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Daniel Birchall

Showing results (21-30 of 25) with videos related to

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Neuromuscular Disorders : NMD|February 8, 2005
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contracturesEugenio Mercuri, Kate Bushby, Enzo Ricci, et al.
Tropical Medicine & International Health : TM & IH|May 6, 2015
Cysticercosis and epilepsy in rural Tanzania: a community-based case-control and imaging studyEwan Hunter, Kathryn Burton, Ahmed Iqbal, et al.
Brain : a Journal of Neurology|December 5, 2006
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationPatrick F Chinnery, Douglas E Crompton, Daniel Birchall, et al.
Neuromuscular Disorders : NMD|May 23, 2013
Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: extending the clinical and pathological phenotypeRos Quinlivan, Satomi Mitsuahashi, Caroline Sewry, et al.
Nature Communications|July 4, 2014
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasiaVeronika Boczonadi, Juliane S Müller, Angela Pyle, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Neuromuscular Disorders : NMD|February 8, 2005
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contracturesEugenio Mercuri, Kate Bushby, Enzo Ricci, et al.
Tropical Medicine & International Health : TM & IH|May 6, 2015
Cysticercosis and epilepsy in rural Tanzania: a community-based case-control and imaging studyEwan Hunter, Kathryn Burton, Ahmed Iqbal, et al.
Brain : a Journal of Neurology|December 5, 2006
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationPatrick F Chinnery, Douglas E Crompton, Daniel Birchall, et al.
Neuromuscular Disorders : NMD|May 23, 2013
Muscular dystrophy with large mitochondria associated with mutations in the CHKB gene in three British patients: extending the clinical and pathological phenotypeRos Quinlivan, Satomi Mitsuahashi, Caroline Sewry, et al.
Nature Communications|July 4, 2014
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasiaVeronika Boczonadi, Juliane S Müller, Angela Pyle, et al.
Pageof 3