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Retinal and optic nerve degeneration in α-mannosidosis.
Matlach J, Zindel T, Amraoui Y, Arash-Kaps L, Hennermann JB, Pitz S. Matlach J, et al. Among authors: hennermann jb. Orphanet J Rare Dis. 2018 Jun 1;13(1):88. doi: 10.1186/s13023-018-0829-z. Orphanet J Rare Dis. 2018. PMID: 29859105 Free PMC article.
Enzyme replacement therapy with velmanase alfa (human recombinant alpha-mannosidase): Novel global treatment response model and outcomes in patients with alpha-mannosidosis.
Harmatz P, Cattaneo F, Ardigò D, Geraci S, Hennermann JB, Guffon N, Lund A, Hendriksz CJ, Borgwardt L. Harmatz P, et al. Among authors: hennermann jb. Mol Genet Metab. 2018 Jun;124(2):152-160. doi: 10.1016/j.ymgme.2018.04.003. Epub 2018 Apr 18. Mol Genet Metab. 2018. PMID: 29716835 Free article.
Saccadic reaction time and ocular findings in phenylketonuria.
Hopf S, Nowak C, Hennermann JB, Schmidtmann I, Pfeiffer N, Pitz S. Hopf S, et al. Among authors: hennermann jb. Orphanet J Rare Dis. 2020 May 25;15(1):124. doi: 10.1186/s13023-020-01407-7. Orphanet J Rare Dis. 2020. PMID: 32450880 Free PMC article.
Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease.
Lenders M, Hennermann JB, Kurschat C, Rolfs A, Canaan-Kühl S, Sommer C, Üçeyler N, Kampmann C, Karabul N, Giese AK, Duning T, Stypmann J, Krämer J, Weidemann F, Brand SM, Wanner C, Brand E. Lenders M, et al. Among authors: hennermann jb. Orphanet J Rare Dis. 2016 Jun 29;11(1):88. doi: 10.1186/s13023-016-0473-4. Orphanet J Rare Dis. 2016. PMID: 27356758 Free PMC article.
The cardiovascular phenotype of adult patients with phenylketonuria.
Azabdaftari A, van der Giet M, Schuchardt M, Hennermann JB, Plöckinger U, Querfeld U. Azabdaftari A, et al. Among authors: hennermann jb. Orphanet J Rare Dis. 2019 Sep 6;14(1):213. doi: 10.1186/s13023-019-1188-0. Orphanet J Rare Dis. 2019. PMID: 31492166 Free PMC article.
112 results