Houshmand M - Search Results

1

De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring.

Tulinius MH, Houshmand M, Larsson NG, Holme E, Oldfors A, Holmberg E, Wahlström J. Tulinius MH, et al. Among authors: houshmand m. Hum Genet. 1995 Sep;96(3):290-4. doi: 10.1007/BF00210409. Hum Genet. 1995. PMID: 7649544

2

Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne.

Houshmand M, Larsson NG, Oldfors A, Tulinius M, Holme E. Houshmand M, et al. Hum Genet. 1996 Mar;97(3):269-73. doi: 10.1007/BF02185750. Hum Genet. 1996. PMID: 8786060

3

A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encephalomyopathy: de novo mutation and no transmission to the offspring.

Houshmand M, Lindberg C, Moslemi AR, Oldfors A, Holme E. Houshmand M, et al. Hum Mutat. 1999;13(3):203-9. doi: 10.1002/(SICI)1098-1004(1999)13:3<203::AID-HUMU4>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10090475

4

Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood.

Houshmand M, Gardner A, Hällström T, Müntzing K, Oldfors A, Holme E. Houshmand M, et al. Neuromuscul Disord. 2004 Mar;14(3):195-201. doi: 10.1016/j.nmd.2003.12.002. Neuromuscul Disord. 2004. PMID: 15036329

5

Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions.

Tulinius MH, Oldfors A, Holme E, Larsson NG, Houshmand M, Fahleson P, Sigström L, Kristiansson B. Tulinius MH, et al. Among authors: houshmand m. Eur J Pediatr. 1995 Jan;154(1):35-42. doi: 10.1007/BF01972970. Eur J Pediatr. 1995. PMID: 7895754

6

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.

Houshmand M, Larsson NG, Holme E, Oldfors A, Tulinius MH, Andersen O. Houshmand M, et al. Biochim Biophys Acta. 1994 Apr 12;1226(1):49-55. doi: 10.1016/0925-4439(94)90058-2. Biochim Biophys Acta. 1994. PMID: 8155739

7

Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?

Houshmand M, Holme E, Hanson C, Wennerholm UB, Hamberger L. Houshmand M, et al. J Assist Reprod Genet. 1997 Apr;14(4):223-7. doi: 10.1007/BF02766114. J Assist Reprod Genet. 1997. PMID: 9130071 Free PMC article.

8

No mitochondrial DNA deletions but more D-loop point mutations in repeated pregnancy loss.

Seyedhassani SM, Houshmand M, Kalantar SM, Modabber G, Aflatoonian A. Seyedhassani SM, et al. Among authors: houshmand m. J Assist Reprod Genet. 2010 Nov;27(11):641-8. doi: 10.1007/s10815-010-9435-2. Epub 2010 May 25. J Assist Reprod Genet. 2010. PMID: 20499271 Free PMC article.

9

Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia.

Pala M, Olivieri A, Achilli A, Accetturo M, Metspalu E, Reidla M, Tamm E, Karmin M, Reisberg T, Hooshiar Kashani B, Perego UA, Carossa V, Gandini F, Pereira JB, Soares P, Angerhofer N, Rychkov S, Al-Zahery N, Carelli V, Sanati MH, Houshmand M, Hatina J, Macaulay V, Pereira L, Woodward SR, Davies W, Gamble C, Baird D, Semino O, Villems R, Torroni A, Richards MB. Pala M, et al. Among authors: houshmand m. Am J Hum Genet. 2012 May 4;90(5):915-24. doi: 10.1016/j.ajhg.2012.04.003. Am J Hum Genet. 2012. PMID: 22560092 Free PMC article.

10

BAX pro-apoptotic gene alterations in repeated pregnancy loss.

Mohammad Seyedhassani S, Houshmand M, Mehdi Kalantar S, Aflatoonian A, Modabber G, Hashemi-Gorji F, Hadipour Z. Mohammad Seyedhassani S, et al. Among authors: houshmand m. Arch Med Sci. 2011 Feb;7(1):117-22. doi: 10.5114/aoms.2011.20614. Epub 2011 Mar 8. Arch Med Sci. 2011. PMID: 22291743 Free PMC article.

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