R. Murphy

发表

Isolated trochlear infarction: an uncommon cause of acquired diplopia.

R. Walsh, R. Murphy, D. Moore, 2010, Archives of neurology.

Pathogenic ATM mutations occur rarely in a subset of multiple myeloma patients

T. Stankovic, P. Byrd, A. Taylor, 2008, British journal of haematology.

Carnitine palmitoyl transferase deficiency with an atypical presentation and ultrastructural mitochondrial abnormalities.

C. Hawkins, R. Murphy, M. Carey, 1987, Journal of neurology, neurosurgery, and psychiatry.

Waardenburg syndrome: a rare cause of inherited neuropathy due to SOX10 mutation

S. Murphy, R. Murphy, P. Bogdanova-Mihaylova, 2017, Journal of the peripheral nervous system : JPNS.

Increased thrombin generation potential in symptomatic versus asymptomatic moderate or severe carotid stenosis and relationship with cerebral microemboli

J. Harbison, D. Collins, T. Coughlan, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Assessment of ‘on-treatment platelet reactivity’ and relationship with cerebral micro-embolic signals in asymptomatic and symptomatic carotid stenosis

J. Harbison, D. Collins, T. Coughlan, 2017, Journal of the Neurological Sciences.

Increased endothelial activation in recently symptomatic versus asymptomatic carotid artery stenosis and in cerebral microembolic‐signal‐negative patient subgroups

J. Harbison, T. Coughlan, C. Doherty, 2014, European journal of neurology.

Increased platelet activation in early symptomatic vs. asymptomatic carotid stenosis and relationship with microembolic status: results from the Platelets and Carotid Stenosis Study

J. Harbison, D. Collins, T. Coughlan, 2013, Journal of thrombosis and haemostasis : JTH.

Broadening the phenotype of childhood-onset dopa-responsive dystonia.

N. Delanty, R. Murphy, D. McCabe, 2006, Archives of neurology.

Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C

K., Stevens, A. Vanderver, 2020, The Journal of clinical endocrinology and metabolism.

Acute pseudobulbar palsy due to methotrexate with rapid response to intravenous immunoglobulin

R. Murphy, H. Enright, P. Kinirons, 2005, Journal of neurology.

S. Murphy, R. Walsh, R. Murphy, 2017, Movement disorders clinical practice.

High on‐treatment platelet reactivity on commonly prescribed antiplatelet agents following transient ischaemic attack or ischaemic stroke: results from the Trinity Antiplatelet Responsiveness (TRAP) study

D. Collins, T. Coughlan, S. Tierney, 2013, European journal of neurology.

A novel locus for episodic ataxia:UBR4 the likely candidate

J. Conroy, S. Ennis, P. McGettigan, 2013, European Journal of Human Genetics.

Dysmorphic features and learning disability in an adult male with pure partial trisomy 17q24-q25 due to a terminal duplication.

A. Green, R. Stallings, B. Kelly, 2002, American journal of medical genetics.

Spinal subdural abscess.

R. Murphy, J. McCabe, 2013, JAMA neurology.

A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns

J. Casey, S. Ennis, K. Mikoshiba, 2017, Journal of Neurology.

Aciclovir-induced acute kidney injury in patients with ‘suspected viral encephalitis’ encountered on a liaison neurology service

S. Cronin, J. O'Dwyer, S. Murphy, 2018, Irish Journal of Medical Science (1971 -).

Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene.

D. Barton, N. Wood, M. Hanna, 2002, Archives of neurology.

X inactivation in females with X-linked Charcot–Marie–Tooth disease

H. Houlden, M. Shy, C. Siskind, 2012, Neuromuscular Disorders.

Microsatellite instability in sporadic colorectal carcinoma is not an indicator of prognosis

Terry J. Smith, J. Fullard, M. Heneghan, 1999, The Journal of pathology.

Clinical spectrum of AIFM1‐associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindness

D. Healy, S. Murphy, R. Walsh, 2019, Journal of the peripheral nervous system : JPNS.

Prevalence of ex vivo high on-treatment platelet reactivity on antiplatelet therapy after transient ischemic attack or ischemic stroke on the PFA-100(®) and VerifyNow(®).

T. Coughlan, D. Cox, R. Collins, 2013, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylenetetrahydrofolate reductase polymorphisms in pregnancy.

D. Fitzgerald, A. Whitehead, R. Murphy, 2000, Arteriosclerosis, thrombosis, and vascular biology.

Babinski, Pseudo-Babinski, and Dystonia—Reply

N. Delanty, R. Murphy, D. McCabe, 2007 .

Typical Friedreich's ataxia without GAA expansions and GAA expansions without typical Friedreich's ataxia

D. Barton, M. King, A. Kelly, 2000, Journal of Neurology.

Longitudinal assessment of von Willebrand factor antigen and von Willebrand factor propeptide in response to alteration of antiplatelet therapy after TIA or ischaemic stroke

D. Collins, T. Coughlan, R. McGrath, 2014, Journal of Neurology.

Enhanced ex vivo inhibition of platelet function following addition of dipyridamole to aspirin after transient ischaemic attack or ischaemic stroke: First results from the TRinity AntiPlatelet responsiveness (TrAP) study

D. Collins, T. Coughlan, S. Tierney, 2011, British journal of haematology.

Spastic ataxia associated with colour vision deficiency due to DDHD2 mutations

S. Murphy, R. Walsh, R. Murphy, 2020, European journal of neurology.

Hashimoto's encephalopathy; an unusual cause of status epilepticus.

R. Murphy, D. McCabe, E. Casey, 2000, Irish medical journal.

Liaison neurologists facilitate accurate neurological diagnosis and management, resulting in substantial savings in the cost of inpatient care

R. Murphy, D. McCabe, L. Costelloe, 2011, Irish Journal of Medical Science.

X inactivation in females with X-linked Charcot–Marie–Tooth disease

H. Houlden, M. Shy, C. Siskind, 2012, Neuromuscular Disorders.