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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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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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S Pensiero

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Journal of Pediatric Ophthalmology and Strabismus|March 1, 1992

Normal intraocular pressure in childrenS Pensiero, S Da Pozzo, P Perissutti, et al.

Neurology|December 14, 2005

Saccade testing in the diagnosis and treatment of type 3 Gaucher diseaseS Pensiero, A Accardo, M G Pittis, et al.

International Journal of Pediatric Otorhinolaryngology|May 14, 2013

Bilateral orbital preseptal cellulitis after combined adenotonsillectomy and strabismus surgery--case report and pathogenetic hypothesisE Muzzi, F Parentin, G Pelos, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|October 1, 2014

A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian familyM Callea, P Nieminen, C E Willoughby, et al.

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Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Journal of Pediatric Ophthalmology and Strabismus|March 1, 1992

Normal intraocular pressure in childrenS Pensiero, S Da Pozzo, P Perissutti, et al.

Neurology|December 14, 2005

Saccade testing in the diagnosis and treatment of type 3 Gaucher diseaseS Pensiero, A Accardo, M G Pittis, et al.

International Journal of Pediatric Otorhinolaryngology|May 14, 2013

Bilateral orbital preseptal cellulitis after combined adenotonsillectomy and strabismus surgery--case report and pathogenetic hypothesisE Muzzi, F Parentin, G Pelos, et al.

Journal of the European Academy of Dermatology and Venereology : JEADV|October 1, 2014

A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian familyM Callea, P Nieminen, C E Willoughby, et al.

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