Results 81 to 90 of about 163,801 (186)
Letter from Usher Burdick to Emma Adams Regarding Beaded Vest, June 2, 1933 [PDF]
This letter dated June 2, 1933, from Usher Burdick to Emma Adams, requests information concerning the completion of a beaded vest. Burdick notes that Adams did not have it finished the last time he saw her and further asserts she has had time enough now
Burdick, Usher
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The molecular genetics of Usher syndrome: Genetics of Usher syndrome
Association of sensorineural deafness and progressive retinitis pigmentosa with and without a vestibular abnormality is the hallmark of Usher syndrome and involves at least 12 loci among three different clinical subtypes. Genes identified for the more commonly inherited loci are USH2A (encoding usherin), MYO7A (encoding myosin VIIa), CDH23 (encoding ...
Ahmed, Zm +3 more
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Norte, Maria Carolina Braga +4 more
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Atrial arrhythmias associated with J wave syndromes
Atrial arrhythmias including atrial fibrillation, atrial flutter and paroxysmal supraventricular tachycardias (atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia, and atrial tachycardia) frequently coexist with J wave ...
Can Hasdemir, Hasdemir C.
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Comorbid Bipolar Disorder and Usher Syndrome
To the Editor: Co-occurrence of psychiatric disorder and rare syndromes with known gene loci can facilitate critical pathophysiologic insights and might have important therapeutic implications as well.1 Usher syndrome is the most common type of deaf ...
Gangadhar, Bangalore N. +4 more
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Anupam, Verma, O P, Shukla
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Clinical and molecular genetics of Usher syndrome
Usher syndrome is an autosomal-recessive disorder manifested by hearing impairment, retinitis pigmentosa (RP), and variable vestibular deficit. Recent progress in the characterization of the genetics of Usher syndrome has shown that this disorder is ...
Kimberling, William J., Möller, Claes,
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Current and future gene‐based therapies for Usher syndromes
International audienceAbstract Inherited retinal dystrophies are a group of genetically and clinically heterogeneous disorders characterized by photoreceptor degeneration.
Vasiliki Kalatzis, Kalatzis, Vasiliki
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