Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lada Cindro Heberle"'
Autor:
Jamila K. Abdulla, Musuwadi S. Gopinath, Asma A. Al-Tawari, Lada Cindro-Heberle, David Neubauer
Publikováno v:
Journal of Pediatric Neurology. :257-260
Neurocysticercosis is the most common parasitic central nervous system disease and the major cause of epilepsy in non-Muslim developing countries. Cases also occur in non-endemic regions reflecting pattern of immigration from highly endemic areas. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7d56830477823dfbb960baf49105b27
https://doi.org/10.1055/s-0035-1557338
https://doi.org/10.1055/s-0035-1557338
Autor:
Delphine Trochet, Yanick J. Crow, Graziella Pinto, Isabelle Desguerre, Othman A Abou Shenab, Loïc de Pontual, Pierre Bougnères, Blandine Esteva, Steve Cunningham, Ha Trang, Magdy Helmy Shafik, Christian Straus, Lada Cindro Heberle, Michel Polak, Juliane Léger, Stanislas Lyonnet, Arnold Munnich, Jeanne Amiel, Sophie Caillat-Zucman
Publikováno v:
Pediatric Research. 64:689-694
Late Onset Central Hypoventilation Syndrome associated with Hypothalamic Dysfunction (LO-CHS/HD) is a distinct entity among the clinical and genetic heterogeneous group of patients with late onset central hypoventilation. Here we report a series of 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d7e3e52c686212e5b154b3f0e6ba576
https://doi.org/10.1203/pdr.0b013e318187dd0e
https://doi.org/10.1203/pdr.0b013e318187dd0e
Publikováno v:
European Journal of Paediatric Neurology. 21:e81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca7470df7dd52e7718dde5dd86326e42
https://doi.org/10.1016/j.ejpn.2017.04.1278
https://doi.org/10.1016/j.ejpn.2017.04.1278
Publikováno v:
Pediatric neurology. 51(4)
Background Microcephaly-capillary malformation syndrome is a newly described neurocutaneous entity that is characterized by congenital and progressive microcephaly, intractable epilepsy, profound developmental delay, multiple small capillary malforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::380d4de253f279f42fa2bc3286773146
https://pubmed.ncbi.nlm.nih.gov/25266620
https://pubmed.ncbi.nlm.nih.gov/25266620
Publikováno v:
Braindevelopment. 28(5)
Ethylmalonic encephalopathy is a rare metabolic disease presenting in infancy with developmental delay, acrocyanosis, petechiae, chronic diarrhea and early death. The biochemical characteristics of this autosomal recessive disease are urinary organic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02025b4269c8b327c2aad2ab62955e6d
https://pubmed.ncbi.nlm.nih.gov/16376514
https://pubmed.ncbi.nlm.nih.gov/16376514
Publikováno v:
Developmental Medicine & Child Neurology. 47:504-504
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::905c4fd217db5120f5d631cae40ed5ee
https://doi.org/10.1017/s0012162205000988
https://doi.org/10.1017/s0012162205000988
Publikováno v:
Developmental Medicine & Child Neurology; Jul2005, Vol. 47 Issue 7, p504-504, 1p