169th ENMC International Workshop Rare Structural Congenital Myopathies 6–8 November 2009, Naarden, The Netherlands

Por Goebel, Hans H., Bönnemann, Carsten G.
Publicado no Neuromuscul Disord (2011)

Primary desminopathies

Por Schröder, Rolf, Vrabie, Alexandra, Goebel, Hans H
Publicado em 2007

Intermediate Filament Diseases: Desminopathy

Por Goldfarb, Lev G., Olivé, Montse, Vicart, Patrick, Goebel, Hans H.
Publicado em 2008

M2 Polarized Macrophages and Giant Cells Contribute to Myofibrosis in Neuromuscular Sarcoidosis

Por Prokop, Stefan, Heppner, Frank L., Goebel, Hans H., Stenzel, Werner
Publicado em 2011

Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson’s disease

Por Wrede, Arne, Margraf, Nils G., Goebel, Hans H., Deuschl, Günther, Schulz-Schaeffer, Walter J.
Publicado em 2011

Neuronal loss and brain atrophy in mice lacking cathepsins B and L

Por Felbor, Ute, Kessler, Benedikt, Mothes, Walther, Goebel, Hans H., Ploegh, Hidde L., Bronson, Roderick T., Olsen, Bjorn R.
Publicado em 2002

The lymphoid follicle variant of dermatomyositis

Por Radke, Josefine, Pehl, Debora, Aronica, Eleonora, Schonenberg-Meinema, Dieneke, Schneider, Udo, Heppner, Frank L., de Visser, Marianne, Goebel, Hans H., Stenzel, Werner
Publicado em 2014

De Novo Prion Aggregates Trigger Autophagy in Skeletal Muscle

Por Joshi-Barr, Shivanjali, Bett, Cyrus, Chiang, Wei-Chieh, Trejo, Margarita, Goebel, Hans H., Sikorska, Beata, Liberski, Pawel, Raeber, Alex, Lin, Jonathan H., Masliah, Eliezer, Sigurdson, Christina J.
Publicado em 2014

Ubiquitin ligase defect by DCAF8 mutation causes HMSN2 with giant axons

Por Klein, Christopher J., Wu, Yanhong, Vogel, Peter, Goebel, Hans H., Bönnemann, Carsten, Zukosky, Kristen, Botuyan, Maria-Victoria, Duan, Xiaohui, Middha, Sumit, Atkinson, Elizabeth J., Mer, Georges, Dyck, Peter J.
Publicado em 2014

Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy

Por Hess, Barbara, Saftig, Paul, Hartmann, Dieter, Coenen, Ruth, Lüllmann-Rauch, Renate, Goebel, Hans H., Evers, Meike, von Figura, Kurt, D’Hooge, Rudi, Nagels, Guy, De Deyn, Peter, Peters, Christoph, Gieselmann, Volkmar
Publicado em 1996

ATP Synthase Deficiency due to TMEM70 Mutation Leads to Ultrastructural Mitochondrial Degeneration and Is Amenable to Treatment

Por Braczynski, Anne K., Vlaho, Stefan, Müller, Klaus, Wittig, Ilka, Blank, Anna-Eva, Tews, Dominique S., Drott, Ulrich, Kleinle, Stephanie, Abicht, Angela, Horvath, Rita, Plate, Karl H., Stenzel, Werner, Goebel, Hans H., Schulze, Andreas, Harter, Patrick N., Kieslich, Matthias, Mittelbronn, Michel
Publicado no Biomed Res Int (2015)

In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy

Por Shatunov, Alexey, Olivé, Montse, Odgerel, Zagaa, Stadelmann-Nessler, Christine, Irlbacher, Kerstin, van Landeghem, Frank, Bayarsaikhan, Munkhuu, Lee, Hee-Suk, Goudeau, Bertrand, Chinnery, Patrick F, Straub, Volker, Hilton-Jones, David, Damian, Maxwell S, Kaminska, Anna, Vicart, Patrick, Bushby, Kate, Dalakas, Marinos C, Sambuughin, Nyamkhishig, Ferrer, Isidro, Goebel, Hans H, Goldfarb, Lev G
Publicado em 2009