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Nicholson(G A),Yeung(L),Corbett(A) Neurology 1998-12-03

...PMP22, Po, or connexin 32) should be screened for mutations.,The yield of connexin 32 mutations was compared in possible...

Pareyson(D),Solari(A),Taroni(F),Botti(S),F... Muscle Nerve 1998-12-23

...PMP22) gene. We tried to identify criteria distinguishing HNPP among patients with acute painless mononeuropathy/plexopa...

Gabriel(C M),Hughes(R A),Moore(S E),Smith(... Brain 1998-11-20

...PMP22), the gene for which is duplicated in hereditary motor sensory neuropathy type la, can also induce EAN. PMP22 cDNA...

Hagen(K),Boman(H),Mellgren(S I),Lindal(S),... Arch Neurol 1998-12-01

...PMP22 (17q), APP (21q), CMTX1 (Xq), or PLP (Xq).,Progressive central and peripheral demyelinating disease seems to be a ...

Murakami(T),Sun(Z S),Lee(C C),Lupski(J R) Genomics 1997-03-31

...PMP22), which lies within the critical region. To identify additional genes rapidly, we used a cosmid contig of this reg...

Nelis(E),Warner(L E),Vriendt(E D),Chance(P... Eur J Hum Genet 1997-05-28

...PMP22, MPZ and Cx32. In total, 21 samples showed 13 distinct altered migration patterns by one or both methods. Ten alte...

Marrosu(M G),Vaccargiu(S),Marrosu(G),Vanne... Neurology 1997-03-26

...PMP22, predicted to determine a valine for glycine substitution at codon 107, which could be plotted in the center of th...

Young(P),Wiebusch(H),Stögbauer(F),Ringelst... Neurology 1997-03-26

Peripheral myelin protein PMP22 deficiency is associated with hereditary neuropathy with liability to pressure palsies (...

Zoidl(G),D'Urso(D),Blass-Kampmann(S),Schma... Cell Tissue Res 1997-04-10

...PMP22 is as a negative growth modulator. We have investigated the influence of rat PMP22 (rPMP22) and a mutant of PMP22 ...

Zlotogora(J) Am J Med Genet 1997-04-25

...PMP22 and further over-expression lead to a more severe disorder. In diseases in which the mutation leads to an abnormal...