Roggendorf W - Search Results

1

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses.

Harzer K, Paton BC, Poulos A, Kustermann-Kuhn B, Roggendorf W, Grisar T, Popp M. Harzer K, et al. Among authors: roggendorf w. Eur J Pediatr. 1989 Oct;149(1):31-9. doi: 10.1007/BF02024331. Eur J Pediatr. 1989. PMID: 2514102 Review.

2

A case of combined Farber and Sandhoff disease.

Fusch C, Huenges R, Moser HW, Sewell AC, Roggendorf W, Kustermann-Kuhn B, Poulos A, Carey WF, Harzer K. Fusch C, et al. Among authors: roggendorf w. Eur J Pediatr. 1989 Apr;148(6):558-62. doi: 10.1007/BF00441558. Eur J Pediatr. 1989. PMID: 2744019

3

Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage disease.

Bradová V, Smíd F, Ulrich-Bott B, Roggendorf W, Paton BC, Harzer K. Bradová V, et al. Among authors: roggendorf w. Hum Genet. 1993 Sep;92(2):143-52. doi: 10.1007/BF00219682. Hum Genet. 1993. PMID: 8370580

4

Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.

Peiffer J, Kustermann-Kuhn B, Mortier W, Poremba M, Roggendorf W, Scholte HR, Schröder JM, Wendtland B, Wessel K, Zimmermann C. Peiffer J, et al. Among authors: roggendorf w. Pathol Res Pract. 1988 Nov;183(6):706-16. doi: 10.1016/S0344-0338(88)80056-6. Pathol Res Pract. 1988. PMID: 3222173

5

Normomorphic sialidosis in two female adults with severe neurologic disease and without sialyl oligosacchariduria.

Harzer K, Cantz M, Sewell AC, Dhareshwar SS, Roggendorf W, Heckl RW, Schofer O, Thumler R, Peiffer J, Schlote W. Harzer K, et al. Among authors: roggendorf w. Hum Genet. 1986 Nov;74(3):209-14. doi: 10.1007/BF00282535. Hum Genet. 1986. PMID: 3096875

6

Molecular analysis of medulloblastomas occurring simultaneously in monozygotic twins.

Scheurlen W, Sörensen N, Roggendorf W, Kühl J. Scheurlen W, et al. Among authors: roggendorf w. Eur J Pediatr. 1996 Oct;155(10):880-4. doi: 10.1007/BF02282838. Eur J Pediatr. 1996. PMID: 8891558

7

Altered expression of collagen type VI in brain vessels of patients with chronic hypertension. A comparison with the distribution of collagen IV and procollagen III.

Roggendorf W, Opitz H, Schuppan D. Roggendorf W, et al. Acta Neuropathol. 1988;77(1):55-60. doi: 10.1007/BF00688243. Acta Neuropathol. 1988. PMID: 3239376

8

Localization of basic fibroblast growth factor, a mitogen and angiogenic factor, in human brain tumors.

Paulus W, Grothe C, Sensenbrenner M, Janet T, Baur I, Graf M, Roggendorf W. Paulus W, et al. Among authors: roggendorf w. Acta Neuropathol. 1990;79(4):418-23. doi: 10.1007/BF00308718. Acta Neuropathol. 1990. PMID: 2339593

9

Meningio-angiomatosis.

Paulus W, Peiffer J, Roggendorf W, Schuppan D. Paulus W, et al. Among authors: roggendorf w. Pathol Res Pract. 1989 Apr;184(4):446-54. doi: 10.1016/S0344-0338(89)80043-3. Pathol Res Pract. 1989. PMID: 2498857 Review.

10

Adult-onset rod disease with abundant intranuclear rods.

Paulus W, Peiffer J, Becker I, Roggendorf W, Schumm F. Paulus W, et al. Among authors: roggendorf w. J Neurol. 1988 Jul;235(6):343-7. doi: 10.1007/BF00314229. J Neurol. 1988. PMID: 2845006

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