Udd B - Search Results

1

Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus.

Hackman P, Sandell S, Sarparanta J, Luque H, Huovinen S, Palmio J, Paetau A, Kalimo H, Mahjneh I, Udd B. Hackman P, et al. Among authors: udd b. Neuromuscul Disord. 2011 May;21(5):338-44. doi: 10.1016/j.nmd.2011.02.008. Epub 2011 Mar 3. Neuromuscul Disord. 2011. PMID: 21376592

2

Imaging methods reveal unexpected patchy lesions in late onset distal myopathy.

Udd B, Lamminen A, Somer H. Udd B, et al. Neuromuscul Disord. 1991;1(4):279-85. doi: 10.1016/0960-8966(91)90102-x. Neuromuscul Disord. 1991. PMID: 1822807

3

Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients.

Udd B, Partanen J, Halonen P, Falck B, Hakamies L, Heikkilä H, Ingo S, Kalimo H, Kääriäinen H, Laulumaa V, et al. Udd B, et al. Arch Neurol. 1993 Jun;50(6):604-8. doi: 10.1001/archneur.1993.00540060044015. Arch Neurol. 1993. PMID: 8503797

4

Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?

Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H. Udd B, et al. Neuromuscul Disord. 1997 Jun;7(4):217-28. doi: 10.1016/s0960-8966(97)00041-2. Neuromuscul Disord. 1997. PMID: 9196902

5

Assignment of the tibial muscular dystrophy locus to chromosome 2q31.

Haravuori H, Mäkelä-Bengs P, Udd B, Partanen J, Pulkkinen L, Somer H, Peltonen L. Haravuori H, et al. Among authors: udd b. Am J Hum Genet. 1998 Mar;62(3):620-6. doi: 10.1086/301752. Am J Hum Genet. 1998. PMID: 9497249 Free PMC article.

6

Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31.

Udd B, Haravuori H, Kalimo H, Partanen J, Pulkkinen L, Paetau A, Peltonen L, Somer H. Udd B, et al. Neuromuscul Disord. 1998 Jun;8(5):327-32. doi: 10.1016/s0960-8966(98)00024-8. Neuromuscul Disord. 1998. PMID: 9673987

7

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.

Haravuori H, Vihola A, Straub V, Auranen M, Richard I, Marchand S, Voit T, Labeit S, Somer H, Peltonen L, Beckmann JS, Udd B. Haravuori H, et al. Among authors: udd b. Neurology. 2001 Apr 10;56(7):869-77. doi: 10.1212/wnl.56.7.869. Neurology. 2001. PMID: 11294923

8

Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.

Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B. Rantamäki M, et al. Among authors: udd b. Neurology. 2001 Sep 25;57(6):1043-9. doi: 10.1212/wnl.57.6.1043. Neurology. 2001. PMID: 11571332

9

Electrophysiological findings in X-linked myopathy with excessive autophagy.

Jääskeläinen SK, Juel VC, Udd B, Villanova M, Liguori R, Minassian BA, Falck B, Niemi P, Kalimo H. Jääskeläinen SK, et al. Among authors: udd b. Ann Neurol. 2002 May;51(5):648-52. doi: 10.1002/ana.10173. Ann Neurol. 2002. PMID: 12112116

10

Welander distal myopathy outside the Swedish population: phenotype and genotype.

von Tell D, Somer H, Udd B, Edström L, Borg K, Ahlberg G. von Tell D, et al. Among authors: udd b. Neuromuscul Disord. 2002 Aug;12(6):544-7. doi: 10.1016/s0960-8966(01)00338-8. Neuromuscul Disord. 2002. PMID: 12117477

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