C. Wetzburger

发表

Le suivi systématique des grands prématurés Systematic follow-up of infants born preterm

A. Aeby, P. Bogaert, V. Wermenbol, 2015 .

Postinfectious immune-mediated encephalitis after pediatric herpes simplex encephalitis

B. Dan, C. Christophe, X. Tiège, 2005, Brain and Development.

Acquired auditory agnosia in childhood and normal sleep electroencephalography subsequently diagnosed as Landau–Kleffner syndrome: a report of three cases

P. Paquier, P. van Bogaert, M. King, 2013, Developmental medicine and child neurology.

Gray matter heterotopia and acute necrotizing encephalopathy in trichothiodystrophy.

M. Abramowicz, P. van Bogaert, H. Szliwowski, 1998, Pediatric neurology.

Perisylvian dysgenesis. Clinical, EEG, MRI and glucose metabolism features in 10 patients.

T Metens, S Goldman, H B Szliwowski, 1998, Brain : a journal of neurology.

Critical evaluation of lung scintigraphy in cystic fibrosis: study of 113 patients.

D. Machin, H. Ham, A. Piepsz, 1980, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Levetiracetam Efficacy in Epileptic Syndromes with Continuous Spikes and Waves during Slow Sleep: Experience in 12 Cases

Denis Verheulpen, Patrick Van Bogaert, Alec Aeby, 2005, Epilepsia.

Regional cerebral glucose metabolism in epilepsies with continuous spikes and waves during sleep

Steven Laureys, P. Paquier, I. Jambaqué, 2004, Neurology.

Uncommon Leber “Plus” Disease Associated With Mitochondrial Mutation m.11778G>A in a Premature Child

V. Benoit, I. Maystadt, F. Meire, 2014, Journal of child neurology.

Mental retardation with blepharo‐naso‐facial abnormalities and hand malformations: a new syndrome?

Y. Gillerot, A. Verloes, L. Maldergem, 1992, Clinical genetics.

The geneticist and the so-called "socio cultural" familial mental retardation.

Y. Gillerot, L. Koulischer, C. Wetzburger, 1989, Journal de genetique humaine.