Contents Vol. 98, 2010

Autor: J.F. Felix, Anna Koskinen, Bryan S. Richardson, Kevin P. Lally, N. Laforgia, C.F. Poets, James N. MacLachlan, M.J. Butel, Luciana Porto, Mete Akisu, Pekka Kääpä, Kathleen Ayers, M. Gorett Silva, Bilin Cakmak, N. Kalach, Guillaume Emeriaud, Payam Vali, Doris Fischer, Cherrie D. Welch, Gunnel Hellgren, Xiaoping Luo, K. Allegaert, Gulin Erdemir, W.C.J. Hop, T. Schaible, Thierry Debillon, Charles Turner, Sarah E. Fleming, Thomas Pranikoff, Eva Engström, Hüseyin Onay, Gila Benchetrit, Pascale Calabrese, I. Reiss, Ana Remesal, Hanna Soukka, Keirnan L. Willett, Lex W. Doyle, L. van den Hout, Sanjeev Aggarwal, Brad Matushewski, Nasser Chegini, F. Campeotto, Hildegard Stoll, Dolores Ludeña, Girija Natarajan, A. van Heijst, D. Tibboel, Bo Jacobsson, Jeremy D. McCallum, Henry L. Halliday, Patricia M. Schnulle, D. Bassler, N. Kapel, Caroline N. Nguyen, Asta Laiho, I. Capolupo, Nilgün Kültürsay, Elsa Kermorvant-Duchemin, Qing Yang, Laura San Feliciano, Sreedhar Reddy Anne, Alexandre Lapillonne, David M. Hougaard, Joyce M. Koenig, Heikki Lukkarinen, Christof Geisen, Sergio Eleni dit Trolli, Poul Thorsen, Pamela A. Lally, Pierre Baconnier, M. Baldassarre, Jae H. Kim, Richard A. Ehrenkranz, Chatarina Löfqvist, Mehmet Yalaz, André Eberhard, Rolf L. Schloesser, C. Maas, C. Dupont, María Isidoro-García, A. Greenough, L. Amati, Ann Hellström, Norman B. Smith, Ferda Ozkinay, Ozge Altun Koroglu, V. Viallon

Publikováno v: Neonatology. 98:I-IV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d7b650b2be1c1597e692618ce3839810
https://doi.org/10.1159/000313652

Pharmacokinetics of plasma-derived C1-esterase inhibitor after subcutaneous versus intravenous administration in subjects with mild or moderate hereditary angioedema: the PASSION study

Autor: Chiara Suffritti, Wolfhart Kreuz, Hildegard Stoll, Tanja Rossmanith, Emel Aygören-Pürsün, Inmaculada Martinez-Saguer, E. Rusicke, Uwe Kalina, Marco Cicardi, Annette Feussner

Publikováno v: Transfusion

Hereditary angioedema (HAE), caused by functional deficiency of C1-esterase inhibitor1 (C1-INH), is a rare disease characterized by recurrent, spontaneous, nonallergic edema in subcutaneous (SC) tissues and mucous membranes. In case of laryngeal edem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba677533df4ad87a65811f76143b03b
https://pubmed.ncbi.nlm.nih.gov/24266596

Early long-term FEIBA prophylaxis in haemophilia A patients with inhibitor after failing immune tolerance induction: A prospective clinical case series.

Autor: ETTINGSHAUSEN, C. ESCURIOLA¹ carmen.escuriola@kgu.de, KREUZ, W.¹

Publikováno v: Haemophilia. Jan2010, Vol. 16 Issue 1, p90-100. 11p. 5 Charts, 2 Graphs.

Immune tolerance induction with mycophenolate-mofetil in two children with haemophilia B and inhibitor.

Autor: KLARMANN, DIETER¹ dieter.klarmann@kgu.de, MARTINEZ Saguer, I.¹, FUNK, M. B.¹, KNOEFLER, R.², VON HENTIG, N.³, HELLER, C.¹, KREUZ, W.¹

Publikováno v: Haemophilia. Jan2008, Vol. 14 Issue 1, p44-49. 6p. 1 Chart, 1 Graph.

Intracerebral Mass Bleeding in a Term Neonate: Manifestation of Hereditary Protein S Deficiency with a New Mutation in the PROS1 Gene.

Autor: Fischer, Doris, Porto, Luciana, Stoll, Hildegard, Geisen, Christof, Schloesser, Rolf L.

Publikováno v: Neonatology (16617800); Nov2010, Vol. 98 Issue 4, p337-340, 4p