Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Larbrisseau, A."'
Publikováno v:
In Pediatric Neurology July 2016 60:24-29
Autor:
Aaron Spahr, E. Malvey-Dorn, S. Chandratre, F Pelletier, B. Osterman, M. Desmeules, G. Roedde, Marie Emmanuelle Dilenge, S. Chenier, Albert Larbrisseau, P. Marois, A Mirchi, Luan Tran, Elsa Rossignol, K. Y. Lim, Nancy Braverman, E. Dermer, Michael Shevell, J. Reggin, Mark A. Tarnopolsky, Guillaume Sébire, J. Laflamme, Kether Guerrero, Catalina Maftei, Geneviève Legault, Soad M. Ahmed, Sunita Venkateswaran, Daniela Pohl, Daniela Buhas, Philippe Major, I. Paradis, John J. Mitchell, Geneviève Bernard, M. Sullivan, Bernard Brais, Nicolas Chrestian, Myriam Srour, Michel Sylvain, EM Riou, A. Nadeau
Publikováno v:
Journal of Child Neurology. 35:901-907
Genetically determined leukoencephalopathies comprise a group of rare inherited white matter disorders. The majority are progressive diseases resulting in early death. We performed a cross-sectional pilot study including 55 parents from 36 families t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f960a9c3c06818684c86c6b2dd83c196
https://doi.org/10.1177/0883073820938645
https://doi.org/10.1177/0883073820938645
Autor:
Albert L. Larbrisseau
Publikováno v:
The Medical Treatment of Epilepsy ISBN: 9781003066736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2b25b35f8205ec1cb0eab51901a2564
https://doi.org/10.1201/9781003066736-39
https://doi.org/10.1201/9781003066736-39
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Philippe Major, Lionel Carmant, Albert Larbrisseau, Anne Lortie, Paola Diadori, Elsa Rossignol, Ala Birca, Guy D'Anjou, Sébastien Perreault, Michel Vanasse, Jean-François Toupin
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 17(4)
Lacosamide is an antiepileptic drug approved for the treatment of focal epilepsy in adult patients. The aim of this observational study was to review our centre's experience with lacosamide and to characterize its effectiveness and tolerability as an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06f1392a909af4afee581f84a28675f7
https://pubmed.ncbi.nlm.nih.gov/26609635
https://pubmed.ncbi.nlm.nih.gov/26609635
Publikováno v:
International Journal of Production Research; Jun96, Vol. 34 Issue 6, p1603, 21p
Autor:
T. Thomas, A. M. Gagnon, M. Lambert, Bernard Brais, Guy A. Rouleau, Albert Larbrisseau, Michel Vanasse, G. Marleau, I. Gosselin, A. M. Sarrazin, A. St-Denis, Marie-Josée Dicaire, D. Gaudet, K. Roddier
Publikováno v:
Neurology. 64:1762-1767
Background: Hereditary sensory and autonomic neuropathy type 2 (HSAN2; MIM 201300) is a rare recessive neuropathy typically diagnosed in the first decade. The 1973 study of a French Canadian family led to the definition of HSAN2. Objectives: To demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a59a411b65641b9e6e2158a016f991b
https://doi.org/10.1212/01.wnl.0000161849.29944.43
https://doi.org/10.1212/01.wnl.0000161849.29944.43
Publikováno v:
International Journal of Production Research. 34:1603-1623
This paper presents a method to generate 3-axis NC programs for rough milling processes, when the free-form surface is modelled parametrically by dual kriging. This general and powerful interpolation technique presents several advantages, since it in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e2d2c42c3a8f990cc0f8d313cc49194
https://doi.org/10.1080/00207549608904986
https://doi.org/10.1080/00207549608904986
Publikováno v:
Pediatric Neurology. 60:24-29.e1
Background The first sign of neurofibromatosis type 1 (NF1) in a child is often the presence of multiple cafe-au-lait macules. Although previous studies reported that almost individuals with multiple cafe-au-lait macules will eventually develop NF1 b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6a528857f6b4d84b82b45e3586bc89
https://doi.org/10.1016/j.pediatrneurol.2016.03.003
https://doi.org/10.1016/j.pediatrneurol.2016.03.003
Publikováno v:
European Journal of Pediatrics. 152:526-529
We report the case of a 9-year-old girl with multiple problems due to hypothalamic dysfunction of obscure origin: apnoeic spells, behavioural problems, developmental delay, hypodipsia with bouts of hypernatraemia, episodes of spontaneous hypothermia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef2a326160c11c8c9da9f398342ac140
https://doi.org/10.1007/bf01955066
https://doi.org/10.1007/bf01955066