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Udd, B
Juvonen, V
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Cederquist, K
Davis, M
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Sperfeld, AD
Sorensen, SA
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Van Maldergem, L
Watanabe, M
Weber, M
Yeung, L
Savontaus, ML
Citation: A. Lund et al., Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world, EUR J HUM G, 9(6), 2001, pp. 431-436
Authors:
Haravuori, H
Vihola, A
Straub, V
Auranen, M
Richard, I
Marchand, S
Voit, T
Labeit, S
Somer, H
Peltonen, L
Beckmann, JS
Udd, B
Citation: H. Haravuori et al., Secondary calpain3 deficiency in 2q-linked muscular dystrophy - Titin is the candidate gene, NEUROLOGY, 56(7), 2001, pp. 869-877
Authors:
Ohno, K
Tsujino, A
Brengman, JM
Harper, CM
Bajzer, Z
Udd, B
Beyring, R
Robb, S
Kirkham, FJ
Engel, AG
Citation: K. Ohno et al., Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans (vol 98, pg 2017, 2001), P NAS US, 98(9), 2001, pp. 5369-5369
Authors:
Ohno, K
Tsujino, A
Brengman, JM
Harper, CM
Bajzer, Z
Udd, B
Beyring, R
Robb, S
Kirkham, FJ
Engel, AG
Citation: K. Ohno et al., Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans, P NAS US, 98(4), 2001, pp. 2017-2022
Authors:
de Seze, J
Udd, B
Haravuori, H
Sablonniere, B
Maurage, CA
Hurtevent, JF
Boutry, N
Stojkovic, T
Schraen, S
Petit, H
Vermersch, P
Citation: J. De Seze et al., The first European family with tibial muscular dystrophy outside the Finnish population, NEUROLOGY, 51(6), 1998, pp. 1746-1748