Lampe C - Search Results

Year	Number of Results
1953	2
1956	1
1957	4
1959	2
1960	2
1961	1
1968	1
1971	4
1974	1
1980	1
1986	1
1996	1
1997	2
2004	1
2006	1
2007	1
2008	1
2009	1
2010	2
2011	5
2012	4
2013	11
2014	8
2015	5
2016	6
2017	5
2018	5
2019	8
2020	5
2021	8
2022	9
2023	7
2024	1

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

Energy Transfer in Stability-Optimized Perovskite Nanocrystals.

Greiner MG, Singldinger A, Henke NA, Lampe C, Leo U, Gramlich M, Urban AS. Greiner MG, et al. Among authors: lampe c. Nano Lett. 2022 Aug 24;22(16):6709-6715. doi: 10.1021/acs.nanolett.2c02108. Epub 2022 Aug 8. Nano Lett. 2022. PMID: 35939043

3

Surgical management of neurological manifestations of mucopolysaccharidosis disorders.

Alden TD, Amartino H, Dalla Corte A, Lampe C, Harmatz PR, Vedolin L. Alden TD, et al. Among authors: lampe c. Mol Genet Metab. 2017 Dec;122S:41-48. doi: 10.1016/j.ymgme.2017.09.011. Epub 2017 Sep 28. Mol Genet Metab. 2017. PMID: 29153846 Free article. Review.

4

Practical management of behavioral problems in mucopolysaccharidoses disorders.

Escolar ML, Jones SA, Shapiro EG, Horovitz DDG, Lampe C, Amartino H. Escolar ML, et al. Among authors: lampe c. Mol Genet Metab. 2017 Dec;122S:35-40. doi: 10.1016/j.ymgme.2017.09.010. Epub 2017 Sep 27. Mol Genet Metab. 2017. PMID: 29170079 Free article. Review.

5

Mucopolysaccharidoses and other lysosomal storage diseases.

Lampe C, Bellettato CM, Karabul N, Scarpa M. Lampe C, et al. Rheum Dis Clin North Am. 2013 May;39(2):431-55. doi: 10.1016/j.rdc.2013.03.004. Rheum Dis Clin North Am. 2013. PMID: 23597973 Review.

6

The Inflammation in the Cytopathology of Patients With Mucopolysaccharidoses- Immunomodulatory Drugs as an Approach to Therapy.

Wiesinger AM, Bigger B, Giugliani R, Scarpa M, Moser T, Lampe C, Kampmann C, Lagler FB. Wiesinger AM, et al. Among authors: lampe c. Front Pharmacol. 2022 May 13;13:863667. doi: 10.3389/fphar.2022.863667. eCollection 2022. Front Pharmacol. 2022. PMID: 35645812 Free PMC article. Review.

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

An Innovative Tool for Evidence-Based, Personalized Treatment Trials in Mucopolysaccharidosis.

Wiesinger AM, Bigger B, Giugliani R, Lampe C, Scarpa M, Moser T, Kampmann C, Zimmermann G, Lagler FB. Wiesinger AM, et al. Among authors: lampe c. Pharmaceutics. 2023 May 22;15(5):1565. doi: 10.3390/pharmaceutics15051565. Pharmaceutics. 2023. PMID: 37242808 Free PMC article. Retracted.

9

Social and medical needs of rare metabolic patients: results from a MetabERN survey.

Sestini S, Paneghetti L, Lampe C, Betti G, Bond S, Bellettato CM, Maurizio S. Sestini S, et al. Among authors: lampe c. Orphanet J Rare Dis. 2021 Aug 3;16(1):336. doi: 10.1186/s13023-021-01948-5. Orphanet J Rare Dis. 2021. PMID: 34344397 Free PMC article. Review.

10

European Achondroplasia Forum guiding principles for the detection and management of foramen magnum stenosis.

Irving M, AlSayed M, Arundel P, Baujat G, Ben-Omran T, Boero S, Cormier-Daire V, Fredwall S, Guillen-Navarro E, Hoyer-Kuhn H, Kunkel P, Lampe C, Maghnie M, Mohnike K, Mortier G, Sousa SB. Irving M, et al. Among authors: lampe c. Orphanet J Rare Dis. 2023 Jul 27;18(1):219. doi: 10.1186/s13023-023-02795-2. Orphanet J Rare Dis. 2023. PMID: 37501185 Free PMC article.

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