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Franco Laccone

Showing results (11-20 of 99) with videos related to

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Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 31, 2016
Schmerzhafte KnotenTeresa Valero, Oliver Brandau, Franco Laccone, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 31, 2016
Painful nodulesTeresa Valero, Oliver Brandau, Franco Laccone, et al.
Brain & Development|July 10, 2003
The spectrum of phenotypes in females with Rett SyndromePeter Huppke, Melanie Held, Franco Laccone, et al.
Assay and Drug Development Technologies|April 8, 2015
Detection of survival motor neuron protein in buccal cells through electrochemiluminescence-based assayHannes Steinkellner, Julia Etzler, Bernhard M Gmeiner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2003
Chronic thalamic stimulation in a patient with spinocerebellar ataxia type 2Walter Pirker, Claude Back, Willibald Gerschlager, et al.
American Journal of Medical Genetics. Part A|August 9, 2005
Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2Peter Huppke, Andreas Ohlenbusch, Cornelia Brendel, et al.
Clinics and Practice|February 5, 2021
Simpson-Golabi-Behmel-Syndrome in Dichorionic-Diamniotic Twin PregnancyTheresa Reischer, Franco Laccone, Gregor J Kasprian, et al.
Human Mutation|March 17, 2004
Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dyeDetlef Boehm, Sabine Herold, Alma Kuechler, et al.
Cardiology|December 16, 2014
Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>AJosef Finsterer, Claudia Stöllberger, Ernst Sehnal, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Autosomal dominant Carvajal plus syndrome due to the novel desmoplakin mutation c.1678A > T (p.Ile560Phe)Josef Finsterer, Claudia Stöllberger, Eva Wollmann, et al.
Pageof 10

Showing results (11-20 of 99) with videos related to

Sort By:
Pageof 10
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 31, 2016
Schmerzhafte KnotenTeresa Valero, Oliver Brandau, Franco Laccone, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|May 31, 2016
Painful nodulesTeresa Valero, Oliver Brandau, Franco Laccone, et al.
Brain & Development|July 10, 2003
The spectrum of phenotypes in females with Rett SyndromePeter Huppke, Melanie Held, Franco Laccone, et al.
Assay and Drug Development Technologies|April 8, 2015
Detection of survival motor neuron protein in buccal cells through electrochemiluminescence-based assayHannes Steinkellner, Julia Etzler, Bernhard M Gmeiner, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 23, 2003
Chronic thalamic stimulation in a patient with spinocerebellar ataxia type 2Walter Pirker, Claude Back, Willibald Gerschlager, et al.
American Journal of Medical Genetics. Part A|August 9, 2005
Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2Peter Huppke, Andreas Ohlenbusch, Cornelia Brendel, et al.
Clinics and Practice|February 5, 2021
Simpson-Golabi-Behmel-Syndrome in Dichorionic-Diamniotic Twin PregnancyTheresa Reischer, Franco Laccone, Gregor J Kasprian, et al.
Human Mutation|March 17, 2004
Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dyeDetlef Boehm, Sabine Herold, Alma Kuechler, et al.
Cardiology|December 16, 2014
Dilated, arrhythmogenic cardiomyopathy in emery-dreifuss muscular dystrophy due to the emerin splice-site mutation c.449 + 1G>AJosef Finsterer, Claudia Stöllberger, Ernst Sehnal, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Autosomal dominant Carvajal plus syndrome due to the novel desmoplakin mutation c.1678A > T (p.Ile560Phe)Josef Finsterer, Claudia Stöllberger, Eva Wollmann, et al.
Pageof 10