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Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

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USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

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Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.

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Ventricular mapping during atrial and ventricular pacing. Relationship of multipotential electrograms to ventricular tachycardia reentry circuits after myocardial infarction.

European heart journal·2002

Electrophysiology and anatomic characterization of an epicardial accessory pathway.

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Atrial fibrillation after cardiac surgery.

Annals of internal medicine·2001

Clinical Uses of Common Genetic Variants Associated with Common Diseases.

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No detectable effect of P2 neurons on female post-mating changes in sleep and feeding in Drosophila melanogaster.

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Unsustained ventricular tachycardia--to treat or not to treat

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Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.

Ventricular mapping during atrial and ventricular pacing. Relationship of multipotential electrograms to ventricular tachycardia reentry circuits after myocardial infarction.

Electrophysiology and anatomic characterization of an epicardial accessory pathway.

Atrial fibrillation after cardiac surgery.

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Phase 1 Study of Anito-cel, a d-Domain BCMA CAR T Cell for Refractory or Recurrent Myeloma.

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No detectable effect of P2 neurons on female post-mating changes in sleep and feeding in Drosophila melanogaster.

"He would not only be my partner in the relationship but also a partner in the research": the role of male partners in women's PrEP research.

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Text Message Delivery of a Digital Tool for Reproductive Health Discussions in Primary Care: A Cluster Randomized Clinical Trial.

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