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.
136 related articles for article (PubMed ID: 2175847)
1. Presence of inclusion body myositis-like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases. Coquet M; Vital C; Julien J Neuropathol Appl Neurobiol; 1990 Oct; 16(5):393-400. PubMed ID: 2175847 [TBL] [Abstract][Full Text] [Related]
2. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy. Askanas V; Serdaroglu P; Engel WK; Alvarez RB Neurosci Lett; 1991 Sep; 130(1):73-6. PubMed ID: 1660975 [TBL] [Abstract][Full Text] [Related]
3. Nuclear inclusions in oculopharyngeal dystrophy. An ultrastructural study of six cases. Coquet M; Vallat JM; Vital C; Fournier M; Barat M; Orgogozo JM; Julien J; Loiseau P J Neurol Sci; 1983 Jul; 60(1):151-6. PubMed ID: 6308176 [TBL] [Abstract][Full Text] [Related]
4. Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews. Blumen SC; Sadeh M; Korczyn AD; Rouche A; Nisipeanu P; Asherov A; Tomé FM Neurology; 1996 May; 46(5):1324-8. PubMed ID: 8628475 [TBL] [Abstract][Full Text] [Related]
5. Nuclear inclusions in innervated cultured muscle fibers from patients with oculopharyngeal muscular dystrophy. Tomé FM; Askanas V; Engel WK; Alvarez RB; Lee CS Neurology; 1989 Jul; 39(7):926-32. PubMed ID: 2544827 [TBL] [Abstract][Full Text] [Related]
6. Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type. Schröder JM; Krabbe B; Weis J Neuropathol Appl Neurobiol; 1995 Feb; 21(1):68-73. PubMed ID: 7770123 [TBL] [Abstract][Full Text] [Related]