Leonardis L - Search Results

1

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.

Leonardis L, Zidar J, Popovič M, Timmerman V, Löfgren A, Broeckhoven CV, Butinar D. Leonardis L, et al. Pflugers Arch. 2000 Jan;439(Suppl 1):r208-r210. doi: 10.1007/s004240000148. Pflugers Arch. 2000. PMID: 28176125

2

Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey.

El-Hassar L, Amara A, Sanson B, Lacatus O, Amir Belhouchet A, Kroneman M, Claeys K, Plançon JP, Rodolico C, Primiano G, Trojsi F, Filosto M, Mongini TE, Bortolani S, Monforte M, Carraro E, Maggi L, Ricci F, Silani V, Orsucci D, Créange A, Péréon Y, Stojkovic T, van der Beek NAME, Toscano A, Pareyson D, Attarian S, Van den Bergh PYK, Remiche G, Hoeijmakers JGJ, Badrising U, Voermans NC, Kaindl AM, Schara-Schmidt U, Schoser B, Gazzerro E, Haberlová J, Voháňka S, Pál E, Molnar MJ, Leonardis L, Tournev IL, Osorio AN, Olivé M, Muelas N, Alonso-Perez J, Plá F, de Visser M, Siciliano G, Sacconi S. El-Hassar L, et al. Among authors: leonardis l. J Neuromuscul Dis. 2023;10(2):173-184. doi: 10.3233/JND-221525. J Neuromuscul Dis. 2023. PMID: 36373291 Free article.

3

Correlations between clinical, electrophysiological and genetic findings in hereditary motor and sensory neuropathy type I (HMSN I).

Leonardis L, Zidar J, Trontelj J, Peterlin B. Leonardis L, et al. Pflugers Arch. 1996;431(6 Suppl 2):R195-6. doi: 10.1007/BF02346335. Pflugers Arch. 1996. PMID: 8739331 Clinical Trial.

4

Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutation.

Leonardis L, Zidar J, Ekici A, Peterlin B, Rautenstrauss B. Leonardis L, et al. Int J Mol Med. 1998 Feb;1(2):495-501. doi: 10.3892/ijmm.1.2.495. Int J Mol Med. 1998. PMID: 9852256

5

Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.

Butinar D, Zidar J, Leonardis L, Popovic M, Kalaydjieva L, Angelicheva D, Sininger Y, Keats B, Starr A. Butinar D, et al. Among authors: leonardis l. Ann Neurol. 1999 Jul;46(1):36-44. doi: 10.1002/1531-8249(199907)46:1<36::aid-ana7>3.0.co;2-j. Ann Neurol. 1999. PMID: 10401778

6

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.

Leonardis L, Zidar J, Popovic M, Timmerman V, Löfgren A, Van Broeckhoven C, Butinar D. Leonardis L, et al. Pflugers Arch. 2000;439(3 Suppl):R208-10. Pflugers Arch. 2000. PMID: 10653194

7

Relapses and remissions of hypokalaemic periodic paralysis and multiple sclerosis in the same patient.

Leonardis L, Zidar J, Le Bail A, Sternberg D. Leonardis L, et al. Clin Neurol Neurosurg. 2011 Oct;113(8):683-5. doi: 10.1016/j.clineuro.2011.04.008. Epub 2011 May 31. Clin Neurol Neurosurg. 2011. PMID: 21621912 No abstract available.

8

The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features.

Leonardis L, Auer-Grumbach M, Papić L, Zidar J. Leonardis L, et al. Eur J Neurol. 2012 Jul;19(7):992-8. doi: 10.1111/j.1468-1331.2012.03665.x. Epub 2012 Feb 16. Eur J Neurol. 2012. PMID: 22340599

9

Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population.

Vrabec K, Koritnik B, Leonardis L, Dolenc-Grošelj L, Zidar J, Smith B, Vance C, Shaw C, Rogelj B, Glavač D, Ravnik-Glavač M. Vrabec K, et al. Among authors: leonardis l. Neurobiol Aging. 2015 Mar;36(3):1601.e17-20. doi: 10.1016/j.neurobiolaging.2014.11.011. Epub 2014 Dec 18. Neurobiol Aging. 2015. PMID: 25585530

10

Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls.

Kovanda A, Leonardis L, Zidar J, Koritnik B, Dolenc-Groselj L, Ristic Kovacic S, Curk T, Rogelj B. Kovanda A, et al. Among authors: leonardis l. Sci Rep. 2018 Apr 4;8(1):5609. doi: 10.1038/s41598-018-23139-2. Sci Rep. 2018. PMID: 29618798 Free PMC article.

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