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Neurology
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August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
March 5, 2019
Influence of the Insertion Method of Aryl-Extended Calix[4]pyrroles into Liposomal Membranes on Their Properties as Anion Carriers
Luis Martínez-Crespo, Jia Liang Sun-Wang, Pedro Ferreira, et al.
Acta Diabetologica
|
December 31, 2011
Trans fatty acids consumption in type 1 diabetic patients: evaluation by dietary records and measurement in serum phospholipids
M Vitale, D Luongo, D Naviglio, et al.
Annals of Neurology
|
November 15, 2001
Relapsing-remitting autoimmune agrypnia
A P Batocchi, G Della Marca, M Mirabella, et al.
Neuromuscular Disorders : NMD
|
March 6, 2022
Upper body involvement in GNE myopathy assessed by muscle imaging
E Torchia, M Lucchini, S Bortolani, et al.
Journal of the Neurological Sciences
|
March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family
G Manfredi, G Silvestri, S Servidei, et al.
Neurology
|
February 19, 2000
GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy
M Mirabella, G Silvestri, G de Rosa, et al.
Neurology
|
August 15, 2001
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency
S Di Giovanni, M Mirabella, A Spinazzola, et al.
International Journal of Transgender Health
|
April 25, 2025
"<i>The third table where I would sit comfortably</i>": narratives of nonbinary identity routes
B Di Giannantonio, K Milanese, M Mirabella, et al.
European Journal of Neurology
|
May 16, 2012
Muscle MRI in female carriers of dystrophinopathy
G Tasca, M Monforte, E Iannaccone, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Neurology
|
August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy
M Mirabella, G Galluzzi, G Manfredi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
March 5, 2019
Influence of the Insertion Method of Aryl-Extended Calix[4]pyrroles into Liposomal Membranes on Their Properties as Anion Carriers
Luis Martínez-Crespo, Jia Liang Sun-Wang, Pedro Ferreira, et al.
Acta Diabetologica
|
December 31, 2011
Trans fatty acids consumption in type 1 diabetic patients: evaluation by dietary records and measurement in serum phospholipids
M Vitale, D Luongo, D Naviglio, et al.
Annals of Neurology
|
November 15, 2001
Relapsing-remitting autoimmune agrypnia
A P Batocchi, G Della Marca, M Mirabella, et al.
Neuromuscular Disorders : NMD
|
March 6, 2022
Upper body involvement in GNE myopathy assessed by muscle imaging
E Torchia, M Lucchini, S Bortolani, et al.
Journal of the Neurological Sciences
|
March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family
G Manfredi, G Silvestri, S Servidei, et al.
Neurology
|
February 19, 2000
GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy
M Mirabella, G Silvestri, G de Rosa, et al.
Neurology
|
August 15, 2001
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency
S Di Giovanni, M Mirabella, A Spinazzola, et al.
International Journal of Transgender Health
|
April 25, 2025
"<i>The third table where I would sit comfortably</i>": narratives of nonbinary identity routes
B Di Giannantonio, K Milanese, M Mirabella, et al.
European Journal of Neurology
|
May 16, 2012
Muscle MRI in female carriers of dystrophinopathy
G Tasca, M Monforte, E Iannaccone, et al.
Page
of 5