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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1994 1
1996 3
1998 1
1999 2
2000 1
2001 3
2002 3
2003 3
2004 3
2005 3
2006 4
2007 2
2009 1
2010 2
2011 1
2012 3
2013 3
2014 1
2016 1
2019 1
2021 1
2022 0
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40 results
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Page 1
Decreased Aerobic Capacity in ANO5-Muscular Dystrophy.
Ylikallio E, Auranen M, Mahjneh I, Lamminen A, Kousi M, Träskelin AL, Muurinen T, Löfberg M, Salmi T, Paetau A, Lehesjoki AE, Piirilä P, Kiuru-Enari S. Ylikallio E, et al. Among authors: mahjneh i. J Neuromuscul Dis. 2016 Nov 29;3(4):475-485. doi: 10.3233/JND-160186. J Neuromuscul Dis. 2016. PMID: 27911336
Hartia-lantiodystrofioiden molekyyligenetiikka Suomessa.
Raheem O, Suominen T, Hackman P, Vihola A, Auranen M, Kalimo H, Mahjneh I, Kärppä M, Haapasalo H, Udd B. Raheem O, et al. Among authors: mahjneh i. Duodecim. 2006;122(17):2130-6. Duodecim. 2006. PMID: 17115630 Finnish. No abstract available.
Dysregulated calcium homeostasis prevents plasma membrane repair in Anoctamin 5/TMEM16E-deficient patient muscle cells.
Chandra G, Defour A, Mamchoui K, Pandey K, Mishra S, Mouly V, Sreetama S, Mahad Ahmad M, Mahjneh I, Morizono H, Pattabiraman N, Menon AK, Jaiswal JK. Chandra G, et al. Among authors: mahjneh i. Cell Death Discov. 2019 Jul 18;5:118. doi: 10.1038/s41420-019-0197-z. eCollection 2019. Cell Death Discov. 2019. PMID: 31341644 Free PMC article.
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene.
Hackman P, Rusanen SM, Johari M, Vihola A, Jonson PH, Sarparanta J, Donner K, Lahermo P, Koivunen S, Luque H, Soininen M, Mahjneh I, Auranen M, Arumilli M, Savarese M, Udd B. Hackman P, et al. Among authors: mahjneh i. Neurol Genet. 2021 Oct 27;7(6):e632. doi: 10.1212/NXG.0000000000000632. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34722876 Free PMC article.
Axial myopathy--an unrecognised entity.
Mahjneh I, Marconi G, Paetau A, Saarinen A, Salmi T, Somer H. Mahjneh I, et al. J Neurol. 2002 Jun;249(6):730-4. doi: 10.1007/s00415-002-0701-9. J Neurol. 2002. PMID: 12111307
Hereditary myopathy with early respiratory failure: occurrence in various populations.
Palmio J, Evilä A, Chapon F, Tasca G, Xiang F, Brådvik B, Eymard B, Echaniz-Laguna A, Laporte J, Kärppä M, Mahjneh I, Quinlivan R, Laforêt P, Damian M, Berardo A, Taratuto AL, Bueri JA, Tommiska J, Raivio T, Tuerk M, Gölitz P, Chevessier F, Sewry C, Norwood F, Hedberg C, Schröder R, Edström L, Oldfors A, Hackman P, Udd B. Palmio J, et al. Among authors: mahjneh i. J Neurol Neurosurg Psychiatry. 2014 Mar;85(3):345-53. doi: 10.1136/jnnp-2013-304965. Epub 2013 Apr 19. J Neurol Neurosurg Psychiatry. 2014. PMID: 23606733
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.
Sarparanta J, Jonson PH, Golzio C, Sandell S, Luque H, Screen M, McDonald K, Stajich JM, Mahjneh I, Vihola A, Raheem O, Penttilä S, Lehtinen S, Huovinen S, Palmio J, Tasca G, Ricci E, Hackman P, Hauser M, Katsanis N, Udd B. Sarparanta J, et al. Among authors: mahjneh i. Nat Genet. 2012 Feb 26;44(4):450-5, S1-2. doi: 10.1038/ng.1103. Nat Genet. 2012. PMID: 22366786 Free PMC article.
40 results