Zerres K - Search Results

1

Heterogeneity in proximal spinal muscular atrophy.

Zerres K, Rudnik-Schöneborn S, Rietschel M. Zerres K, et al. Lancet. 1990 Sep 22;336(8717):749-50. doi: 10.1016/0140-6736(90)92243-b. Lancet. 1990. PMID: 1975919 No abstract available.

2

Genetic basis of adult-onset spinal muscular atrophy.

Zerres K, Rudnik-Schöneborn S, Forkert R, Wirth B. Zerres K, et al. Lancet. 1995 Oct 28;346(8983):1162. doi: 10.1016/s0140-6736(95)91835-3. Lancet. 1995. PMID: 7475624 No abstract available.

3

Pregnancy and spinal muscular atrophy.

Rudnik-Schöneborn S, Zerres K, Ignatius J, Rietschel M. Rudnik-Schöneborn S, et al. Among authors: zerres k. J Neurol. 1992 Jan;239(1):26-30. doi: 10.1007/BF00839207. J Neurol. 1992. PMID: 1541965 Review.

4

Clinical variability of autosomal dominant spinal muscular atrophy.

Rietschel M, Rudnik-Schöneborn S, Zerres K. Rietschel M, et al. Among authors: zerres k. J Neurol Sci. 1992 Jan;107(1):65-73. doi: 10.1016/0022-510x(92)90210-c. J Neurol Sci. 1992. PMID: 1578236

5

No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.

Kausch K, Müller CR, Grimm T, Ricker K, Rietschel M, Rudnik-Schöneborn S, Zerres K. Kausch K, et al. Among authors: zerres k. Hum Genet. 1991 Jan;86(3):317-8. doi: 10.1007/BF00202419. Hum Genet. 1991. PMID: 1997389

6

Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases.

Wirth B, Rudnik-Schöneborn S, Hahnen E, Röhrig D, Zerres K. Wirth B, et al. Among authors: zerres k. Prenat Diagn. 1995 May;15(5):407-17. doi: 10.1002/pd.1970150503. Prenat Diagn. 1995. PMID: 7644431

7

Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications.

Zerres K, Rudnik-Schöneborn S. Zerres K, et al. Arch Neurol. 1995 May;52(5):518-23. doi: 10.1001/archneur.1995.00540290108025. Arch Neurol. 1995. PMID: 7733848

8

Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy.

Rudnik-Schöneborn S, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Am J Hum Genet. 1994 Jul;55(1):112-9. Am J Hum Genet. 1994. PMID: 8023839 Free PMC article.

9

Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications.

Rudnik-Schöneborn S, Röhrig D, Morgan G, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Am J Med Genet. 1994 May 15;51(1):70-6. doi: 10.1002/ajmg.1320510115. Am J Med Genet. 1994. PMID: 8030672

10

Spinal muscular atrophy--clinical and genetic correlations.

Zerres K, Wirth B, Rudnik-Schöneborn S. Zerres K, et al. Neuromuscul Disord. 1997 May;7(3):202-7. doi: 10.1016/s0960-8966(97)00459-8. Neuromuscul Disord. 1997. PMID: 9185186 Review.

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