Georgiou DM - Search Results

1

A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.

Georgiou DM, Nicolaou P, Chitayat D, Koutsou P, Babul-Hirji R, Vajsar J, Murphy J, Christodoulou K. Georgiou DM, et al. Can J Neurol Sci. 2006 Aug;33(3):311-6. doi: 10.1017/s0317167100005199. Can J Neurol Sci. 2006. PMID: 17001820

2

A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes.

Kleopa KA, Georgiou DM, Nicolaou P, Koutsou P, Papathanasiou E, Kyriakides T, Christodoulou K. Kleopa KA, et al. Among authors: georgiou dm. Neurogenetics. 2004 Sep;5(3):171-5. doi: 10.1007/s10048-004-0184-1. Epub 2004 Jun 17. Neurogenetics. 2004. PMID: 15205993

3

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.

Kleopa KA, Zamba-Papanicolaou E, Alevra X, Nicolaou P, Georgiou DM, Hadjisavvas A, Kyriakides T, Christodoulou K. Kleopa KA, et al. Among authors: georgiou dm. Neurology. 2006 Feb 14;66(3):396-402. doi: 10.1212/01.wnl.0000196479.93722.59. Neurology. 2006. PMID: 16476939

4

A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.

Georgiou DM, Zidar J, Korosec M, Middleton LT, Kyriakides T, Christodoulou K. Georgiou DM, et al. Neurogenetics. 2002 Oct;4(2):93-6. doi: 10.1007/s10048-002-0138-4. Neurogenetics. 2002. PMID: 12481988

5

Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity.

Christodoulou K, Deymeer F, Serdaroğlu P, Ozdemir C, Poda M, Georgiou DM, Ioannou P, Tsingis M, Zamba E, Middleton LT. Christodoulou K, et al. Among authors: georgiou dm. Neurogenetics. 2001 Jul;3(3):127-32. doi: 10.1007/s100480100112. Neurogenetics. 2001. PMID: 11523563

6

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.

Bolino A, Muglia M, Conforti FL, LeGuern E, Salih MA, Georgiou DM, Christodoulou K, Hausmanowa-Petrusewicz I, Mandich P, Schenone A, Gambardella A, Bono F, Quattrone A, Devoto M, Monaco AP. Bolino A, et al. Among authors: georgiou dm. Nat Genet. 2000 May;25(1):17-9. doi: 10.1038/75542. Nat Genet. 2000. PMID: 10802647

7

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. Among authors: georgiou dm. Genomics. 2000 Jan 15;63(2):271-8. doi: 10.1006/geno.1999.6088. Genomics. 2000. PMID: 10673338

8

Distal hereditary motor neuronopathy of the Jerash type.

Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: georgiou dm. Ann N Y Acad Sci. 1999 Sep 14;883:439-42. Ann N Y Acad Sci. 1999. PMID: 10586267 No abstract available.

9

Distal hereditary motor neuronopathy of the Jerash type.

Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: georgiou dm. Ann N Y Acad Sci. 1999 Sep 14;883:65-8. Ann N Y Acad Sci. 1999. PMID: 10586232

10

Distal Hereditary Motor Neuronopathy of the Jerash Type.

Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, El-Khateeb M, Al-Qudan A, Horany K. Middleton LT, et al. Among authors: georgiou dm. Ann N Y Acad Sci. 1999 Oct;883(1):65-68. doi: 10.1111/j.1749-6632.1999.tb08569.x. Ann N Y Acad Sci. 1999. PMID: 29086969

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