Krenn M - Search Results

1

Bilateral foot drop as presenting feature of facioscapulohumeral muscular dystrophy type 1.

Krenn M, Vetchy V, Kasprian G, Grisold W. Krenn M, et al. eNeurologicalSci. 2024 Dec 13;38:100546. doi: 10.1016/j.ensci.2024.100546. eCollection 2025 Mar. eNeurologicalSci. 2024. PMID: 39802033 Free PMC article.

2

Spinal muscular atrophy presenting with mild limb-girdle weakness in adulthood: Diagnostic pitfalls in the era of disease-modifying therapies.

Krenn M, Jengojan S, Grisold W. Krenn M, et al. J Neurol Sci. 2022 Sep 15;440:120347. doi: 10.1016/j.jns.2022.120347. Epub 2022 Jul 25. J Neurol Sci. 2022. PMID: 35908306 No abstract available.

3

A de novo truncating variant in CSDE1 in an adult-onset neuropsychiatric phenotype without intellectual disability.

Krenn M, Kepa S, Kasprian G, Riedhammer KM, Wagner M, Goedl-Fleischhacker U, Milenkovic I. Krenn M, et al. Eur J Med Genet. 2022 Mar;65(3):104423. doi: 10.1016/j.ejmg.2022.104423. Epub 2022 Jan 11. Eur J Med Genet. 2022. PMID: 35026469 Free article.

4

Connectome Analysis in an Individual with SETD1B -Related Neurodevelopmental Disorder and Epilepsy.

Weng R, Nenning KH, Schwarz M, Riedhammer KM, Brunet T, Wagner M, Kasprian G, Lehrner J, Zimprich F, Bonelli SB, Krenn M. Weng R, et al. Among authors: krenn m. J Dev Behav Pediatr. 2022 Aug 1;43(6):e419-e422. doi: 10.1097/DBP.0000000000001079. Epub 2022 Apr 6. J Dev Behav Pediatr. 2022. PMID: 35385430

5

Developmental, Cognitive, Ocular Motor, and Neuroimaging Findings Related to SUFU Haploinsufficiency: Unraveling Subtle and Highly Variable Phenotypes.

Siegert S, Grisold A, Pal-Handl K, Lilja S, Kepa S, Silvaieh S, Laccone F, Wiest G, Pogledic I, Schmook MT, Boltshauser E, Schmidt WM, Krenn M. Siegert S, et al. Among authors: krenn m. Pediatr Neurol. 2024 Nov;160:38-44. doi: 10.1016/j.pediatrneurol.2024.07.015. Epub 2024 Jul 30. Pediatr Neurol. 2024. PMID: 39181021 Free article.

6

A Homozygous PTRHD1 Missense Variant (p.Arg122Gln) in an Individual with Intellectual Disability, Generalized Epilepsy, and Juvenile Parkinsonism.

Gebert J, Brunet T, Wagner M, Rath J, Aull-Watschinger S, Pataraia E, Krenn M. Gebert J, et al. Among authors: krenn m. Neuropediatrics. 2024 Jun;55(3):209-212. doi: 10.1055/a-2256-0722. Epub 2024 Jan 29. Neuropediatrics. 2024. PMID: 38286424

7

[No title available]

[No authors listed] [No authors listed] PMID: 38346691

8

Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnoses.

Krenn M, Wagner M, Zulehner G, Weng R, Jäger F, Keritam O, Sener M, Brücke C, Milenkovic I, Langer A, Buchinger D, Habersam R, Mayerhanser K, Brugger M, Brunet T, Jacob M, Graf E, Berutti R, Cetin H, Hoefele J, Winkelmann J, Zimprich F, Rath J. Krenn M, et al. J Neurol. 2024 Apr;271(4):1937-1946. doi: 10.1007/s00415-023-12101-6. Epub 2023 Dec 21. J Neurol. 2024. PMID: 38127101 Free PMC article.

9

Estimation of patent foramen ovale size using transcranial Doppler ultrasound in patients with ischemic stroke.

Grisold A, Rinner W, Paul A, Gabriel H, Klickovic U, Wolzt M, Krenn M, Zimprich F, Bsteh G, Sycha T. Grisold A, et al. Among authors: krenn m. J Neuroimaging. 2022 Jan;32(1):97-103. doi: 10.1111/jon.12935. Epub 2021 Sep 30. J Neuroimaging. 2022. PMID: 34591348 Free PMC article.

10

CANOMAD responding to weekly treatment with intravenous immunoglobulin (IVIg).

Krenn M, Keir G, Wieshmann UC. Krenn M, et al. BMJ Case Rep. 2014 Apr 10;2014:bcr2013202545. doi: 10.1136/bcr-2013-202545. BMJ Case Rep. 2014. PMID: 24722712 Free PMC article.

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