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Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular GeneticsV. TIMMERMAN; J. BEUTEN; J. IROBI; P. De JONGHE; J.-J. MARTIN; C. VAN BROECKHOVEN · 1999
108. Genetic heterogeneity of distal hereditary motor neuropathy type IIS. Lee; S. Moon; C. Ki · 2009
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeVincent Timmerman; Peter Raeymaekers; Eva Nelis; Peter De Jonghe; Ludo Muylle; Chantal Ceuterick; Jean-Jacques Martin; Christine Van Broeckhoven · 1992
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3J. IROBI; E. NELIS; J. MEULEMAN; K. VENKEN; P. DE JONGHE; C. VAN BROECKHOVEN; V. TIMMERMAN · 2001
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3Joy Irobi; Eva Nelis; Kristien Verhoeven; Els De Vriendt; Ines Dierick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman · 2002
A Clone Contig of 12q24.3 Encompassing the Distal Hereditary Motor Neuropathy Type II GeneJoy Irobi; Fadel Tissir; Peter De Jonghe; Els De Vriendt; Christine Van Broeckhoven; Vincent Timmerman; Joke Beuten · 2000
A CLONE CONTIG OF 12Q24.3 ENCOMPASSING THE DISTAL HEREDITARY MOTOR NEUROPATHY TYPE II GENEJ Irobi; F Tissir; P De Jonghe; E De Vriendt; C Van Broeckhoven; V Timmerman; J. Beuten · 2000
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegiaN Ivanova; A Löfgren; I Tournev; R Rousev; A Andreeva; A Jordanova; V Georgieva; T Deconinck; V Timmerman; I Kremensky; P De Jonghe; V Mitev · 2006
Promising riboflavin treatment for motor neuron disorderTimmerman, V.; De Jonghe, P. · Brain · 2014
Storage and retrieval of slides and angiogramsSiertsema, J. V.; Blanksma, L. J.; Timmerman, Z. · Journal of Visual Communication in Medicine · 1980
Andermann Syndrome in a Turkish PatientDemir, E.; Irobi, J.; Erdem, S.; Demirci, M.; Tan, E.; Timmerman, V.; De Jonghe, P.; Topaloglu, H. · Journal of Child Neurology · 2003
Clinical gene panel in UNIFE patients orphans of genetic diagnosisNeri, M.; Selvatici, R.; Scotton, C.; Storbeck, M.; Vezyroglou, K.; Heller, R.; Tugnoli, V.; Bigoni, S.; Timmerman, V.; Wirth, B.; De, D.; Gualandi, F.; Ferlini, A. · Neuromuscular Disorders · 2017
G.P.237Peeters, K.; Litvinenko, I.; Chamova, T.; Asselbergh, B.; Almeida-Souza, L.; Geuens, T.; Ydens, E.; Zimon, M.; Irobi, J.; Vriendt, E. De; Winter, V. De; Ooms, T.; Timmerman, V.; Tournev, I.; Jordanova, A. · Neuromuscular Disorders · 2014
Autosomal dominant burning feet syndromeStogbauer, F.; Young, P.; Kuhlenbaumer, G.; Kiefer, R.; Timmerman, V.; Ringelstein, E B.; Wang, J.-F.; Schroder, J M.; Van Broeckhoven, C.; Weis, J. · Journal of Neurology, Neurosurgery & Psychiatry · 1999
455 – Antibiomania, acute manic psychosis following the use of antibioticsKlain, V.; Timmerman, L. · European Psychiatry · 2013
Replication timing of the human genomeWoodfine, K. · Human Molecular Genetics · 2003
Chromosome painting: a useful artRied, T · Human Molecular Genetics · 1998
Molecular pathogenesis of Parkinson's diseaseGandhi, S. · Human Molecular Genetics · 2005
Gene therapy for leukodystrophiesBiffi, A.; Aubourg, P.; Cartier, N. · Human Molecular Genetics · 2011
Epigenetic reprogramming in mammalsMorgan, H. D. · Human Molecular Genetics · 2005
The evolving epigenomeWeichenhan, D.; Plass, C. · Human Molecular Genetics · 2013
Susceptibility genes for complex epilepsyMulley, J. C. · Human Molecular Genetics · 2005
Mouse ENU MutagenesisJustice, M. J. · Human Molecular Genetics · 1999