Pages that link to "Q35859588"

The following pages link to Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy (Q35859588):

Displaying 15 items.

• SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophy (Q30009101) (← links)
• Facioscapulohumeral Dystrophy (Q30250223) (← links)
• Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study (Q35061314) (← links)
• Diagnostic evaluation of rhabdomyolysis (Q35624916) (← links)
• Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry (Q36472254) (← links)
• New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients (Q36523111) (← links)
• Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy (Q37256202) (← links)
• What's in a name? The clinical features of facioscapulohumeral muscular dystrophy (Q38728144) (← links)
• Clinical and genetic features of patients with facial-sparing facioscapulohumeral muscular dystrophy. (Q48349062) (← links)
• Facioscapulohumeral Muscular Dystrophy. (Q52506936) (← links)
• A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1 (Q57174014) (← links)
• Differential diagnosis of idiopathic inflammatory myopathies in adults - the first step when approaching a patient with muscle weakness. (Q64948091) (← links)
• A Pediatric Review of Facioscapulohumeral Muscular Dystrophy (Q92688891) (← links)
• DUX4 Signalling in the Pathogenesis of Facioscapulohumeral Muscular Dystrophy (Q92921881) (← links)
• Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy (Q94478957) (← links)