Dohrn MF - Search Results

1

A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1A.

Xu IRL, Danzi MC, Ruiz A, Raposo J, De Jesus YA, Reilly MM, Cortese A, Shy ME, Scherer SS, Herrmann DN, Fridman V, Baets J, Saporta M, Seyedsadjadi R, Stojkovic T, Claeys KG, Patel P, Feely S, Rebelo AP; Inherited Neuropathy Consortium; Dohrn MF, Züchner S. Xu IRL, et al. Among authors: dohrn mf. J Peripher Nerv Syst. 2024 Jun;29(2):202-212. doi: 10.1111/jns.12621. Epub 2024 Apr 5. J Peripher Nerv Syst. 2024. PMID: 38581130

2

Progressive multifocal leukoencephalopathy and immune reconstitution inflammatory syndrome in seven patients with sarcoidosis: a critical discussion of treatment and prognosis.

Dohrn MF, Ellrichmann G, Pjontek R, Lukas C, Panse J, Gold R, Schulz JB, Gess B, Tauber SC. Dohrn MF, et al. Ther Adv Neurol Disord. 2021 Jul 31;14:17562864211035543. doi: 10.1177/17562864211035543. eCollection 2021. Ther Adv Neurol Disord. 2021. PMID: 34377151 Free PMC article.

3

[Neuropathic pain syndromes and channelopathies].

Dohrn MF, Lampert A, Üçeyler N, Kurth I. Dohrn MF, et al. Internist (Berl). 2019 Jan;60(1):90-97. doi: 10.1007/s00108-018-0535-x. Internist (Berl). 2019. PMID: 30564884 Review. German.

4

Avoiding in hospital delays and eliminating the three-hour effect in thrombolysis for stroke.

Köhrmann M, Schellinger PD, Breuer L, Dohrn M, Kuramatsu JB, Blinzler C, Schwab S, Huttner HB. Köhrmann M, et al. Int J Stroke. 2011 Dec;6(6):493-7. doi: 10.1111/j.1747-4949.2011.00585.x. Epub 2011 Feb 17. Int J Stroke. 2011. PMID: 21609415

5

Does APC/C^CDH1 control the human brain size?: An Editorial Highlight for 'A novel human Cdh1 mutation impairs anaphase-promoting complex/cyclosome (APC/C) activity resulting in microcephaly, psychomotor retardation, and epilepsy' on page 103.

Dohrn MF, Bolaños JP. Dohrn MF, et al. J Neurochem. 2019 Oct;151(1):8-10. doi: 10.1111/jnc.14835. Epub 2019 Aug 23. J Neurochem. 2019. PMID: 31441503 Free PMC article.

6

Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy.

Dohrn MF, Röcken C, De Bleecker JL, Martin JJ, Vorgerd M, Van den Bergh PY, Ferbert A, Hinderhofer K, Schröder JM, Weis J, Schulz JB, Claeys KG. Dohrn MF, et al. J Neurol. 2013 Dec;260(12):3093-108. doi: 10.1007/s00415-013-7124-7. Epub 2013 Oct 8. J Neurol. 2013. PMID: 24101130

7

Elevation of plasma 1-deoxy-sphingolipids in type 2 diabetes mellitus: a susceptibility to neuropathy?

Dohrn MF, Othman A, Hirshman SK, Bode H, Alecu I, Fähndrich E, Karges W, Weis J, Schulz JB, Hornemann T, Claeys KG. Dohrn MF, et al. Eur J Neurol. 2015 May;22(5):806-14, e55. doi: 10.1111/ene.12663. Epub 2015 Jan 26. Eur J Neurol. 2015. PMID: 25623782

8

Metabolic Syndrome, Neurotoxic 1-Deoxysphingolipids and Nervous Tissue Inflammation in Chronic Idiopathic Axonal Polyneuropathy (CIAP).

Hube L, Dohrn MF, Karsai G, Hirshman S, Van Damme P, Schulz JB, Weis J, Hornemann T, Claeys KG. Hube L, et al. Among authors: dohrn mf. PLoS One. 2017 Jan 23;12(1):e0170583. doi: 10.1371/journal.pone.0170583. eCollection 2017. PLoS One. 2017. PMID: 28114358 Free PMC article.

9

Hereditary motor neuropathies.

Dohrn MF, Saporta M. Dohrn MF, et al. Curr Opin Neurol. 2020 Oct;33(5):568-574. doi: 10.1097/WCO.0000000000000848. Curr Opin Neurol. 2020. PMID: 32796276 Review.

10

Targeting transthyretin - Mechanism-based treatment approaches and future perspectives in hereditary amyloidosis.

Dohrn MF, Ihne S, Hegenbart U, Medina J, Züchner SL, Coelho T, Hahn K. Dohrn MF, et al. J Neurochem. 2021 Mar;156(6):802-818. doi: 10.1111/jnc.15233. Epub 2020 Dec 3. J Neurochem. 2021. PMID: 33155274 Free article.

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