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B Meissner

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Articles 34
Citations 863
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Recent Articles
1.
Costa S, Regier D, Meissner B, Cromwell I, Ben-Neriah S, Chavez E, et al.
Curr Oncol . 2016 Nov; 23(5):304-313. PMID: 27803594
Background: Genomic technologies are increasingly used to guide clinical decision-making in cancer control. Economic evidence about the cost-effectiveness of genomic technologies is limited, in part because of a lack of...
2.
Zaliova M, Zimmermannova O, Dorge P, Eckert C, Moricke A, Zimmermann M, et al.
Leukemia . 2015 May; 29(5):1222. PMID: 25945612
No abstract available.
3.
Zaliova M, Zimmermannova O, Dorge P, Eckert C, Moricke A, Zimmermann M, et al.
Leukemia . 2013 Sep; 28(1):182-5. PMID: 24072102
No abstract available.
4.
Ellinghaus E, Stanulla M, Richter G, Ellinghaus D, Te Kronnie G, Cario G, et al.
Leukemia . 2011 Nov; 26(5):902-9. PMID: 22076464
Acute lymphoblastic leukemia (ALL) is a malignant disease of the white blood cells. The etiology of ALL is believed to be multifactorial and likely to involve an interplay of environmental...
5.
Zerr I, Kallenberg K, Summers D, Romero C, Taratuto A, Heinemann U, et al.
Brain . 2009 Sep; 132(Pt 10):2659-68. PMID: 19773352
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype....
6.
Meissner B, Kallenberg K, Sanchez-Juan P, Collie D, Summers D, Almonti S, et al.
Neurology . 2009 Jun; 72(23):1994-2001. PMID: 19506221
Background: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six molecular subtypes (MM1, MM2, MV1, MV2, VV1, and VV2) have been described, which vary with respect to age at disease onset,...
7.
Meissner B, Kallenberg K, Sanchez-Juan P, Ramljak S, Krasnianski A, Heinemann U, et al.
J Neurol . 2009 Jan; 256(3):355-63. PMID: 19159063
Objective: Iatrogenic Creutzfeldt-Jakob disease (iCJD) is mainly associated with dura mater (DM) grafts and administration of human growth hormones (hGH). Data on disease course in DM-CJD are limited. We describe...
8.
Sauer M, Meissner B, Fuchs D, Gruhn B, Kabisch H, Erttmann R, et al.
Bone Marrow Transplant . 2008 Oct; 43(5):375-81. PMID: 18850023
Hurler's syndrome is an inborn error of mucopolysaccharide metabolism leading to premature death in childhood. Allogeneic hematopoietic SCT can achieve long-term survival by correcting the enzymatic deficiency. In an attempt...
9.
Krasnianski A, Kallenberg K, Collie D, Meissner B, Schulz-Schaeffer W, Heinemann U, et al.
Eur J Neurol . 2008 Aug; 15(8):762-71. PMID: 18684308
Background And Purpose: To establish radiological features in the atypical MV2 subtype of sCJD compared with the classical MM1 subtype, as well as region- and sequence-dependent inter-observer correlation. Methods: MRI...
10.
Meissner B, Kallenberg K, Sanchez-Juan P, Krasnianski A, Heinemann U, Varges D, et al.
AJNR Am J Neuroradiol . 2008 Jul; 29(8):1519-24. PMID: 18599580
Background And Purpose: Hyperintense basal ganglia on MR imaging support the diagnosis of sporadic Creutzfeldt-Jakob disease (CJD). Our aim was to study the frequency of patients with sporadic CJD presenting...