171 related articles for article (PubMed ID: 16901430)
1. Facioscapulohumeral muscular dystrophy can be a cause of isolated childhood cognitive dysfunction.
Hobson-Webb LD; Caress JB
J Child Neurol; 2006 Mar; 21(3):252-3. PubMed ID: 16901430
[TBL] [Abstract][Full Text] [Related]
2. Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy.
Grosso S; Mostardini R; Di Bartolo RM; Balestri P; Verrotti A
Eur J Paediatr Neurol; 2011 Sep; 15(5):456-60. PubMed ID: 21763164
[TBL] [Abstract][Full Text] [Related]
3. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
Trevisan CP; Pastorello E; Tomelleri G; Vercelli L; Bruno C; Scapolan S; Siciliano G; Comacchio F
Eur J Neurol; 2008 Dec; 15(12):1353-8. PubMed ID: 19049553
[TBL] [Abstract][Full Text] [Related]
4. Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy.
Saito Y; Miyashita S; Yokoyama A; Komaki H; Seki A; Maegaki Y; Ohno K
Brain Dev; 2007 May; 29(4):231-3. PubMed ID: 17010549
[TBL] [Abstract][Full Text] [Related]
5. Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.
Chen TH; Lai YH; Lee PL; Hsu JH; Goto K; Hayashi YK; Nishino I; Lin CW; Shih HH; Huang CC; Liang WC; Wang WF; Jong YJ
Neuromuscul Disord; 2013 Apr; 23(4):298-305. PubMed ID: 23434070
[TBL] [Abstract][Full Text] [Related]
6. Absence of hearing impairment in adult onset facioscapulohumeral muscular dystrophy.
Rogers MT; Zhao F; Harper PS; Stephens D
Neuromuscul Disord; 2002 May; 12(4):358-65. PubMed ID: 12062253
[TBL] [Abstract][Full Text] [Related]
7. Facioscapulohumeral muscular dystrophy (landouzy-dejerine type) in a Nigerian female: a case report.
Anisiuba BC; Onwuekwe I; Ejim EC
Niger J Med; 2006; 15(3):329-32. PubMed ID: 17111772
[TBL] [Abstract][Full Text] [Related]
8. Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Dorobek M; van der Maarel SM; Lemmers RJ; Ryniewicz B; Kabzińska D; Frants RR; Gawel M; Walecki J; Hausmanowa-Petrusewicz I
J Child Neurol; 2015 Apr; 30(5):580-7. PubMed ID: 24717985
[TBL] [Abstract][Full Text] [Related]
9. Cognitive impairment and cerebellar atrophy in typical onset 4Q35 fascioscapulohumeral dystrophy.
Zouvelou V; Rentzos M; Zalonis I; Filippopolitis K; Manta P; Evdokimidis I
Muscle Nerve; 2008 Nov; 38(5):1523-1524. PubMed ID: 18816620
[No Abstract] [Full Text] [Related]
10. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.
Goto K; Nishino I; Hayashi YK
Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566
[TBL] [Abstract][Full Text] [Related]
11. A pediatric case report and literature review of facioscapulohumeral muscular dystrophy type1.
Xiao T; Yang H; Gan S; Wu L
Medicine (Baltimore); 2021 Nov; 100(47):e27907. PubMed ID: 34964760
[TBL] [Abstract][Full Text] [Related]
12. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
[TBL] [Abstract][Full Text] [Related]
13. Diagnostic challenges in facioscapulohumeral muscular dystrophy.
Sacconi S; Salviati L; Bourget I; Figarella D; Péréon Y; Lemmers R; van der Maarel S; Desnuelle C
Neurology; 2006 Oct; 67(8):1464-6. PubMed ID: 17060574
[TBL] [Abstract][Full Text] [Related]
14. Facioscapulohumeral muscular dystrophy.
Fitzsimons RB
Curr Opin Neurol; 1999 Oct; 12(5):501-11. PubMed ID: 10590886
[TBL] [Abstract][Full Text] [Related]
15. Severe fascioscapulohumeral muscular dystrophy presenting with Coats' disease and mental retardation.
Bindoff LA; Mjellem N; Sommerfelt K; Krossnes BK; Roberts F; Krohn J; Tranheim RS; Haggerty ID
Neuromuscul Disord; 2006 Oct; 16(9-10):559-63. PubMed ID: 16935506
[TBL] [Abstract][Full Text] [Related]
16. Two cases of chromosome 4q35-linked early onset facioscapulohumeral muscular dystrophy with mental retardation and epilepsy.
Miura K; Kumagai T; Matsumoto A; Iriyama E; Watanabe K; Goto K; Arahata K
Neuropediatrics; 1998 Oct; 29(5):239-41. PubMed ID: 9810558
[TBL] [Abstract][Full Text] [Related]
17. Early onset facioscapulohumeral muscular dystrophy - Long-term follow-up of a patient with total facial diplegia.
Rudnik-Schöneborn S; Huemer M; Weis J; Sauer E; Meng G
Neuromuscul Disord; 2019 Dec; 29(12):973-976. PubMed ID: 31708336
[TBL] [Abstract][Full Text] [Related]
18. Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.
Krasnianski M; Eger K; Neudecker S; Jakubiczka S; Zierz S
Arch Neurol; 2003 Oct; 60(10):1421-5. PubMed ID: 14568813
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophy.
Lutz KL; Holte L; Kliethermes SA; Stephan C; Mathews KD
Neurology; 2013 Oct; 81(16):1374-7. PubMed ID: 24042093
[TBL] [Abstract][Full Text] [Related]
20. A "Triple Trouble" Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy.
Lin XD; He JJ; Lin F; Chen HZ; Xu LQ; Hu W; Cai NQ; Lin MT; Wang N; Wang ZQ; Xu GR
Chin Med J (Engl); 2018 Sep; 131(18):2164-2171. PubMed ID: 30203790
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]