Zerres K - Search Results

1

Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Rudnik-Schöneborn S, Stolz P, Varon R, Grohmann K, Schächtele M, Ketelsen UP, Stavrou D, Kurz H, Hübner C, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Neuropediatrics. 2004 Jun;35(3):174-82. doi: 10.1055/s-2004-820994. Neuropediatrics. 2004. PMID: 15248100

2

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

3

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

4

Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.

Rudnik-Schöneborn S, Forkert R, Hahnen E, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Neuropediatrics. 1996 Feb;27(1):8-15. doi: 10.1055/s-2007-973741. Neuropediatrics. 1996. PMID: 8677029

5

Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseases.

Spranger S, Rudnik-Schöneborn S, Spranger M, Schächtele M, Zerres K, Wirth B. Spranger S, et al. Among authors: zerres k. J Med Genet. 1997 Apr;34(4):340-2. doi: 10.1136/jmg.34.4.340. J Med Genet. 1997. PMID: 9138162 Free PMC article.

6

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.

7

The predictive value of achieved motor milestones assessed in 441 patients with infantile spinal muscular atrophy types II and III.

Rudnik-Schöneborn S, Hausmanowa-Petrusewicz I, Borkowska J, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Eur Neurol. 2001;45(3):174-81. doi: 10.1159/000052118. Eur Neurol. 2001. PMID: 11306862

8

Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy.

Rudnik-Schöneborn S, Goebel HH, Schlote W, Molaian S, Omran H, Ketelsen U, Korinthenberg R, Wenzel D, Lauffer H, Kreiss-Nachtsheim M, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Neurology. 2003 Mar 25;60(6):983-7. doi: 10.1212/01.wnl.0000052788.39340.45. Neurology. 2003. PMID: 12654964

9

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.

10

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

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