V. van Gerwen

发表

A method for quantifying limbal stem cell niches using OCT imaging

Sorcha Ní Dhubhghaill, Nadia Zakaria, J. Rozema, 2017, British Journal of Ophthalmology.

Proteomic analysis of posterior capsular plaques in congenital unilateral cataract

K. Laukens, G. Baggerman, K. Schildermans, 2018, Acta ophthalmologica.

The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V.

N. Verpoorten, V. Timmerman, P. de Jonghe, 2004, Brain : a journal of neurology.

Mutations in GDAP1

C. van Broeckhoven, F. Palau, V. Timmerman, 2002, Neurology.

Immunohistochemical characteristics of the vitreolenticular interface in congenital unilateral posterior cataract

J. Timmermans, M. Tassignon, V. van Gerwen, 2016, Journal of cataract and refractive surgery.

Mutations in GDAP1: Autosomal recessive CMT with demyelination and axonopathy

C. van Broeckhoven, F. Palau, V. Timmerman, 2002 .

Pterygium Pathology: A Prospective Case-Control Study on Tear Film Cytokine Levels

E. Roelant, J. Rozema, M. Tassignon, 2019, Mediators of inflammation.

Limbal Stem Cell Deficiency: Current Treatment Options and Emerging Therapies

M. Tassignon, M. Haagdorens, V. van Gerwen, 2015, Stem cells international.

Corneal epithelial restoration after penetrating keratoplasty in repeated failed cultivated limbal stem cell grafts

M. Tassignon, J. Behaegel, V. van Gerwen, 2019, Journal of EuCornea.

A Rapid Method for Simultaneous Detection of Phenotypic Resistance to Inhibitors of Protease and Reverse Transcriptase in Recombinant Human Immunodeficiency Virus Type 1 Isolates from Patients Treated with Antiretroviral Drugs

Brendan Larder, Stuart Bloor, Frank Peeters, 1998, Antimicrobial Agents and Chemotherapy.

The importance of the epithelial fibre cell interface to lens regeneration in an in vivo rat model and in a human bag-in-the-lens (BiL) sample.

S. Richards, A. Prescott, N. Lois, 2021, Experimental eye research.

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.

H. Hartung, D. Fitzpatrick, N. Verpoorten, 2003, American journal of human genetics.

Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10.

D. Huylebroeck, N. Verpoorten, K. Verhoeven, 2003, American journal of human genetics.

SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I

J. Martín, K. Verhoeven, V. Timmerman, 2004, Neurology.

Xeno-Free Cultivation of Mesenchymal Stem Cells From the Corneal Stroma.

V. van Gerwen, S. Ní Dhubhghaill, N. Zakaria, 2017, Investigative ophthalmology & visual science.

Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

O. Combarros, N. Verpoorten, V. Timmerman, 2004, Journal of Medical Genetics.

Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene

S. Züchner, Y. Parman, E. Battaloğlu, 2004, Neurology.

Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?

H. Hartung, V. Timmerman, B. Plecko, 2002, Brain : a journal of neurology.

Limbal Stem Cell Deficiency: Current Treatment Options and Emerging Therapies

M. Tassignon, M. Haagdorens, V. van Gerwen, 2015, Stem cells international.

Belgian Endothelial Surgical Transplant of the Cornea (BEST cornea) protocol: clinical and patient-reported outcomes of Ultra-Thin Descemet Stripping Automated Endothelial Keratoplasty (UT-DSAEK) versus Descemet Membrane Endothelial Keratoplasty (DMEK) – a multicentric, randomised, parallel group pr

V. van Gerwen, S. Ní Dhubhghaill, R. Wisse, 2023, BMJ Open.

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.

H. Hartung, D. Fitzpatrick, N. Verpoorten, 2003, American journal of human genetics.