Houshmand M - Search Results

1

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

2

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

3

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

4

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

Hassani-Kumleh H, Houshmand M, Panahi MS, Riazi GH, Sanati MH, Gharagozli K, Ghabaee M. Hassani-Kumleh H, et al. Among authors: houshmand m. Cell Mol Neurobiol. 2006 Mar;26(2):119-25. doi: 10.1007/s10571-006-9026-z. Epub 2006 May 6. Cell Mol Neurobiol. 2006. PMID: 16763779

5

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.

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

Do haplogroups H and U act to increase the penetrance of Alzheimer's disease?

Fesahat F, Houshmand M, Panahi MS, Gharagozli K, Mirzajani F. Fesahat F, et al. Among authors: houshmand m. Cell Mol Neurobiol. 2007 May;27(3):329-34. doi: 10.1007/s10571-006-9126-9. Epub 2006 Dec 21. Cell Mol Neurobiol. 2007. PMID: 17186363

10

Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients.

Ahari SE, Houshmand M, Panahi MS, Kasraie S, Moin M, Bahar MA. Ahari SE, et al. Among authors: houshmand m. Cell Mol Neurobiol. 2007 Sep;27(6):695-700. doi: 10.1007/s10571-007-9160-2. Epub 2007 Jul 6. Cell Mol Neurobiol. 2007. PMID: 17619138

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