E-LIB Suche - Ergebnisse für: Vill, K.

1

P206 Impaired neurodevelopment in children with 5q-SMA - 2 ..:

Kölbel, H. ; Kopka, M. ; Modler, L....
Neuromuscular Disorders. 33 (2023) - p. S86 , 2023

Link: https://doi.org/10.1016/..

2

Neugeborenenscreening auf spinale Muskelatrophie; Newborn s..:

Müller-Felber, W. ; Vill, K. ; Schwartz, O....
Monatsschrift Kinderheilkunde. 172 (2021) 7 - p. 595-600 , 2021

Link: https://doi.org/10.1007/..

3

Qualitative and quantitative muscle ultrasound in patients ..:

Vill, K. ; Sehri, M. ; Müller, C....
European Journal of Paediatric Neurology. 28 (2020) - p. 142-150 , 2020

Link: https://doi.org/10.1016/..

4

P.211Pilot study of genetic newborn screening for spinal mu..:

Mueller-Felber, W. ; Kölbel, H. ; Schwartz, O....
Neuromuscular Disorders. 29 (2019) - p. S128 , 2019

Link: https://doi.org/10.1016/..

5

Three by three weeks of robot-enhanced repetitive gait ther..:

Weinberger, R. ; Warken, B. ; König, H....
European Journal of Paediatric Neurology. 23 (2019) 4 - p. 581-588 , 2019

Link: https://doi.org/10.1016/..

6

Novel SBF2 mutations and clinical spectrum of Charcot‐Marie..:

Laššuthová, P. ; Vill, K. ; Erdem‐Ozdamar, S....
Clinical Genetics. 94 (2018) 5 - p. 467-472 , 2018

Link: https://doi.org/10.1111/..

7

Spinale Muskelatrophie: Zeit für das Neugeborenenscreening?:

Vill, K. ; Blaschek, A. ; Schara, U....
Der Nervenarzt. 88 (2017) 12 - p. 1358-1366 , 2017

Link: https://doi.org/10.1007/..

8

Children with migraine: Provocation of headache via pressur..:

Landgraf, M.N. ; Biebl, J.T. ; Langhagen, T....
European Journal of Pain. 22 (2017) 2 - p. 385-392 , 2017

Link: https://doi.org/10.1002/..

9

Proximal muscular atrophy and weakness: An unusual adverse ..:

Vill, K. ; Müller-Felber, W. ; Teusch, V....
Neuromuscular Disorders. 26 (2016) 4-5 - p. 322-325 , 2016

Link: https://doi.org/10.1016/..

10

Muscle ultrasound in classic infantile and adult Pompe dise..:

Vill, K. ; Schessl, J. ; Teusch, V....
Neuromuscular Disorders. 25 (2015) 2 - p. 120-126 , 2015

Link: https://doi.org/10.1016/..

11

De novo stop-loss variants in CLDN11 cause hypomyelinating ..:

Riedhammer, K.M ; Stockler, S ; Ploski, R...
info:eu-repo/semantics/altIdentifier/doi/10.1093/brain/awaa410. , 2021

Link: https://push-zb.helmholt..

12

Neugeborenenscreening auf spinale Muskelatrophie:

Müller-Felber, W ; Vill, K ; Schwartz, O...
https://repository.publisso.de/resource/frl:6448245. , 2021

Link: https://repository.publi..

13

Sequential targeted exome sequencing of 1001 patients affec..:

Töpf, A ; Johnson, K ; Bates, A...
Genetics in medicine. , 2020

Link: https://ddd.uab.cat/reco..

14

Monogenic variants in dystonia: an exome-wide sequencing st..:

Zech M ; Jech R ; Boesch S...
14744465. , 2020

Link: https://doi.org/10.1016/..

15

Monogenic variants in dystonia: An exome-wide sequencing st..:

Zech, M ; Jech, R ; Boesch, S...
info:eu-repo/semantics/altIdentifier/doi/10.1016/S1474-4422(20)30312-4. , 2020

Link: https://push-zb.helmholt..