Dagvadorj A - Search Results

1

Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.

Olivé M, Goldfarb L, Dagvadorj A, Sambuughin N, Paulin D, Li Z, Goudeau B, Vicart P, Ferrer I. Olivé M, et al. Among authors: dagvadorj a. Acta Neuropathol. 2003 Jul;106(1):1-7. doi: 10.1007/s00401-003-0695-0. Epub 2003 Apr 1. Acta Neuropathol. 2003. PMID: 12669240

2

Olivé M, Goldfarb L, Moreno D, Laforet E, Dagvadorj A, Sambuughin N, Martínez-Matos JA, Martínez F, Alió J, Farrero E, Vicart P, Ferrer I. Olivé M, et al. Among authors: dagvadorj a. J Neurol Sci. 2004 Apr 15;219(1-2):125-37. doi: 10.1016/j.jns.2004.01.007. J Neurol Sci. 2004. PMID: 15050448

3

Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segment.

Dagvadorj A, Goudeau B, Hilton-Jones D, Blancato JK, Shatunov A, Simon-Casteras M, Squier W, Nagle JW, Goldfarb LG, Vicart P. Dagvadorj A, et al. Muscle Nerve. 2003 Jun;27(6):669-75. doi: 10.1002/mus.10370. Muscle Nerve. 2003. PMID: 12766977

4

Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy.

Kaminska A, Strelkov SV, Goudeau B, Olivé M, Dagvadorj A, Fidzianska A, Simon-Casteras M, Shatunov A, Dalakas MC, Ferrer I, Kwiecinski H, Vicart P, Goldfarb LG. Kaminska A, et al. Among authors: dagvadorj a. Hum Genet. 2004 Feb;114(3):306-13. doi: 10.1007/s00439-003-1057-7. Epub 2003 Nov 27. Hum Genet. 2004. PMID: 14648196

5

A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.

Dagvadorj A, Olivé M, Urtizberea JA, Halle M, Shatunov A, Bönnemann C, Park KY, Goebel HH, Ferrer I, Vicart P, Dalakas MC, Goldfarb LG. Dagvadorj A, et al. J Neurol. 2004 Feb;251(2):143-9. doi: 10.1007/s00415-004-0289-3. J Neurol. 2004. PMID: 14991347

6

Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations.

Dalakas MC, Dagvadorj A, Goudeau B, Park KY, Takeda K, Simon-Casteras M, Vasconcelos O, Sambuughin N, Shatunov A, Nagle JW, Sivakumar K, Vicart P, Goldfarb LG. Dalakas MC, et al. Among authors: dagvadorj a. Neuromuscul Disord. 2003 Mar;13(3):252-8. doi: 10.1016/s0960-8966(02)00271-7. Neuromuscul Disord. 2003. PMID: 12609507

7

Structural and functional analysis of a new desmin variant causing desmin-related myopathy.

Goudeau B, Dagvadorj A, Rodrigues-Lima F, Nédellec P, Casteras-Simon M, Perret E, Langlois S, Goldfarb L, Vicart P. Goudeau B, et al. Among authors: dagvadorj a. Hum Mutat. 2001 Nov;18(5):388-96. doi: 10.1002/humu.1210. Hum Mutat. 2001. PMID: 11668632

8

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG. Shatunov A, et al. Among authors: dagvadorj a. Brain. 2006 Sep;129(Pt 9):2318-31. doi: 10.1093/brain/awl120. Epub 2006 May 15. Brain. 2006. PMID: 16702189 Free article.

9

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG. Dagvadorj A, et al. Ann Neurol. 2002 Sep;52(3):355-9. doi: 10.1002/ana.10267. Ann Neurol. 2002. PMID: 12205650

10

Persisting risk factors for preeclampsia among high-risk pregnancies already using prophylactic aspirin: a multi-country retrospective investigation.

Muldoon KA, McLean C, El-Chaár D, Corsi DJ, Rybak N, Dagvadorj A, Guo Y, Rennicks White R, Dingwall-Harvey ALJ, Gaudet LM, Walker MC, Wen SW; FACT Collaborating Group. Muldoon KA, et al. Among authors: dagvadorj a. J Matern Fetal Neonatal Med. 2023 Dec;36(1):2200879. doi: 10.1080/14767058.2023.2200879. J Matern Fetal Neonatal Med. 2023. PMID: 37073421 Free article. Clinical Trial.

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