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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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M Astuto

Showing results (21-30 of 26) with videos related to

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American Journal of Medical Genetics|May 7, 2002

Searching for evidence of DFNB2Lisa M Astuto, Philip M Kelley, James W Askew, et al.

Minerva Anestesiologica|October 24, 2007

Epidural analgesia in children: planning, organization and development of a new programP M Ingelmo, C Gelsumino, A P Acosta, et al.

American Journal of Human Genetics|November 4, 2000

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.

Minerva Anestesiologica|November 7, 2013

Preoperative evaluation in infants and children: recommendations of the Italian Society of Pediatric and Neonatal Anesthesia and Intensive Care (SARNePI)G Serafini, P M Ingelmo, M Astuto, et al.

Human Genetics|January 11, 2003

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one familyArjan P M de Brouwer, Ronald J E Pennings, Marjolijn Roeters, et al.

American Journal of Human Genetics|June 21, 2002

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.

Pageof 3

Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

American Journal of Medical Genetics|May 7, 2002

Searching for evidence of DFNB2Lisa M Astuto, Philip M Kelley, James W Askew, et al.

Minerva Anestesiologica|October 24, 2007

Epidural analgesia in children: planning, organization and development of a new programP M Ingelmo, C Gelsumino, A P Acosta, et al.

American Journal of Human Genetics|November 4, 2000

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type IL M Astuto, M D Weston, C A Carney, et al.

Minerva Anestesiologica|November 7, 2013

Preoperative evaluation in infants and children: recommendations of the Italian Society of Pediatric and Neonatal Anesthesia and Intensive Care (SARNePI)G Serafini, P M Ingelmo, M Astuto, et al.

Human Genetics|January 11, 2003

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one familyArjan P M de Brouwer, Ronald J E Pennings, Marjolijn Roeters, et al.

American Journal of Human Genetics|June 21, 2002

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.

Pageof 3