461 related articles for article (PubMed ID: 19923170)
1. Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A.
Saporta MA; Katona I; Lewis RA; Masse S; Shy ME; Li J
Brain; 2009 Dec; 132(Pt 12):3263-73. PubMed ID: 19923170
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Internodal length variability of dermal myelinated fibres.
Nolano M; Provitera V; Santoro L
Brain; 2010 Jun; 133(Pt 6):e142; author reply e143. PubMed ID: 20157010
[No Abstract] [Full Text] [Related]
4. Charcot-Marie-Tooth disease: New insights from skin biopsy.
Manganelli F; Nolano M; Pisciotta C; Provitera V; Fabrizi GM; Cavallaro T; Stancanelli A; Caporaso G; Shy ME; Santoro L
Neurology; 2015 Oct; 85(14):1202-8. PubMed ID: 26362287
[TBL] [Abstract][Full Text] [Related]
5. Intraepidermal nerve fibre density as biomarker in Charcot-Marie-Tooth disease type 1A.
Hartmannsberger B; Doppler K; Stauber J; Schlotter-Weigel B; Young P; Sereda MW; Sommer C
Brain Commun; 2020; 2(1):fcaa012. PubMed ID: 32954280
[TBL] [Abstract][Full Text] [Related]
6. Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.
Li J; Bai Y; Ghandour K; Qin P; Grandis M; Trostinskaia A; Ianakova E; Wu X; Schenone A; Vallat JM; Kupsky WJ; Hatfield J; Shy ME
Brain; 2005 May; 128(Pt 5):1168-77. PubMed ID: 15774502
[TBL] [Abstract][Full Text] [Related]
7. Diagnostic value of sural nerve demyelination in chronic inflammatory demyelinating polyneuropathy.
Bosboom WM; van den Berg LH; Franssen H; Giesbergen PC; Flach HZ; van Putten AM; Veldman H; Wokke JH
Brain; 2001 Dec; 124(Pt 12):2427-38. PubMed ID: 11701597
[TBL] [Abstract][Full Text] [Related]
8. A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients.
Fledrich R; Schlotter-Weigel B; Schnizer TJ; Wichert SP; Stassart RM; Meyer zu Hörste G; Klink A; Weiss BG; Haag U; Walter MC; Rautenstrauss B; Paulus W; Rossner MJ; Sereda MW
Brain; 2012 Jan; 135(Pt 1):72-87. PubMed ID: 22189569
[TBL] [Abstract][Full Text] [Related]
9. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
Klein D; Patzkó Á; Schreiber D; van Hauwermeiren A; Baier M; Groh J; West BL; Martini R
Brain; 2015 Nov; 138(Pt 11):3193-205. PubMed ID: 26297559
[TBL] [Abstract][Full Text] [Related]
10. Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases.
Hong SM; Ha H; Suh JH; Kim KK; Khang SK; Ro JY; Park SH
J Korean Med Sci; 2000 Apr; 15(2):211-6. PubMed ID: 10803700
[TBL] [Abstract][Full Text] [Related]
11. [Charcot-Marie-Tooth disease type 2 caused by homozygous MME gene mutation superimposed by chronic inflammatory demyelinating polyneuropathy].
Fujisawa M; Sano Y; Omoto M; Ogasawara JI; Koga M; Takashima H; Kanda T
Rinsho Shinkeigaku; 2017 Sep; 57(9):515-520. PubMed ID: 28855494
[TBL] [Abstract][Full Text] [Related]
12. Small axons relative to number of myelin lamellae in Charcot-Marie-Tooth disease 1A with peripheral myelin protein 22 gene duplication.
Ohnishi A; Yamamoto T; Ikeda M
J UOEH; 2000 Jun; 22(2):107-17. PubMed ID: 10862406
[TBL] [Abstract][Full Text] [Related]
13. Preliminary study of large and small peripheral nerve fibers in Charcot-Marie-Tooth disease, type I.
Hanson P; Deltombe T
Am J Phys Med Rehabil; 1998; 77(1):45-8. PubMed ID: 9482378
[TBL] [Abstract][Full Text] [Related]
14. Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype.
Malandrini A; Gambelli S; Muglia M; Berti G; Patitucci A; Sugie K; Umehara F; Quattrone A; Dotti MT; Federico A
Neurology; 2005 Sep; 65(5):776. PubMed ID: 16157924
[No Abstract] [Full Text] [Related]
15. Cation binding at the node of Ranvier in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies.
Yoshikawa H; Nishimura T; Kaido M; Toyooka K; Fujimura H; Sakoda S; Yanagihara T
Acta Neuropathol; 1996; 91(6):587-94. PubMed ID: 8781657
[TBL] [Abstract][Full Text] [Related]
16. Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.
Li J; Bai Y; Ianakova E; Grandis M; Uchwat F; Trostinskaia A; Krajewski KM; Garbern J; Kupsky WJ; Shy ME
J Comp Neurol; 2006 Sep; 498(2):252-65. PubMed ID: 16856127
[TBL] [Abstract][Full Text] [Related]
17. Simulating mild systematic and focal demyelinating neuropathies: membrane property abnormalities.
Stephanova DI; Alexandrov AS
J Integr Neurosci; 2006 Dec; 5(4):595-623. PubMed ID: 17245824
[TBL] [Abstract][Full Text] [Related]
18. Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination.
Hu B; McCollum M; Ravi V; Arpag S; Moiseev D; Castoro R; Mobley B; Burnette B; Siskind C; Day J; Yawn R; Feely S; Li Y; Yan Q; Shy M; Li J
Ann Neurol; 2018 Apr; 83(4):756-770. PubMed ID: 29518270
[TBL] [Abstract][Full Text] [Related]
19. Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves.
Behse F; Buchthal F
Brain; 1977 Mar; 100 Pt 1():67-85. PubMed ID: 861716
[TBL] [Abstract][Full Text] [Related]
20. The natural history of Charcot-Marie-Tooth type 1A in adults: a 5-year follow-up study.
Verhamme C; van Schaik IN; Koelman JH; de Haan RJ; de Visser M
Brain; 2009 Dec; 132(Pt 12):3252-62. PubMed ID: 19843647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
