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4. [A case of facioscapulohumeral muscular dystrophy with sensorineural hearing loss and retinal angioma]. Fujimura H, Yoshikawa H, Ueno S, Yorifuji S, Tarui S. Rinsho Shinkeigaku; 1989 Nov; 29(11):1387-91. PubMed ID: 2625025 [Abstract] [Full Text] [Related]
5. Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels. Gieron MA, Korthals JK, Kousseff BG. Am J Med Genet; 1985 Sep; 22(1):143-7. PubMed ID: 4050849 [Abstract] [Full Text] [Related]
6. Facioscapulohumeral syndrome with sensorineural hearing loss and abnormality of retinal vessels. Kamata T, Miyajima H, Shimizu T, Fujimoto M, Takahashi Y, Kaneko E. Intern Med; 1993 Aug; 32(8):678-80. PubMed ID: 8312672 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. Facioscapulohumeral muscular dystrophy and accompanying hearing loss. Meyerson MD, Lewis E, Ill K. Arch Otolaryngol; 1984 Apr; 110(4):261-6. PubMed ID: 6704043 [Abstract] [Full Text] [Related]
9. Facioscapulohumeral dystrophy associated with sensorineural hearing loss, tortuosity of retinal arterioles, and an early onset and rapid progression of respiratory failure. Yasukohchi S, Yagi Y, Akabane T, Terauchi A, Tamagawa K, Mizuno Y. Brain Dev; 1988 Apr; 10(5):319-24. PubMed ID: 3239698 [Abstract] [Full Text] [Related]
10. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness. Korf BR, Bresnan MJ, Shapiro F, Sotrel A, Abroms IF. Ann Neurol; 1985 May; 17(5):513-6. PubMed ID: 4004175 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
12. 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 20; 131(18):2164-2171. PubMed ID: 30203790 [Abstract] [Full Text] [Related]
14. Locomotor problems in infantile facioscapulohumeral muscular dystrophy. Retrospective study of 9 patients. Shapiro F, Specht L, Korf BR. Acta Orthop Scand; 1991 Aug 20; 62(4):367-71. PubMed ID: 1882679 [Abstract] [Full Text] [Related]
15. 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 20; 15(12):1353-8. PubMed ID: 19049553 [Abstract] [Full Text] [Related]
16. Hearing loss in facioscapulohumeral muscular dystrophy. Brouwer OF, Padberg GW, Ruys CJ, Brand R, de Laat JA, Grote JJ. Neurology; 1991 Dec 20; 41(12):1878-81. PubMed ID: 1745341 [Abstract] [Full Text] [Related]
17. [A case of facioscapulohumeral muscular atrophy presenting unusual squatting gait, associated with tongue atrophy and sensorineural hearing loss]. Goto K, Sugihara R. Rinsho Shinkeigaku; 1994 Nov 20; 34(11):1157-61. PubMed ID: 7729099 [Abstract] [Full Text] [Related]
18. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). Jardine PE, Koch MC, Lunt PW, Maynard J, Bathke KD, Harper PS, Upadhyaya M. Arch Dis Child; 1994 Sep 20; 71(3):221-7. PubMed ID: 7979495 [Abstract] [Full Text] [Related]