Search research articles
Contact Us
Filters
Showing results (11-20 of 24) with videos related to
Page
of 3
Sort By:
Annales De Dermatologie Et De Venereologie
|
March 1, 2017
[Cutaneous involvement in T-lymphoblastic lymphoma]
C Nascimbeni, S Chantepie, C Brugiere, et al.
The American Journal of Pathology
|
March 28, 2006
Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease
Marina Fanin, Anna C Nascimbeni, Luigi Fulizio, et al.
Journal of Medical Genetics
|
May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A
M Fanin, L Nardetto, A C Nascimbeni, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 4, 2006
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C Pizzanelli, M Mancuso, R Galli, et al.
Muscle & Nerve
|
December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1F
Marina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
International Ophthalmology
|
February 19, 2026
Loading dose and 12-month outcomes in treatment-naïve patients with neovascular age-related macular degeneration treated with faricimab, with AI-based analysis of fluid dynamics
Mickael Barbosa, Nicolò Bartolomeo, Yannic Pannatier Schuetz, et al.
European Journal of Ophthalmology
|
December 17, 2025
Pigment epithelial detachment as a biomarker for faricimab treatment outcomes in naïve neovascular age-related macular degeneration
Nicolò Bartolomeo, Mickael Barbosa, Yannic Pannatier Schuetz, et al.
Clinical Genetics
|
April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps
M Fanin, F Benedicenti, C Fritegotto, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Annales De Dermatologie Et De Venereologie
|
March 1, 2017
[Cutaneous involvement in T-lymphoblastic lymphoma]
C Nascimbeni, S Chantepie, C Brugiere, et al.
The American Journal of Pathology
|
March 28, 2006
Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease
Marina Fanin, Anna C Nascimbeni, Luigi Fulizio, et al.
Journal of Medical Genetics
|
May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A
M Fanin, L Nardetto, A C Nascimbeni, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 4, 2006
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C Pizzanelli, M Mancuso, R Galli, et al.
Muscle & Nerve
|
December 10, 2014
Incomplete penetrance in limb-girdle muscular dystrophy type 1F
Marina Fanin, Enrico Peterle, Chiara Fritegotto, et al.
International Ophthalmology
|
February 19, 2026
Loading dose and 12-month outcomes in treatment-naïve patients with neovascular age-related macular degeneration treated with faricimab, with AI-based analysis of fluid dynamics
Mickael Barbosa, Nicolò Bartolomeo, Yannic Pannatier Schuetz, et al.
European Journal of Ophthalmology
|
December 17, 2025
Pigment epithelial detachment as a biomarker for faricimab treatment outcomes in naïve neovascular age-related macular degeneration
Nicolò Bartolomeo, Mickael Barbosa, Yannic Pannatier Schuetz, et al.
Clinical Genetics
|
April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps
M Fanin, F Benedicenti, C Fritegotto, et al.
Page
of 3