Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons
Schapira, Anthony H. V., Cleeter, Michael W. J., Muddle, John R., Workman, Jane M., Cooper, J. Mark, King, Rosalind H. M.
Published in Annals of neurology (01.08.2006)
Published in Annals of neurology (01.08.2006)
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Journal Article
A novel RAB7 mutation associated with ulcero-mutilating neuropathy
Houlden, Henry, King, Rosalind H. M., Muddle, John R., Warner, Thomas T., Reilly, Mary M., Orrell, Richard W., Ginsberg, Lionel
Published in Annals of neurology (01.10.2004)
Published in Annals of neurology (01.10.2004)
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Journal Article
High Incidence of Spontaneous Disease in an HLA-DR15 and TCR Transgenic Multiple Sclerosis Model
Ellmerich, Stephan, Mycko, Marcin, Takacs, Katalin, Waldner, Hanspeter, Wahid, Faisal N, Boyton, Rosemary J, King, Rosalind H. M, Smith, Paul A, Amor, Sandra, Herlihy, Amy H, Hewitt, Rachel E, Jutton, Mark, Price, David A, Hafler, David A, Kuchroo, Vijay K, Altmann, Daniel M
Published in The Journal of immunology (1950) (15.02.2005)
Published in The Journal of immunology (1950) (15.02.2005)
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Journal Article
Coexistent hereditary and inflammatory neuropathy
Ginsberg, Lionel, Malik, Omar, Kenton, Anthony R., Sharp, David, Muddle, John R., Davis, Mary B., Winer, John B., Orrell, Richard W., King, Rosalind H. M.
Published in Brain (London, England : 1878) (01.01.2004)
Published in Brain (London, England : 1878) (01.01.2004)
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Journal Article
Ndrg1 in development and maintenance of the myelin sheath
King, Rosalind H.M, Chandler, David, Lopaticki, Sash, Huang, Dexing, Blake, Julian, Muddle, John R, Kilpatrick, Trevor, Nourallah, Michelle, Miyata, Toshiyuki, Okuda, Tomohiko, Carter, Kim W, Hunter, Michael, Angelicheva, Dora, Morahan, Grant, Kalaydjieva, Luba
Published in Neurobiology of disease (01.06.2011)
Published in Neurobiology of disease (01.06.2011)
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Journal Article
The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy
Houlden, Henry, Laura, Matilde, Ginsberg, Lionel, Jungbluth, Heinz, Robb, Stephanie A, Blake, Julian, Robinson, Susan, King, Rosalind H.M, Reilly, Mary M
Published in Neuromuscular disorders : NMD (01.04.2009)
Published in Neuromuscular disorders : NMD (01.04.2009)
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Journal Article
The phagocytic capacity of neurones
Bowen, Samantha, Ateh, Davidson D., Deinhardt, Katrin, Bird, Margaret M., Price, Karen M., Baker, Cathy S., Robson, Joanna C., Swash, Michael, Shamsuddin, Wassim, Kawar, Shalini, El-Tawil, Tariq, Roos, Jesper, Hoyle, Andrew, Nickols, Carole D., Knowles, Charles H., Pullen, Anthony H., Luthert, Phillip J., Weller, Roy O., Hafezparast, Majid, Franklin, Robin J. M., Revesz, Tamas, King, Rosalind H. M., Berninghausen, Otto, Fisher, Elizabeth M. C., Schiavo, Giampietro, Martin, Joanne E.
Published in The European journal of neuroscience (01.05.2007)
Published in The European journal of neuroscience (01.05.2007)
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Journal Article
Increased axonal ribosome numbers in CMT diseases
Verheijen, Mark H. G., Lammens, Martin, Ceuterick-de Groote, Chantal, Timmerman, Vincent, De Jonghe, Peter, King, Rosalind H. M., Smit, August B., van Minnen, Jan
Published in Journal of the peripheral nervous system (01.03.2011)
Published in Journal of the peripheral nervous system (01.03.2011)
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Journal Article
Myelin and Axon Pathology in a Long-Term Study of PMP22-Overexpressing Mice
Verhamme, Camiel, King, Rosalind H.M, ten Asbroek, Anneloor L.M.A, Muddle, John R, Nourallah, Michelle, Wolterman, Ruud, Baas, Frank, van Schaik, Ivo N
Published in Journal of neuropathology and experimental neurology (01.05.2011)
Published in Journal of neuropathology and experimental neurology (01.05.2011)
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Journal Article
YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit
Cemal, Cemal K., Carroll, Christopher J., Lawrence, Lorraine, Lowrie, Margaret B., Ruddle, Piers, Al-Mahdawi, Sahar, King, Rosalind H.M., Pook, Mark A., Huxley, Clare, Chamberlain, Susan
Published in Human molecular genetics (01.05.2002)
Published in Human molecular genetics (01.05.2002)
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Journal Article
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2
Colomer, Jaume, Gooding, Rebecca, Angelicheva, Dora, King, Rosalind H.M., Guillén-Navarro, Encarna, Parman, Yesim, Nascimento, Andres, Conill, Joan, Kalaydjieva, Luba
Published in Neuromuscular disorders : NMD (01.07.2006)
Published in Neuromuscular disorders : NMD (01.07.2006)
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Journal Article
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve
Previtali, Stefano C., Zerega, Barbara, Sherman, Diane L., Brophy, Peter J., Dina, Giorgia, King, Rosalind H.M., Salih, Mustafa M., Feltri, Laura, Quattrini, Angelo, Ravazzolo, Roberto, Wrabetz, Lawrence, Monaco, Anthony P., Bolino, Alessandra
Published in Human molecular genetics (15.07.2003)
Published in Human molecular genetics (15.07.2003)
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Journal Article
Hereditary motor and sensory neuropathy-russe: New autosomal recessive neuropathy in balkan gypsies
Thomas, P. K., Kalaydjieva, Luba, Youl, Brian, Rogers, Tamara, Angelicheva, Dora, King, Rosalind H. M., Guergueltcheva, Velina, Colomer, Jaume, Lupu, Constantin, Corches, Axinia, Popa, Gabriela, Merlini, Luciano, Shmarov, Alex, Muddle, John R., Nourallah, Michelle, Tournev, Ivailo
Published in Annals of neurology (01.10.2001)
Published in Annals of neurology (01.10.2001)
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Journal Article
The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D [version 1; peer review: 3 approved]
Chandler, David, Lopaticki, Sash, Huang, Dexing, Hunter, Michael, Angelicheva, Dora, Kilpatrick, Trevor, King, Rosalind HM, Kalaydjieva, Luba, Morahan, Grant
Published in F1000 research (2013)
Published in F1000 research (2013)
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Journal Article
N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom
Kalaydjieva, Luba, Gresham, David, Gooding, Rebecca, Heather, Lisa, Baas, Frank, de Jonge, Rosalein, Blechschmidt, Karin, Angelicheva, Dora, Chandler, David, Worsley, Penelope, Rosenthal, Andre, King, Rosalind H.M., Thomas, P.K.
Published in American journal of human genetics (01.07.2000)
Published in American journal of human genetics (01.07.2000)
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