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Yoko Aoki

Showing results (241-250 of 255) with videos related to

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JMA Journal|May 25, 2022
A Pilot Study for Return of Individual Pharmacogenomic Results to Population-Based Cohort Study ParticipantsKinuko Ohneda, Masahiro Hiratsuka, Hiroshi Kawame, et al.
Gastroenterology|January 14, 2020
Variants That Affect Function of Calcium Channel TRPV6 Are Associated With Early-Onset Chronic PancreatitisAtsushi Masamune, Hiroshi Kotani, Franziska Lena Sörgel, et al.
The Journal of Dermatology|March 23, 2020
Japanese Clinical Practice Guidelines for Vascular Anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Japanese Journal of Radiology|March 25, 2020
Japanese clinical practice guidelines for vascular anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 24, 2020
Japanese clinical practice guidelines for vascular anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Journal of Medical Genetics|November 24, 2021
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in <i>CHST14</i> (mcEDS-<i>CHST14</i>)Mari Minatogawa, Ai Unzaki, Hiroko Morisaki, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and backKatherine A Rauen, Lisa Schoyer, Frank McCormick, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discoveryMaria I Kontaridis, Amy E Roberts, Lisa Schill, et al.
Human Molecular Genetics|April 8, 2014
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesisElisabetta Flex, Mamta Jaiswal, Francesca Pantaleoni, et al.
Nature Communications|May 19, 2018
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Hiroki Kudo, Jia Rao, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
JMA Journal|May 25, 2022
A Pilot Study for Return of Individual Pharmacogenomic Results to Population-Based Cohort Study ParticipantsKinuko Ohneda, Masahiro Hiratsuka, Hiroshi Kawame, et al.
Gastroenterology|January 14, 2020
Variants That Affect Function of Calcium Channel TRPV6 Are Associated With Early-Onset Chronic PancreatitisAtsushi Masamune, Hiroshi Kotani, Franziska Lena Sörgel, et al.
The Journal of Dermatology|March 23, 2020
Japanese Clinical Practice Guidelines for Vascular Anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Japanese Journal of Radiology|March 25, 2020
Japanese clinical practice guidelines for vascular anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 24, 2020
Japanese clinical practice guidelines for vascular anomalies 2017Hidefumi Mimura, Sadanori Akita, Akihiro Fujino, et al.
Journal of Medical Genetics|November 24, 2021
Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in <i>CHST14</i> (mcEDS-<i>CHST14</i>)Mari Minatogawa, Ai Unzaki, Hiroko Morisaki, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and backKatherine A Rauen, Lisa Schoyer, Frank McCormick, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discoveryMaria I Kontaridis, Amy E Roberts, Lisa Schill, et al.
Human Molecular Genetics|April 8, 2014
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesisElisabetta Flex, Mamta Jaiswal, Francesca Pantaleoni, et al.
Nature Communications|May 19, 2018
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatmentShazia Ashraf, Hiroki Kudo, Jia Rao, et al.
Pageof 26