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.
5. 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]
6. 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]
7. SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy. Klein CJ; Wu Y; Cunningham JM; Windebank AJ; Dyck PJ; Friedenberg SM; Klein DM; Dyck PJ Arch Neurol; 2009 Feb; 66(2):238-43. PubMed ID: 19204161 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families. Watts GD; O'Briant KC; Chance PF Hum Genet; 2002 Feb; 110(2):166-72. PubMed ID: 11935323 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA). Meuleman J; Kuhlenbäumer G; Audenaert D; Hünermund G; Hor H; Young P; Stögbauer F; Ringelstein EB; Van Broeckhoven C; De Jonghe P; Timmerman V Hum Genet; 2001 May; 108(5):390-3. PubMed ID: 11409865 [TBL] [Abstract][Full Text] [Related]
14. Translational control of SEPT9 isoforms is perturbed in disease. McDade SS; Hall PA; Russell SE Hum Mol Genet; 2007 Apr; 16(7):742-52. PubMed ID: 17468182 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. Spectrum of Clinical Variability with SEPT9 Gene Mutation in Hereditary Neuralgic Amyotrophy: Understanding the Pathogenesis Using Molecular Dynamics Simulation Study. Bhatti A; Ravat S; Desai K; Shekhar BR; Menon SR; Kumbhar BV; Kunwar A; Jain N; Das DK Neurol India; 2024 Sep; 72(5):1021-1026. PubMed ID: 39428775 [TBL] [Abstract][Full Text] [Related]
18. Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25. Meulemann J; Kuhlenbäumer G; Schirmacher A; Wehnert M; De Jonghe P; De Vriendt E; Young P; Airaksinen E; Pou-Serradell A; Prats JM; Ringelstein B; Stögbauer F; Van Broeckhoven C; Timmerman V Eur J Hum Genet; 1999 Dec; 7(8):920-7. PubMed ID: 10602368 [TBL] [Abstract][Full Text] [Related]