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Medientyp
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Erscheinungsjahr
Autor/in
- Johannsen, Jessika
- Denecke, Jonas 2
- Altmeppen, Hermann Clemens 1
- Barkmann, Claus 1
- Becker, Lena-Luise 1
- alle zeigen
Sprache
- Englisch 4
4 Einträge gefunden
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Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala)
- Holling, Tess
- Lisfeld, Jasmin
- Johannsen, Jessika
- Matschke, Jakob
- Song, Feizhi
- Altmeppen, Hermann Clemens
- Kutsche, Kerstin
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Health-Related Quality of Life and mental health of families with children and adolescents affected by rare diseases and high disease burden: the perspective of affected children and their siblings
- Wiegand-Grefe, Silke
- Liedtke, Anna
- Morgenstern, Lydia
- Hoff, Antonia
- Csengoe-Norris, Anikó
- Johannsen, Jessika
- Denecke, Jonas
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Mucha-Habermann disease: a pediatric case report and proposal of a risk score
- Blohm, Martin Ernst
- Ebenebe, Chinedu Ulrich
- Rau, Cornelius
- Escherich, Carolin
- Johannsen, Jessika
- Escherich, Gabriele
- Driemeyer, Joenna
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Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study
- Weiß, Claudia
- Ziegler, Andreas
- Becker, Lena-Luise
- Johannsen, Jessika
- Brennenstuhl, Heiko
- Schreiber, Gudrun
- Flotats-Bastardas, Marina