Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory Neuropathy (English)
- New search for: Vill, Katharina
- New search for: Ille, Lena
- New search for: Blaschek, Astrid
- New search for: Rawer, Rainer
- New search for: Landgraf, Mirjam N.
- New search for: Gerstl, Lucia
- New search for: Schroeder, Sebastian A.
- New search for: Müller-Felber, Wolfgang
- New search for: Vill, Katharina
- New search for: Ille, Lena
- New search for: Blaschek, Astrid
- New search for: Rawer, Rainer
- New search for: Landgraf, Mirjam N.
- New search for: Gerstl, Lucia
- New search for: Schroeder, Sebastian A.
- New search for: Müller-Felber, Wolfgang
In:
Neuropediatrics
;
48
, 06
;
420-425
;
2017
- Article (Journal) / Electronic Resource
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Title:Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory Neuropathy
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Contributors:Vill, Katharina ( author ) / Ille, Lena ( author ) / Blaschek, Astrid ( author ) / Rawer, Rainer ( author ) / Landgraf, Mirjam N. ( author ) / Gerstl, Lucia ( author ) / Schroeder, Sebastian A. ( author ) / Müller-Felber, Wolfgang ( author )
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Published in:Neuropediatrics ; 48, 06 ; 420-425
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Publisher:
- New search for: Georg Thieme Verlag KG
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Place of publication:Stuttgart · New York
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Publication date:2017-12-01
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Size:6 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 48, Issue 06
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 403
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Congenital Glioblastoma Multiforme: An Unusual and Challenging TumorAnestis, Dimitrios M. / Tsitsopoulos, Parmenion P. / Ble, Christina A. / Tsitouras, Vassilios / Tsonidis, Christos A. et al. | 2017
- 413
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The Role of Amplitude Integrated Electroencephalogram in Very Low-Birth-Weight Preterm Infants: A Literature ReviewMagalhães, Luiza Vieira da Silva / Winckler, Maria Isabel Bragatti / Bragatti, José Augusto / Procianoy, Renato / Silveira, Rita de Cássia Santos et al. | 2017
- 420
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Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory NeuropathyVill, Katharina / Ille, Lena / Blaschek, Astrid / Rawer, Rainer / Landgraf, Mirjam N. / Gerstl, Lucia / Schroeder, Sebastian A. / Müller-Felber, Wolfgang et al. | 2017
- 426
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Different Mutations of Gap Junction Connexin 47 Lead to Discrepant Activation of Unfolded Protein Response Pathway in Pelizaeus–Merzbacher-Like DiseaseChen, Na / Wang, Jingmin / Jiang, Yuwu / Wu, Ye / Hao, Hongjun / Ji, Taoyun et al. | 2017
- 432
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Normal Head Shape Parameters in the First 2 Years of Life and Effect of Helmet TherapyWilbrand, Jan-Falco / Kaps, Kerstin / Tabak, Darko / Bierther, Uta / Wilbrand, Martina / Neubauer, Bernd Axel / Pons-Kuehnemann, Joern / Howaldt, Hans-Peter / Hahn, Andreas et al. | 2017
- 442
-
Molecular Analysis Confirms that FKRP-Related Disorders are Underdiagnosed in Mexican Patients with Neuromuscular DiseasesNavarro-Cobos, María José / González-del Angel, Ariadna / Estandia-Ortega, Bernardette / Ruiz-Herrera, Adriana / Becerra, Arturo / Vargas-Ramírez, Guadalupe / Bermúdez-López, Cesárea / Alcántara-Ortigoza, Miguel Angel et al. | 2017
- 451
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Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American MyopathyGrzybowski, Michelle / Schänzer, Anne / Pepler, Alexander / Heller, Corina / Neubauer, Bernd A. / Hahn, Andreas et al. | 2017
- 456
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Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the LiteratureKropach, Nesia / Shkalim-Zemer, Vered / Orenstein, Naama / Scheuerman, Oded / Straussberg, Rachel et al. | 2017
- 463
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Morning Glory Disc Anomaly Associated with Ipsilateral Optic Nerve and Chiasm Thickening: Three Cases and Review of the LiteratureDoneda, Chiara / Pinelli, Lorenzo / Scaramuzzi, Matteo / Galli, Jessica / Fazzi, Elisa / Parazzini, Cecilia / Righini, Andrea / Nucci, Paolo et al. | 2017
- 467
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Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine AnalysisKomulainen-Ebrahim, Jonna / Saastamoinen, Eemeli / Rahikkala, Elisa / Helander, Heli / Hinttala, Reetta / Risteli, Leila / Rantala, Heikki / Uusimaa, Johanna et al. | 2017
- 473
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Anti-HMGCR Antibody–Related Necrotizing Autoimmune Myopathy Mimicking Muscular DystrophyTard, Céline / Tiffreau, Vincent / Jaillette, Emmanuelle / Jouen, Fabienne / Nelson, Isabelle / Bonne, Gisèle / Yaou, Rabah Ben / Romero, Norma / Vallée, Louis / Vermersch, Patrick et al. | 2017
- 477
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Neonatal-Onset Recurrent Guillain–Barré Syndrome-Like Disease: Clues for Inherited CD59 DeficiencyArdicli, Didem / Taskiran, Ekim Z. / Kosukcu, Can / Temucin, Cagri / Oguz, Kader K. / Haliloglu, Goknur / Alikasifoglu, Mehmet / Topaloglu, Haluk et al. | 2017
- 482
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Chorea Minor Associated with Anti-Neurochondrin AutoantibodiesRommel, Frank R. / Miske, Ramona / Stöcker, Winfried / Arneth, Borros / Neubauer, Bernd A. / Hahn, Andreas et al. | 2017
- 484
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The Epilepsy-Aphasia Spectrum: From Landau–Kleffner Syndrome to Rolandic EpilepsyBölsterli Heinzle, Bigna Katrin et al. | 2017