Loitzsch, A; Bartsch, O
Healthy 12-year-old boy with mosaic inv dup(15)(q13).Am J Med Genet. Bd. 140. H. 6. 2006 S. 640-3
Hegemann, S; Hajioff, D; Conti, G et al.
Hearing loss in Fabry disease: data from FOS -; the Fabry Outcome SurveyEur J Clin Invest. Bd. 36. H. 9. 2006 S. 654-662
Pitton, MB; Kemmerich, G; Herber, S et al.
Hemodynamic effects of monomeric nonionic contrast media in pulmonary angiography in chronic thromboembolic pulmonary hypertension.Am J Roentgenol. Bd. 187. H. 1. 2006 S. 128-34
Kunz-Kostomanolakis, M; Runkel, S; Hitzler, WE
Hemolysis in a liver transplant recipient by donor Anti-Rh(D) and anti-CTransfus Med Hemother. Bd. 33. H. supp. 2006 S. 47
Böcher, WO; Nienhaus, A
Hepatitis A: Relevantes Infektionsrisiko durch akzidentelle Nadelstichverletzung?Ergo Med. Bd. 4. 2006 S. 14-19
Sprinzl, MF; Otto, G; Galle, PR et al.
Hepatitis C virus re-infection: new perspectives.Clin Transplant. Bd. 20 Suppl 17. 2006 S. 117-123
Brambrink, AM; Kurz, S
Hereditäre Malformationssyndrome - LuftwegeWappler F, Tonner PH, Bürkle H (Hrsg). Anästhesie und Begleiterkrankungen. Perioperatives Management des kranken Patienten. Stuttgart: Thieme 2006
Lasarzik, I; Turial, S; Kretz, FJ
Hereditäre Malformationssyndrome - Thorax: Trichterbrust, SkolioseWappler F, Tonner PH, Bürkle H (Hrsg). Anästhesie und Begleiterkrankungen. Perioperatives Management des kranken Patienten. Stuttgart: Thieme 2006
Bork, K; Gül, D; Dewald, G
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men.Br J Dermatol. Bd. 154. H. 3. 2006 S. 542-545
Bork, K
Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations.Immunol Allergy Clin North Am. Bd. 26. H. 4. 2006 S. 709-24