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A Maw

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Proceedings of the National Academy of Sciences of the United States of America|May 18, 2005

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activationAriana Hemara-Wahanui, Stanislav Berjukow, Carolyn I Hope, et al.

Eclinicalmedicine|July 29, 2025

Dynamic versus fixed cerebral perfusion pressure targets in paediatric traumatic brain injury: a STARSHIP analysisC A Smith, S Y Bögli, M M Placek, et al.

Human Molecular Genetics|October 23, 1997

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.

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Search research articles

Showing results (41-50 of 43) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 43 results.

Proceedings of the National Academy of Sciences of the United States of America|May 18, 2005

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activationAriana Hemara-Wahanui, Stanislav Berjukow, Carolyn I Hope, et al.

Eclinicalmedicine|July 29, 2025

Dynamic versus fixed cerebral perfusion pressure targets in paediatric traumatic brain injury: a STARSHIP analysisC A Smith, S Y Bögli, M M Placek, et al.

Human Molecular Genetics|October 23, 1997

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.

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