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351 results

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Page 1
Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor function.
Pane M, Palermo C, Messina S, Sansone VA, Bruno C, Catteruccia M, Sframeli M, Albamonte E, Pedemonte M, D'Amico A, Brigati G, de Sanctis R, Coratti G, Lucibello S, Bertini E, Vita G, Tiziano FD, Mercuri E; Italian EAP working group. Pane M, et al. Neuromuscul Disord. 2018 Jul;28(7):582-585. doi: 10.1016/j.nmd.2018.05.010. Epub 2018 Jun 1. Neuromuscul Disord. 2018. PMID: 29960818
Muscle MRI in Ullrich congenital muscular dystrophy and Bethlem myopathy.
Mercuri E, Lampe A, Allsop J, Knight R, Pane M, Kinali M, Bonnemann C, Flanigan K, Lapini I, Bushby K, Pepe G, Muntoni F. Mercuri E, et al. Among authors: pane m. Neuromuscul Disord. 2005 Apr;15(4):303-10. doi: 10.1016/j.nmd.2005.01.004. Neuromuscul Disord. 2005. PMID: 15792870
The neurological examination of the newborn baby.
Mercuri E, Ricci D, Pane M, Baranello G. Mercuri E, et al. Among authors: pane m. Early Hum Dev. 2005 Dec;81(12):947-56. doi: 10.1016/j.earlhumdev.2005.10.007. Epub 2005 Nov 7. Early Hum Dev. 2005. PMID: 16274943 Review.
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric study.
Mercuri E, Messina S, Battini R, Berardinelli A, Boffi P, Bono R, Bruno C, Carboni N, Cini C, Colitto F, D'Amico A, Minetti C, Mirabella M, Mongini T, Morandi L, Dlamini N, Orcesi S, Pelliccioni M, Pane M, Pini A, Swan AV, Villanova M, Vita G, Main M, Muntoni F, Bertini E. Mercuri E, et al. Among authors: pane m. Neuromuscul Disord. 2006 Feb;16(2):93-8. doi: 10.1016/j.nmd.2005.11.010. Epub 2006 Jan 20. Neuromuscul Disord. 2006. PMID: 16427782
Thalamic atrophy in infants with PVL and cerebral visual impairment.
Ricci D, Anker S, Cowan F, Pane M, Gallini F, Luciano R, Donvito V, Baranello G, Cesarini L, Bianco F, Rutherford M, Romagnoli C, Atkinson J, Braddick O, Guzzetta F, Mercuri E. Ricci D, et al. Among authors: pane m. Early Hum Dev. 2006 Sep;82(9):591-5. doi: 10.1016/j.earlhumdev.2005.12.007. Epub 2006 Feb 24. Early Hum Dev. 2006. PMID: 16500047
POMT2 mutation in a patient with 'MEB-like' phenotype.
Mercuri E, D'Amico A, Tessa A, Berardinelli A, Pane M, Messina S, van Reeuwijk J, Bertini E, Muntoni F, Santorelli FM. Mercuri E, et al. Among authors: pane m. Neuromuscul Disord. 2006 Jul;16(7):446-8. doi: 10.1016/j.nmd.2006.03.016. Epub 2006 May 15. Neuromuscul Disord. 2006. PMID: 16701995
Expanding the clinical spectrum of POMT1 phenotype.
D'Amico A, Tessa A, Bruno C, Petrini S, Biancheri R, Pane M, Pedemonte M, Ricci E, Falace A, Rossi A, Mercuri E, Santorelli FM, Bertini E. D'Amico A, et al. Among authors: pane m. Neurology. 2006 May 23;66(10):1564-7; discussion 1461. doi: 10.1212/01.wnl.0000216145.66476.36. Neurology. 2006. PMID: 16717220
351 results