Zhu D - Search Results

1

Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.

Zhu D, Kennerson ML, Walizada G, Züchner S, Vance JM, Nicholson GA. Zhu D, et al. Neurology. 2005 Aug 9;65(3):496-7. doi: 10.1212/01.wnl.0000171345.62270.29. Neurology. 2005. PMID: 16087932 No abstract available.

2

Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2.

Kennerson ML, Zhu D, Gardner RJ, Storey E, Merory J, Robertson SP, Nicholson GA. Kennerson ML, et al. Among authors: zhu d. Am J Hum Genet. 2001 Oct;69(4):883-8. doi: 10.1086/323743. Epub 2001 Aug 28. Am J Hum Genet. 2001. PMID: 11533912 Free PMC article.

3

Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?

De Jonghe P, Auer-Grumbach M, Irobi J, Wagner K, Plecko B, Kennerson M, Zhu D, De Vriendt E, Van Gerwen V, Nicholson G, Hartung HP, Timmerman V. De Jonghe P, et al. Among authors: zhu d. Brain. 2002 Jun;125(Pt 6):1320-5. doi: 10.1093/brain/awf127. Brain. 2002. PMID: 12023320

4

Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion.

Zhu D, Burke C, Leslie A, Nicholson GA. Zhu D, et al. Mov Disord. 2002 May;17(3):585-9. doi: 10.1002/mds.10175. Mov Disord. 2002. PMID: 12112211

5

CMT with pyramidal features. Charcot-Marie-Tooth.

Vucic S, Kennerson M, Zhu D, Miedema E, Kok C, Nicholson GA. Vucic S, et al. Among authors: zhu d. Neurology. 2003 Feb 25;60(4):696-9. doi: 10.1212/01.wnl.0000048561.61921.71. Neurology. 2003. PMID: 12601114

6

Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region.

Zhu D, Kennerson M, Merory J, Chrast R, Verheijen M, Lemke G, Nicholson G. Zhu D, et al. Neurogenetics. 2003 Aug;4(4):179-83. doi: 10.1007/s10048-003-0147-y. Epub 2003 May 22. Neurogenetics. 2003. PMID: 12761657

7

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.

Züchner S, Noureddine M, Kennerson M, Verhoeven K, Claeys K, De Jonghe P, Merory J, Oliveira SA, Speer MC, Stenger JE, Walizada G, Zhu D, Pericak-Vance MA, Nicholson G, Timmerman V, Vance JM. Züchner S, et al. Among authors: zhu d. Nat Genet. 2005 Mar;37(3):289-94. doi: 10.1038/ng1514. Epub 2005 Jan 30. Nat Genet. 2005. PMID: 15731758

8

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations.

Nicholson GA, Magdelaine C, Zhu D, Grew S, Ryan MM, Sturtz F, Vallat JM, Ouvrier RA. Nicholson GA, et al. Among authors: zhu d. Neurology. 2008 May 6;70(19):1678-81. doi: 10.1212/01.wnl.0000311275.89032.22. Neurology. 2008. PMID: 18458227

9

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.

Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, Grew S, Ryan MM, Funalot B. Vallat JM, et al. Among authors: zhu d. J Neuropathol Exp Neurol. 2008 Nov;67(11):1097-102. doi: 10.1097/NEN.0b013e31818b6cbc. J Neuropathol Exp Neurol. 2008. PMID: 18957892

10

Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.

Drew AP, Zhu D, Kidambi A, Ly C, Tey S, Brewer MH, Ahmad-Annuar A, Nicholson GA, Kennerson ML. Drew AP, et al. Among authors: zhu d. Mol Genet Genomic Med. 2015 Mar;3(2):143-54. doi: 10.1002/mgg3.126. Epub 2015 Jan 14. Mol Genet Genomic Med. 2015. PMID: 25802885 Free PMC article.

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