Classification and diagnosis of the inherited neuropathies

af Reilly, Mary M.
Udgivet 2009

Early detection of nerve injury in transthyretin-related familial amyloid polyneuropathy

af Morrow, Jasper M., Reilly, Mary M.
Udgivet i Brain (2015)

Humans: the ultimate animal models

af Reilly, Mary M, Rossor, Alexander M
Udgivet i J Neurol Neurosurg Psychiatry (2020)

Knee bobbing in Charcot–Marie-Tooth disease

af Rossor, Alexander M., Murphy, Sinead, Reilly, Mary M.
Udgivet 2012

A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H

af Houlden, Henry, Hammans, Simon, Katifi, Haider, Reilly, Mary M.
Udgivet 2009

Sensory neuronopathy associated with cholangiocarcinoma diagnosed 6 years after symptom onset

af Rossor, Alexander M, Blake, Julian, Pissanou, Theodora, Reilly, Mary M
Udgivet i BMJ Case Rep (2017)

Clinical Presentation, Diagnosis and Treatment of TTR Amyloidosis

af Kapoor, Mahima, Rossor, Alexander M., Laura, Matilde, Reilly, Mary M.
Udgivet i J Neuromuscul Dis (2019)

Cervical spinal cord compression complicating the clinical course of Charcot-Marie-Tooth type 1

af Evans, Matthew R B, Laurá, Matilde, Chandrashekar, Hoskote, Reilly, Mary M
Udgivet i BMJ Case Rep (2015)

Hip flexor fatigue limits walking in Charcot-Marie-Tooth disease

af RAMDHARRY, GITA M., DAY, BRIAN L., REILLY, MARY M., MARSDEN, JONATHAN F.
Udgivet 2009

Mutation in FAM134B causing severe hereditary sensory neuropathy

af Murphy, Sinead M, Davidson, Gabrielle L, Brandner, Sebastian, Houlden, Henry, Reilly, Mary M
Udgivet 2010

An observational study of asymmetry in CMT1A

af Pelayo-Negro, Ana L, Carr, Aisling S, Laura, Matilde, Skorupinska, Mariola, Reilly, Mary M
Udgivet i J Neurol Neurosurg Psychiatry (2015)

TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN

af Rossor, Alexander M., Jaunmuktane, Zane, Rossor, Martin N., Hoti, Glen, Reilly, Mary M.
Udgivet i Neurology (2019)

Ascorbic acid for the treatment of Charcot‐Marie‐Tooth disease

af Gess, Burkhard, Baets, Jonathan, De Jonghe, Peter, Reilly, Mary M, Pareyson, Davide, Young, Peter
Udgivet i Cochrane Database Syst Rev (2015)

Rydel-Seiffer fork revisited: Beyond a simple case of black and white

af Panosyan, Francis B., Mountain, Joan M., Reilly, Mary M., Shy, Michael E., Herrmann, David N.
Udgivet i Neurology (2016)

A novel mutation in the FGD4 gene causing Charcot‐Marie‐Tooth disease

af Zis, Panagiotis, Reilly, Mary M., Rao, Dasappaiah G., Tomaselli, Pedro, Rossor, Alex M., Hadjivassiliou, Marios
Udgivet i J Peripher Nerv Syst (2017)

New mutations, genotype phenotype studies and manifesting carriers in giant axonal neuropathy

af Houlden, Henry, Groves, Mike, Miedzybrodzka, Zosia, Roper, Helen, Willis, Tracey, Winer, John, Cole, Gaynor, Reilly, Mary M
Udgivet 2007

Severe axonal neuropathy is a late manifestation of SPG11

af Manole, Andreea, Chelban, Viorica, Haridy, Nourelhoda A., Hamed, Sherifa A., Berardo, Andrés, Reilly, Mary M., Houlden, Henry
Udgivet i J Neurol (2016)

A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorder

af Tomaselli, Pedro J., Rossor, Alexander M., Horga, Alejandro, Laura, Matilde, Blake, Julian C., Houlden, Henry, Reilly, Mary M.
Udgivet i J Peripher Nerv Syst (2017)

Plasma neurofilament light chain concentration in the inherited peripheral neuropathies

af Sandelius, Åsa, Zetterberg, Henrik, Blennow, Kaj, Adiutori, Rocco, Malaspina, Andrea, Laura, Matilde, Reilly, Mary M., Rossor, Alexander M.
Udgivet i Neurology (2018)

Loss of BICD2 in muscle drives motor neuron loss in a developmental form of spinal muscular atrophy

af Rossor, Alexander M., Sleigh, James N., Groves, Michael, Muntoni, Francesco, Reilly, Mary M., Hoogenraad, Casper C., Schiavo, Giampietro
Udgivet i Acta Neuropathol Commun (2020)