Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marie Böhm"'
Autor:
Irene Moor, Max Herke, Jenny Markert, Marie Böhm, Franziska Reiß, Ludwig Bilz, Gorden Sudeck, Kristina Winter, for the HBSC Study Group Germany
Publikováno v:
Journal of Health Monitoring, Vol 9, Iss 1, Pp 79-98 (2024)
Background: Many studies have identified health inequalities in childhood and adolescence. However, it is unclear how these have developed in recent years, particularly since the COVID-19 pandemic. Methods: Analyses are based on the German data from
Externí odkaz:
https://doaj.org/article/38940cdac52547abbf8b480311a97a03
Autor:
Christoph Klein, László Maródi, Adrian Schwarzer, Ali Nowrouzi, Claudia R. Ball, Klaus Kühlcke, Ricardo A Dewey, Manfred Schmidt, Irina Kondratenko, Sonja Naundorf, Marie Böhm, Rainer Blasczyk, Christof von Kalle, Kaan Boztug, Jordan S. Orange, Inés Avedillo Díez, Hanno Glimm, Pinaki P. Banerjee
Publikováno v:
The New England journal of medicine. 363(20)
The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive primary immunodeficiency disorder associated with thrombocytopenia, eczema, and autoimmunity. We treated two patients who had this disorder with a transfusion of autologous, genetically modi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0866144beff8940c6648ea18f0077610
https://pubmed.ncbi.nlm.nih.gov/21067383
https://pubmed.ncbi.nlm.nih.gov/21067383
Autor:
Kaan Boztug, Thomas Moulton, Simona Gatti, Blanche P. Alter, Julie Curtin, Nima Parvaneh, P. J. Darbyshire, Nima Rezaei, Jeffrey W. Innis, Jean Donadieu, Zekai Avci, Karl Welte, Rachel Fruge, Christoph Klein, George R. Buchanan, John Corns, Larry Boxer, Philip S. Rosenberg, Hung Chi Tran, Marie Böhm, Isabelle Pellier
Publikováno v:
Blood. 116:1495-1495
Abstract 1495 Severe congenital neutropenia (SCN) is a heterogenous group of disorders characterized by an increased susceptibility to bacterial infections. Recently, our discovery of G6PC3 deficiency in 12 patients with SCN and various developmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c97989a065b4e705075b18dd9397c58c
https://doi.org/10.1182/blood.v116.21.1495.1495
https://doi.org/10.1182/blood.v116.21.1495.1495
Autor:
Rudolf Ferrari, Marie Böhm, Miguel R. Abboud, Claudia R. Ball, Christoph Klein, Martina Rose, Sonja Naundorf, Rainer Blasczyk, László Maródi, Rita Beier, Ali Nowrouzi, Mathias Liesl, Inés Avedillo Díez, von Kalle Christof, Waleed Al-Herz, Pinaki P. Banerjee, Kaan Boztug, Irina Kondratenko, Ricardo A Dewey, Adrian Schwarzer, Manfred Schmidt, Chris Fraser, Jordan S. Orange, Klaus Küuhlcke
Publikováno v:
Blood. 116:5-5
Abstract 5 Wiskott Aldrich Syndrome is a life-threatening immune-disorder characterized by bleeding secondary to microthrombocytopenia, immunodeficiency, autoimmunity, and susceptibility to lymphoma. A clinical gene therapy protocol using a GALV pseu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5336ccdbd5647eb89c3987399d3fd967
https://doi.org/10.1182/blood.v116.21.5.5
https://doi.org/10.1182/blood.v116.21.5.5