These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 15519918)

  • 1. Spinal muscular atrophy and progressive myoclonic epilepsy: one case report and characteristics of the epileptic syndrome.
    Striano P; Boccella P; Sarappa C; Striano S
    Seizure; 2004 Dec; 13(8):582-6. PubMed ID: 15519918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.
    Haliloglu G; Chattopadhyay A; Skorodis L; Manzur A; Mercuri E; Talim B; Akçören Z; Renda Y; Muntoni F; Topaloğlu H
    Neuropediatrics; 2002 Dec; 33(6):314-9. PubMed ID: 12571787
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of type IV spinal muscular atrophy (SMA) with myoclonic epilepsy within a single family.
    Liyanage DS; Pathberiya LS; Gooneratne IK; Vithanage KK; Gamage R
    Int Arch Med; 2014; 7(1):42. PubMed ID: 25278999
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Early myoclonic encephalopathy and spinal muscular atrophy type I].
    Bado M; Bruno C; Morreale G; Parisi F; Minetti C; Cordone G
    Minerva Pediatr; 1995 Jun; 47(6):233-8. PubMed ID: 7476749
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.
    Rubboli G; Veggiotti P; Pini A; Berardinelli A; Cantalupo G; Bertini E; Tiziano FD; D'Amico A; Piazza E; Abiusi E; Fiori S; Pasini E; Darra F; Gobbi G; Michelucci R
    Epilepsia; 2015 May; 56(5):692-8. PubMed ID: 25847462
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of progressive myoclonic epilepsy and spinal muscular atrophy.
    Marjanovic B; Todorovic S; Dozic S
    Pediatr Neurol; 1993; 9(2):147-50. PubMed ID: 8499046
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An unusual case of benign reflex myoclonic epilepsy of infancy.
    Kurian MA; King MD
    Neuropediatrics; 2003 Jun; 34(3):152-5. PubMed ID: 12910440
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Myoclonic epilepsies in infancy].
    Palencia R
    Rev Neurol; 2000 Jun; 30 Suppl 1():S15-24. PubMed ID: 10904965
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood.
    Yang Z; Liu X; Qin J; Zhang Y; Bao X; Chang X; Wang S; Wu Y; Xiong H
    Brain Dev; 2009 Apr; 31(4):274-81. PubMed ID: 18562140
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Eyelid myoclonia with absences occurring during the clinical course of cryptogenic myoclonic epilepsy of early childhood.
    Ohya T; Yamashita Y; Shibuya I; Hara M; Nagamitsu S; Matsuishi T
    Eur J Paediatr Neurol; 2012 Jul; 16(4):399-401. PubMed ID: 22153876
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy.
    Gan JJ; Garcia V; Tian J; Tagliati M; Parisi JE; Chung JM; Lewis R; Baloh R; Levade T; Pierson TM
    Neuromuscul Disord; 2015 Dec; 25(12):959-63. PubMed ID: 26526000
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adult-onset autosomal dominant myoclonic epilepsy: report of a family with an overlooked epileptic syndrome.
    Hsin YL; Chuang MF; Shyu WC; Lin CY; Chen YH; Harnod T
    Seizure; 2007 Mar; 16(2):160-5. PubMed ID: 17174115
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unusual clinical features in infantile Spinal Muscular Atrophies.
    Guillot N; Cuisset JM; Cuvellier JC; Hurtevent JF; Joriot S; Vallee L
    Brain Dev; 2008 Mar; 30(3):169-78. PubMed ID: 17804187
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial occurrence of myoclonic epilepsy syndrome and acute intermittent porphyria.
    Varsik P; Buranová D; Kollár B; Traubner P; Bozek P; Mikulecký M
    Neuro Endocrinol Lett; 2005 Feb; 26(1):7-12. PubMed ID: 15726012
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy.
    Dyment DA; Sell E; Vanstone MR; Smith AC; Garandeau D; Garcia V; Carpentier S; Le Trionnaire E; Sabourdy F; Beaulieu CL; Schwartzentruber JA; McMillan HJ; ; Majewski J; Bulman DE; Levade T; Boycott KM
    Clin Genet; 2014 Dec; 86(6):558-63. PubMed ID: 24164096
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Progressive familial myoclonic epilepsy with bulbo-spinal amyotrophy. Clinical, electrophysiological study, and biopsy of a case].
    Taglioli M; Bartolini S; Volpi G; Alberti G; Ambrosetto G
    Riv Neurol; 1990; 60(5):201-6. PubMed ID: 2151603
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Myoclonus and epilepsies in children].
    Fejerman N
    Rev Neurol (Paris); 1991; 147(12):782-97. PubMed ID: 1780607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reflex myoclonic epilepsy in infancy: a critical review.
    Verrotti A; Matricardi S; Pavone P; Marino R; Curatolo P
    Epileptic Disord; 2013 Jun; 15(2):114-22. PubMed ID: 23770486
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.
    Rudnik-Schöneborn S; Forkert R; Hahnen E; Wirth B; Zerres K
    Neuropediatrics; 1996 Feb; 27(1):8-15. PubMed ID: 8677029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital segmental spinal muscular atrophy: a case report.
    Savaş T; Erol I; Özkale Y; Saygi S
    J Child Neurol; 2015 Mar; 30(4):509-12. PubMed ID: 25300987
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.