Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders

J. M. Burgunder, L. Schöls, J. Baets, P. Andersen, T. Gasser, Z. Szolnoki, B. Fontaine, C. Van Broeckhoven, S. Di Donato, P. De Jonghe, T. Lynch, C. Mariotti, A. Spinazzola, S. J. Tabrizi, C. Tallaksen, M. Zeviani, H. F. Harbo, J. Finsterer

Research output: Chapter

Original languageEnglish
Title of host publicationEuropean Handbook of Neurological Management
PublisherWiley-Blackwell
Pages97-109
Number of pages13
Volume2
ISBN (Print)9781405185349
DOIs
Publication statusPublished - szept. 21 2011

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Motor Neurons
Muscular Diseases
Peripheral Nerves

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Burgunder, J. M., Schöls, L., Baets, J., Andersen, P., Gasser, T., Szolnoki, Z., ... Finsterer, J. (2011). Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders. In European Handbook of Neurological Management (Vol. 2, pp. 97-109). Wiley-Blackwell. https://doi.org/10.1002/9781444346268.ch8

Molecular Diagnosis of Neurogenetic Disorders : Motoneuron, Peripheral Nerve and Muscle Disorders. / Burgunder, J. M.; Schöls, L.; Baets, J.; Andersen, P.; Gasser, T.; Szolnoki, Z.; Fontaine, B.; Van Broeckhoven, C.; Di Donato, S.; De Jonghe, P.; Lynch, T.; Mariotti, C.; Spinazzola, A.; Tabrizi, S. J.; Tallaksen, C.; Zeviani, M.; Harbo, H. F.; Finsterer, J.

European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. p. 97-109.

Research output: Chapter

Burgunder, JM, Schöls, L, Baets, J, Andersen, P, Gasser, T, Szolnoki, Z, Fontaine, B, Van Broeckhoven, C, Di Donato, S, De Jonghe, P, Lynch, T, Mariotti, C, Spinazzola, A, Tabrizi, SJ, Tallaksen, C, Zeviani, M, Harbo, HF & Finsterer, J 2011, Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders. in European Handbook of Neurological Management. vol. 2, Wiley-Blackwell, pp. 97-109. https://doi.org/10.1002/9781444346268.ch8
Burgunder JM, Schöls L, Baets J, Andersen P, Gasser T, Szolnoki Z et al. Molecular Diagnosis of Neurogenetic Disorders: Motoneuron, Peripheral Nerve and Muscle Disorders. In European Handbook of Neurological Management. Vol. 2. Wiley-Blackwell. 2011. p. 97-109 https://doi.org/10.1002/9781444346268.ch8
Burgunder, J. M. ; Schöls, L. ; Baets, J. ; Andersen, P. ; Gasser, T. ; Szolnoki, Z. ; Fontaine, B. ; Van Broeckhoven, C. ; Di Donato, S. ; De Jonghe, P. ; Lynch, T. ; Mariotti, C. ; Spinazzola, A. ; Tabrizi, S. J. ; Tallaksen, C. ; Zeviani, M. ; Harbo, H. F. ; Finsterer, J. / Molecular Diagnosis of Neurogenetic Disorders : Motoneuron, Peripheral Nerve and Muscle Disorders. European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. pp. 97-109
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T2 - Motoneuron, Peripheral Nerve and Muscle Disorders

AU - Burgunder, J. M.

AU - Schöls, L.

AU - Baets, J.

AU - Andersen, P.

AU - Gasser, T.

AU - Szolnoki, Z.

AU - Fontaine, B.

AU - Van Broeckhoven, C.

AU - Di Donato, S.

AU - De Jonghe, P.

AU - Lynch, T.

AU - Mariotti, C.

AU - Spinazzola, A.

AU - Tabrizi, S. J.

AU - Tallaksen, C.

AU - Zeviani, M.

AU - Harbo, H. F.

AU - Finsterer, J.

PY - 2011/9/21

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KW - EFNS guidelines, and motoneuron disorders-polyneuropathies and myopathies

KW - Genetic basis for DM1-a CTG repeats expansion in dmpk gene on 19q13

KW - Molecular diagnosis of inherited neuropathies

KW - Molecular diagnosis of neurogenetic disorders-motoneuron, muscle disorders

KW - Muscle dystrophies-Duchenne/Becker muscular dystrophy (dmd/bmd), X-linked recessive condition

KW - Myofibrillar myopathies-and specific cytoplasmatic inclusions

KW - Other myopathies-distal myopathies, muscular dystrophies with distal upper and lower extremities

KW - Proximal spinal muscular atrophy (SMA)-common and severe autosomal-recessive diseases of children

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