Stålberg E - Search Results

1

Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset.

Melberg A, Kretz C, Kalimo H, Wallgren-Pettersson C, Toussaint A, Böhm J, Stålberg E, Laporte J. Melberg A, et al. Among authors: stalberg e. Neuromuscul Disord. 2010 Jan;20(1):53-6. doi: 10.1016/j.nmd.2009.10.006. Epub 2009 Nov 22. Neuromuscul Disord. 2010. PMID: 19932619

2

Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism.

Melberg A, Lundberg PO, Henriksson KG, Olsson Y, Stålberg E. Melberg A, et al. Among authors: stalberg e. Muscle Nerve. 1996 Jun;19(6):751-7. doi: 10.1002/(SICI)1097-4598(199606)19:6<751::AID-MUS10>3.0.CO;2-O. Muscle Nerve. 1996. PMID: 8609926

3

Charcot-marie-tooth disease with cerebellar atrophy.

Melberg A, Raininko R, Dahl N, Olsson Y, Stålberg E. Melberg A, et al. Among authors: stalberg e. J Clin Neuromuscul Dis. 2000 Sep;2(1):24-6. doi: 10.1097/00131402-200009000-00007. J Clin Neuromuscul Dis. 2000. PMID: 19078599

4

A patient with two mitochondrial DNA mutations causing PEO and LHON.

Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A. Melberg A, et al. Among authors: stalberg e. Eur J Med Genet. 2009 Jan-Feb;52(1):47-8. doi: 10.1016/j.ejmg.2008.10.004. Epub 2008 Nov 5. Eur J Med Genet. 2009. PMID: 19015050

5

Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers.

Sundblom J, Stålberg E, Osterdahl M, Rücker F, Montelius M, Kalimo H, Nennesmo I, Islander G, Smits A, Dahl N, Melberg A. Sundblom J, et al. Among authors: stalberg e. Muscle Nerve. 2010 Jun;41(6):751-7. doi: 10.1002/mus.21589. Muscle Nerve. 2010. PMID: 20229577

6

Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q.

Melberg A, Oldfors A, Blomström-Lundqvist C, Stålberg E, Carlsson B, Larrson E, Lidell C, Eeg-Olofsson KE, Wikström G, Henriksson G, Dahl N. Melberg A, et al. Among authors: stalberg e. Ann Neurol. 1999 Nov;46(5):684-92. doi: 10.1002/1531-8249(199911)46:5<684::aid-ana2>3.0.co;2-#. Ann Neurol. 1999. PMID: 10970245

7

Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes.

Rostedt Punga A, Ahlqvist K, Bartoccioni E, Scuderi F, Marino M, Suomalainen A, Kalimo H, Stålberg EV. Rostedt Punga A, et al. Among authors: stalberg ev. Clin Neurophysiol. 2006 Jul;117(7):1434-43. doi: 10.1016/j.clinph.2006.03.028. Epub 2006 Jun 5. Clin Neurophysiol. 2006. PMID: 16737845

8

Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism.

Melberg A, Arnell H, Dahl N, Stålberg E, Raininko R, Oldfors A, Bakall B, Lundberg PO, Holme E. Melberg A, et al. Among authors: stalberg e. Muscle Nerve. 1996 Dec;19(12):1561-9. doi: 10.1002/(SICI)1097-4598(199612)19:12<1561::AID-MUS5>3.0.CO;2-8. Muscle Nerve. 1996. PMID: 8941270

9

Tubular aggregates in congenital myasthenic syndrome.

Feresiadou A, Casar-Borota O, Dragomir A, Oldfors CH, Stålberg E, Oldfors A. Feresiadou A, et al. Among authors: stalberg e. Neuromuscul Disord. 2018 Feb;28(2):174-175. doi: 10.1016/j.nmd.2017.11.009. Epub 2017 Nov 24. Neuromuscul Disord. 2018. PMID: 29311015 No abstract available.

10

The difficulty in confirming clinical diagnosis of myasthenia gravis in a seronegative patient: a possible neurophysiological approach.

Caliandro P, Evoli A, Stålberg E, Granata G, Tonali P, Padua L. Caliandro P, et al. Among authors: stalberg e. Neuromuscul Disord. 2009 Dec;19(12):825-7. doi: 10.1016/j.nmd.2009.09.005. Epub 2009 Oct 28. Neuromuscul Disord. 2009. PMID: 19846306

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