Grimm A - Search Results

1

Phenotypic spectrum of autosomal recessive retinitis pigmentosa without posterior column ataxia caused by mutations in the FLVCR1 gene.

Kuehlewein L, Schöls L, Llavona P, Grimm A, Biskup S, Zrenner E, Kohl S. Kuehlewein L, et al. Among authors: grimm a. Graefes Arch Clin Exp Ophthalmol. 2019 Mar;257(3):629-638. doi: 10.1007/s00417-018-04233-7. Epub 2019 Jan 17. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 30656474

2

Thickening of the peripheral nerves in metachromatic leukodystrophy.

Grimm A, Schäffer E, Just J, Schöls L, Kehrer C, Bevot A, Ziemann U, Krageloh-Mann I. Grimm A, et al. J Neurol Sci. 2016 Sep 15;368:399-401. doi: 10.1016/j.jns.2016.07.030. Epub 2016 Jul 14. J Neurol Sci. 2016. PMID: 27538671 No abstract available.

3

Nerve enlargement in an unusual case of inflammatory neuropathy and new gene mutation-morphology is the key.

Grimm A, Winter N, Wolking S, Vittore D, Biskup S, Axer H. Grimm A, et al. Neurol Sci. 2017 Aug;38(8):1525-1527. doi: 10.1007/s10072-017-2960-3. Epub 2017 Apr 19. Neurol Sci. 2017. PMID: 28424919 No abstract available.

4

Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.

Dohrn MF, Glöckle N, Mulahasanovic L, Heller C, Mohr J, Bauer C, Riesch E, Becker A, Battke F, Hörtnagel K, Hornemann T, Suriyanarayanan S, Blankenburg M, Schulz JB, Claeys KG, Gess B, Katona I, Ferbert A, Vittore D, Grimm A, Wolking S, Schöls L, Lerche H, Korenke GC, Fischer D, Schrank B, Kotzaeridou U, Kurlemann G, Dräger B, Schirmacher A, Young P, Schlotter-Weigel B, Biskup S. Dohrn MF, et al. Among authors: grimm a. J Neurochem. 2017 Dec;143(5):507-522. doi: 10.1111/jnc.14217. Epub 2017 Nov 7. J Neurochem. 2017. PMID: 28902413 Free article.

5

Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophic.

Rattay TW, Just J, Röben B, Hengel H, Schüle R, Synofzik M, Söhn AS, Winter N, Dammeier N, Schöls L, Grimm A. Rattay TW, et al. Among authors: grimm a. Orphanet J Rare Dis. 2018 Nov 3;13(1):194. doi: 10.1186/s13023-018-0939-7. Orphanet J Rare Dis. 2018. PMID: 30390710 Free PMC article.

6

Multifocal, hypoechogenic nerve thickening in Cerebrotendinous Xanthomatosis.

Roeben B, Just J, Hengel H, Bender F, Pöschl P, Synofzik M, Schöls L, Grimm A. Roeben B, et al. Among authors: grimm a. Clin Neurophysiol. 2020 Aug;131(8):1798-1803. doi: 10.1016/j.clinph.2020.04.162. Epub 2020 May 21. Clin Neurophysiol. 2020. PMID: 32531740

7

Neuropathy in ARSACS is demyelinating but without typical nerve enlargement in nerve ultrasound.

Kneer K, Straub S, Wittlinger J, Stahl JH, Winter N, Timmann D, Schöls L, Synofzik M, Bender F, Grimm A. Kneer K, et al. Among authors: grimm a. J Neurol. 2024 Jan 23. doi: 10.1007/s00415-023-12159-2. Online ahead of print. J Neurol. 2024. PMID: 38261029

8

De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy.

Park J, Flores BR, Scherer K, Kuepper H, Rossi M, Rupprich K, Rautenberg M, Deininger N, Weichselbaum A, Grimm A, Sturm M, Grasshoff U, Delpire E, Haack TB. Park J, et al. Among authors: grimm a. J Med Genet. 2020 Apr;57(4):283-288. doi: 10.1136/jmedgenet-2019-106273. Epub 2019 Aug 22. J Med Genet. 2020. PMID: 31439721

9

Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis.

Zimmermann M, Deininger N, Willikens S, Haack TB, Grundmann-Hauser K, Streubel B, Schreiber M, Lerche H, Grimm A. Zimmermann M, et al. Among authors: grimm a. Neurol Sci. 2021 Apr;42(4):1523-1525. doi: 10.1007/s10072-020-04896-3. Epub 2020 Nov 13. Neurol Sci. 2021. PMID: 33188503 Free PMC article.

10

[Critical illness polyneuropathy and critical illness myopathy].

Grimm A, Günther A, Witte OW, Axer H. Grimm A, et al. Med Klin Intensivmed Notfmed. 2012 Nov;107(8):649-58; quiz 659. doi: 10.1007/s00063-012-0186-y. Epub 2012 Oct 28. Med Klin Intensivmed Notfmed. 2012. PMID: 23104463 Review. German.

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