Publications by authors named "Julie Perrier"

Claim this Profile
A
Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues.
Valérie Biancalana, Sophie Scheidecker, Marguerite Miguet, Annie Laquerrière, Norma B Romero, Julie Perrier

Acta Neuropathol· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of an in vivo orally active dual-binding protein-protein interaction inhibitor targeting TNFα through combined in silico/in vitro/in vivo screening.
Hadley Mouhsine, Hélène Guillemain, Gabriel Moreau, Najla Fourati, Chouki Zerrouki, Julie Perrier

Sci Rep· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.
Sandra Mercier, Sébastien Küry, Emmanuelle Salort-Campana, Armelle Magot, Uchenna Agbim, Julie Perrier

Orphanet J Rare Dis· October 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and electrophysiological features in a French family presenting with seipinopathy.
Yolaine Ollivier, Armelle Magot, Philippe Latour, Julie Perrier, Sandra Mercier

Neuromuscul Disord· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Type I interferon potentiates T-cell receptor mediated induction of IL-10-producing CD4⁺ T cells.
Béatrice Corre, Julie Perrier, Margueritte El Khouri, Silvia Cerboni, Sandra Pellegrini

Eur J Immunol· October 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Palmo-Plantar hyperkeratosis, intellectual disability, and spastic paraplegia in two maternal half brothers: further evidence for an X-linked inheritance.
Bertrand Isidor, Tiphaine Lefebvre, Sébastien Barbarot, Julie Perrier, Sandra Mercier

Am J Med Genet A· June 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.
Mathieu Milh, Nadia Boutry-Kryza, Julie Sutera-Sardo, Cyril Mignot, Stéphane Auvin, Julie Perrier

Orphanet J Rare Dis· May 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Ring 14 chromosome presenting as early-onset isolated partial epilepsy.
Dorothée Ville, Julitta DE Bellescize, Marie Ange Nguyen, Hervé Testard, Agnès Gautier, Julie Perrier

Dev Med Child Neurol· November 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
Derek E Neilson, Mark D Adams, Caitlin M D Orr, Deborah K Schelling, Robert M Eiben, Julie Perrier

Am J Hum Genet· January 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis