Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michelle Nourallah"'
Autor:
Rosalind H.M. King, David Chandler, Sash Lopaticki, Dexing Huang, Julian Blake, John R. Muddle, Trevor Kilpatrick, Michelle Nourallah, Toshiyuki Miyata, Tomohiko Okuda, Kim W. Carter, Michael Hunter, Dora Angelicheva, Grant Morahan, Luba Kalaydjieva
Publikováno v:
Neurobiology of Disease, Vol 42, Iss 3, Pp 368-380 (2011)
CMT4D disease is a severe autosomal recessive demyelinating neuropathy with extensive axonal loss leading to early disability, caused by mutations in the N-myc downstream regulated gene 1 (NDRG1). NDRG1 is expressed at particularly high levels in the
Externí odkaz:
https://doaj.org/article/025929e759604c54813529023ccc2f1a
Autor:
Rosalind H.M. King, J. R. Muddle, Anneloor L.M.A. ten Asbroek, Camiel Verhamme, R. A. Wolterman, Michelle Nourallah, Ivo N. van Schaik, Frank Baas
Publikováno v:
Journal of neuropathology and experimental neurology, 70(5), 386-398. Lippincott Williams and Wilkins
We analyzed clinical and pathological disease in 2 peripheral myelin protein-22 (PMP22) overexpressing mouse models for 1.5 years. C22 mice have 7 and C3-PMP mice have 3 to 4 copies of the human PMP22 gene. C3-PMP mice showed no overt clinical signs
Autor:
Tomohiko Okuda, Dexing Huang, Rosalind H.M. King, Trevor J. Kilpatrick, Julian Blake, Kim W. Carter, David Chandler, Luba Kalaydjieva, Grant Morahan, Michael Hunter, J. R. Muddle, Sash Lopaticki, Dora Angelicheva, Toshiyuki Miyata, Michelle Nourallah
Publikováno v:
Neurobiology of Disease, Vol 42, Iss 3, Pp 368-380 (2011)
CMT4D disease is a severe autosomal recessive demyelinating neuropathy with extensive axonal loss leading to early disability, caused by mutations in the N-myc downstream regulated gene 1 (NDRG1). NDRG1 is expressed at particularly high levels in the
Autor:
J. R. Muddle, Dora Angelicheva, Constantin Lupu, Axinia Corches, Brian Youl, Tamara Rogers, Michelle Nourallah, Luba Kalaydjieva, Velina Guergueltcheva, Jaume Colomer, Ivailo Tournev, P. K. Thomas, Alex Shmarov, Luciano Merlini, Rosalind H.M. King, Gabriela Popa
Publikováno v:
Annals of neurology. 50(4)
A novel peripheral neuropathy of autosomal recessive inheritance has been identified in Balkan Gypsies and termed hereditary motor and sensory neuropathy-Russe (HMSN-R). We investigated 21 affected individuals from 10 families. Distal lower limb weak