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1

Predominant fiber atrophy and fiber type disproportion in early ullrich disease

Joachim Schessl, Nathalie M. Goemans, Alexandra I. Magold, Yaqun Zou, Ying Hu, Janbernd Kirschner, Raf Sciot, Carsten G. Bönnemann

Journal:

Year:

2008

Language:

english

File:

PDF, 1.36 MB

english, 2008

2

Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and miyoshi type of muscular dystrophy

Joachim Schessl, Wolfram Kress, Benedikt Schoser

Journal:

Year:

2012

Language:

english

File:

PDF, 928 KB

english, 2012

3

P2.42 Cys150Arg FHL1 mutation in two brothers affected by the Emery-Dreifuss muscular dystrophy phenotype

C. Ortez, A. Nascimento, C. Jimenez-Mallabrera, S. Feldkirchner, C. Kubny, J. Schessl, C. Jou, J. Corbera, M. Roig, J. Colomer

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

4

Novel recessive myotilin mutation causes severe myofibrillar myopathy

Schessl, Joachim, Bach, Elisa, Rost, Simone, Feldkirchner, Sarah, Kubny, Christiana, Müller, Stefan, Hanisch, Franz-Georg, Kress, Wolfram, Schoser, Benedikt

Journal:

Year:

2014

Language:

english

File:

PDF, 5.65 MB

english, 2014

5

Familial Reducing Body Myopathy with Cytoplasmic Bodies and Rigid Spine Revisited: Identification of a Second LIM Domain Mutation in FHL1

Schessl, J., Columbus, A., Hu, Y., Zou, Y., Voit, T., Goebel, H. H., Bönnemann, C. G.

Journal:

Neuropediatrics

Year:

2010

Language:

english

File:

PDF, 244 KB

english, 2010

6

Clinical Presentation and Course of Childhood Guillain-Barré Syndrome: A Prospective Multicentre Study

Korinthenberg, R., Schessl, J., Kirschner, J.

Journal:

Neuropediatrics

Year:

2007

Language:

english

File:

PDF, 271 KB

english, 2007

7

Relationship between vegetation and environmental conditions in the northern Pantanal of Mato Grosso, Brazil

Peter Zeilhofer, Michael Schessl

Journal:

Journal of Biogeography

Year:

2000

Language:

english

File:

PDF, 426 KB

english, 2000

8

Orthodontic Procedures in the Treatment of Obstructive Sleep Apnea in Children

Edmund Rose, Joachim Schessl

Journal:

Journal of Orofacial Orthopedics/Fortschritte der Kieferorthopädie

Year:

2006

Language:

english

File:

PDF, 740 KB

english, 2006

9

Aszites und Abmagerung bei intrakranieller Raumforderung

J. Schessl, V. Mall, V. van Velthoven, R. Korinthenberg

Journal:

Monatsschrift Kinderheilkunde

Year:

2007

Language:

german

File:

PDF, 258 KB

german, 2007

10

Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration

J. Schessl, M. Schuberth, P. Reilich, P. Schneiderat, N. Strigl-Pill, M. C. Walter, B. Schlotter-Weigel, B. Schoser

Journal:

Journal of Neurology

Year:

2011

Language:

english

File:

PDF, 123 KB

english, 2011

11

Infections and vaccinations preceding childhood Guillain-Barré syndrome: a prospective study

Joachim Schessl, Birgit Luther, Janbernd Kirschner, Gottfried Mauff, Rudolf Korinthenberg

Journal:

European Journal of Pediatrics

Year:

2006

Language:

english

File:

PDF, 132 KB

english, 2006

12

Maturation of inhibitory and excitatory motor cortex pathways in children

Michael Walther, Steffen Berweck, Joachim Schessl, Michaela Linder-Lucht, Urban M. Fietzek, Franz X. Glocker, Florian Heinen, Volker Mall

Journal:

Brain and Development

Year:

2009

Language:

english

File:

PDF, 237 KB

english, 2009

13

Congenital Muscular Dystrophies and the Extracellular Matrix

Joachim Schessl, Yaqun Zou, Carsten G. Bönnemann

Journal:

Seminars in Pediatric Neurology

Year:

2006

Language:

english

File:

PDF, 1.14 MB

english, 2006

14

Reducing Body Myopathy and Other FHL1-Related Muscular Disorders

Joachim Schessl, Sarah Feldkirchner, Christiana Kubny, Benedikt Schoser

Journal:

Seminars in Pediatric Neurology

Year:

2011

Language:

english

File:

PDF, 787 KB

english, 2011

15

Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial

Janbernd Kirschner, Joachim Schessl, Ulrike Schara, Bernd Reitter, Georg M Stettner, Elke Hobbiebrunken, Ekkehard Wilichowski, Günther Bernert, Simone Weiss, Florian Stehling, Gert Wiegand, Wolfgang M

Journal:

The Lancet Neurology

Year:

2010

Language:

english

File:

PDF, 219 KB

english, 2010

16

Electrical Power Net Systems in Cars—Impedance Modeling and Measurement

Bechteler, M.S., Schessl, C.M., Bechteler, T.F.

Journal:

IEEE Transactions on Vehicular Technology

Year:

2010

Language:

english

File:

PDF, 397 KB

english, 2010

17

Effects of fragmentation on forest structure and litter dynamics in Atlantic rainforest in Pernambuco, Brazil

Michael Schessl, Wilkilane Luiz Da Silva, Gerhard Gottsberger

Journal:

Flora - Morphology, Distribution, Functional Ecology of Plants

Year:

2008

Language:

english

File:

PDF, 512 KB

english, 2008

18

P.P.7 08 Early changes in muscle fiber size and type distribution in congenital muscular dystrophy type Ullrich

J. Schessl, A.I. Magold, Y. Zou, C.G. Bönnemann

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 42 KB

english, 2006

19

MRI in DNM2-related centronuclear myopathy: Evidence for highly selective muscle involvement

Joachim Schessl, Livija Medne, Ying Hu, Yaqun Zou, Mark J. Brown, Jason T. Huse, Drew A. Torigian, Heinz Jungbluth, Hans-Hilmar Goebel, Carsten G. Bönnemann

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 1.14 MB

english, 2007

20

G.P.4.14 Clinical variability in siblings with calpainopathy (LGMD2A)

J. Kirschner, J. Schessl, M. Walter, G. Schreiber, C. Müller-Reible, U. Schara, C. Bönnemann, R. Korinthenberg

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

21

C.P.2.04 Skipping of exon 16 in COL6A3 is a recurrent mutation causing severe congenital muscular dystrophy type Ullrich

Y. Zou, J. Schessl, A. Lampe, Y. Hu, C. Jiménez-Mallebrera, G. Schreiber, I. Stolte-Dijkstra, A. Fock, M. Chu, K. Bushby, R. Weiss, K. Flanigan, F. Muntoni, C. Bönnemann

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 51 KB

english, 2007

22

G.P.1.05 siRNA mediated allele specific selective silencing of a dominant negative COL6A3 mutation causing UCMD

Y. Zou, J. Schessl, C. Bonnemann

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 46 KB

english, 2008

23

G.O.2 Proteomic identification of the LIM domain protein FHL1 as the gene-product mutated in reducing body myopathy

J. Schessl, Y. Zou, M.J. McGrath, B.S. Cowling, B. Maiti, S.S. Chin, C. Sewry, R. Battini, Y. Hu, D.L. Cottle, M. Rosenblatt, L. Spruce, A. Ganguly, J. Kirschner, A.R. Judkins, J.A. Golden, H.H. Goebe

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 63 KB

english, 2008

24

G.P.5.10 Novel FHL1 mutation in familial mixed reducing body myopathy with rigid spine

J. Schessl, A. Columbus, Y. Hu, Y. Zou, T. Voit, H.H. Goebel, C.G. Bönnemann

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 52 KB

english, 2009

25

G.P.13.04 In-frame deletion of the entire dystrophin rod domain prevents compensation by utrophin and causes an unusually severe muscular dystrophy

J. Schessl, M.L. Yang, P.T. Heydemann, R.L. Sufit, L. Medne, A. Attia, R.S. Finkel, C.G. Bönnemann

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 39 KB

english, 2009

26

Muscle MRI in FHL1-linked reducing body myopathy

G. Astrea, J. Schessl, E. Clement, M. Tosetti, E. Mercuri, M. Rutherford, G. Cioni, C.G. Bönnemann, F. Muntoni, R. Battini

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 700 KB

english, 2009

27

The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy

Peter Reilich, Benedikt Schoser, Nicolai Schramm, Sabine Krause, Joachim Schessl, Wolfram Kress, Josef Müller-Höcker, Maggie C. Walter, Hanns Lochmuller

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 490 KB

english, 2010

28

P5.51 Evaluation of standardized protein pattern of skeletal muscle fibers via laser microdissection

S. Feldkirchner, S. Müller, W. Kress, F.G. Hanisch, B. Schoser, J. Schessl

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 59 KB

english, 2011

29

P5.53 The C224W FHL1 mutation is causing a protein aggregation disorder of muscle: Two brothers revisited

S. Feldkirchner, M.C. Walter, C. Kubny, S. Mueller, W. Kress, F.G. Hanisch, B. Schoser, J. Schessl

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

30

Anti-GT1a IgG Antibodies in a Child With Severe Guillain-Barré Syndrome

Joachim Schessl, Kei Funakoshi, Keiichiro Susuki, Ralf Gold, Rudolf Korinthenberg

Journal:

Pediatric Neurology

Year:

2006

Language:

english

File:

PDF, 67 KB

english, 2006

31

Patient-specific protein aggregates in myofibrillar myopathies: Laser microdissection and differential proteomics for identification of plaque components

Feldkirchner, Sarah, Schessl, Joachim, Müller, Stefan, Schoser, Benedikt, Hanisch, Franz-Georg

Journal:

Year:

2012

Language:

english

File:

PDF, 1.13 MB

english, 2012

32

Deafferentation of neighbouring motor cortex areas does not further enhance saturated practice-dependent plasticity in healthy adults

Michael Walther, Nicola Kuhnke, Joachim Schessl, Igor Delvendahl, Nikolai Jung, Dirk Kreml, Ulf Ziemann, Volker Mall

Journal:

Clinical Neurophysiology

Year:

2008

Language:

english

File:

PDF, 131 KB

english, 2008

33

G.P.123 Identification of molecular effects of FHL1 mutations on protein assembly in reducing body myopathy

Kubny, C., Bulst, S., Levin, J., Krause, S., Schoser, B., Giese, A., Walter, M.C., Schessl, J.

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 50 KB

english, 2012

34

Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy

Feldkirchner, Sarah, Walter, Maggie C., Müller, Stefan, Kubny, Christiana, Krause, Sabine, Kress, Wolfram, Hanisch, Franz-Georg, Schoser, Benedikt, Schessl, Joachim

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 1.72 MB

english, 2013

35

Relationship between Vegetation and Environmental Conditions in the Northern Pantanal of Mato Grosso, Brazil

Peter Zeilhofer and Michael Schessl

Journal:

Journal of Biogeography

Year:

2000

Language:

english

File:

PDF, 1.62 MB

english, 2000

36

Identification of FHL1 as a Regulator of Skeletal Muscle Mass: Implications for Human Myopathy

Belinda S. Cowling, Meagan J. McGrath, Mai-Anh Nguyen, Denny L. Cottle, Anthony J. Kee, Susan Brown, Joachim Schessl, Yaqun Zou, Josephine Joya, Carsten G. Bönnemann, Edna C. Hardeman and Christina A.

Journal:

The Journal of Cell Biology

Year:

2008

Language:

english

File:

PDF, 2.58 MB

english, 2008

37

A.P.5

Schessl, J., Bach, E., Rost, S., Feldkirchner, S., Kubny, C., Müller, S., Hanisch, F.G., Kress, W., Schoser, B.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 45 KB

english, 2014

38

A.P.1

Maerkens, A., Olivé, M., Tasca, G., Claeys, K., Barresi, R., Sarkozy, A., Pfeffer, G., Evangelista, T., Feldkirchner, S., Reimann, J., Hanisch, F., Stenzel, W., Schessl, J., Schoser, B., Goldfarb, L.,

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 51 KB

english, 2014

39

G.P.148

Schessl, J., Kress, W., Feldkirchner, S., Schoser, B.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 46 KB

english, 2014

40

G.P.151

Keßler, M., Kieltsch, A., Kayvanpour, E., Schoser, B., Schessl, J., Rottbauer, W., Just, S.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 46 KB

english, 2014

41

Muscle ultrasound in classic infantile and adult Pompe disease: A useful screening tool in adults but not in infants

Vill, K., Schessl, J., Teusch, V., Schroeder, S., Blaschek, A., Schoser, B., Müller-Felber, W.

Journal:

Neuromuscular Disorders

Year:

2015

Language:

english

File:

PDF, 1.04 MB

english, 2015

42

Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy

Cowling, B. S., McGrath, M. J., Nguyen, M.-A., Cottle, D. L., Kee, A. J., Brown, S., Schessl, J., Zou, Y., Joya, J., Bonnemann, C. G., Hardeman, E. C., Mitchell, C. A.

Journal:

The Journal of Cell Biology

Year:

2008

Language:

english

File:

PDF, 3.59 MB

english, 2008

43

In vivo characterization of human myofibrillar myopathy genes in zebrafish

Bührdel, John B., Hirth, Sofia, Keßler, Mirjam, Westphal, Sören, Forster, Monika, Manta, Linda, Wiche, Gerhard, Schoser, Benedikt, Schessl, Joachim, Schröder, Rolf, Clemen, Christoph S., Eichinger, Lu

Journal:

Biochemical and Biophysical Research Communications

Year:

2015

Language:

english

File:

PDF, 2.05 MB

english, 2015

44

A novel role for Lef-1, a central transcription mediator of Wnt signaling, in leukemogenesis

Petropoulos, K., Arseni, N., Schessl, C., Stadler, C. R., Rawat, V. P.S., Deshpande, A. J., Heilmeier, B., Hiddemann, W., Quintanilla-Martinez, L., Bohlander, S. K., Feuring-Buske, M., Buske, C.

Journal:

Journal of Experimental Medicine

Year:

2008

Language:

english

File:

PDF, 3.89 MB

english, 2008

45

Severe Obstructive Sleep Apnea Alleviated by Oral Appliance in a Three-Year-Old Boy

Schessl, Joachim, Rose, Edmund, Korinthenberg, Rudolf, Henschen, Matthias

Journal:

Year:

2008

Language:

english

File:

PDF, 257 KB

english, 2008

46

Role of GluR1 in Activity-Dependent Motor System Development

Zhang, L., Schessl, J., Werner, M., Bonnemann, C., Xiong, G., Mojsilovic-Petrovic, J., Zhou, W., Cohen, A., Seeburg, P., Misawa, H., Jayaram, A., Personius, K., Hollmann, M., Sprengel, R., Kalb, R.

Journal:

Journal of Neuroscience

Year:

2008

Language:

english

File:

PDF, 879 KB

english, 2008

47

Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models

Aigner, B., Rathkolb, B., Herbach, N., Kemter, E., Schessl, C., Klaften, M., Klempt, M., de Angelis, M. H., Wanke, R., Wolf, E.

Journal:

AJP Renal Physiology

Year:

2007

Language:

english

File:

PDF, 402 KB

english, 2007

48

Prospective study on anti-ganglioside antibodies in childhood Guillain-Barre syndrome

Schessl, J, Koga, M, Funakoshi, K, Kirschner, J, Muellges, W, Weishaupt, A, Gold, R, Korinthenberg, R

Journal:

Archives of Disease in Childhood

Year:

2007

Language:

english

File:

PDF, 183 KB

english, 2007

49

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1

Schessl, J., Taratuto, A. L., Sewry, C., Battini, R., Chin, S. S., Maiti, B., Dubrovsky, A. L., Erro, M. G., Espada, G., Robertella, M., Saccoliti, M., Olmos, P., Bridges, L. R., Standring, P., Hu, Y.

Journal:

Year:

2008

Language:

english

File:

PDF, 1.09 MB

english, 2008

50

New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses

Maerkens, A., Olivé, M., Schreiner, A., Feldkirchner, S., Schessl, J., Uszkoreit, J., Barkovits, K., Güttsches, A. K., Theis, V., Eisenacher, M., Tegenthoff, M., Goldfarb, L. G., Schröder, R., Schoser

Journal:

Acta Neuropathologica Communications

Year:

2016

Language:

english

File:

PDF, 8.18 MB

english, 2016