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Connection

Michal Vytopil to Adult

This is a "connection" page, showing publications Michal Vytopil has written about Adult.
Connection Strength

0.174
  1. Vytopil M, Mani R, Adlakha A, Zhu JJ. Acute chorea and hyperthermia after concurrent use of modafinil and tranylcypromine. Am J Psychiatry. 2007 Apr; 164(4):684.
    View in: PubMed
    Score: 0.020
  2. Bareja N, Desai B, Vytopil M, Srinivasan J, Ghasemi M. Cancer and benign tumors in myotonic dystrophy, facioscapulohumeral muscular dystrophy, and oculopharyngeal muscular dystrophy: a 23-year, single-center, retrospective study. Acta Myol. 2025 Jun; 44(2):49-56.
    View in: PubMed
    Score: 0.018
  3. Vytopil M, Jones HR. Mogul-clonus. Neurology. 2004 Sep 28; 63(6):1130.
    View in: PubMed
    Score: 0.017
  4. Vytopil M, Vohanka S, Vlasinova J, Toman J, Novak M, Toniolo D, Ricotti R, Lukas Z. The screening for X-linked Emery-Dreifuss muscular dystrophy amongst young patients with idiopathic heart conduction system disease treated by a pacemaker implant. Eur J Neurol. 2004 Aug; 11(8):531-4.
    View in: PubMed
    Score: 0.017
  5. Arends S, Drenthen J, de Koning L, van den Bergh P, Hadden RDM, Kuwabara S, Reisin RC, Shahrizaila N, Ajroud-Driss S, Antonini G, Attarian S, Balducci C, Bertorini T, Brannagan TH, Cavaletti G, Chao CC, Chavada G, Dillmann KU, Dimachkie MM, Galassi G, Guti?rrez-Guti?rrez G, Harbo T, Islam B, Islam Z, Katzberg H, Kusunoki S, Manganelli F, Miller JAL, Pardo J, Pereon Y, Rajabally YA, Sindrup S, Stettner M, Uncini A, Verhamme C, Vytopil M, Waheed W, Jacobs BC, Cornblath DR. Electrodiagnostic subtyping in Guillain-Barr? syndrome patients in the International Guillain-Barr? Outcome Study. Eur J Neurol. 2024 Sep; 31(9):e16335.
    View in: PubMed
    Score: 0.017
  6. Vytopil M, Benedetti S, Ricci E, Galluzzi G, Dello Russo A, Merlini L, Boriani G, Gallina M, Morandi L, Politano L, Moggio M, Chiveri L, Hausmanova-Petrusewicz I, Ricotti R, Vohanka S, Toman J, Toniolo D. Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. J Med Genet. 2003 Dec; 40(12):e132.
    View in: PubMed
    Score: 0.016
  7. Al-Hakem H, Doets AY, Stino AM, Zivkovic SA, Andersen H, Willison HJ, Cornblath DR, Gorson KC, Islam Z, Mohammad QD, Sindrup SH, Kusunoki S, Davidson A, Casasnovas C, Bateman K, Miller JAL, van den Berg B, Verboon C, Roodbol J, Leonhard SE, Arends S, Luijten LWG, Benedetti L, Kuwabara S, Van den Bergh P, Monges S, Marfia GA, Shahrizaila N, Galassi G, Pereon Y, B?rmann J, Kuitwaard K, Kleyweg RP, Marchesoni C, Sedano Tous MJ, Querol L, Mart?n-Aguilar L, Wang Y, Nobile-Orazio E, Rinaldi S, Schenone A, Pardo J, Vermeij FH, Waheed W, Lehmann HC, Granit V, Stein B, Cavaletti G, Guti?rrez-Guti?rrez G, Barroso FA, Visser LH, Katzberg HD, Dardiotis E, Attarian S, van der Kooi AJ, Eftimov F, Wirtz PW, Samijn JPA, Gilhuis HJ, Hadden RDM, Holt JKL, Sheikh KA, Kolb N, Karafiath S, Vytopil M, Antonini G, Feasby TE, Faber C, Kramers H, Busby M, Roberts RC, Silvestri NJ, Fazio R, van Dijk GW, Garssen MPJ, Verschuuren J, Harbo T, Jacobs BC. CSF Findings in Relation to Clinical Characteristics, Subtype, and Disease Course in Patients With Guillain-Barr? Syndrome. Neurology. 2023 06 06; 100(23):e2386-e2397.
    View in: PubMed
    Score: 0.015
  8. Vytopil M, Ricci E, Dello Russo A, Hanisch F, Neudecker S, Zierz S, Ricotti R, Demay L, Richard P, Wehnert M, Bonne G, Merlini L, Toniolo D. Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy. Neuromuscul Disord. 2002 Dec; 12(10):958-63.
    View in: PubMed
    Score: 0.015
  9. Elnahry AG, Asal ZB, Shaikh N, Dennett K, Abd Elmohsen MN, Elnahry GA, Shehab A, Vytopil M, Ghaffari L, Athappilly GK, Ramsey DJ. Optic neuropathy after COVID-19 vaccination: a report of two cases. Int J Neurosci. 2023 Dec; 133(8):901-907.
    View in: PubMed
    Score: 0.014
  10. Limbekar NS, Soong MC, Vytopil MM, Blanchet DT, Paci GM, Ho DT. High-Resolution Ultrasound in the Diagnosis and Surgical Management of Ulnar Neuropathy at the Elbow. Orthopedics. 2021 Sep-Oct; 44(5):285-288.
    View in: PubMed
    Score: 0.014
  11. Sanna T, Dello Russo A, Toniolo D, Vytopil M, Pelargonio G, De Martino G, Ricci E, Silvestri G, Giglio V, Messano L, Zachara E, Bellocci F. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations. Eur Heart J. 2003 Dec; 24(24):2227-36.
    View in: PubMed
    Score: 0.004
  12. Spinarov? L, Toman J, Hude P, Voh?nka S, Vytopil M, Luk?s Z, Nov?k M, V?tovec J. [Disorders of laminins in diseases of myocardial and skeletal muscles]. Vnitr Lek. 2003 Aug; 49(8):637-41.
    View in: PubMed
    Score: 0.004
  13. Vohanka S, Vytopil M, Bednarik J, Lukas Z, Kadanka Z, Schildberger J, Ricotti R, Bione S, Toniolo D. A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy. Neuromuscul Disord. 2001 May; 11(4):411-3.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.