Publications by authors named "Fatima Jaffer"

Claim this Profile
I
Improving specialised care for neuromuscular patients reduces the frequency of preventable emergency hospital admissions.
Renata S Scalco, Rosaline M Quinlivan, Laura Nastasi, Fatima Jaffer, Michael G Hanna

Neuromuscul Disord· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Letter to the Editor: NMDA receptor autoimmunity in mania following HSV encephalitis.
Graham Blackman, Nicholas Moran, Eli Silber, Christopher Symeon, Franz Brunnhuber, Fatima Jaffer

Psychol Med· May 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Atypical periodic paralysis and myalgia: A novel phenotype.
Emma Matthews, Christoph Neuwirth, Fatima Jaffer, Renata S Scalco, Doreen Fialho

Neurology· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial childhood-onset progressive cerebellar syndrome associated with the mutation.
Fatima Jaffer, Katherine Fawcett, David Sims, Andreas Heger, Henry Houlden

Neurol Genet· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spontaneously Fluctuating Motor Cortex Excitability in Alternating Hemiplegia of Childhood: A Transcranial Magnetic Stimulation Study.
William M Stern, Mahalekshmi Desikan, Damon Hoad, Fatima Jaffer, Gionata Strigaro

PLoS One· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro

Brain· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Fatima Jaffer, Andreja Avbersek, Rosaria Vavassori, Carmen Fons, Jaume Campistol

Brain· October 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L Heinzen, Carmen Fons, Fatima Jaffer

Orphanet J Rare Dis· September 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.
Merel Klaassens, Deborah Morrogh, Elisabeth M Rosser, Fatima Jaffer, Maaike Vreeburg

Eur J Hum Genet· May 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
BAG3 mutations: another cause of giant axonal neuropathy.
Fatima Jaffer, Sinéad M Murphy, Mariacristina Scoto, Estelle Healy, Alexander M Rossor

J Peripher Nerv Syst· June 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis