Similar articles for PMID: 15744041

Year	Number of Results
1971	2
1972	1
1976	1
1980	2
1982	2
1988	1
1990	1
1992	1
1993	1
1994	2
1995	1
1996	6
1997	4
1998	7
1999	17
2000	7
2001	5
2002	9
2003	4
2004	7
2005	19
2006	16
2007	14
2008	10
2009	6
2011	1
2012	6
2013	2
2014	1
2015	1
2016	1
2017	1
2021	1
2022	1
2024	0

1

Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11.

De Sandre-Giovannoli A, Delague V, Hamadouche T, Chaouch M, Krahn M, Boccaccio I, Maisonobe T, Chouery E, Jabbour R, Atweh S, Grid D, Mégarbané A, Lévy N. De Sandre-Giovannoli A, et al. J Med Genet. 2005 Mar;42(3):260-5. doi: 10.1136/jmg.2004.024364. J Med Genet. 2005. PMID: 15744041 Free PMC article. No abstract available.

2

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

Gambardella A, Bono F, Muglia M, Valentino P, Quattrone A. Gambardella A, et al. Ann N Y Acad Sci. 1999 Sep 14;883:47-55. Ann N Y Acad Sci. 1999. PMID: 10586229

3

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Othmane KB, et al. Genomics. 1999 Dec 15;62(3):344-9. doi: 10.1006/geno.1999.6028. Genomics. 1999. PMID: 10644431

4

The autosomal recessive form of CMT disease linked to 5q31-q33.

Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, LeGuern E. Guilbot A, et al. Ann N Y Acad Sci. 1999 Sep 14;883:453-6. Ann N Y Acad Sci. 1999. PMID: 10586271 No abstract available.

5

The autosomal recessive form of CMT disease linked to 5q31-q33.

Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, Leguern E. Guilbot A, et al. Ann N Y Acad Sci. 1999 Sep 14;883:56-9. Ann N Y Acad Sci. 1999. PMID: 10586230 No abstract available.

6

Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.

Guilbot A, Ravisé N, Bouhouche A, Coullin P, Birouk N, Maisonobe T, Kuntzer T, Vial C, Grid D, Brice A, LeGuern E. Guilbot A, et al. Eur J Hum Genet. 1999 Dec;7(8):849-59. doi: 10.1038/sj.ejhg.5200382. Eur J Hum Genet. 1999. PMID: 10602360

7

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.

Ismailov SM, Fedotov VP, Dadali EL, Polyakov AV, Van Broeckhoven C, Ivanov VI, De Jonghe P, Timmerman V, Evgrafov OV. Ismailov SM, et al. Eur J Hum Genet. 2001 Aug;9(8):646-50. doi: 10.1038/sj.ejhg.5200686. Eur J Hum Genet. 2001. PMID: 11528513

8

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

LeGuern E, Guilbot A, Kessali M, Ravisé N, Tassin J, Maisonobe T, Grid D, Brice A. LeGuern E, et al. Hum Mol Genet. 1996 Oct;5(10):1685-8. doi: 10.1093/hmg/5.10.1685. Hum Mol Genet. 1996. PMID: 8894708

9

Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22.

Bolino A, Levy ER, Muglia M, Conforti FL, LeGuern E, Salih MA, Georgiou DM, Christodoulou RK, Hausmanowa-Petrusewicz I, Mandich P, Gambardella A, Quattrone A, Devoto M, Monaco AP. Bolino A, et al. Genomics. 2000 Jan 15;63(2):271-8. doi: 10.1006/geno.1999.6088. Genomics. 2000. PMID: 10673338

10

The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4.

Claramunt R, Sevilla T, Lupo V, Cuesta A, Millán JM, Vílchez JJ, Palau F, Espinós C. Claramunt R, et al. Clin Genet. 2007 Apr;71(4):343-9. doi: 10.1111/j.1399-0004.2007.00774.x. Clin Genet. 2007. PMID: 17470135

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