skip to main content
Primo Advanced Search
Advanced search    Note: Search terms must be in lower case
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search prefilters
Date range searching is not available for Article, Issue and Archived Website records; nor does it work for Audio records.

Results 1 - 10 of 11  for Everything in this catalogue

results 1 2 next page
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Material Type:
Article
Add to My workspace

DRG Neuron/Schwann Cells Myelinating Cocultures

Taveggia, Carla; Bolino, Alessandra

Methods in molecular biology. Volume 1791 (2018); pp 115-130

Check library holdings

2
Material Type:
Article
Add to My workspace

A novel homozygous mutation in the MTMR2 gene in two siblings with 'hypermyelinating neuropathy'

Luigetti, Marco et al.

Journal of the peripheral nervous system: JPNS. Volume 18:Issue 2 (2013); pp 192-194 -- John Wiley & Sons

Online access

3
Material Type:
Article
Add to My workspace

A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2

Scarlato, Marina et al.

Journal of the peripheral nervous system: JPNS. Volume 20:Issue 4 (2015); pp 419-421 -- John Wiley & Sons

Online access

4
Material Type:
Article
Add to My workspace

Meeting Report: 2013 Peripheral Nerve Society Biennial Meeting, Saint‐Malo, France, June 29–July 3, 2013

Nobile‐Orazio, Eduardo et al.

Journal of the peripheral nervous system: JPNS. Volume 18:Issue 3 (2013); pp 197-198 -- John Wiley & Sons

Online access

5
Material Type:
Article
Add to My workspace

Vocal cord paralysis in Charcot–Marie–Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature

Zambon, Alberto Andrea et al.

NEUROMUSCULAR DISORDERS -- Volume: 27 5; (pages 487-491) -- 2017

Online access

6
Material Type:
Article
Add to My workspace

Vocal cord paralysis in Charcot–Marie–Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature

Zambon, Alberto Andrea et al.

NEUROMUSCULAR DISORDERS. Volume 27:Issue 5 (2017); pp 487-491

Online access

7
Material Type:
Article
Add to My workspace

Niacin‐mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination

Bolino, Alessandra et al.

EMBO molecular medicine. Volume 8:Issue 12 (2016); pp 1438-1454 -- Wiley Europe

Online access

8
Material Type:
Article
Add to My workspace

A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs)

Pareyson, Davide et al.

Annals of neurology. Volume 86:Issue 1 (2019); pp 55-67 -- John Wiley & Sons

Online access

9
Material Type:
Article
Add to My workspace

A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs)

Pareyson, Davide et al.

Annals of neurology. Volume 86:Issue 1 (2019); pp 55-67 -- John Wiley & Sons

Online access

10
Material Type:
Article
Add to My workspace

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Klionsky, Daniel J et al.

Autophagy. Volume 12:Issue 1 (2016, January); pp 1-222 -- Taylor & Francis

Online access

Results 1 - 10 of 11  for Everything in this catalogue

results 1 2 next page

Refine Search Results

Creation date 

From To
  1. Before2015  (2)
  2. 2015To2015  (1)
  3. 2016To2016  (3)
  4. 2017To2018  (3)
  5. After 2018  (2)
  6. Refine further open sub menu

Additional Features 

  1. Abstract  (5)
  2. No Abstract  (6)
  3. Refine further open sub menu

Searching Remote Databases, Please Wait