Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Drac

Showing results (31-40 of 43) with videos related to

Pageof 5
Sort By:
European Journal of Neurology|August 28, 2003
Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short reportA Kochański, H Drac, H Jedrzejowska, et al.
Folia Neuropathologica|November 1, 2000
Paraneoplastic syndrome in the course of lung adenocarcinoma: morphological picture and immunohistochemical analysis of the inflammatory infiltrates and PECAM-1 expressionD Dziewulska, H Drac, W Michej, et al.
Neurologia I Neurochirurgia Polska|July 10, 1999
[Hereditary neuropathy with liability to pressure palsies caused by 17p11.2 chromosome deletion]M Dorobek, E Szmidt-Sałkowska, H Drac, et al.
Neurologia I Neurochirurgia Polska|March 1, 1986
[Hereditary motor-sensory neuropathy. II. Electrophysiological studies]B Ryniewicz, T Nowak-Michalska, B Badurska, et al.
Neuropediatrics|June 10, 2005
Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 geneD Kabzińska, A Kochański, H Drac, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 17, 2006
Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 geneD Kabzinska, H Drac, K Rowinska-Marcinska, et al.
Neurology|June 9, 2004
A novel MPZ gene mutation in congenital neuropathy with hypomyelinationA Kochanski, H Drac, D Kabzińska, et al.
Polskie Archiwum Medycyny Wewnetrznej|February 1, 1986
[Changes in the peripheral nerves in chronic renal failure]K Rowińska, J Juskowa, H Drac, et al.
Neurology|March 15, 2006
Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX geneD Kabzinska, H Drac, D L Sherman, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 22, 2008
Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 geneD Kabzińska, G M Saifi, H Drac, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
European Journal of Neurology|August 28, 2003
Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short reportA Kochański, H Drac, H Jedrzejowska, et al.
Folia Neuropathologica|November 1, 2000
Paraneoplastic syndrome in the course of lung adenocarcinoma: morphological picture and immunohistochemical analysis of the inflammatory infiltrates and PECAM-1 expressionD Dziewulska, H Drac, W Michej, et al.
Neurologia I Neurochirurgia Polska|July 10, 1999
[Hereditary neuropathy with liability to pressure palsies caused by 17p11.2 chromosome deletion]M Dorobek, E Szmidt-Sałkowska, H Drac, et al.
Neurologia I Neurochirurgia Polska|March 1, 1986
[Hereditary motor-sensory neuropathy. II. Electrophysiological studies]B Ryniewicz, T Nowak-Michalska, B Badurska, et al.
Neuropediatrics|June 10, 2005
Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 geneD Kabzińska, A Kochański, H Drac, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 17, 2006
Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 geneD Kabzinska, H Drac, K Rowinska-Marcinska, et al.
Neurology|June 9, 2004
A novel MPZ gene mutation in congenital neuropathy with hypomyelinationA Kochanski, H Drac, D Kabzińska, et al.
Polskie Archiwum Medycyny Wewnetrznej|February 1, 1986
[Changes in the peripheral nerves in chronic renal failure]K Rowińska, J Juskowa, H Drac, et al.
Neurology|March 15, 2006
Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX geneD Kabzinska, H Drac, D L Sherman, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 22, 2008
Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 geneD Kabzińska, G M Saifi, H Drac, et al.
Pageof 5