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M B Delatycki

Showing results (21-30 of 58) with videos related to

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Clinical Genetics|May 11, 2007
Newborn screening for mucopolysaccharidoses: opinions of patients and their familiesI M Hayes, V Collins, M Sahhar, et al.
Neuroscience|September 21, 2010
Successful treatment of auditory perceptual disorder in individuals with Friedreich ataxiaG Rance, L A Corben, E Du Bourg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2006
How is disease progress in Friedreich's ataxia best measured? A study of four rating scalesM C Fahey, L Corben, V Collins, et al.
Neurology|February 28, 2007
The 25-foot walk velocity accurately measures real world ambulation in Friedreich ataxiaM C Fahey, L A Corben, V Collins, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Reproductive Biomedicine Online|January 16, 2019
Germ cell arrest associated with aSETX mutation in ataxia oculomotor apraxia type 2S R Catford, M K O'Bryan, R I McLachlan, et al.
Journal of Neurology|October 14, 2009
A comparison of three measures of upper limb function in Friedreich ataxiaL A Corben, G Tai, C Wilson, et al.
Clinical Genetics|February 1, 2005
Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosisA A Gason, M A Aitken, S A Metcalfe, et al.
Journal of Medical Genetics|January 15, 2000
46,XX/46,XY at amniocentesis in a fetus with true hermaphroditismD Amor, M B Delatycki, M Susman, et al.
Clinical Genetics|November 6, 2012
To tell or not to tell - what to do about p.C282Y heterozygotes identified by HFE screeningM B Delatycki, M Wolthuizen, M A Aitken, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Clinical Genetics|May 11, 2007
Newborn screening for mucopolysaccharidoses: opinions of patients and their familiesI M Hayes, V Collins, M Sahhar, et al.
Neuroscience|September 21, 2010
Successful treatment of auditory perceptual disorder in individuals with Friedreich ataxiaG Rance, L A Corben, E Du Bourg, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2006
How is disease progress in Friedreich's ataxia best measured? A study of four rating scalesM C Fahey, L Corben, V Collins, et al.
Neurology|February 28, 2007
The 25-foot walk velocity accurately measures real world ambulation in Friedreich ataxiaM C Fahey, L A Corben, V Collins, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Reproductive Biomedicine Online|January 16, 2019
Germ cell arrest associated with aSETX mutation in ataxia oculomotor apraxia type 2S R Catford, M K O'Bryan, R I McLachlan, et al.
Journal of Neurology|October 14, 2009
A comparison of three measures of upper limb function in Friedreich ataxiaL A Corben, G Tai, C Wilson, et al.
Clinical Genetics|February 1, 2005
Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosisA A Gason, M A Aitken, S A Metcalfe, et al.
Journal of Medical Genetics|January 15, 2000
46,XX/46,XY at amniocentesis in a fetus with true hermaphroditismD Amor, M B Delatycki, M Susman, et al.
Clinical Genetics|November 6, 2012
To tell or not to tell - what to do about p.C282Y heterozygotes identified by HFE screeningM B Delatycki, M Wolthuizen, M A Aitken, et al.
Pageof 6