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Ingo Kennerknecht

Showing results (11-20 of 32) with videos related to

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I-Perception|August 3, 2016
Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven TestsJanina Esins, Johannes Schultz, Claudia Stemper, et al.
Atherosclerosis Plus|August 20, 2024
Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/IndonesiaIngo Kennerknecht, Johannes M Hämmerle, Manfred Fobker, et al.
Case Reports in Genetics|May 20, 2017
Neoplasia in Cri du Chat Syndrome from Italian and German DatabasesAndrea Guala, Marianna Spunton, Silvia Kalantari, et al.
Frontiers in Human Neuroscience|June 16, 2015
Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?Janina Esins, Johannes Schultz, Claudia Stemper, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2010
Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)Martino Ruggieri, Mario Roggini, Ingo Kennerknecht, et al.
Molecular Vision|December 15, 2006
A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophyArseni Markoff, Nadia Bogdanova, Constantin E Uhlig, et al.
Neuropsychologia|April 8, 2014
A family at risk: congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one familyAndreas Johnen, Stefan C Schmukle, Judith Hüttenbrink, et al.
American Journal of Medical Genetics. Part A|July 4, 2006
First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)Ingo Kennerknecht, Thomas Grueter, Brigitte Welling, et al.
Psychological Research|June 13, 2006
Gaze behaviour in hereditary prosopagnosiaGudrun Schwarzer, Susanne Huber, Martina Grüter, et al.
Genetics|March 28, 2024
Human genetics of face recognition: discovery of MCTP2 mutations in humans with face blindness (congenital prosopagnosia)Yun Sun, Weiwei Men, Ingo Kennerknecht, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
I-Perception|August 3, 2016
Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven TestsJanina Esins, Johannes Schultz, Claudia Stemper, et al.
Atherosclerosis Plus|August 20, 2024
Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/IndonesiaIngo Kennerknecht, Johannes M Hämmerle, Manfred Fobker, et al.
Case Reports in Genetics|May 20, 2017
Neoplasia in Cri du Chat Syndrome from Italian and German DatabasesAndrea Guala, Marianna Spunton, Silvia Kalantari, et al.
Frontiers in Human Neuroscience|June 16, 2015
Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?Janina Esins, Johannes Schultz, Claudia Stemper, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2010
Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)Martino Ruggieri, Mario Roggini, Ingo Kennerknecht, et al.
Molecular Vision|December 15, 2006
A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophyArseni Markoff, Nadia Bogdanova, Constantin E Uhlig, et al.
Neuropsychologia|April 8, 2014
A family at risk: congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one familyAndreas Johnen, Stefan C Schmukle, Judith Hüttenbrink, et al.
American Journal of Medical Genetics. Part A|July 4, 2006
First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)Ingo Kennerknecht, Thomas Grueter, Brigitte Welling, et al.
Psychological Research|June 13, 2006
Gaze behaviour in hereditary prosopagnosiaGudrun Schwarzer, Susanne Huber, Martina Grüter, et al.
Genetics|March 28, 2024
Human genetics of face recognition: discovery of MCTP2 mutations in humans with face blindness (congenital prosopagnosia)Yun Sun, Weiwei Men, Ingo Kennerknecht, et al.
Pageof 4