Publications by authors named "Claes Moller"

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Usher Syndrome.
Alessandro Castiglione, Claes Möller

Audiol Res· January 2022

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The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2.
Mattias Ehn, Moa Wahlqvist, Claes Möller, Agneta Anderzén-Carlsson

Int J Qual Stud Health Well-being· December 2020

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[Possibilities to diagnose hearing impairment in children].
Inger Uhlén, Bea Kovacsovics, Claes Möller

Lakartidningen· October 2020

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Similarities and Differences in Health, Social Trust, and Financial Situation in People With Usher Syndrome, a Bio-Psychosocial Perspective.
Moa Wahlqvist, Claes Möller, Kerstin Möller, Berth Danermark

Front Psychol· August 2020

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Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes.
Eva Lindberg, Claes Moller, Juha Kere, Satu Wedenoja, Agneta Anderzén-Carlsson

BMC Med Genet· April 2020

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Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study.
Mattias Ehn, Agneta Anderzén-Carlsson, Claes Möller, Moa Wahlqvist

Int J Qual Stud Health Well-being· December 2019

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Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
Sorina Gorcenco, Frédéric M Vaz, Anna Tracewska-Siemiatkowska, Lisbeth Tranebjærg, Frans P M Cremers

Parkinsonism Relat Disord· April 2019

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Health, work, social trust, and financial situation in persons with Usher syndrome type 1.
Mattias Ehn, Moa Wahlqvist, Berth Danermark, Örjan Dahlström, Claes Möller

Work· January 2019

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Headphone listening habits, hearing thresholds and listening levels in Swedish adolescents with severe to profound HL and adolescents with normal hearing.
Stephen E Widén, Claes Möller, Kim Kähäri

Int J Audiol· October 2018

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Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Lisbeth Tranebjærg, Nicola Strenzke, Sture Lindholm, Nanna D Rendtorff, Hanne Poulsen

Hum Genet· March 2018

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The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Lisbeth Tranebjærg, Nicola Strenzke, Sture Lindholm, Nanna D Rendtorff, Hanne Poulsen

Hum Genet· February 2018

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An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS.
Anna Tracewska-Siemiątkowska, Lonneke Haer-Wigman, Danielle G M Bosch, Deborah Nickerson, Michael J Bamshad

Genes (Basel)· December 2017

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Putative digenic inheritance of heterozygous RP1L1 and C2orf71 null mutations in syndromic retinal dystrophy.
Yangfan P Liu, Daniëlle G M Bosch, Anna M Siemiatkowska, Nanna Dahl Rendtorff, F Nienke Boonstra

Ophthalmic Genet· November 2017

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Headphone listening habits and hearing thresholds in swedish adolescents.
Stephen E Widen, Sara Båsjö, Claes Möller, Kim Kähäri

Noise Health· August 2017

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Physical functioning in older persons with dizziness: a population-based study.
Lena Kollén, Helena Hörder, Claes Möller, Kerstin Frändin

Aging Clin Exp Res· April 2017

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Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC.
Angèle Tingaud-Sequeira, Demetrio Raldúa, Julie Lavie, Guilaine Mathieu, Magali Bordier

Neurobiol Dis· February 2017

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Aspects of learning from the perspective of people with Alström syndrome.
Berit Rönnåsen, Kerstin Möller, Claes Möller, Björn Lyxell, Agneta Anderzen-Carlsson

Disabil Rehabil· October 2016

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Hearing thresholds, tinnitus, and headphone listening habits in nine-year-old children.
Sara Båsjö, Claes Möller, Stephen Widén, Göran Jutengren, Kim Kähäri

Int J Audiol· October 2016

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A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa.
Bas P Hartel, Maria Löfgren, Patrick L M Huygen, Iris Guchelaar, Nicole Lo-A-Njoe Kort

Hear Res· September 2016

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Long-term follow-up in patients treated with curative electrochemotherapy for cancer in the oral cavity and oropharynx.
Fredrik J Landström, Johan Reizenstein, Gun-Britt Adamsson, Mathias von Beckerath, Claes Möller

Acta Otolaryngol· May 2016

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Electrochemotherapy - Evidence for Cell-type Selectivity In Vitro.
Fredrik Landström, Mikael Ivarsson, Anita Koskela Von Sydow, Anders Magnuson, Mathias Von Beckerath

Anticancer Res· November 2015

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Theory-of-mind in individuals with Alström syndrome is related to executive functions, and verbal ability.
Hans-Erik Frölander, Claes Möller, Mary Rudner, Sushmit Mishra, Jan D Marshall

Front Psychol· October 2015

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Cognitive skills and reading in adults with Usher syndrome type 2.
Cecilia Henricson, Björn Lidestam, Björn Lyxell, Claes Möller

Front Psychol· April 2015

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Electrochemotherapy - possible benefits and limitations to its use in the head and neck region.
Fredrik J Landström, Johan A Reizenstein, Christer O S Nilsson, Mathias Von Beckerath, A Lennart Löfgren

Acta Otolaryngol· January 2015

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall

J Hum Genet· January 2015

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