspirin intolerant asthma (AIA) in Australian asthmatic patients. Thorax 2002;57:569–574. 3. Matucci A, Parronchi P, Vultaggio A, Rossi O, Brugnolo F, Maggi E, et al. Partial safety of the new COX-2 inhibitor rofecoxib in NSAIDs high sensitive patients. Allergy 2004;59:1133–1134. 4. Nettis E, Colanardi MC, Ferrannini A, Tursi A. Short-term and long-term tolerability of rofecoxib in patients with prior reactions to nonsteroidal anti-inflammatory drugs. Ann Allergy Asthma Immunol 2005;94:29–33. 5. Fontaine C, Bousquet PJ, Demoly P. Anaphylactic shock caused by a selective allergy to celecoxib, with no allergy to rofecoxib or sulfamethoxazole. J Allergy Clin Immunol 2005;115:633–634. 6. Matsumoto AK, Cavanaugh PF Jr. Etoricoxib. Drugs Today 2004;40:395–414. 7. Leclercq P, Malaise MG. Etoricoxib (Arcoxia). Rev Med Liege 2004;59: 345–349. Vesicular and bullous eczema in response to intravenous immunoglobulins (IVIG)
Allergy | 2005
Lars Alexander Schneider; Julia Maetzke; Gyde Staib; Karin Scharffetter-Kochanek
References 1. Johri S, Shetty S, Soni A, Kumar S. Anaphylaxis from intravenous thiamine-long forgotton? Am J Emerg Med 2000;18:642– 643. 2. Proebestle TM, Gall H, Jugert FK, Merk HF, Sterry W. Specific IgE and IgG serum antibodies to thiamine associated with anaphylactic reaction. J Allergy Clin Immunol 1995;95:1059–1060. 3. Stephen JM, Grant R, Yeh CS. Anaphylaxis from administration of intravenous thiamine. Am J Emerg Med 1992;10:61–63. 4. Van Haecke P, Ramaekers D, Vanderwegen L, Boonen S. Thiamine-induced anaphylactic shock. Am J Emerg Med 1995;13:371–372. 5. Wrenn KD, Slovis CM. Is intravenous thiamine safe? Am J Emerg Med 1992;10:165. 6. Burge PS, Pantin CF, Newton DT et al. Development of an expert system for the interpretation of serial peak expiratory flow measurements in the diagnosis of occupational asthma. Occup Env Med 1999;56:758–764.
Hautarzt | 2009
V. Mayer; Julia Maetzke; Karin Scharffetter-Kochanek
A 44-year-old woman developed punctate erythematous maculae on the backs of her hands, arms and shoulders following a pregnancy. Laboratory evaluation was unremarkable. Our differential diagnosis includes idiopathic teleangiectases, teleangiectasia eruptiva perstans, angioma serpiginosum and angiokeratoma corporis diffusum Fabry. Microscopic examination showed increased numbers of the small vessels of the upper vascular plexus with dilated capillaries. This coupled with the clinical findings led us to the diagnosis of angioma serpiginosum with symmetrical distribution involving the shoulder girdle, upper aspects of the arms, and the backs of the hands. We treated with a pulsed dye laser and noted some regression after two sessions.ZusammenfassungBei einer 44-jährigen Patientin traten nach einer Schwangerschaft scharf umschriebene punktförmige erythematöse Makulae im Bereich der Handrücken, Oberarme und Schultern auf. Die Labordiagnostik zeigte unauffällige Befunde. Wir dachten differenzialdiagnostisch unter anderem an idiopathische Teleangiektasien, eine Teleangiectasia eruptiva perstans, ein Angioma serpiginosum und ein Angiokeratoma corporis diffusum Fabry. Histologisch zeigte sich eine Vermehrung der kleinen Gefäße des oberen Gefäßplexus mit Nachweis dilatierter Kapillaren, sodass wir in Zusammenschau des klinischen Bildes und der histopathologischen Befunde die Diagnose eines Angioma serpiginosum mit einer symmetrischen Lokalisation im Bereich von Schultergürtel, Oberarmen und Handrücken stellten. Wir behandelten mit einem gepulsten Farbstofflaser und konnten nach 2-maliger Therapie eine diskrete Rückbildung der purpurfarbenen punktförmigen Makulae erreichen.AbstractA 44-year-old woman developed punctate erythematous maculae on the backs of her hands, arms and shoulders following a pregnancy. Laboratory evaluation was unremarkable. Our differential diagnosis includes idiopathic teleangiectases, teleangiectasia eruptiva perstans, angioma serpiginosum and angiokeratoma corporis diffusum Fabry. Microscopic examination showed increased numbers of the small vessels of the upper vascular plexus with dilated capillaries. This coupled with the clinical findings led us to the diagnosis of angioma serpiginosum with symmetrical distribution involving the shoulder girdle, upper aspects of the arms, and the backs of the hands. We treated with a pulsed dye laser and noted some regression after two sessions.
Hautarzt | 2009
V. Mayer; Julia Maetzke; Karin Scharffetter-Kochanek
A 44-year-old woman developed punctate erythematous maculae on the backs of her hands, arms and shoulders following a pregnancy. Laboratory evaluation was unremarkable. Our differential diagnosis includes idiopathic teleangiectases, teleangiectasia eruptiva perstans, angioma serpiginosum and angiokeratoma corporis diffusum Fabry. Microscopic examination showed increased numbers of the small vessels of the upper vascular plexus with dilated capillaries. This coupled with the clinical findings led us to the diagnosis of angioma serpiginosum with symmetrical distribution involving the shoulder girdle, upper aspects of the arms, and the backs of the hands. We treated with a pulsed dye laser and noted some regression after two sessions.ZusammenfassungBei einer 44-jährigen Patientin traten nach einer Schwangerschaft scharf umschriebene punktförmige erythematöse Makulae im Bereich der Handrücken, Oberarme und Schultern auf. Die Labordiagnostik zeigte unauffällige Befunde. Wir dachten differenzialdiagnostisch unter anderem an idiopathische Teleangiektasien, eine Teleangiectasia eruptiva perstans, ein Angioma serpiginosum und ein Angiokeratoma corporis diffusum Fabry. Histologisch zeigte sich eine Vermehrung der kleinen Gefäße des oberen Gefäßplexus mit Nachweis dilatierter Kapillaren, sodass wir in Zusammenschau des klinischen Bildes und der histopathologischen Befunde die Diagnose eines Angioma serpiginosum mit einer symmetrischen Lokalisation im Bereich von Schultergürtel, Oberarmen und Handrücken stellten. Wir behandelten mit einem gepulsten Farbstofflaser und konnten nach 2-maliger Therapie eine diskrete Rückbildung der purpurfarbenen punktförmigen Makulae erreichen.AbstractA 44-year-old woman developed punctate erythematous maculae on the backs of her hands, arms and shoulders following a pregnancy. Laboratory evaluation was unremarkable. Our differential diagnosis includes idiopathic teleangiectases, teleangiectasia eruptiva perstans, angioma serpiginosum and angiokeratoma corporis diffusum Fabry. Microscopic examination showed increased numbers of the small vessels of the upper vascular plexus with dilated capillaries. This coupled with the clinical findings led us to the diagnosis of angioma serpiginosum with symmetrical distribution involving the shoulder girdle, upper aspects of the arms, and the backs of the hands. We treated with a pulsed dye laser and noted some regression after two sessions.
Hautarzt | 2007
Julia Maetzke; Ralf Hinrichs; A. Sigge; Karin Scharffetter-Kochanek
Bei einem 83-jährigen Patienten waren innerhalb der letzten 8 Monate Erytheme mit entzündlichen Knötchen an Wangen und Nase aufgetreten. Des Weiteren berichtete der Patient von täglicher Epistaxis und einem chronischen Hustenreiz. Seit dem 20. Lebensjahr bestünde eine unklare Entzündung im Bereich der Nase und der Nasennebenhöhlen. Es sei diesbezüglich mehrfach eine operative Sanierung erfolgt, wobei die Diagnose bisher weder klinisch noch histopathologisch zugeordnet werden konnte.
Allergy | 2004
Julia Maetzke; R. Hinrichs; G. Staib; Karin Scharffetter-Kochanek
Journal Der Deutschen Dermatologischen Gesellschaft | 2005
Lars Alexander Schneider; Lutz Weber; Julia Maetzke; Karin Scharffetter-Kochanek
Hautarzt | 2009
Volker Mayer; Julia Maetzke; Karin Scharffetter-Kochanek
Hautarzt | 2007
Julia Maetzke; Ralf Hinrichs; Anja Sigge; Karin Scharffetter-Kochanek