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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 0
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39 results
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Page 1
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.
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
Muscle CT in peripheral neuropathies.
Marconi G, Mahjneh I, Pizzi A. Marconi G, et al. Among authors: mahjneh i. Acta Neurol Scand. 2001 Sep;104(3):156-61. doi: 10.1034/j.1600-0404.2001.00087.x. Acta Neurol Scand. 2001. PMID: 11551235
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.
A new distal myopathy with mutation in anoctamin 5.
Mahjneh I, Jaiswal J, Lamminen A, Somer M, Marlow G, Kiuru-Enari S, Bashir R. Mahjneh I, et al. Neuromuscul Disord. 2010 Dec;20(12):791-5. doi: 10.1016/j.nmd.2010.07.270. Epub 2010 Aug 7. Neuromuscul Disord. 2010. PMID: 20692837 Free PMC article.
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