158 related articles for article (PubMed ID: 34708324)
1. New Keys to Early Diagnosis: Muscle Echogenicity, Nerve Ultrasound Patterns, Electrodiagnostic, and Clinical Parameters in 150 Patients with Hereditary Polyneuropathies.
Winter N; Vittore D; Gess B; Schulz JB; Grimm A; Dohrn MF
Neurotherapeutics; 2021 Oct; 18(4):2425-2435. PubMed ID: 34708324
[TBL] [Abstract][Full Text] [Related]
2. The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies.
Grimm A; Rasenack M; Athanasopoulou IM; Dammeier NM; Lipski C; Wolking S; Vittore D; Décard BF; Axer H
J Neurol; 2016 Feb; 263(2):221-230. PubMed ID: 26559821
[TBL] [Abstract][Full Text] [Related]
3. Ultrasound pattern sum score, homogeneity score and regional nerve enlargement index for differentiation of demyelinating inflammatory and hereditary neuropathies.
Grimm A; Vittore D; Schubert V; Lipski C; Heiling B; Décard BF; Axer H
Clin Neurophysiol; 2016 Jul; 127(7):2618-24. PubMed ID: 27291881
[TBL] [Abstract][Full Text] [Related]
4. Different nerve ultrasound patterns in charcot-marie-tooth types and hereditary neuropathy with liability to pressure palsies.
Padua L; Coraci D; Lucchetta M; Paolasso I; Pazzaglia C; Granata G; Cacciavillani M; Luigetti M; Manganelli F; Pisciotta C; Piscosquito G; Pareyson D; Briani C
Muscle Nerve; 2018 Jan; 57(1):E18-E23. PubMed ID: 28802056
[TBL] [Abstract][Full Text] [Related]
5. Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP.
Schreiber S; Oldag A; Kornblum C; Kollewe K; Kropf S; Schoenfeld A; Feistner H; Jakubiczka S; Kunz WS; Scherlach C; Tempelmann C; Mawrin C; Dengler R; Schreiber F; Goertler M; Vielhaber S
Muscle Nerve; 2013 Mar; 47(3):385-95. PubMed ID: 23381770
[TBL] [Abstract][Full Text] [Related]
6. Charcot-Marie-Tooth disease and related inherited neuropathies.
Murakami T; Garcia CA; Reiter LT; Lupski JR
Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346
[TBL] [Abstract][Full Text] [Related]
7. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
Chance PF
Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374
[TBL] [Abstract][Full Text] [Related]
8. Distinctive patterns of sonographic nerve enlargement in Charcot-Marie-Tooth type 1A and hereditary neuropathy with pressure palsies.
Goedee SH; Brekelmans GJ; van den Berg LH; Visser LH
Clin Neurophysiol; 2015 Jul; 126(7):1413-20. PubMed ID: 25454274
[TBL] [Abstract][Full Text] [Related]
9. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.
Taioli F; Cabrini I; Cavallaro T; Acler M; Fabrizi GM
Brain; 2011 Feb; 134(Pt 2):608-17. PubMed ID: 21252112
[TBL] [Abstract][Full Text] [Related]
10. Genetic evaluation of inherited motor/sensory neuropathy.
Chance PF
Suppl Clin Neurophysiol; 2004; 57():228-42. PubMed ID: 16106622
[TBL] [Abstract][Full Text] [Related]
11. Molecular basis of hereditary neuropathies.
Chance PF
Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007
[TBL] [Abstract][Full Text] [Related]
12. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.
van Paassen BW; van der Kooi AJ; van Spaendonck-Zwarts KY; Verhamme C; Baas F; de Visser M
Orphanet J Rare Dis; 2014 Mar; 9():38. PubMed ID: 24646194
[TBL] [Abstract][Full Text] [Related]
13. Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A.
Bjelica B; Peric S; Bozovic I; Jankovic M; Brankovic M; Palibrk A; Rakocevic Stojanovic V
Acta Neurol Belg; 2021 Dec; 121(6):1481-1486. PubMed ID: 32335868
[TBL] [Abstract][Full Text] [Related]
14. Inherited neuropathies: from gene to disease.
Keller MP; Chance PF
Brain Pathol; 1999 Apr; 9(2):327-41. PubMed ID: 10219749
[TBL] [Abstract][Full Text] [Related]
15. Dispersion of compound muscle action potential in hereditary neuropathies and chronic inflammatory demyelinating polyneuropathy.
Stanton M; Pannoni V; Lewis RA; Logigian EL; Naguib D; Shy ME; Cleland J; Herrmann DN
Muscle Nerve; 2006 Oct; 34(4):417-22. PubMed ID: 16823858
[TBL] [Abstract][Full Text] [Related]
16. Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease.
Noto Y; Shiga K; Tsuji Y; Mizuta I; Higuchi Y; Hashiguchi A; Takashima H; Nakagawa M; Mizuno T
J Neurol Neurosurg Psychiatry; 2015 Apr; 86(4):378-84. PubMed ID: 25091364
[TBL] [Abstract][Full Text] [Related]
17. Nerve ultrasound findings differentiate Charcot-Marie-Tooth disease (CMT) 1A from other demyelinating CMTs.
Zanette G; Fabrizi GM; Taioli F; Lauriola MF; Badari A; Ferrarini M; Cavallaro T; Tamburin S
Clin Neurophysiol; 2018 Nov; 129(11):2259-2267. PubMed ID: 30216910
[TBL] [Abstract][Full Text] [Related]
18. Inherited peripheral neuropathy.
Keller MP; Chance PF
Semin Neurol; 1999; 19(4):353-62. PubMed ID: 10716658
[TBL] [Abstract][Full Text] [Related]
19. New evidence for secondary axonal degeneration in demyelinating neuropathies.
Moss KR; Bopp TS; Johnson AE; Höke A
Neurosci Lett; 2021 Jan; 744():135595. PubMed ID: 33359733
[TBL] [Abstract][Full Text] [Related]
20. Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs.
Seeman P; Mazanec R; Zidar J; Hrusáková S; Ctvrtecková M; Rautenstrauss B
Int J Mol Med; 2000 Oct; 6(4):421-6. PubMed ID: 10998431
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]