BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 22981636)

  • 1. Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene.
    Leshinsky-Silver E; Ginzberg M; Dabby R; Sadeh M; Lev D; Lerman-Sagie T
    Eur J Paediatr Neurol; 2013 Jan; 17(1):64-7. PubMed ID: 22981636
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Severe form of hereditary neuralgic amyotrophy without SEPT9 gene mutation].
    Cosson A; Mathieu A; Sevrin P; Nollet S; Tatu L
    Rev Neurol (Paris); 2011 Feb; 167(2):169-72. PubMed ID: 20800251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study.
    Neubauer K; Boeckelmann D; Koehler U; Kracht J; Kirschner J; Pendziwiat M; Zieger B
    Cytoskeleton (Hoboken); 2019 Jan; 76(1):131-136. PubMed ID: 30019529
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic spectrum of hereditary neuralgic amyotrophy caused by the SEPT9 R88W mutation.
    Ueda M; Kawamura N; Tateishi T; Sakae N; Motomura K; Ohyagi Y; Kira JI
    J Neurol Neurosurg Psychiatry; 2010 Jan; 81(1):94-6. PubMed ID: 20019224
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Painful brachial plexopathies in SEPT9 mutations: adverse outcome related to comorbid states.
    Hoque R; Schwendimann RN; Kelley RE; Bien-Willner R; Sivakumar K
    J Clin Neuromuscul Dis; 2008 Jun; 9(4):379-84. PubMed ID: 18525421
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.
    Hannibal MC; Ruzzo EK; Miller LR; Betz B; Buchan JG; Knutzen DM; Barnett K; Landsverk ML; Brice A; LeGuern E; Bedford HM; Worrall BB; Lovitt S; Appel SH; Andermann E; Bird TD; Chance PF
    Neurology; 2009 May; 72(20):1755-9. PubMed ID: 19451530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.
    Chance PF
    Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neuralgic amyotrophy presenting with bilateral vocal cord paralysis in a child: a case report.
    To WC; Traquina DN
    Int J Pediatr Otorhinolaryngol; 1999 May; 48(3):251-4. PubMed ID: 10402122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study.
    Laccone F; Hannibal MC; Neesen J; Grisold W; Chance PF; Rehder H
    Clin Genet; 2008 Sep; 74(3):279-83. PubMed ID: 18492087
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
    Kuhlenbäumer G; Hannibal MC; Nelis E; Schirmacher A; Verpoorten N; Meuleman J; Watts GD; De Vriendt E; Young P; Stögbauer F; Halfter H; Irobi J; Goossens D; Del-Favero J; Betz BG; Hor H; Kurlemann G; Bird TD; Airaksinen E; Mononen T; Serradell AP; Prats JM; Van Broeckhoven C; De Jonghe P; Timmerman V; Ringelstein EB; Chance PF
    Nat Genet; 2005 Oct; 37(10):1044-6. PubMed ID: 16186812
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bilateral neuralgic amyotrophy presenting with left vocal cord and phrenic nerve paralysis.
    Chen YM; Hu GC; Cheng SJ
    J Formos Med Assoc; 2007 Aug; 106(8):680-4. PubMed ID: 17711804
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A rare cause of brachial plexopathy: hereditary neuralgic amyotrophy.
    Serin HM; Yılmaz S; Kanmaz S; Şimşek E; Aktan G; Tekgül H; Gökben S
    Turk Pediatri Ars; 2019; 54(3):189-191. PubMed ID: 31619932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.
    Landsverk ML; Ruzzo EK; Mefford HC; Buysse K; Buchan JG; Eichler EE; Petty EM; Peterson EA; Knutzen DM; Barnett K; Farlow MR; Caress J; Parry GJ; Quan D; Gardner KL; Hong M; Simmons Z; Bird TD; Chance PF; Hannibal MC
    Hum Mol Genet; 2009 Apr; 18(7):1200-8. PubMed ID: 19139049
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary neuralgic amyotrophy.
    Chance PF; Windebank AJ
    Curr Opin Neurol; 1996 Oct; 9(5):343-7. PubMed ID: 8894409
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy.
    Collie AM; Landsverk ML; Ruzzo E; Mefford HC; Buysse K; Adkins JR; Knutzen DM; Barnett K; Brown RH; Parry GJ; Yum SW; Simpson DA; Olney RK; Chinnery PF; Eichler EE; Chance PF; Hannibal MC
    J Med Genet; 2010 Sep; 47(9):601-7. PubMed ID: 19939853
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary neuralgic amyotrophy: a paediatric and familial presentation of Parsonage-Turner syndrome].
    Husson M; Goizet C; Rivera S; Lacombe D; Pedespan JM
    Arch Pediatr; 2004 Nov; 11(11):1336-8. PubMed ID: 15519832
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extended Neuralgic Amyotrophy Syndrome: voice therapy in one case of vocal fold paralysis.
    Oliveira AG; Pinho MM
    Codas; 2014; 26(2):175-80. PubMed ID: 24918513
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuralgic amyotrophy associated with temporary vocal fold paralysis: successful treatment by vocal fold augmentation with hyaluronic acid.
    Geißler K; Klingner CM; Guntinas-Lichius O; Bitter T
    J Laryngol Otol; 2015 Apr; 129(4):e1. PubMed ID: 25776098
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pediatric Hereditary Neuralgic Amyotrophy: Successful Treatment With Intravenous Immunoglobulin and Insights Into
    Chuk R; Sheppard M; Wallace G; Coman D
    Child Neurol Open; 2016; 3():2329048X16668970. PubMed ID: 28503616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling.
    Sudo K; Ito H; Iwamoto I; Morishita R; Asano T; Nagata K
    Hum Mutat; 2007 Oct; 28(10):1005-13. PubMed ID: 17546647
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.