Peter De Jonghe
Antwerp University Hospital(BE)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurological diseases and metabolism, Neurogenetic and Muscular Disorders Research, Mitochondrial Function and Pathology
Most-Cited Works
- → Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia(2012)129 cited
- Charcot-Marie-Tooth disease and related peripheral neuropathies.(1997)
- → A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21(2001)73 cited
- → Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1(2001)67 cited
- → Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree(1992)41 cited
- → Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations(1997)33 cited
- → Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous(2001)25 cited
- → Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy(1988)10 cited
- → Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24(1997)4 cited
- → A CLONE CONTIG OF 12Q24.3 ENCOMPASSING THE DISTAL HEREDITARY MOTOR NEUROPATHY TYPE II GENE(2000)1 cited