Houshmand M - Search Results

1

Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia.

Houshmand M, Panahi MS, Hosseini BN, Dorraj GH, Tabassi AR. Houshmand M, et al. Neurol India. 2006 Jun;54(2):182-5. Neurol India. 2006. PMID: 16804265 Free article.

2

Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.

Houshmand M, Sanati MH, Rashedi I, Sharifpanah F, Asghari E, Lotfi J. Houshmand M, et al. Eur Neurol. 2004;51(2):68-71. doi: 10.1159/000075518. Epub 2003 Dec 10. Eur Neurol. 2004. PMID: 14671420

3

Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.

Houshmand M, Sharifpanah F, Tabasi A, Sanati MH, Vakilian M, Lavasani SH, Joughehdoust S. Houshmand M, et al. Ann N Y Acad Sci. 2004 Apr;1011:345-9. doi: 10.1007/978-3-662-41088-2_35. Ann N Y Acad Sci. 2004. PMID: 15126312

4

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.

Houshmand M, Sanati MH, Babrzadeh F, Ardalan A, Teimori M, Vakilian M, Akuchekian M, Farhud D, Lotfi J. Houshmand M, et al. Mult Scler. 2005 Dec;11(6):728-30. doi: 10.1191/1352458505ms1228sr. Mult Scler. 2005. PMID: 16320736

5

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.

Houshmand M, Panahi MS, Nafisi S, Soltanzadeh A, Alkandari FM. Houshmand M, et al. Mitochondrion. 2006 Apr;6(2):82-8. doi: 10.1016/j.mito.2006.01.005. Epub 2006 Apr 3. Mitochondrion. 2006. PMID: 16581313

6

Delta mtDNA4977 is more common in non-tumoral cells from gastric cancer sample.

Kamalidehghan B, Houshmand M, Ismail P, Panahi MS, Akbari MH. Kamalidehghan B, et al. Among authors: houshmand m. Arch Med Res. 2006 Aug;37(6):730-5. doi: 10.1016/j.arcmed.2006.02.005. Arch Med Res. 2006. PMID: 16824932

7

Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer.

Kamalidehghan B, Houshmand M, Panahi MS, Abbaszadegan MR, Ismail P, Shiroudi MB. Kamalidehghan B, et al. Among authors: houshmand m. Arch Med Res. 2006 Oct;37(7):848-53. doi: 10.1016/j.arcmed.2006.03.007. Arch Med Res. 2006. PMID: 16971224

8

Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.

Shafa Shariat Panahi M, Houshmand M, Tabassi AR. Shafa Shariat Panahi M, et al. Among authors: houshmand m. Arch Med Res. 2006 Nov;37(8):1028-33. doi: 10.1016/j.arcmed.2006.04.009. Arch Med Res. 2006. PMID: 17045122

9

Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!

Banoei MM, Houshmand M, Panahi MS, Shariati P, Rostami M, Manshadi MD, Majidizadeh T. Banoei MM, et al. Among authors: houshmand m. Cell Mol Neurobiol. 2007 Nov;27(7):867-75. doi: 10.1007/s10571-007-9206-5. Epub 2007 Oct 20. Cell Mol Neurobiol. 2007. PMID: 17952586

10

Application of multiplex PCR with histopathologic features for detection of familial breast cancer in formalin-fixed, paraffin-embedded histologic specimens.

Rassi H, Houshmand M, Hashemi M, Majidzadeh K, Akbari MH, Panahi MS. Rassi H, et al. Among authors: houshmand m. Tsitol Genet. 2008 Mar-Apr;42(2):55-62. Tsitol Genet. 2008. PMID: 18630122

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