Bilateral posterior cerebral artery infarction

od Ryan, Davinia, Murphy, Sinead M, Hennessey, Michael J
Izdano 2010

An unusual cause of cavernous sinus syndrome

od Smyth, Andrew, Murphy, Sinead M, Counihan, Timothy J
Izdano 2009

Unintended Effects of Orphan Product Designation for Rare Neurological Diseases

od Murphy, Sinéad M, Puwanant, Araya, Griggs, Robert C.
Izdano 2012

Mutation in FAM134B causing severe hereditary sensory neuropathy

od Murphy, Sinead M, Davidson, Gabrielle L, Brandner, Sebastian, Houlden, Henry, Reilly, Mary M
Izdano 2010

Anoctamin 10‐Related Autosomal Recessive Cerebellar Ataxia: Comprehensive Clinical Phenotyping of an Irish Sibship

od Bogdanova‐Mihaylova, Petya, Austin, Neil, Alexander, Michael D., Cassidy, Lorraine, Early, Anne, Murphy, Raymond P., Murphy, Sinéad M., Walsh, Richard A.
izdano v Mov Disord Clin Pract (2016)

Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene

od Rossor, Alexander M., Morrow, Jasper M., Polke, James M., Murphy, Sinead M., Houlden, Henry, Laura, Matilde, Manji, Hadi, Blake, Julian, Reilly, Mary M.
izdano v Neuromuscul Disord (2017)

Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2

od Murphy, Sinéad M., Ernst, Daniela, Wei, Yu, Laurà, Matilde, Liu, Yo-Tsen, Polke, James, Blake, Julian, Winer, John, Houlden, Henry, Hornemann, Thorsten, Reilly, Mary M.
Izdano 2013

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

od Murphy, Sinéad M., Ovens, Richard, Polke, James, Siskind, Carly E., Laurà, Matilde, Bull, Karen, Ramdharry, Gita, Houlden, Henry, Murphy, Raymond P.J., Shy, Michael E., Reilly, Mary M.
Izdano 2012

Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland

od Bansagi, Boglarka, Antoniadi, Thalia, Burton-Jones, Sarah, Murphy, Sinead M., McHugh, John, Alexander, Michael, Wells, Richard, Davies, Joanna, Hilton-Jones, David, Lochmüller, Hanns, Chinnery, Patrick, Horvath, Rita
izdano v J Neurol (2015)

Novel HSAN1 Mutation in Serine Palmitoyltransferase Resides at a Putative Phosphorylation Site That Is Involved in Regulating Substrate Specificity

od Ernst, Daniela, Murphy, Sinéad M., Sathiyanadan, Karthik, Wei, Yu, Othman, Alaa, Laurá, Matilde, Liu, Yo-Tsen, Penno, Anke, Blake, Julian, Donaghy, Michael, Houlden, Henry, Reilly, Mary M., Hornemann, Thorsten
izdano v Neuromolecular Med (2015)

A novel locus for episodic ataxia:UBR4 the likely candidate

od Conroy, Judith, McGettigan, Paul, Murphy, Raymond, Webb, David, Murphy, Sinéad M, McCoy, Blathnaid, Albertyn, Christine, McCreary, Dara, McDonagh, Cara, Walsh, Orla, Lynch, SallyAnn, Ennis, Sean
Izdano 2014

Anti Ma2-associated myeloradiculopathy: expanding the phenotype of anti-Ma2 associated paraneoplastic syndromes

od Murphy, Sinead M, Khan, Usman, Alifrangis, Constantine, Hazell, Steven, Hrouda, David, Blake, Julian, Ball, Joanna, Gabriel, Carolyn, Markarian, Pierre, Rees, Jeremy, Karim, Abid, Seckl, Michael J, Lunn, Michael P, Reilly, Mary M
Izdano 2011

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

od Murphy, Sinead M., Laura, Matilde, Fawcett, Katherine, Pandraud, Amelie, Liu, Yo-Tsen, Davidson, Gabrielle L, Rossor, Alexander M, Polke, James M, Castleman, Victoria, Manji, Hadi, Lunn, Michael P T, Bull, Karen, Ramdharry, Gita, Davis, Mary, Blake, Julian C, Houlden, Henry, Reilly, Mary M
Izdano 2012

Simultaneous assessment of plaque morphology, cerebral micro-embolic signal status and platelet biomarkers in patients with recently symptomatic and asymptomatic carotid stenosis

od Murphy, Stephen J, Lim, Soon T, Kinsella, Justin A, Tierney, Sean, Egan, Bridget, Feeley, Tim M, Dooley, Clare, Kelly, James, Murphy, Sinead M, Walsh, Richard A, Collins, Ronan, Coughlan, Tara, O’Neill, Desmond, Harbison, Joseph A, Madhavan, Prakash, O’Neill, Sean M, Colgan, Mary P, Meaney, Jim F, Hamilton, George, McCabe, Dominick JH
izdano v J Cereb Blood Flow Metab (2019)

Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease

od Pitceathly, Robert D.S., Murphy, Sinéad M., Cottenie, Ellen, Chalasani, Annapurna, Sweeney, Mary G., Woodward, Cathy, Mudanohwo, Ese E., Hargreaves, Iain, Heales, Simon, Land, John, Holton, Janice L., Houlden, Henry, Blake, Julian, Champion, Michael, Flinter, Frances, Robb, Stephanie A., Page, Rupert, Rose, Michael, Palace, Jacqueline, Crowe, Carol, Longman, Cheryl, Lunn, Michael P., Rahman, Shamima, Reilly, Mary M., Hanna, Michael G.
Izdano 2012

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

od Rossor, Alexander M., Oates, Emily C., Salter, Hannah K., Liu, Yang, Murphy, Sinead M., Schule, Rebecca, Gonzalez, Michael A., Scoto, Mariacristina, Phadke, Rahul, Sewry, Caroline A., Houlden, Henry, Jordanova, Albena, Tournev, Iyailo, Chamova, Teodora, Litvinenko, Ivan, Zuchner, Stephan, Herrmann, David N., Blake, Julian, Sowden, Janet E., Acsadi, Gyuda, Rodriguez, Michael L., Menezes, Manoj P., Clarke, Nigel F., Auer Grumbach, Michaela, Bullock, Simon L., Muntoni, Francesco, Reilly, Mary M., North, Kathryn N.
izdano v Brain (2015)

Reply: The p.Ser107Leu in BICD2 is a mutation ‘hot spot’ causing distal spinal muscular atrophy

od Rossor, Alexander M., Oates, Emily C., Salter, Hannah K., Liu, Yang, Murphy, Sinead M., Schule, Rebecca, Gonzales, Michael A., Scoto, Mariacristina, Phadke, Rahul, Sewry, Caroline A., Houlden, Henry, Jordanova, Albena, Tournev, Iyailo, Chamova, Teodora, Litvinenko, Ivan, Zuchner, Stephan, Herrmann, David N., Blake, Julian, Sowden, Janet E., Acsadi, Gyuda, Rodriguez, Michael L., Menezes, Manoj P., Clarke, Nigel F., Auer Grumbach, Michaela, Bullock, Simon L., Muntoni, Francesco, Reilly, Mary M., North, Kathryn N.
izdano v Brain (2015)

Transcriptional regulator PRDM12 is essential for human pain perception

od Chen, Ya-Chun, Auer-Grumbach, Michaela, Matsukawa, Shinya, Zitzelsberger, Manuela, Themistocleous, Andreas C, Strom, Tim M, Samara, Chrysanthi, Moore, Adrian W, Cho, Lily Ting-Yin, Young, Gareth T, Weiss, Caecilia, Schabhüttl, Maria, Stucka, Rolf, Schmid, Annina B, Parman, Yesim, Graul-Neumann, Luitgard, Heinritz, Wolfram, Passarge, Eberhard, Watson, Rosemarie M, Hertz, Jens Michael, Moog, Ute, Baumgartner, Manuela, Valente, Enza Maria, Pereira, Diego, Restrepo, Carlos M, Katona, Istvan, Dusl, Marina, Stendel, Claudia, Wieland, Thomas, Stafford, Fay, Reimann, Frank, von Au, Katja, Finke, Christian, Willems, Patrick J, Nahorski, Michael S, Shaikh, Samiha S, Carvalho, Ofélia P, Nicholas, Adeline K, Karbani, Gulshan, McAleer, Maeve A, Cilio, Maria Roberta, McHugh, John C, Murphy, Sinead M, Irvine, Alan D, Jensen, Uffe Birk, Windhager, Reinhard, Weis, Joachim, Bergmann, Carsten, Rautenstrauss, Bernd, Baets, Jonathan, De Jonghe, Peter, Reilly, Mary M, Kropatsch, Regina, Kurth, Ingo, Chrast, Roman, Michiue, Tatsuo, Bennett, David L H, Woods, C Geoffrey, Senderek, Jan
izdano v Nat Genet (2015)