Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Herman Willekens"'
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 101, Iss 1 (2017)
We present a case of a 2-year-old boy with chronic suppurative osteomyelitis of the left jaw. A computed tomography (CT) scan demonstrated a periosteal reaction on the left side of the mandible with cortical destruction of the left mandibular head. T
Externí odkaz:
https://doaj.org/article/5590151a33de4a77bdb0f870fd01fed5
Publikováno v:
Journal of child neurology
Severe myoclonic epilepsy in infancy, or Dravet syndrome, is one of the catastrophic epilepsy syndromes. In the past, treatment was mainly based on valproate and phenobarbital. Recently, some of the new antiepilepsy drugs, such as topiramate and stir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e05942ea5fc63ef5b6c19e3c232967d2
https://pubmed.ncbi.nlm.nih.gov/15526956
https://pubmed.ncbi.nlm.nih.gov/15526956
Autor:
J. Gheuens, Berten Ceulemans, I. Buntinx, Bernadette Van Roy, Jan E. Dumon, Franki Speleman, Patrick Willems, Marie-Noëlle Van Thienen, Nadine Van Roy, Herman Willekens, Kathelijne Mangelschots, Joke Beuten
Publikováno v:
Human genetics
We describe two female siblings with similar clinical features consisting of hydrocephalus, scaphocephaly, hypotonia, mongoloid eye slant, blepharophimosis, micrognathia, supernumerary mouth frenula and mental retardation. Routine cytogenetic studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e1dfea979f2b57fe963b39b66f03a17
https://pubmed.ncbi.nlm.nih.gov/1352272
https://pubmed.ncbi.nlm.nih.gov/1352272
Publikováno v:
Pediatric Research. 24:266-266
Two daughters of related Turkish parents were investigated at the ages of 11 8/12 and 16 8/12 years for severe neurologic disease. This was characterised by pronounced psychomotor retardation, ataxia, dysmetria, dystonia and choreiform movements. Bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acc5d78d38af7fe6791735a65d68dffe
https://doi.org/10.1203/00006450-198808000-00060
https://doi.org/10.1203/00006450-198808000-00060