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Pascal Cintas

Showing results (21-30 of 80) with videos related to

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Neurology. Genetics|November 7, 2024
Early Peripheral Nerve Involvement at the Time of Coughing in Patients With <i>RFC1</i> Intronic ExpansionSimon Frachet, Pauline Chazelas, Laurent Magy, et al.
Clinical Immunology (Orlando, Fla.)|July 8, 2024
Store-operated calcium entry dysfunction in CRAC channelopathy: Insights from a novel STIM1 mutationBenedicte Alary, Pascal Cintas, Corentin Claude, et al.
Nature Reviews. Neurology|December 30, 2015
Hepatitis E virus and neurological injuryHarry R Dalton, Nassim Kamar, Jeroen J J van Eijk, et al.
Vaccines|October 26, 2021
Hepatitis E Virus Quasispecies in Cerebrospinal Fluid with Neurological ManifestationsFlorence Abravanel, Florence Nicot, Sébastien Lhomme, et al.
Brain Sciences|December 18, 2020
One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal FormFederica Miressi, Corinne Magdelaine, Pascal Cintas, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|October 1, 2017
Transfusion-acquired hepatitis E infection misdiagnosed as severe critical illness polyneuromyopathy in a heart transplant patientJulie Belliere, Florence Abravanel, Marie Béatrice Nogier, et al.
ESC Heart Failure|June 27, 2020
Gateway and journey of patients with cardiac amyloidosisDaniel Dang, Pauline Fournier, Eve Cariou, et al.
Emerging Infectious Diseases|February 5, 2011
Hepatitis E virus and neurologic disordersNassim Kamar, Richard P Bendall, Jean Marie Peron, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 8, 2019
Atrial fibrillation and subtype of atrial fibrillation in cardiac amyloidosis: clinical and echocardiographic features, impact on mortalityKevin Sanchis, Eve Cariou, Magali Colombat, et al.
Orphanet Journal of Rare Diseases|March 2, 2025
Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective studyYann Péréon, David Adams, Jean-Philippe Camdessanché, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Neurology. Genetics|November 7, 2024
Early Peripheral Nerve Involvement at the Time of Coughing in Patients With <i>RFC1</i> Intronic ExpansionSimon Frachet, Pauline Chazelas, Laurent Magy, et al.
Clinical Immunology (Orlando, Fla.)|July 8, 2024
Store-operated calcium entry dysfunction in CRAC channelopathy: Insights from a novel STIM1 mutationBenedicte Alary, Pascal Cintas, Corentin Claude, et al.
Nature Reviews. Neurology|December 30, 2015
Hepatitis E virus and neurological injuryHarry R Dalton, Nassim Kamar, Jeroen J J van Eijk, et al.
Vaccines|October 26, 2021
Hepatitis E Virus Quasispecies in Cerebrospinal Fluid with Neurological ManifestationsFlorence Abravanel, Florence Nicot, Sébastien Lhomme, et al.
Brain Sciences|December 18, 2020
One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal FormFederica Miressi, Corinne Magdelaine, Pascal Cintas, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|October 1, 2017
Transfusion-acquired hepatitis E infection misdiagnosed as severe critical illness polyneuromyopathy in a heart transplant patientJulie Belliere, Florence Abravanel, Marie Béatrice Nogier, et al.
ESC Heart Failure|June 27, 2020
Gateway and journey of patients with cardiac amyloidosisDaniel Dang, Pauline Fournier, Eve Cariou, et al.
Emerging Infectious Diseases|February 5, 2011
Hepatitis E virus and neurologic disordersNassim Kamar, Richard P Bendall, Jean Marie Peron, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 8, 2019
Atrial fibrillation and subtype of atrial fibrillation in cardiac amyloidosis: clinical and echocardiographic features, impact on mortalityKevin Sanchis, Eve Cariou, Magali Colombat, et al.
Orphanet Journal of Rare Diseases|March 2, 2025
Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective studyYann Péréon, David Adams, Jean-Philippe Camdessanché, et al.
Pageof 8