Visual Universitätsmedizin Mainz

Publikationen 2015

1

Braczynski AK, Vlaho S, Müller K, Wittig I, Blank AE, Tews DS, Drott U, Kleinle S, Abicht A, Horvath R, Plate KH, Stenzel W, Goebel HH, Schulze A, Harter PN, Kieslich M, Mittelbronn M:
ATP synthase deficiency due to TMEM70 mutation leads to ultrastructural mitochondrial Degeneration and is amenable to Treatment.
Biomed Res Int (2015) 2015: 462592

2

De Bleecker JL, De Paepe B, Aronica E, de Visser M, ENMC Myositis Muscle Biopsy Study Group, Amato A, Aronica E, Benveniste O, De Bleecker J, de Boer O, De Paepe B, de Visser M, Dimachkie M, Gherardi R, Goebel HH, Hilton-Jones D, Holton J, Lundberg IE, Mammen A, Mastaglia F, Nishino I, Rushing E, Daa Schroder H, Selcen D, Stenzel W:
205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies part II 28-30 March 2014, Naarden, The Netherlands.
Neuromuscul Disord (201) 25 (3): 268-272

3

Frauenknecht K, Katzav A, Weiss Lavi R, Sabaq A, Otten S, Chapman J, Sommer CJ:
Mice with experimental antiphospholipid syndrome display hippocampal dysfunction and a reduction of dendritic complexity in hippocampal CA1 neurones.
Neuropathol Appl Neurobiol (2015) 41 (5): 657-71

4

Mayer A, Schwabeck C, Sommer C, Stockinger M, Giese A, Renovanz M, Vaupel P, Schmidtberger H:
Adjuvant temozolomide-based chemoradiotherapy versus radiotherapy alone in patients with WHO III astrocytoma: The Mainz experience.
Strahlenther Onkol (2015) 191 (8): 665-671

5

Preusse C, Goebel HH, Pehl D, Rinnenthal JL, Kley RA, Allenbach Y, Heppner FL, Vorgerd M, Authier FJ, Gherardi R, Stenzel W:
Th2-M2-immunity in lesions of muscular sarcoidosis and macrophagic mofasciitis.
Neuropathol Appl Neurobiol (2015) 1 (7): 952-63

6

Radke J, Stenzel W, Goebel HH:
Human NCL neuropatholoy.
Biochim Biophys Acta (2015) 1852 (10 PtB): 2262-6

7

Stenzel W, Preuße C, Allenbach Y, Pehl D, Junckerstorff R, Heppnr FL, Nolte K, Aronica E, Kana V, Rushing E, Schneider U, Claeys KG, Benveniste O, Weis J, Goebel HH:
Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy.
Neurology (2015) 84 (13): 1346-54