Author/Creator: Reilly, MM - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Reilly, MM

1. 099 High relapse rate with steroid monotherapy in non-systemic vasculitic neuropathy. Issue 6 (27th May 2022)

Authors:: Bunting, Eva; Cooper, Rebecca; Seral, M; Manji, H; Rossor, A; Reilly, MM; Lunn, MP; Bennett, D; Hadden, R; Carr, AS
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 93:Issue 6(2022)
Page Start:: A42
Record Type:: Journal Article
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2. AVOIDING UNPLANNED HOSPITAL ADMISSIONS IN PATIENTS WITH NEUROMUSCULAR DISEASES: A REGIONAL COLLABORATIVE AUDIT OF HOSPITAL ADMISSIONS. (29th November 2012)

Authors:: Jaffer, F; Reilly, MM; Quinlivan, RR; Muntoni, F; Orrell, R; Wraige, E; Saha, R; Radunovic, A; Mummery, C; Parton, M; Hanna, M
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83(2012)Supplement 2
Page Start:: A23
Record Type:: Journal Article
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3. CARDIAC AND EXTRACARDIAC AMYLOIDOSIS IN V122I ATTR. Issue 10 (9th September 2014)

Authors:: Carr, Aisling; Jaunmuktane, Z; Pelayo, Healy; Hutt, D; Brandner Holton, S; Blake, J; Whelan, CJ; Wechalekar, AD; Gilmore, JD; Hawkins, PN; Reilly, MM
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 85:Issue 10(2014)
Page Start:: e4
Record Type:: Journal Article
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4. ELECTROLYTE IMBALANCE TRIGGERING RELAPSE OF INFLAMMATORY NEUROPATHY. Issue 11 (9th October 2013)

Authors:: Keshavan, A; Gandhi, S; Lunn, MP; Reilly, MM
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 84:Issue 11(2013)
Page Start:: e2
Record Type:: Journal Article
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5. MFN2 DELETION FOUNDER MUTATION IN THE UK POPULATION. Issue 10 (9th September 2014)

Authors:: Carr, Aisling; Polke, JM; Wilson, J; Nanji, T; Laura, M; Pelayo, AL; Lecky, B; Vaughan, J; Rankin, J; Sweeny, M; Reilly, MM
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 85:Issue 10(2014)
Page Start:: e4
Record Type:: Journal Article
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6. Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot–Marie–Tooth type 1 patients. (19th April 2013)

Authors:: Koutsis, G; Pandraud, A; Karadima, G; Panas, M; Reilly, MM; Floroskufi, P; Wood, NW; Houlden, H
Journal:: Clinical genetics
Issue:: Volume 83:Number 4(2013:Apr.)
Page Start:: 388
Record Type:: Journal Article
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7. Mutational analysis of PMP22, EGR2, LITAF and NEFL in Greek Charcot–Marie–Tooth type 1 patients. (5th July 2012)

Authors:: Koutsis, G; Pandraud, A; Karadima, G; Panas, M; Reilly, MM; Floroskufi, P; Wood, NW; Houlden, H
Journal:: Clinical genetics
Issue:: Volume 83:Number 4(2013:Apr.)
Page Start:: 388
Record Type:: Journal Article
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8. NEUROPATHY PHENOTYPE IN HEREDITARY TRANSTHYRETIN AMYLOIDOSIS. Issue 10 (9th September 2014)

Authors:: Carr, Aisling; Pelayo, Ana; Wechalekar, AD; Whelan, CJ; Gilmore, JD; Hawkins, PN; Reilly, MM
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 85:Issue 10(2014)
Page Start:: e4
Record Type:: Journal Article
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9. P71 Neurosurgical presentation of hereditary transthyretin (ATTR) amyloidosis: early recognition for earlier genetic therapies. Issue 3 (14th February 2019)

Authors:: Kapoor, M; Quaegebeur, Annelies; Shah, Sachit; Carr, AS; Reilly, MM
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 90:Issue 3(2019)
Page Start:: e40
Record Type:: Journal Article
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10. PO207 Thromboembolic risk in inflammatory neuromuscular disease patients on long-term ivig. (1st December 2017)

Authors:: Spillane, J; Englezou, C; Sarri-Gonzalez, S; Rossor, A; Lunn, MP; Manji, H; Reilly, MM; Carr, AS
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 88(2017)Supplement 1
Page Start:: A66
Record Type:: Journal Article
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