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30 in total

Review 1. Schwann cells as a therapeutic target for peripheral neuropathies.

Authors: Helmar C Lehmann; Ahmet Höke
Journal: CNS Neurol Disord Drug Targets Date: 2010-12 Impact factor: 4.388

Review 2. The proteolipid protein gene: double, double, ... and trouble.

Authors: M E Hodes; S R Dlouhy
Journal: Am J Hum Genet Date: 1996-07 Impact factor: 11.025

3. Peripheral myelin protein 22 is a constituent of intercellular junctions in epithelia.

Authors: L Notterpek; K J Roux; S A Amici; A Yazdanpour; C Rahner; B S Fletcher
Journal: Proc Natl Acad Sci U S A Date: 2001-11-20 Impact factor: 11.205

4. Connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease show two distinct behaviors: loss of function and altered gating properties.

Authors: C Ressot; D Gomès; A Dautigny; D Pham-Dinh; R Bruzzone
Journal: J Neurosci Date: 1998-06-01 Impact factor: 6.167

5. Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin.

Authors: D D'Urso; P Ehrhardt; H W Müller
Journal: J Neurosci Date: 1999-05-01 Impact factor: 6.167

Review 6. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.

Authors: Axel Niemann; Philipp Berger; Ueli Suter
Journal: Neuromolecular Med Date: 2006 Impact factor: 3.843

7. Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy.

Authors: K Adlkofer; R Frei; D H Neuberg; J Zielasek; K V Toyka; U Suter
Journal: J Neurosci Date: 1997-06-15 Impact factor: 6.167

Biology and genetics of hereditary motor and sensory neuropathies.