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Claes Möller

Showing results (41-50 of 61) with videos related to

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International Journal of Audiology|June 17, 2004
Audiological findings in Usher syndrome types IIa and II (non-IIa)Mehdi Sadeghi, Edward S Cohn, William J Kelly, et al.
Human Mutation|February 15, 2008
Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type IIBo Dreyer, Vigdis Brox, Lisbeth Tranebjaerg, et al.
Anticancer Research|October 28, 2015
Electrochemotherapy - Evidence for Cell-type Selectivity In VitroFredrik Landström, Mikael Ivarsson, Anita Koskela Von Sydow, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2014
Theory-of-mind in adolescents and young adults with Alström syndromeHans Erik Frölander, Claes Möller, Jan D Marshall, et al.
Frontiers in Psychology|October 7, 2015
Theory-of-mind in individuals with Alström syndrome is related to executive functions, and verbal abilityHans-Erik Frölander, Claes Möller, Mary Rudner, et al.
International Journal of Audiology|October 15, 2014
The ICF core sets for hearing loss project: functioning and disability from the patient perspectiveSarah Granberg, Marieke Pronk, De Wet Swanepoel, et al.
American Journal of Human Genetics|July 30, 2002
Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutationsRandall R Fields, Guimei Zhou, Dali Huang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 16, 2008
Full-field electroretinography and marked variability in clinical phenotype of Alström syndromeEva Malm, Vesna Ponjavic, Patsy M Nishina, et al.
Acta Oto-Laryngologica|December 16, 2014
Electrochemotherapy - possible benefits and limitations to its use in the head and neck regionFredrik J Landström, Johan A Reizenstein, Christer O S Nilsson, et al.
Ophthalmic Genetics|April 1, 2016
Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophyYangfan P Liu, Daniëlle G M Bosch, Anna M Siemiatkowska, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
International Journal of Audiology|June 17, 2004
Audiological findings in Usher syndrome types IIa and II (non-IIa)Mehdi Sadeghi, Edward S Cohn, William J Kelly, et al.
Human Mutation|February 15, 2008
Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type IIBo Dreyer, Vigdis Brox, Lisbeth Tranebjaerg, et al.
Anticancer Research|October 28, 2015
Electrochemotherapy - Evidence for Cell-type Selectivity In VitroFredrik Landström, Mikael Ivarsson, Anita Koskela Von Sydow, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2014
Theory-of-mind in adolescents and young adults with Alström syndromeHans Erik Frölander, Claes Möller, Jan D Marshall, et al.
Frontiers in Psychology|October 7, 2015
Theory-of-mind in individuals with Alström syndrome is related to executive functions, and verbal abilityHans-Erik Frölander, Claes Möller, Mary Rudner, et al.
International Journal of Audiology|October 15, 2014
The ICF core sets for hearing loss project: functioning and disability from the patient perspectiveSarah Granberg, Marieke Pronk, De Wet Swanepoel, et al.
American Journal of Human Genetics|July 30, 2002
Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutationsRandall R Fields, Guimei Zhou, Dali Huang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 16, 2008
Full-field electroretinography and marked variability in clinical phenotype of Alström syndromeEva Malm, Vesna Ponjavic, Patsy M Nishina, et al.
Acta Oto-Laryngologica|December 16, 2014
Electrochemotherapy - possible benefits and limitations to its use in the head and neck regionFredrik J Landström, Johan A Reizenstein, Christer O S Nilsson, et al.
Ophthalmic Genetics|April 1, 2016
Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophyYangfan P Liu, Daniëlle G M Bosch, Anna M Siemiatkowska, et al.
Pageof 7