Quantification of Specific Urinary Oligosaccharide Biomarkers for Diagnosis and Treatment Monitoring of Alpha-Mannosidosis
Dörfel D, Dreyer B, Lindschau M, Barbato A, Altavilla N, la Marca G, Marten L, Bürger F, Botti M, Sevenich L, Spiegel R, Schumann A, Herrmann M, Fielitz D, Muschol N, Santer R, Murko S
J INHERIT METAB DIS. 2026;49(3):e70208.

Automated bone age assessment in rare pediatric growth disorders: a comparative study using Deeplasia
Skaf K, Fardipour M, Schmidt P, Bolmer E, Keller A, Lampe C, Jurgens J, Lindschau M, Palm K, Ruckdeschel S, Javanmardi B, Mohnike K
FRONT ENDOCRINOL. 2026;17:1741927.

Delayed diagnosis of mucopolysaccharidosis type I in a patient with spinopelvic instability, short stature, and skeletal dysplasia
Windels O, Lindschau M, Boschann F, Oheim R, Muschol N
JBMR PLUS. 2026;10(6):ziag065.

Spinal cord compression in patients with mucopolysaccharidosis
Pantel T, Lindschau M, Luebke A, Kunkel P, Dreimann M, Muschol N, Eicker S
EUR SPINE J. 2022;31(7):1693-1699.

Mucopolysaccharidosis type I due to maternal uniparental disomy of chromosome 4 with partial isodisomy of 4p16.3p15.2
Kloth K, Vater I, Lindschau R, Rau I, Caliebe A, Muschol N
MOL GENET METAB REP. 2020;25:.

Letzte Aktualisierung aus dem FIS: 25.09.2026 - 00:32 Uhr