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Geir J Braathen

Showing results (1-10 of 21) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 16, 2005
[Episodic ataxias]Antje Herrmann, Geir J Braathen, Michael Bjørn Russell
BMC Research Notes|April 14, 2010
Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndromeGeir J Braathen, Jette C Sand, Michael B Russell
Analytical and Quantitative Cytology and Histology|October 8, 2011
Simplification of grading papillary urothelial neoplasia using a reduced set of diagnostic featuresBjörn L Isfoss, Bernard Majak, Christer Busch, et al.
Analytical and Quantitative Cytology and Histology|October 8, 2011
Diagnosis of intraurothelial neoplasia. Interobserver variation and the value of individual histopathologic attributesBjörn L Isfoss, Bernard Majak, Christer Busch, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 16, 2005
[Cerebral cavernous malformations]Jeanette Koht, Geir J Braathen, Dirk Neubert, et al.
BMC Neurology|July 11, 2007
Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth diseaseGeir J Braathen, Jette C Sand, Geir Bukholm, et al.
BMC Medical Genetics|March 31, 2010
MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT familiesGeir J Braathen, Jette C Sand, Ana Lobato, et al.
European Journal of Medical Genetics|July 27, 2011
Charcot-Marie-Tooth caused by a copy number variation in myelin protein zeroHelle Høyer, Geir J Braathen, Anette K Eek, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 13, 2022
A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
International Journal of Dermatology|December 15, 2020
Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 geneHilal Al Mandhari, Buthaina Al-Musalhi, Nouh Al Mahroqi, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 16, 2005
[Episodic ataxias]Antje Herrmann, Geir J Braathen, Michael Bjørn Russell
BMC Research Notes|April 14, 2010
Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndromeGeir J Braathen, Jette C Sand, Michael B Russell
Analytical and Quantitative Cytology and Histology|October 8, 2011
Simplification of grading papillary urothelial neoplasia using a reduced set of diagnostic featuresBjörn L Isfoss, Bernard Majak, Christer Busch, et al.
Analytical and Quantitative Cytology and Histology|October 8, 2011
Diagnosis of intraurothelial neoplasia. Interobserver variation and the value of individual histopathologic attributesBjörn L Isfoss, Bernard Majak, Christer Busch, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 16, 2005
[Cerebral cavernous malformations]Jeanette Koht, Geir J Braathen, Dirk Neubert, et al.
BMC Neurology|July 11, 2007
Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth diseaseGeir J Braathen, Jette C Sand, Geir Bukholm, et al.
BMC Medical Genetics|March 31, 2010
MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT familiesGeir J Braathen, Jette C Sand, Ana Lobato, et al.
European Journal of Medical Genetics|July 27, 2011
Charcot-Marie-Tooth caused by a copy number variation in myelin protein zeroHelle Høyer, Geir J Braathen, Anette K Eek, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|January 13, 2022
A woman in her fifties with chronic muscle weaknessCecilie F Rustad, Kristian Tveten, Geir J Braathen, et al.
International Journal of Dermatology|December 15, 2020
Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 geneHilal Al Mandhari, Buthaina Al-Musalhi, Nouh Al Mahroqi, et al.
Pageof 3