-
1
-
-
0035800434
-
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
-
Liquori C.L., Ricker K., Moseley M.L., et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 293 (2001) 864-867
-
(2001)
Science
, vol.293
, pp. 864-867
-
-
Liquori, C.L.1
Ricker, K.2
Moseley, M.L.3
-
2
-
-
0033653152
-
Clinical and genetic heterogeneity in myotonic dystrophies
-
Meola G. Clinical and genetic heterogeneity in myotonic dystrophies. Muscle Nerve 23 12 (2000) 1789-1799
-
(2000)
Muscle Nerve
, vol.23
, Issue.12
, pp. 1789-1799
-
-
Meola, G.1
-
3
-
-
0032192323
-
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness
-
Phillips M.F., Rogers M.T., Barnetson R., et al. PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness. Neuromuscul Disord 8 (1998) 439-446
-
(1998)
Neuromuscul Disord
, vol.8
, pp. 439-446
-
-
Phillips, M.F.1
Rogers, M.T.2
Barnetson, R.3
-
4
-
-
0032995065
-
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)
-
Day J.W., Roelofs R., Leroy B., et al. Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2). Neuromuscul Disord 9 (1999) 19-27
-
(1999)
Neuromuscul Disord
, vol.9
, pp. 19-27
-
-
Day, J.W.1
Roelofs, R.2
Leroy, B.3
-
5
-
-
3142720352
-
Clinical and genetic analysis of a family with PROMM
-
Grewal R.P., Zhang S., Ma W., et al. Clinical and genetic analysis of a family with PROMM. J Clin Neurosci 11 (2004) 603-605
-
(2004)
J Clin Neurosci
, vol.11
, pp. 603-605
-
-
Grewal, R.P.1
Zhang, S.2
Ma, W.3
-
6
-
-
48549094945
-
Gastrointestinal involvement is frequent in myotonic dystrophy type 2
-
Tieleman A.A., van Vliet J., Jansen J.B.M.J., et al. Gastrointestinal involvement is frequent in myotonic dystrophy type 2. Neuromuscul Disord 18 (2008) 646-649
-
(2008)
Neuromuscul Disord
, vol.18
, pp. 646-649
-
-
Tieleman, A.A.1
van Vliet, J.2
Jansen, J.B.M.J.3
-
7
-
-
33344462063
-
Evaluation of a Gastrointestinal Symptoms Questionnaire
-
Bovenschen H.J., Janssen M.J., van Oijen M.G., et al. Evaluation of a Gastrointestinal Symptoms Questionnaire. Dig Dis Sci 51 (2006) 1509-1515
-
(2006)
Dig Dis Sci
, vol.51
, pp. 1509-1515
-
-
Bovenschen, H.J.1
Janssen, M.J.2
van Oijen, M.G.3
-
8
-
-
33745914230
-
Dysphagia in facioscapulohumeral muscular dystrophy
-
Wohlgemuth M., de Swart B.J.M., Kalf F.B.M., et al. Dysphagia in facioscapulohumeral muscular dystrophy. Neurology 66 (2006) 1926-1928
-
(2006)
Neurology
, vol.66
, pp. 1926-1928
-
-
Wohlgemuth, M.1
de Swart, B.J.M.2
Kalf, F.B.M.3
-
10
-
-
33750960352
-
Flexible endoscopic evaluation of swallowing with sensory testing
-
Rees C.J. Flexible endoscopic evaluation of swallowing with sensory testing. Curr Opin Otolaryngol Head Neck Surg 14 6 (2006) 425-430
-
(2006)
Curr Opin Otolaryngol Head Neck Surg
, vol.14
, Issue.6
, pp. 425-430
-
-
Rees, C.J.1
-
11
-
-
0033057079
-
The dysphagia outcome and severity scale
-
O'Neil K.H., Purdy M., Falk J., et al. The dysphagia outcome and severity scale. Dysphagia 14 (1999) 139-145
-
(1999)
Dysphagia
, vol.14
, pp. 139-145
-
-
O'Neil, K.H.1
Purdy, M.2
Falk, J.3
-
12
-
-
0030052755
-
Clinical measurement of swallowing in health and in neurogenic dysphagia
-
Hughes T.A., and Wiles C.M. Clinical measurement of swallowing in health and in neurogenic dysphagia. Q J Med 89 (1996) 109-116
-
(1996)
Q J Med
, vol.89
, pp. 109-116
-
-
Hughes, T.A.1
Wiles, C.M.2
-
13
-
-
0035088042
-
Electrophysiological evaluation of oropharyngeal swallowing in myotonic dystrophy
-
Ertekin C., Yüceyar N., Aydoǧdu I., et al. Electrophysiological evaluation of oropharyngeal swallowing in myotonic dystrophy. J Neurol Neurosurg Psychiatry 70 3 (2001) 363-371
-
(2001)
J Neurol Neurosurg Psychiatry
, vol.70
, Issue.3
, pp. 363-371
-
-
Ertekin, C.1
Yüceyar, N.2
Aydoǧdu, I.3
|