gms | German Medical Science

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)

Hypoxia related molecular mechanisms in adult and juvenile dermatomyositis

Preuße C, Goebel HH, Schoser B, Heppner FL, Schara U, Stenzel W
Meeting Abstract (12dgnnPP1.2)

Differential analysis of protein aggregates in myofibrillar myopathies – a proteomic approach

Maerkens A, Kley R, Theis V, Vorgerd M, Müller T, Marcus K
Meeting Abstract (12dgnnPP1.3)

The Modified Procedure and its Experimental study Treating the Compartment Syndrome as well as the established Volkmmann contracture

Wang X
Meeting Abstract (12dgnnPP1.4)

LMD-assisted Comparison of Muscle Proteome in Patients with Filaminopathy and matched Controls

Theis V, Maerkens A, Kley RA, Vorgerd M, Marcus K
Meeting Abstract (12dgnnPP1.5)

“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
Meeting Abstract (12dgnnPP1.6)

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
Meeting Abstract (12dgnnPP1.7)

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
Meeting Abstract (12dgnnPP1.8)

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
Meeting Abstract (12dgnnPP1.9)

Gastrointestinal dysmotility as initial symptom of RET mutation-associated MEN2B syndrome

Rolle U, Gfrörer S, Harter PN, Müller K, Mittelbronn M
Meeting Abstract (12dgnnPP1.10)

Mitochondrial degeneration in familial ATP synthetase defect

Vlaho S, Müller K, Selter M, Drott U, Harter PN, Kieslich M, Mittelbronn M
Meeting Abstract (12dgnnPP1.11)

Teaching neuromuscular structure and functions in undergraduate medical education

Gurpinar E, Alimoglu MK
Meeting Abstract (12dgnnPP1.12)

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
Meeting Abstract (12dgnnPP1.13)

Muscle biopsy: Diagnostic value and spectrum of alterations in 2836 patients

Hagel C, Pfanzelt C, Magnus T, Glatzel M, Kunze K
Meeting Abstract (12dgnnPP1.14)

Palpebral myopathology of congenital ptosis

Sarnat HB, Flores-Sarnat L, Kherani F
Meeting Abstract (12dgnnPP1.15)

Histopathological findings in Pompe disease.

Ortiz A, Ruano Calderón LA, Vargas Cañas S, Fernández Valverde F, Dumar Riaño A
Meeting Abstract (12dgnnPP1.16)

Amyotrophic Lateral Sclerosis.

Fernández Valverde F, Ruano Calderón LA, Sánchez García A, Kasakova E, Dumar Riaño A, Ortiz Saldaña A, Vargas Cañas S
Meeting Abstract (12dgnnPP1.17)

Molecular mechanism of plectin-mediated desmin network anchoring

Staszewska I
Meeting Abstract (12dgnnPP1.18)

Diagnosis of neurosarcoidosis by FDG PET/CT

Blumstein N, Zimmerman R, Permanetter W, Woischneck D, Heckmann J