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Author/Creator Senderek, J.

1. Diagnostic algorithms in Charcot–Marie–Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients. Issue 1 (29th April 2015)

Authors:
Rudnik‐Schöneborn, S.; Tölle, D.; Senderek, J.; Eggermann, K.; Elbracht, M.; Kornak, U.; von der Hagen, M.; Kirschner, J.; Leube, B.; Müller‐Felber, W.; Schara, U.; von Au, K.; Wieczorek, D.; Bußmann, C.; Zerres, K.
Journal:
Clinical genetics
Issue:
Volume 89:Issue 1(2016)
Page Start:
34
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2. Issue 5 (14th August 2018)

Authors:
Laššuthová, P.; Vill, K.; Erdem‐Ozdamar, S.; Schröder, J.M.; Topaloglu, H.; Horvath, R.; Müller‐Felber, W.; Bansagi, B.; Schlotter‐Weigel, B.; Gläser, D.; Neupauerová, J.; Sedláčková, L.; Staněk, D.; Mazanec, R.; Weis, J.; Seeman, P.; Senderek, J.
Journal:
Clinical genetics
Issue:
Volume 94:Issue 5(2018)
Page Start:
467
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Demyelinating Charcot–Marie–Tooth neuropathy associated with FBLN5 mutations. (5th September 2020)

Authors:
Safka Brozkova, D.; Stojkovic, T.; Haberlová, J.; Mazanec, R.; Windhager, R.; Fernandes Rosenegger, P.; Hacker, S.; Züchner, S.; Kochański, A.; Leonard‐Louis, S.; Francou, B.; Latour, P.; Senderek, J.; Seeman, P.; Auer‐Grumbach, M.
Journal:
European journal of neurology
Issue:
Volume 27:Number 12(2020)
Page Start:
2568
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I. Issue 2 (8th November 2017)

Authors:
Braunisch, M.C.; Gallwitz, H.; Abicht, A.; Diebold, I.; Holinski‐Feder, E.; Van Maldergem, L.; Lammens, M.; Kovács‐Nagy, R.; Alhaddad, B.; Strom, T.M.; Meitinger, T.; Senderek, J.; Rudnik‐Schöneborn, S.; Haack, T.B.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 2(2018)
Page Start:
255
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗