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Francesca Magri

Showing results (81-90 of 174) with videos related to

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The Australasian Journal of Dermatology|July 17, 2020
Necrotic acral lesions and lung failure in a fatal case of COVID-19Antonella Tammaro, Camilla Chello, Alvise Sernicola, et al.
Scandinavian Journal of Gastroenterology|December 3, 2016
Anti-sulfatide reactivity in patients with celiac diseaseDomenica Saccomanno, Carolina Tomba, Francesca Magri, et al.
International Journal of Molecular Sciences|December 11, 2025
Recurrent <i>CAPN3</i> p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical ExpressivityGiorgia D'Este, Alejandro Giorgetti, Denise Cassandrini, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.
Frontiers in Neurology|February 2, 2024
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophyMartina Rimoldi, Gloria Romagnoli, Francesca Magri, et al.
Dermatology Reports|February 19, 2025
Lack of communication between dermatologists and histopathologists in real-life settings: a survey of the Italian Association of Hospital Dermatologists (ADOI)Francesca Magri, Luca Fania, Tonia Samela, et al.
BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.
Frontiers in Neurology|December 18, 2018
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientElena Abati, Irene Faravelli, Francesca Magri, et al.
Neurology. Genetics|September 3, 2025
Single Nucleotide <i>SMN1</i> Variants in a Cohort of Individuals With Spinal Muscular AtrophyMartina Rimoldi, Francesca Magri, Megi Meneri, et al.
Pageof 18

Showing results (81-90 of 174) with videos related to

Sort By:
Pageof 18
The Australasian Journal of Dermatology|July 17, 2020
Necrotic acral lesions and lung failure in a fatal case of COVID-19Antonella Tammaro, Camilla Chello, Alvise Sernicola, et al.
Scandinavian Journal of Gastroenterology|December 3, 2016
Anti-sulfatide reactivity in patients with celiac diseaseDomenica Saccomanno, Carolina Tomba, Francesca Magri, et al.
International Journal of Molecular Sciences|December 11, 2025
Recurrent <i>CAPN3</i> p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical ExpressivityGiorgia D'Este, Alejandro Giorgetti, Denise Cassandrini, et al.
Frontiers in Neurology|August 29, 2019
Ophthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisRoberta Brusa, Irene Faravelli, Delia Gagliardi, et al.
Pediatric Neurology|October 18, 2011
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation siteMaria Grazia D'Angelo, Maria Luisa Lorusso, Federica Civati, et al.
Frontiers in Neurology|February 2, 2024
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophyMartina Rimoldi, Gloria Romagnoli, Francesca Magri, et al.
Dermatology Reports|February 19, 2025
Lack of communication between dermatologists and histopathologists in real-life settings: a survey of the Italian Association of Hospital Dermatologists (ADOI)Francesca Magri, Luca Fania, Tonia Samela, et al.
BMC Neurology|December 29, 2018
Subclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeEleonora Mauri, Robertino Dilena, Antonio Boccazzi, et al.
Frontiers in Neurology|December 18, 2018
Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientElena Abati, Irene Faravelli, Francesca Magri, et al.
Neurology. Genetics|September 3, 2025
Single Nucleotide <i>SMN1</i> Variants in a Cohort of Individuals With Spinal Muscular AtrophyMartina Rimoldi, Francesca Magri, Megi Meneri, et al.
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