Kampmann C - Search Results

1

A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations.

Herzog A, Hartung R, Reuser AJ, Hermanns P, Runz H, Karabul N, Gökce S, Pohlenz J, Kampmann C, Lampe C, Beck M, Mengel E. Herzog A, et al. Among authors: kampmann c. Orphanet J Rare Dis. 2012 Jun 7;7:35. doi: 10.1186/1750-1172-7-35. Orphanet J Rare Dis. 2012. PMID: 22676651 Free PMC article.

2

Cardiac involvement in Anderson-Fabry disease.

Kampmann C, Baehner F, Ries M, Beck M. Kampmann C, et al. J Am Soc Nephrol. 2002 Jun;13 Suppl 2:S147-9. J Am Soc Nephrol. 2002. PMID: 12068028 Review. No abstract available.

3

The heart in Anderson Fabry disease.

Kampmann C, Wiethoff CM, Perrot A, Beck M, Dietz R, Osterziel KJ. Kampmann C, et al. Z Kardiol. 2002 Oct;91(10):786-95. doi: 10.1007/s00392-002-0848-5. Z Kardiol. 2002. PMID: 12395219 Review.

4

Cardiac manifestations of Anderson-Fabry disease in heterozygous females.

Kampmann C, Baehner F, Whybra C, Martin C, Wiethoff CM, Ries M, Gal A, Beck M. Kampmann C, et al. J Am Coll Cardiol. 2002 Nov 6;40(9):1668-74. doi: 10.1016/s0735-1097(02)02380-x. J Am Coll Cardiol. 2002. PMID: 12427421 Free article.

5

Fabry disease: focus on cardiac manifestations and molecular mechanisms.

Perrot A, Osterziel KJ, Beck M, Dietz R, Kampmann C. Perrot A, et al. Among authors: kampmann c. Herz. 2002 Nov;27(7):699-702. doi: 10.1007/s00059-002-2429-9. Herz. 2002. PMID: 12439642

6

IgA nephropathy in two adolescent sisters heterozygous for Fabry disease.

Whybra C, Schwarting A, Kriegsmann J, Gal A, Mengel E, Kampmann C, Baehner F, Schaefer E, Beck M. Whybra C, et al. Among authors: kampmann c. Pediatr Nephrol. 2006 Sep;21(9):1251-6. doi: 10.1007/s00467-006-0176-5. Epub 2006 Jul 13. Pediatr Nephrol. 2006. PMID: 16838183

7

Cardiac manifestations of Anderson-Fabry disease in children and adolescents.

Kampmann C, Wiethoff CM, Whybra C, Baehner FA, Mengel E, Beck M. Kampmann C, et al. Acta Paediatr. 2008 Apr;97(4):463-9. doi: 10.1111/j.1651-2227.2008.00700.x. Acta Paediatr. 2008. PMID: 18363956

8

Onset and progression of the Anderson-Fabry disease related cardiomyopathy.

Kampmann C, Linhart A, Baehner F, Palecek T, Wiethoff CM, Miebach E, Whybra C, Gal A, Bultas J, Beck M. Kampmann C, et al. Int J Cardiol. 2008 Nov 28;130(3):367-73. doi: 10.1016/j.ijcard.2008.03.007. Epub 2008 Jun 24. Int J Cardiol. 2008. PMID: 18572264

9

A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry disease.

Whybra C, Miebach E, Mengel E, Gal A, Baron K, Beck M, Kampmann C. Whybra C, et al. Among authors: kampmann c. Genet Med. 2009 Jun;11(6):441-9. doi: 10.1097/GIM.0b013e3181a23bec. Genet Med. 2009. PMID: 19346951 Free article. Clinical Trial.

10

Prevalence and characterization of cardiac involvement in Hunter syndrome.

Kampmann C, Beck M, Morin I, Loehr JP. Kampmann C, et al. J Pediatr. 2011 Aug;159(2):327-31.e2. doi: 10.1016/j.jpeds.2011.01.054. Epub 2011 May 6. J Pediatr. 2011. PMID: 21529823

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