Lampe C - Search Results

1

Künstliche Intelligenz zur diagnostischen Unterstützung ausgewählter seltener lysosomaler Speichererkrankungen: Ergebnisse einer Pilotstudie.

Sieg AL, Martin Das A, Maria Muschol N, Köhn A, Lampe C, Kortum X, Mehmecke S, Blöß S, Lechner W, Klawonn F, Grigull L. Sieg AL, et al. Among authors: lampe c. Klin Padiatr. 2019 Mar;231(2):60-66. doi: 10.1055/a-0816-5681. Epub 2019 Jan 10. Klin Padiatr. 2019. PMID: 30630212 German.

2

[Lysosomal Storage Diseases: Challenges in Multiprofessional Patient Care with Enzyme Replacement Therapy].

Das AM, Lagler F, Beck M, Scarpa M, Lampe C. Das AM, et al. Among authors: lampe c. Klin Padiatr. 2017 May;229(3):168-174. doi: 10.1055/s-0043-103088. Epub 2017 May 2. Klin Padiatr. 2017. PMID: 28464188 German.

3

Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS).

Stepien KM, Gevorkyan AK, Hendriksz CJ, Lobzhanidze TV, Pérez-López J, Tol G, Del Toro Riera M, Vashakmadze ND, Lampe C. Stepien KM, et al. Among authors: lampe c. Orphanet J Rare Dis. 2020 May 14;15(1):114. doi: 10.1186/s13023-020-01382-z. Orphanet J Rare Dis. 2020. PMID: 32410642 Free PMC article.

4

Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis Patients.

Wasielica-Poslednik J, Butsch C, Lampe C, Elflein H, Lamparter J, Weyer V, Pitz S. Wasielica-Poslednik J, et al. Among authors: lampe c. PLoS One. 2015 Aug 28;10(8):e0133586. doi: 10.1371/journal.pone.0133586. eCollection 2015. PLoS One. 2015. PMID: 26317991 Free PMC article.

5

Easy-to-use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment.

Tylki-Szymańska A, De Meirleir L, Di Rocco M, Fathalla WM, Guffon N, Lampe C, Lund AM, Parini R, Wijburg FA, Zeman J, Scarpa M. Tylki-Szymańska A, et al. Among authors: lampe c. Acta Paediatr. 2018 Aug;107(8):1402-1408. doi: 10.1111/apa.14417. Acta Paediatr. 2018. PMID: 29797470 Free PMC article.

6

Spinal cord issues in adult patients with MPS: transition of care survey.

Ghotme KA, Alvarado-Gomez F, Lampe C, White KK, Solano-Villareal M, Giugliani R, Harmatz PR. Ghotme KA, et al. Among authors: lampe c. Childs Nerv Syst. 2018 Sep;34(9):1759-1765. doi: 10.1007/s00381-018-3834-6. Epub 2018 May 27. Childs Nerv Syst. 2018. PMID: 29804213

7

Health-related quality of life in mucopolysaccharidosis: looking beyond biomedical issues.

Hendriksz CJ, Berger KI, Lampe C, Kircher SG, Orchard PJ, Southall R, Long S, Sande S, Gold JI. Hendriksz CJ, et al. Among authors: lampe c. Orphanet J Rare Dis. 2016 Aug 26;11(1):119. doi: 10.1186/s13023-016-0503-2. Orphanet J Rare Dis. 2016. PMID: 27561270 Free PMC article. Review.

8

Stand-alone craniocervical decompression is feasible in children with mucopolysaccharidosis type I, IVA, and VI.

Krenzlin H, Ta-Chih T, Lampe C, Lampe C, Knuf M, Horn P, Schwarz M. Krenzlin H, et al. Among authors: lampe c. Spine J. 2018 Aug;18(8):1455-1459. doi: 10.1016/j.spinee.2018.04.002. Epub 2018 Apr 9. Spine J. 2018. PMID: 29649608

9

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: lampe 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.

10

Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome).

Möllmann C, Lampe CG, Müller-Forell W, Scarpa M, Harmatz P, Schwarz M, Beck M, Lampe C. Möllmann C, et al. Among authors: lampe cg, lampe c. JIMD Rep. 2013;11:65-72. doi: 10.1007/8904_2013_223. Epub 2013 Apr 12. JIMD Rep. 2013. PMID: 23580366 Free PMC article.

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