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

L Merlini

Showing results (191-200 of 209) with videos related to

Pageof 21
Sort By:
Annals of Neurology|October 17, 2001
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan GypsiesP K Thomas, L Kalaydjieva, B Youl, et al.
Journal of Medicinal Chemistry|September 21, 2001
Novel 7-oxyiminomethyl derivatives of camptothecin with potent in vitro and in vivo antitumor activityS Dallavalle, A Ferrari, B Biasotti, et al.
Journal of Medical Genetics|December 20, 2003
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypesM Vytopil, S Benedetti, E Ricci, et al.
Human Mutation|October 15, 2008
Transcriptional behavior of DMD gene duplications in DMD/BMD malesF Gualandi, M Neri, M Bovolenta, et al.
American Journal of Human Genetics|March 31, 2000
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophyM Raffaele Di Barletta, E Ricci, G Galluzzi, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Pageof 21

Showing results (191-200 of 209) with videos related to

Sort By:
Pageof 21
Annals of Neurology|October 17, 2001
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan GypsiesP K Thomas, L Kalaydjieva, B Youl, et al.
Journal of Medicinal Chemistry|September 21, 2001
Novel 7-oxyiminomethyl derivatives of camptothecin with potent in vitro and in vivo antitumor activityS Dallavalle, A Ferrari, B Biasotti, et al.
Journal of Medical Genetics|December 20, 2003
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypesM Vytopil, S Benedetti, E Ricci, et al.
Human Mutation|October 15, 2008
Transcriptional behavior of DMD gene duplications in DMD/BMD malesF Gualandi, M Neri, M Bovolenta, et al.
American Journal of Human Genetics|March 31, 2000
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophyM Raffaele Di Barletta, E Ricci, G Galluzzi, et al.
Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Pageof 21