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Results: 1-11 |
Results: 11
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
Authors: Van Goethem, G Dermaut, B Lofgren, A Martin, JJ Van Broeckhoven, C
Citation: G. Van Goethem et al., Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions, NAT GENET, 28(3), 2001, pp. 211-212
Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy
Authors: Ceuterick-de Groote, C De Jonghe, P Timmerman, V Van Goethem, G Lofgren, A Ceulemans, B Van Broeckhoven, C Martin, JJ
Citation: C. Ceuterick-de Groote et al., Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy, PATH RES PR, 197(3), 2001, pp. 193-198
Euratom Framework Programme research in reactor safety: main achievements of FP-4 ('94-'98), preliminary results of FP-5 ('98-'02) and prospects for beyond 2002
Authors: Van Goethem, G Zurita, A Bermejo, JM Lemaitre, P
Citation: G. Van Goethem et al., Euratom Framework Programme research in reactor safety: main achievements of FP-4 ('94-'98), preliminary results of FP-5 ('98-'02) and prospects for beyond 2002, NUCL ENG DE, 209(1-3), 2001, pp. 1-22
Main achievements of FP-4 research in reactor safety
Authors: Van Goethem, G Zurita, A Bermejo, JM Lemaitre, P Bischoff, H
Citation: G. Van Goethem et al., Main achievements of FP-4 research in reactor safety, NUCL ENG DE, 209(1-3), 2001, pp. 29-37
Euratom framework programme research in reactor safety
Authors: Van Goethem, G Zurita, A Bermejo, JM Lemaitre, P
Citation: G. Van Goethem et al., Euratom framework programme research in reactor safety, ATW-INT Z K, 45(12), 2000, pp. 728
Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism
Authors: Devriendt, K Keymolen, K Roelen, L Van Goethem, G Meireleire, J Fryns, JP
Citation: K. Devriendt et al., Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism, CLIN DYSMOR, 9(2), 2000, pp. 111-114
Novel syndromic form of X-linked complicated spastic paraplegia
Authors: Claes, S Devriendt, K Van Goethem, G Roelen, L Meireleire, J Raeymaekers, P Cassiman, JJ Fryns, JP
Citation: S. Claes et al., Novel syndromic form of X-linked complicated spastic paraplegia, AM J MED G, 94(1), 2000, pp. 1-4
EC-sponsored research activities on innovative passive safety systems
Authors: Bermejo, JM Van Goethem, G
Citation: Jm. Bermejo et G. Van Goethem, EC-sponsored research activities on innovative passive safety systems, NUCL ENG DE, 201(1), 2000, pp. 25-40
Further evidence for genetic heterogeneity of autosomal dominant disorderswith accumulation of multiple deletions of mitochondrial DNA
Authors: Van Goethem, G Lofgren, A Martin, JJ Van Broeckhoven, C
Citation: G. Van Goethem et al., Further evidence for genetic heterogeneity of autosomal dominant disorderswith accumulation of multiple deletions of mitochondrial DNA, J MED GENET, 37(7), 2000, pp. 547-548
Fatal encephalitis caused by Mycoplasma pneumoniae diagnosed by the polymerase chain reaction
Authors: Ieven, M Demey, H Ursi, D Van Goethem, G Cras, P Goossens, H
Citation: M. Ieven et al., Fatal encephalitis caused by Mycoplasma pneumoniae diagnosed by the polymerase chain reaction, CLIN INF D, 27(6), 1998, pp. 1552-1553
Zygodactyly as the most striking physical anomaly in an adult male patientwith pure partial trisomy 1q.
Authors: Lukusa, T Van Buggenhout, G Devriendt, K Meireleire, J Van Goethem, G Roelen, L Fryns, JP
Citation: T. Lukusa et al., Zygodactyly as the most striking physical anomaly in an adult male patientwith pure partial trisomy 1q., ANN GENET, 41(4), 1998, pp. 199-204
Risultati: 1-11 |