148 related articles for article (PubMed ID: 11325885)
1. Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplication.
Latour P; Boutrand L; Levy N; Bernard R; Boyer A; Claustrat F; Chazot G; Boucherat M; Vandenberghe A
Clin Chem; 2001 May; 47(5):829-37. PubMed ID: 11325885
[TBL] [Abstract][Full Text] [Related]
2. Duplication analysis in Turkish Charcot-Marie-Tooth type 1A patients using short tandem repeat markers.
Koç F; Güzel AI; Sarica Y; Kasap H
Int J Neurosci; 2007 Nov; 117(11):1611-9. PubMed ID: 17917930
[TBL] [Abstract][Full Text] [Related]
3. New polymorphic short tandem repeats for PCR-based Charcot-Marie-Tooth disease type 1A duplication diagnosis.
Badano JL; Inoue K; Katsanis N; Lupski JR
Clin Chem; 2001 May; 47(5):838-43. PubMed ID: 11325886
[TBL] [Abstract][Full Text] [Related]
4. Quantitative fluorescence-polymerase chain reaction assay for the detection of the duplication of the Charcot Marie Tooth disease type 1A critical region.
De Toffol S; Bellone E; Dulcetti F; Ruggeri AM; Maggio PP; Pulimeno MR; Mandich P; Maggi F; Simoni G; Grati FR
Genet Test Mol Biomarkers; 2010 Apr; 14(2):225-31. PubMed ID: 20187762
[TBL] [Abstract][Full Text] [Related]
5. Polymorphic short tandem repeats for PCR-based diagnosis of the Charcot-Marie-Tooth 1A duplication in Ukraine.
Hryshchenko NV; Kravchenko SA; Livshits LA
Tsitol Genet; 2005; 39(5):56-61. PubMed ID: 16398147
[TBL] [Abstract][Full Text] [Related]
6. Detection of Charcot-Marie-Tooth type 1A duplication by the polymerase chain reaction.
Blair IP; Kennerson ML; Nicholson GA
Clin Chem; 1995 Aug; 41(8 Pt 1):1105-8. PubMed ID: 7628084
[TBL] [Abstract][Full Text] [Related]
7. Utility of STR markers for the molecular diagnosis of a large Brazilian family with Charcot-Marie-Tooth disease.
Possamai CO; Carvalho FM; Silva MF; Wolfgramm EV; Sartori MP; Malta FS; Ribeiro VP; Spina VP; Gomes KB; Ferreira AC; Louro ID
Genet Mol Res; 2008 Oct; 7(4):1179-85. PubMed ID: 19048496
[TBL] [Abstract][Full Text] [Related]
8. Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats.
Gagic M; Markovic MK; Kecmanovic M; Keckarevic D; Mladenovic J; Dackovic J; Milic-Rasic V; Romac S
Clin Chem Lab Med; 2016 May; 54(5):773-80. PubMed ID: 26479344
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.
Chen SR; Lin KP; Kuo HC; Chen CM; Hsieh ST; Lee MJ; Yang CC; Liu CS; Huang CC; Lyu RK; Ro LS
Clin Neurol Neurosurg; 2008 May; 110(5):466-71. PubMed ID: 18353535
[TBL] [Abstract][Full Text] [Related]
11. [A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12].
Inoue M; Kojima M; Aikoh H; Sugai K; Murakami N; Nonaka I; Hayasaka K; Yamamoto M; Sobue G
No To Hattatsu; 1999 Sep; 31(5):452-7. PubMed ID: 10487071
[TBL] [Abstract][Full Text] [Related]
12. Charcot-Marie-Tooth phenotype produced by a duplicated PMP22 gene as part of a 17p trisomy-translocation to the X chromosome.
King PH; Waldrop R; Lupski JR; Shaffer LG
Clin Genet; 1998 Nov; 54(5):413-6. PubMed ID: 9842994
[TBL] [Abstract][Full Text] [Related]
13. Charcot-Marie-Tooth disease type 1A: molecular mechanisms of gene dosage and point mutation underlying a common inherited peripheral neuropathy.
Roa BB; Garcia CA; Lupski JR
Int J Neurol; 1991-1992; 25-26():97-107. PubMed ID: 11980069
[TBL] [Abstract][Full Text] [Related]
14. Charcot-Marie-Tooth disease type 1A: a family study with microsatellites.
Qu Y; Carpenter NJ; Whetsell L; Smith SP; Say B
J Okla State Med Assoc; 1996 Nov; 89(11):395-9. PubMed ID: 8972170
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Effectiveness of real-time quantitative PCR compare to repeat PCR for the diagnosis of Charcot-Marie-Tooth Type 1A and hereditary neuropathy with liability to pressure palsies.
Choi JR; Lee WH; Sunwoo IN; Lee EK; Lee CH; Lim JB
Yonsei Med J; 2005 Jun; 46(3):347-52. PubMed ID: 15988805
[TBL] [Abstract][Full Text] [Related]
17. Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies.
Stronach EA; Clark C; Bell C; Löfgren A; McKay NG; Timmerman V; Van Broeckhoven C; Haites NE
J Peripher Nerv Syst; 1999; 4(2):117-22. PubMed ID: 10442687
[TBL] [Abstract][Full Text] [Related]
18. [Detection of the PMP22 gene duplication in peripheral neuropathy patients: a study in Mexican population].
Cortés H; Hernández-Hernández Ó; Bautista-Tirado T; Escobar-Cedillo RE; Magaña JJ; Leyva-García N
Rev Neurol; 2014 Aug; 59(3):111-7. PubMed ID: 25030070
[TBL] [Abstract][Full Text] [Related]
19. [Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A].
Hryshchenko NV; Bychkova AM; Pichkur NA; Skyban HV; Dmytrenko VV; Livshyts' LA
Tsitol Genet; 2003; 37(6):55-9. PubMed ID: 15067947
[TBL] [Abstract][Full Text] [Related]
20. Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease.
Mathis S; Corcia P; Tazir M; Camu W; Magdelaine C; Latour P; Biberon J; Guennoc AM; Richard L; Magy L; Funalot B; Vallat JM
Neuromuscul Disord; 2014 Jun; 24(6):524-8. PubMed ID: 24792522
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
