57. Jahrestagung der Deutschen Gesellschaft für Neuropathologie und Neuroanatomie (DGNN)
Deutsche Gesellschaft für Neuropathologie und Neuroanatomie
12. - 15.09.2012, Erlangen
Poster Presentations
Muscle and Nerve pathology
Meeting Abstract
(12dgnnPP1.1)
[Volltext]
Hypoxia related molecular mechanisms in adult and juvenile dermatomyositis
Preuße C, Goebel HH, Schoser B, Heppner FL, Schara U, Stenzel W[Volltext]
Meeting Abstract
(12dgnnPP1.2)
[Volltext]
Differential analysis of protein aggregates in myofibrillar myopathies – a proteomic approach
Maerkens A, Kley R, Theis V, Vorgerd M, Müller T, Marcus K[Volltext]
Meeting Abstract
(12dgnnPP1.3)
[Volltext]
The Modified Procedure and its Experimental study Treating the Compartment Syndrome as well as the established Volkmmann contracture
Wang X[Volltext]
Meeting Abstract
(12dgnnPP1.4)
[Volltext]
LMD-assisted Comparison of Muscle Proteome in Patients with Filaminopathy and matched Controls
Theis V, Maerkens A, Kley RA, Vorgerd M, Marcus K[Volltext]
Meeting Abstract
(12dgnnPP1.5)
[Volltext]
“Woozy” mice are a broad phenocopy of human Marinesco-Sjögren syndrome: an electron microscopic and biochemical longitudinal study
Roos A, Buchkremer S, Goswami A, Nolte K, Senderek J, Brauers E, Weis J[Volltext]
Meeting Abstract
(12dgnnPP1.6)
[Volltext]
Novel INF2 mutation links the FSGS-CMT associated pathophysiology to disturbances in ER homeostasis
Roos A, Buchkremer S, Brauers E, Boor P, Senderek J, Häusler M, Weis J[Volltext]
Meeting Abstract
(12dgnnPP1.7)
[Volltext]
Facial nerve repair: comparison of direct repair and y-tube-conduit repair techniques
Hizay A, Ozsoy U, Demirel BM, Ozsoy O, Angelova S, Ankerne J, Bilmen Sarikcioglu S, Dunlop S, Angelov D, Sarikcioglu L[Volltext]
Meeting Abstract
(12dgnnPP1.8)
[Volltext]
Muscle and nerve pathology in spinal muscular atrophy with respiratory distress (SMARD1). Comparison of human and murine SMARD
Stoltenburg-Didinger G, Jablonka S, Kaindl A, von Au K[Volltext]
Meeting Abstract
(12dgnnPP1.9)
[Volltext]
Gastrointestinal dysmotility as initial symptom of RET mutation-associated MEN2B syndrome
Rolle U, Gfrörer S, Harter PN, Müller K, Mittelbronn M[Volltext]
Meeting Abstract
(12dgnnPP1.10)
[Volltext]
Mitochondrial degeneration in familial ATP synthetase defect
Vlaho S, Müller K, Selter M, Drott U, Harter PN, Kieslich M, Mittelbronn M[Volltext]
Meeting Abstract
(12dgnnPP1.11)
[Volltext]
Teaching neuromuscular structure and functions in undergraduate medical education
Gurpinar E, Alimoglu MK[Volltext]
Meeting Abstract
(12dgnnPP1.12)
[Volltext]
Morphological changes in muscle biopsies from patients with infantile and juvenile Pompe disease as a potential predictive marker for enzyme replacement therapy
Prölß AK, Hahn A, Mühlfeld C, von Pein H, Mengel E, Schänzer A[Volltext]
Meeting Abstract
(12dgnnPP1.13)
[Volltext]
Muscle biopsy: Diagnostic value and spectrum of alterations in 2836 patients
Hagel C, Pfanzelt C, Magnus T, Glatzel M, Kunze K[Volltext]
Meeting Abstract
(12dgnnPP1.14)
[Volltext]
Palpebral myopathology of congenital ptosis
Sarnat HB, Flores-Sarnat L, Kherani F[Volltext]
Meeting Abstract
(12dgnnPP1.15)
[Volltext]
Histopathological findings in Pompe disease.
Ortiz A, Ruano Calderón LA, Vargas Cañas S, Fernández Valverde F, Dumar Riaño A[Volltext]
Meeting Abstract
(12dgnnPP1.16)
[Volltext]
Amyotrophic Lateral Sclerosis.
Fernández Valverde F, Ruano Calderón LA, Sánchez García A, Kasakova E, Dumar Riaño A, Ortiz Saldaña A, Vargas Cañas S[Volltext]
Meeting Abstract
(12dgnnPP1.17)
[Volltext]
Molecular mechanism of plectin-mediated desmin network anchoring
Staszewska I[Volltext]
Meeting Abstract
(12dgnnPP1.18)
[Volltext]
Diagnosis of neurosarcoidosis by FDG PET/CT
Blumstein N, Zimmerman R, Permanetter W, Woischneck D, Heckmann J[Volltext]
