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[Lysosomal storage diseases - update and new therapeutic options].
Schöpfer K, Miebach E, Beck M, Pitz S. Schöpfer K, et al. Among authors: pitz s. Klin Monbl Augenheilkd. 2011 Feb;228(2):144-60. doi: 10.1055/s-0028-1109958. Epub 2010 Mar 22. Klin Monbl Augenheilkd. 2011. PMID: 20309790 Review. German.
Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.
Scarpa M, Almássy Z, Beck M, Bodamer O, Bruce IA, De Meirleir L, Guffon N, Guillén-Navarro E, Hensman P, Jones S, Kamin W, Kampmann C, Lampe C, Lavery CA, Teles EL, Link B, Lund AM, Malm G, Pitz S, Rothera M, Stewart C, Tylki-Szymańska A, van der Ploeg A, Walker R, Zeman J, Wraith JE; Hunter Syndrome Europena Expert Council. Scarpa M, et al. Among authors: pitz s. Orphanet J Rare Dis. 2011 Nov 7;6:72. doi: 10.1186/1750-1172-6-72. Orphanet J Rare Dis. 2011. PMID: 22059643 Free PMC article.
Clinical features of pediatric Graves' orbitopathy.
Eha J, Pitz S, Pohlenz J. Eha J, et al. Among authors: pitz s. Int Ophthalmol. 2010 Dec;30(6):717-21. doi: 10.1007/s10792-010-9351-6. Epub 2010 Feb 27. Int Ophthalmol. 2010. PMID: 20191374
162 results