Uneingeschränkter Zugang

The Importance of Rebalancing Foot Biomechanics by Computerized Podoscopic Assessment - Study in Charcot Marie Tooth Syndroms


Zitieren

https://bestpractice.bmj.com/topics/en-gb/1164 Search in Google Scholar

https://www.healthline.com/health/charcot-marie-tooth-disease Search in Google Scholar

http://www.nhs.uk/Conditions/Charcot-Marie-Tooth-disease/Pages/Diagnosis.aspx Search in Google Scholar

http://patient.info/doctor/charcot-marie-tooth-disease Search in Google Scholar

http://emedicine.medscape.com/article/1232386-differential Search in Google Scholar

http://www.ninds.nih.gov/disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm Search in Google Scholar

https://www.mda.org/disease/charcot-marie-tooth/diagnosis Search in Google Scholar

Saporta, A.S.; Sottile, S.L.; Miller, L.J.; Feely, S.M.; Siskind, C.E.; Shy, M.E. Charcot-marie-tooth disease subtypes and genetic testing strategies. Ann. Neurol. 2011, 69, 22–33. (Google Scholar) (CrossRef) Search in Google Scholar

Harding, A.E.; Thomas, P.K. The clinical features of hereditary motor and sensory neuropathy types i and ii. Brain 1980, 103, 259–280. (Google Scholar) (CrossRef) Search in Google Scholar

Horacek, O.; Mazanec, R.; Morris, C.E.; Kobesova, A. Spinal deformities in hereditary motor and sensory neuropathy: A retrospective qualitative, quantitative, genotypical, and familial analysis of 175 patients. Spine 2007, 32, 2502–2508. (Google Scholar) (CrossRef) Search in Google Scholar

Bamford, N.S.; White, K.K.; Robinett, S.A.; Otto, R.K.; Gospe, S.M. Neuromuscular hip dysplasia in charcot-marie-tooth disease type 1a. Dev. Med. Child Neurol. 2009, 51, 408–411. (Google Scholar) (CrossRef) (PubMed) Search in Google Scholar

Werheid, F.; Azzedine, H.; Zwerenz, E.; Bozkurt, A.; Moeller, M.J.; Lin, L.; Mull, M.; Häusler, M.; Schulz, J.B.; Weis, J.; et al. Underestimated associated features in cmt neuropathies: Clinical indicators for the causative gene? Brain Behav. 2016, 6, e00451. (Google Scholar) (CrossRef) (PubMed) Search in Google Scholar

Saifee, T.A.; Pareés, I.; Kassavetis, P.; Kaski, D.; Bronstein, A.M.; Rothwell, J.C.; Sadnicka, A.; Lunn, M.P.; Manji, H.; Teo, J.T.; et al. Tremor in charcot-marie-tooth disease: No evidence of cerebellar dysfunction. Clin. Neurophysiol. 2015, 126, 1817–1824. (Google Scholar) (CrossRef) (PubMed) Search in Google Scholar

Anzalone, C.L.; Nuhanovic, S.; Olund, A.P.; Carlson, M.L. Cochlear implantation in charcot-marie-tooth disease: Case report and review of the literature. Case Rep. Med. 2018, 2018, 1760978. (Google Scholar) (CrossRef) (PubMed) Search in Google Scholar

Lerat, J.; Magdelaine, C.; Beauvais-Dzugan, H.; Espil, C.; Ghorab, K.; Latour, P.; Derouault, P.; Sturtz, F.; Lia, A.S. A novel pathogenic variant of nefl responsible for deafness associated with peripheral neuropathy discovered through next-generation sequencing and review of the literature. J. Peripher. Nerv. Syst. 2019, 24, 139–144. (Google Scholar) (CrossRef) Search in Google Scholar

J. Morena, A. Gupta, J. C. Hoyle-Charcot-Marie-Tooth: From Molecules to Therapy-MDPI, Int. J. Mol. Sci. 2019, 20(14), 3419; https://doi.org/10.3390/ijms20143419 Search in Google Scholar

Rossor, A.M.; Tomaselli, P.J.; Reilly, M.M. Recent advances in the genetic neuropathies. Curr. Opin. Neurol. 2016, 29, 537–548. (Google Scholar) (CrossRef) (PubMed)(Green Version) Search in Google Scholar

eISSN:
1220-5818
Sprache:
Englisch
Zeitrahmen der Veröffentlichung:
4 Hefte pro Jahr
Fachgebiete der Zeitschrift:
Medizin, Klinische Medizin, Allgemeinmedizin, Innere Medizin, andere, Kardiologie, Gastroenterologie, Pneumologie