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Courses
Courses
Choosing a course is one of the most important decisions you'll ever make! View our courses and see what our students and lecturers have to say about the courses you are interested in at the links below.
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University Life
University Life
Each year more than 4,000 choose University of Galway as their University of choice. Find out what life at University of Galway is all about here.
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About University of Galway
About University of Galway
Since 1845, University of Galway has been sharing the highest quality teaching and research with Ireland and the world. Find out what makes our University so special – from our distinguished history to the latest news and campus developments.
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Colleges & Schools
Colleges & Schools
University of Galway has earned international recognition as a research-led university with a commitment to top quality teaching across a range of key areas of expertise.
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Research & Innovation
Research & Innovation
University of Galway’s vibrant research community take on some of the most pressing challenges of our times.
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Business & Industry
Guiding Breakthrough Research at University of Galway
We explore and facilitate commercial opportunities for the research community at University of Galway, as well as facilitating industry partnership.
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Alumni & Friends
Alumni & Friends
There are 128,000 University of Galway alumni worldwide. Stay connected to your alumni community! Join our social networks and update your details online.
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Community Engagement
Community Engagement
At University of Galway, we believe that the best learning takes place when you apply what you learn in a real world context. That's why many of our courses include work placements or community projects.
Medicine
Prof. Nicholas Allen
Biography
Research Interests
Peer Reviewed Journals
Year | Publication | |
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(2024) | 'The 2017 and 2022 ILAE epilepsy classification systems identify needs and opportunities in care: A paediatric hospital-based study'
Donnellan EP, Kehoe C, Moran A, Ni Chollatain M, Hynes Y, Hennessy M, Reade E, Allen NM (2024) 'The 2017 and 2022 ILAE epilepsy classification systems identify needs and opportunities in care: A paediatric hospital-based study'. Epilepsy Behav, 157 (109804) [DOI] [Details] |
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(2024) | 'Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype'
Donnellan EP, Gorman K, Shahwan A, Allen NM (2024) 'Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype'. Epilepsy & Behavior Case Reports, [DOI] [Details] |
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(2023) | 'The Emerging Spectrum of Fetal Acetylcholine Receptor Antibody-associated Disorders (FARAD)'
Allen NM, O'Rahelly M, Eymard B, Chouchane M, Hahn A, Kearns G, Kim DS, Byun SY, Nguyen CE, Schara-Schmidt U, Kölbel H, Marina AD, Schneider-Gold C, Roefke K, Thieme A, Van den Bergh P, Avalos G, Álvarez-Velasco R, Natera-de Benito D, Cheng MHM, Chan WK, Wan HS, Thomas MA, Borch L, Lauzon J, Kornblum C, Reimann J, Mueller A, Kuntzer T, Norwood F, SRamdas S, Jacobson LW, Jie X, Fernandez-Garcia MA, Wraige E, Lim M, Lin JP, Claeys KG, Aktas S, Oskoui M, Hacohen Y, Masud A, Leite MI, Palace J, De Vivo D, Angela Vincent, Jungbluth H (2023) 'The Emerging Spectrum of Fetal Acetylcholine Receptor Antibody-associated Disorders (FARAD)'. Brain, 146 (10):4233-4246 [DOI] [ARAN Link] [Details] |
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(2023) | 'Macrocephaly Following the Bi-directional Glenn Procedure'
Donnellan EP, O'Brien ST, Allen NM (2023) 'Macrocephaly Following the Bi-directional Glenn Procedure'. Journal Of Pediatrics, [DOI] [Details] |
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(2023) | 'Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C)'
Stewart R, Gadoud C, Krawczyk J, McInerney V, O¿Brien T, Shen S, Allen NM (2023) 'Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C)'. Stem Cell Reports, [DOI] [Details] |
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(2023) | 'Using Ribonucleoprotein-based CRISPR/Cas9 toedit single nucleotide on human induced pluripotent stem cells to model type 3 long QT syndrome (SCN5A+/-)'
Ning Ge; Min Liu; Rui Li; Nicholas M. Allen; Joseph Galvin; Sanbing Shen; Timothy O'Brien; Terence Prendiville (2023) 'Using Ribonucleoprotein-based CRISPR/Cas9 toedit single nucleotide on human induced pluripotent stem cells to model type 3 long QT syndrome (SCN5A+/-)'. Stem Cell Reviews And Reports, [DOI] [Details] |
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(2023) | 'The changing face of reported status dystonicus - A systematic review'
Lumsden DE, Cif L, Capuano A, Allen NM (2023) 'The changing face of reported status dystonicus - A systematic review'. Parkinsonism & Related Disorders, [DOI] [Details] |
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(2023) | 'Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C>T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C)'
Stewart R, Gadoud C, Krawczyk J, McInerney V, O¿Brien T, Shen S, Allen NM (2023) 'Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C>T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C)'. Stem Cell Reports, [Details] |
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(2023) | 'The Learning Effects of Team Handover Report'
Duff C, Nicholson A, Allen NM (2023) 'The Learning Effects of Team Handover Report'. Irish Medical Journal, [Details] |
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(2023) | 'Abnormal liver function tests and improved survival in a child with splice mutation TARP syndrome'
Lane M, Allen NM, Letshwiti J. (2023) 'Abnormal liver function tests and improved survival in a child with splice mutation TARP syndrome'. BMJ Case Reports, [Details] |
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(2022) | 'Clinicians Engagement with Research: Motivating and Impeding Factors'
Morrison JC, Allen NM, Lynch SA, McVeigh TP, O'Grady MJ (2022) 'Clinicians Engagement with Research: Motivating and Impeding Factors'. Ir Med J, 115 (6) [Details] |
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(2022) | 'Mowat-Wilson syndrome presenting with Shone's complex cardiac anomaly'
Musaad W, Lyons A, Allen N, Letshwiti (2022) 'Mowat-Wilson syndrome presenting with Shone's complex cardiac anomaly'. BMJ Case Reports, 9 (15(2)) [DOI] [Details] |
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(2022) | 'Response to treatment and outcomes of infantile spasms in Down syndrome'
Harvey S, Allen NM, King MD, Lynch B, Lynch SA, O'Regan M, O'Rourke D, Shahwan A, Webb D, Gorman KM; Irish Paediatric Neurology Group. (2022) 'Response to treatment and outcomes of infantile spasms in Down syndrome'. Developmental Medicine & Child Neurology, [Details] |
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(2021) | 'Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome'
Weerts MJA, Lanko K, Guzman-Vega FJ, et al. (2021) 'Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome'. Genetics In Medicine : Official Journal Of The American College Of Medical Genetics, [Details] |
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(2021) | '4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy'
Hedrich UBS, Lauxmann S, Wolff M, Synofzik M, Bast T, Binelli A, Serratosa JM, Martínez-Ulloa P, Allen NM, King MD, Gorman KM, Zeev BB, Tzadok M, Wong-Kisiel L, Marjanovic D, Rubboli G, Sisodiya SM, Lutz F, Ashraf HP, Torge K, Yan P, Bosselmann C, Schwarz N, Fudali M, Lerche H (2021) '4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy'. Science Translational Medicine, Sep;13(609):eaaz4957 [Details] |
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(2021) | 'Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1¿ deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B)'
Ding Y;O'Brien A;de la Cruz BM;Yang M;Fitzgerald J;Yang G;Li W;McInerney V;Krawczyk J;Lynch SA;Howard L;Allen NM;O'Brien T;Gallagher L;Shen S; (2021) 'Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1¿ deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B)'. Stem Cell Research, 52 [DOI] [Details] |
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(2021) | 'Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1¿ gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B)'
Ding Y;O'Brien A;Marcó de la Cruz B;Yang M;Lu Y;Qian X;Yang G;McInerney V;Krawczyk J;Lynch SA;Howard L;Allen NM;O'Brien T;Gallagher L;Shen S; (2021) 'Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1¿ gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B)'. Stem Cell Research, 53 [DOI] [Details] |
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(2020) | 'Journal club: old tricks and fresh approaches'
McGlacken-Byrne, SM,O'Rahelly, M,Cantillon, P,Allen, NM (2020) 'Journal club: old tricks and fresh approaches'. Archives Of Disease In Childhood-Education And Practice Edition, 105 :236-241 [DOI] [Details] |
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(2020) | 'Catatonia as a feature of down syndrome: An under-recognised entity?'
Lyons A;Allen NM;Flanagan O;Cahalane D; (2020) 'Catatonia as a feature of down syndrome: An under-recognised entity?'. European Journal Of Paediatric Neurology, 25 [DOI] [Details] |
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(2020) | 'Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A)'
de la Cruz BM;Ding Y;McInerney V;Krawczyk J;Lu Y;Yang G;Qian X;Li W;Howard L;Allen NM;O'Brien T;Gallagher L;Shen S; (2020) 'Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A)'. Stem Cell Research, 44 [DOI] [Details] |
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(2020) | 'A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability'
Benson, KA;White, M;Allen, NM;Byrne, S;Carton, R;Comerford, E;Costello, D;Doherty, C;Dunleavey, B;El-Naggar, H;Gangadharan, N;Heavin, S;Kearney, H;Lench, NJ;Lynch, J;McCormack, M;O'Regan, M;Podesta, K;Power, K;Rogers, AS;Steward, CA;Sweeney, B;Webb, D;Fitzsimons, M;Greally, M;Delanty, N;Cavalleri, GL (2020) 'A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability'. European Journal Of Human Genetics, [DOI] [Details] |
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(2020) | 'Genetic potassium channel-associated epilepsies: Clinical review of the Kv family'
Allen NM;Weckhuysen S;Gorman K;King MD;Lerche H; (2020) 'Genetic potassium channel-associated epilepsies: Clinical review of the Kv family'. European Journal Of Paediatric Neurology, 24 [DOI] [Details] |
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(2020) | 'Identification of a novel cystic fibrosis mutation in three patients of South Asian descent'
Semple, A;Clark, T;Allen, NM;Krishnananthan, T;Nwokoro, C;Girodon, E;Porzio, M;Herzig, M (2020) 'Identification of a novel cystic fibrosis mutation in three patients of South Asian descent'. The Clinical Respiratory Journal, 14 :586-588 [DOI] [Details] |
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(2020) | 'Catatonia as a feature of down syndrome: An under-recognised entity?'
Lyons, A,Allen, NM,Flanagan, O,Cahalane, D (2020) 'Catatonia as a feature of down syndrome: An under-recognised entity?'. European Journal Of Paediatric Neurology, 25 :187-190 [DOI] [Details] |
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(2020) | 'Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C)'
Arbini A;Gilmore J;King MD;Gorman KM;Krawczyk J;McInerney V;O'Brien T;Shen S;Allen NM; (2020) 'Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C)'. Stem Cell Research, 46 [DOI] [Details] |
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(2020) | 'Acute Necrotizing Encephalopathy (ANE) Triggered by Influenza'
Julia C. Morrison, Rebecca Finnegan, Aoife Cleary, Eilish Twomey, Nicholas M. Allen (2020) 'Acute Necrotizing Encephalopathy (ANE) Triggered by Influenza'. American Journal Of Neuroradiology, [Details] |
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(2019) | 'Journal club: old tricks and fresh approaches'
McGlacken-Byrne SM;O'Rahelly M;Cantillon P;Allen NM; (2019) 'Journal club: old tricks and fresh approaches'. Archives Of Disease In Childhood-Education And Practice Edition, [DOI] [Details] |
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(2018) | 'Cost of exome sequencing in epileptic encephalopathy: is it 'worth it'?'
Forman, E. B.,Gorman, K. M.,Conroy, J.,Arthur, N.,Grant, C.,Ennis, S.,Allen, N. M.,Lynch, S. A.,King, M. D. (2018) 'Cost of exome sequencing in epileptic encephalopathy: is it 'worth it'?'. Arch Dis ChildArch Dis Child, 103 (33) [Details] |
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(2018) | 'Interferonopathies in laboratory-negative suspected congenital infection'
Forman, E. B.,King, M. D.,Allen, N. M. (2018) 'Interferonopathies in laboratory-negative suspected congenital infection'. Lancet Infect DisLancet Infect Dis, 18 (11) [Details] |
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(2018) | 'Neck-Tongue Syndrome: An Underrecognized Childhood Onset Cephalalgia'
Allen, NM,Dafsari, HS,Wraige, E,Jungbluth, H (2018) 'Neck-Tongue Syndrome: An Underrecognized Childhood Onset Cephalalgia'. Journal of child neurology, 33 :347-350 [DOI] [Details] |
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(2018) | 'Status dystonicus due to missense variant in ARX: Diagnosis and management'
Gorman, KM,Cary, H,Gaffney, L,Forman, E,Waldron, D,Al-Delami, F,Lynch, BJ,King, MD,Allen, NM (2018) 'Status dystonicus due to missense variant in ARX: Diagnosis and management'. European Journal Of Paediatric Neurology, 22 :862-865 [DOI] [Details] |
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(2018) | 'Unusual Presentations of Dystrophinopathies in Childhood'
Allen, NM,Ewer, A,Nakou, V,Konstantoulaki, E,Wraige, E,Gowda, V,Jungbluth, H (2018) 'Unusual Presentations of Dystrophinopathies in Childhood'. Pediatrics, 141 :510-514 [DOI] [Details] |
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(2018) | 'Rethinking status dystonicus: A welcome start to a challenging problem'
Lumsden, D. E.,Allen, N. M. (2018) 'Rethinking status dystonicus: A welcome start to a challenging problem'. Mov DisordMov Disord, 33 (22) [Details] |
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(2017) | '2015-2016 Influenza Season in an Irish Regional Paediatric Unit: Importance of Influenza Vaccination Highlighted'
Ryan, G.,Cleary, A.,Keady, D.,Allen, N. M.,Moylett, E. (2017) '2015-2016 Influenza Season in an Irish Regional Paediatric Unit: Importance of Influenza Vaccination Highlighted'. Ir Med J, 110 (77) [Details] |
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(2017) | 'Novel SMC1A variant and epilepsy of infancy with migrating focal seizures: Expansion of the phenotype'
Gorman, K. M.,Forman, E.,Conroy, J.,Allen, N. M.,Shahwan, A.,Lynch, S. A.,Ennis, S.,King, M. D. (2017) 'Novel SMC1A variant and epilepsy of infancy with migrating focal seizures: Expansion of the phenotype'. EpilepsiaEpilepsia, 58 (77):1301-1302 [Details] |
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(2017) | 'Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies'
Masnada, S.,Hedrich, U. B. S.,Gardella, E.,Schubert, J.,Kaiwar, C.,Klee, E. W.,Lanpher, B. C.,Gavrilova, R. H.,Synofzik, M.,Bast, T.,Gorman, K.,King, M. D.,Allen, N. M.,Conroy, J.,Ben Zeev, B.,Tzadok, M.,Korff, C.,Dubois, F.,Ramsey, K.,Narayanan, V.,Serratosa, J. M.,Giraldez, B. G.,Helbig, I.,Marsh, E.,O'Brien, M.,Bergqvist, C. A.,Binelli, A.,Porter, B.,Zaeyen, E.,Horovitz, D. D.,Wolff, M.,Marjanovic, D.,Caglayan, H. S.,Arslan, M.,Pena, S. D. J.,Sisodiya, S. M.,Balestrini, S.,Syrbe, S.,Veggiotti, P.,Lemke, J. R.,Moller, R. S.,Lerche, H.,Rubboli, G. (2017) 'Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies'. BrainBrain, 140 (99):2337-2354 [Details] |
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(2017) | 'Novel COL4A2 variant in a large pedigree: Consequences and dilemmas'
McGovern, M.,Flanagan, O.,Lynch, B.,Lynch, S. A.,Allen, N. M. (2017) 'Novel COL4A2 variant in a large pedigree: Consequences and dilemmas'. Clin GenetClin Genet, 92 (44):447-448 [Details] |
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(2017) | 'Activated Platelets Induce Endothelial Cell Activation via an Interleukin-1beta Pathway in Systemic Lupus Erythematosus'
Nhek, S.,Clancy, R.,Lee, K. A.,Allen, N. M.,Barrett, T. J.,Marcantoni, E.,Nwaukoni, J.,Rasmussen, S.,Rubin, M.,Newman, J. D.,Buyon, J. P.,Berger, J. S. (2017) 'Activated Platelets Induce Endothelial Cell Activation via an Interleukin-1beta Pathway in Systemic Lupus Erythematosus'. Arterioscler Thromb Vasc BiolArterioscler Thromb Vasc Biol, 37 (44):707-716 [Details] |
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(2017) | 'Status dystonicus in childhood'
Lumsden, DE;King, MD;Allen, NM (2017) 'Status dystonicus in childhood'. Current opinion in pediatrics, 29 :674-682 [DOI] [Details] |
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(2016) | 'Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder'
Allen, NM,Conroy, J,Deonna, T,McCreary, D,McGettigan, P,Madigan, C,Carter, I,Ennis, S,Lynch, SA,Shahwan, A,King, MD (2016) 'Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder'. Epilepsy & Behavior Case Reports, 6 :42-48 [DOI] [Details] |
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(2016) | 'NAPB - a novel SNARE-associated protein for early-onset epileptic encephalopathy'
Conroy, J.,Allen, N. M.,Gorman, K. M.,Shahwan, A.,Ennis, S.,Lynch, S. A.,King, M. D. (2016) 'NAPB - a novel SNARE-associated protein for early-onset epileptic encephalopathy'. Clin GenetClin Genet, 89 (22) [Details] |
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(2016) | 'Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion'
Allen, N. M.,Conroy, J.,Shahwan, A.,Lynch, B.,Correa, R. G.,Pena, S. D.,McCreary, D.,Magalhaes, T. R.,Ennis, S.,Lynch, S. A.,King, M. D. (2016) 'Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion'. EpilepsiaEpilepsia, 57 (11) [Details] |
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(2016) | 'Salbutamol-responsive fetal acetylcholine receptor inactivation syndrome'
Allen, N. M.,Hacohen, Y.,Palace, J.,Beeson, D.,Vincent, A.,Jungbluth, H. (2016) 'Salbutamol-responsive fetal acetylcholine receptor inactivation syndrome'. NeurologyNeurology, 86 (77):692-4 [Details] |
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(2016) | 'Lyme Neuroborreliosis: A Potentially Preventable Cause of Stroke'
Allen, N. M.,Jungbluth, H. (2016) 'Lyme Neuroborreliosis: A Potentially Preventable Cause of Stroke'. J PediatrJ Pediatr, 170 [Details] |
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(2016) | 'Novel European SLC1A4 variant: infantile spasms and population ancestry analysis'
Conroy, J,Allen, NM,Gorman, K,O'Halloran, E,Shahwan, A,Lynch, B,Lynch, SA,Ennis, S,King, MD (2016) 'Novel European SLC1A4 variant: infantile spasms and population ancestry analysis'. Journal Of Human Genetics, 61 :761-764 [DOI] [Details] |
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(2015) | 'Sydenham's chorea: not gone but perhaps forgotten'
Crealey, M.,Allen, N. M.,Webb, D.,Bouldin, A.,Mc Sweeney, N.,Peake, D.,Tirupathi, S.,Butler, K.,King, M. D. (2015) 'Sydenham's chorea: not gone but perhaps forgotten'. Arch Dis ChildArch Dis Child, 100 (1212):1160-2 [Details] |
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(2015) | 'Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort'
Allen, N. M.,Conroy, J.,Shahwan, A.,Ennis, S.,Lynch, B.,Lynch, S. A.,King, M. D. (2015) 'Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort'. Eur J Paediatr NeurolEur J Paediatr Neurol, 19 (44):390-4 [Details] |
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(2015) | 'Clinical Reasoning: Juvenile neurocognitive decline: A snaky diagnosis'
Allen, N. M.,Shahwan, A.,Madigan, C.,Nestor, T.,King, M. D. (2015) 'Clinical Reasoning: Juvenile neurocognitive decline: A snaky diagnosis'. NeurologyNeurology, 85 (2222) [Details] |
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(2015) | 'The Bhutani Nomogram Reduces Incidence of Severe Hyperbilirubinaemia in Term and Near Term Infants'
O'Reilly, P.,Walsh, O.,Allen, N. M.,Corcoran, J. D. (2015) 'The Bhutani Nomogram Reduces Incidence of Severe Hyperbilirubinaemia in Term and Near Term Infants'. Ir Med JIr Med J, 108 (66):181-2 [Details] |
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(2014) | 'Status dystonicus: a practice guide'
Allen, N. M.,Lin, J. P.,Lynch, T.,King, M. D. (2014) 'Status dystonicus: a practice guide'. Dev Med Child NeurolDev Med Child Neurol, 56 (22):105-12 [Details] |
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(2014) | 'The variable phenotypes of KCNQ-related epilepsy'
Allen, N. M.,Mannion, M.,Conroy, J.,Lynch, S. A.,Shahwan, A.,Lynch, B.,King, M. D. (2014) 'The variable phenotypes of KCNQ-related epilepsy'. EpilepsiaEpilepsia, 55 (99) [Details] |
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(2014) | 'Explosive onset non-epileptic jerks and profound hypotonia in an infant with Alpers-Huttenlocher syndrome'
Allen, N. M.,Winter, T.,Shahwan, A.,King, M. D. (2014) 'Explosive onset non-epileptic jerks and profound hypotonia in an infant with Alpers-Huttenlocher syndrome'. SeizureSeizure, 23 (33):237-9 [Details] |
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(2014) | 'De Novo Interstitial Deletion 2q14.1q22.1: Is There a Recognizable Phenotype?'
Greally, MT,Robinson, E,Allen, NM,O'Donovan, D,Crolla, JA (2014) 'De Novo Interstitial Deletion 2q14.1q22.1: Is There a Recognizable Phenotype?'. American Journal Of Medical Genetics Part A, 164 :3194-3202 [DOI] [Details] |
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(2014) | 'Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms--a further patient'
Allen, N. M.,Conroy, J.,Shahwan, A.,Ennis, S.,Lynch, B.,Lynch, S. A.,King, M. D. (2014) 'Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms--a further patient'. Am J Med Genet AAm J Med Genet A, 164a (77):1863-6 [Details] |
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(2013) | 'Not all twitching is epileptic! Hand myoclonus in a boy with spinal cord tumor'
Allen, N. M.,Moran, M. M.,King, M. D. (2013) 'Not all twitching is epileptic! Hand myoclonus in a boy with spinal cord tumor'. J PediatrJ Pediatr, 162 (22):431-4310 [Details] |
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(2012) | 'Limbic encephalitis in a boy with N-methyl-D-aspartate receptor antibodies'
Allen, N. M.,Lynch, B.,Twomey, E. (2012) 'Limbic encephalitis in a boy with N-methyl-D-aspartate receptor antibodies'. J PediatrJ Pediatr, 160 (66) [Details] |
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(2012) | 'Excessive blinking and ataxia in a child with occult neuroblastoma and voltage-gated potassium channel antibodies'
Allen, N. M.,McKeon, A.,O'Rourke, D. J.,O'Meara, A.,King, M. D. (2012) 'Excessive blinking and ataxia in a child with occult neuroblastoma and voltage-gated potassium channel antibodies'. PediatricsPediatrics, 129 (55) [Details] |
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(2012) | 'Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion'
Allen, N. M.,O'HIci, B.,Anderson, G.,Nestor, T.,Lynch, S. A.,King, M. D. (2012) 'Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion'. Clin GenetClin Genet, 81 (66):602-4 [Details] |
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(2011) | 'Transcutaneous bilirubin - comparing the accuracy of BiliChek (R) and JM 103 (R) in a regional postnatal unit'
Qualter, YM,Allen, NM,Corcoran, JD,O'Donovan, DJ (2011) 'Transcutaneous bilirubin - comparing the accuracy of BiliChek (R) and JM 103 (R) in a regional postnatal unit'. Journal Of Maternal-Fetal & Neonatal Medicine, 24 :267-270 [DOI] [Details] |
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(2011) | 'Stiff neonate with mitochondrial DNA depletion and secondary neurotransmitter defects'
Moran, M. M.,Allen, N. M.,Treacy, E. P.,King, M. D. (2011) 'Stiff neonate with mitochondrial DNA depletion and secondary neurotransmitter defects'. Pediatr NeurolPediatr Neurol, 45 (66):403-5 [Details] |
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(2011) | 'Idiopathic Ventricular Tachycardia in a Newborn: Immediate Response to Lidocaine'
Allen, NM,Azam, M,Dunne, KP,Walsh, KP (2011) 'Idiopathic Ventricular Tachycardia in a Newborn: Immediate Response to Lidocaine'. Pediatric Cardiology, 32 :706-707 [DOI] [Details] |
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(2011) | 'Neonatal therapeutic hypothermia: practice and opinions in the Republic of Ireland'
Allen, NM,Foran, A,O'Donovan, DJ (2011) 'Neonatal therapeutic hypothermia: practice and opinions in the Republic of Ireland'. Archives Of Disease In Childhood-Fetal And Neonatal Edition, 96 :233-233 [DOI] [Details] |
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(2011) | 'Is neonatal group B streptococcal infection preventable?'
Azam, M.,Allen, N. M.,O'Donovan, D.,Moylett, E. (2011) 'Is neonatal group B streptococcal infection preventable?'. Ir Med J, 104 (55):149-51 [Details] |
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(2010) | 'Images in neonatal medicine. Benign tonic downgaze of infancy'
Allen, N. M.,Tibussek, D.,Borusiak, P.,King, M. D. (2010) 'Images in neonatal medicine. Benign tonic downgaze of infancy'. Arch Dis Child Fetal Neonatal EdArch Dis Child Fetal Neonatal Ed, 95 (55) [Details] |
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(2010) | 'Initial assessment of jaundice in otherwise healthy infants--a comparison of methods in two postnatal units'
Allen, N. M.,O'Donnell, S. M.,White, M. J.,Corcoran, J. D. (2010) 'Initial assessment of jaundice in otherwise healthy infants--a comparison of methods in two postnatal units'. Ir Med JIr Med J, 103 (1010):310-3 [Details] |
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(2010) | 'Traumatic delivery, diaphragmatic paresis, and dextrocardia'
Allen, N. M.,Clarke, T.,Ryan, S. P.,Farombi-Oghuvbu, I. (2010) 'Traumatic delivery, diaphragmatic paresis, and dextrocardia'. J PediatrJ Pediatr, 156 (66) [Details] |
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(2009) | 'Severe hyperbilirubinaemia and kernicterus: more caution is needed in newborn jaundice surveillance'
Allen, N. M.,Mohammad, F.,Foran, A.,Corcoran, D.,Clarke, T. (2009) 'Severe hyperbilirubinaemia and kernicterus: more caution is needed in newborn jaundice surveillance'. Ir Med JIr Med J, 102 (77):228-9 [Details] |
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(2007) | 'Foam eater'
Allen, NM;O'Donovan, DJ (2007) 'Foam eater'. Journal Of Pediatrics, 151 :710-710 [DOI] [Details] |
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(2007) | 'Expression and function of protease-activated receptor 4 in human myometrium'
Allen NM, O'Brien M, Friel AM, Smith TJ, Morrison JJ (2007) 'Expression and function of protease-activated receptor 4 in human myometrium'. American Journal Of Obstetrics And Gynecology, 196 (2):1690-1696 [DOI] [Details] |
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(2005) | 'Screening for haemoglobinopathy--a comparison of two methods in an Irish maternity unit'
Allen NM, Ni Riain M, Murray M, Hession M. (2005) 'Screening for haemoglobinopathy--a comparison of two methods in an Irish maternity unit'. Ir Med J, 98 (9):276-278 [Details] |
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(2004) | 'Thrombin and PAR1-activating peptide: effects on human uterine contractility in vitro'
O'Sullivan CJ, Allen NM, O'Loughlin AJ, Friel AM, Morrison JJ (2004) 'Thrombin and PAR1-activating peptide: effects on human uterine contractility in vitro'. American Journal Of Obstetrics And Gynecology, 190 (4):1098-1105 [DOI] [Details] |
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(2004) | 'PAR-4 modulation and thrombin in human pregnant myometrium'
Allen, NM,Friel, AM,Morrison, JJ (2004) 'PAR-4 modulation and thrombin in human pregnant myometrium'. American Journal Of Obstetrics & Gynaecology, :322-323 [Details] |
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(2004) | 'Thrombin and PAR-1 agonism: Effects on human uterine contractility in vitro'
O'Sullivan, C. J., Allen, N. M., O'Loughlin, A. J., Friel, A. M. & Morrison, J. J. (2004) 'Thrombin and PAR-1 agonism: Effects on human uterine contractility in vitro'. American Journal of Obstetrics & Gynaecology, 190 :1098-1105 [Details] |
Professional Associations
Association | Function | From / To | |
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ILAE | Member | / | |
ICNA | member | / | |
BPNA | Member | / |
Teaching Interests
Internal Collaborators
Name | Description of Collaboration | |
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See Research Interests |