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Updated: May 19, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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Asymptomatic Pulmonary Involvement as the Initial Presentation of Vascular Ehlers-Danlos Syndrome with a Novel COL3A1

Hitomi Nogawa1, Hiroki Suzuki1, Yoshinori Kawabata2

  • 1Department of Respiratory Medicine, Yamagata Prefectural Central Hospital, Japan.

Internal Medicine (Tokyo, Japan)
|May 17, 2026
PubMed

Keywords:
COL3A1cavitary lesionspulmonary nodulespulmonary ossificationvascular Ehlers-Danlos syndrome

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