A Larbrisseau
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Explore the profile of A Larbrisseau including associated specialties, affiliations and a list of published articles.
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Articles
29
Citations
298
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Recent Articles
1.
Dermer E, Spahr A, Tran L, Mirchi A, Pelletier F, Guerrero K, et al.
J Child Neurol
. 2020 Jul;
35(13):901-907.
PMID: 32720856
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...
2.
Boulanger J, Larbrisseau A
Can J Neurol Sci
. 2005 Jul;
32(2):225-31.
PMID: 16018159
Background: To date, few pediatric series of neurofibromatosis type 1 (NF-1) have been described in the literature even though it is the most frequently encountered phakomatosis. Methods: We reviewed 987...
3.
Roddier K, Thomas T, Marleau G, Gagnon A, Dicaire M, St-Denis A, et al.
Neurology
. 2005 May;
64(10):1762-7.
PMID: 15911806
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...
4.
Lanthier S, Carmant L, David M, Larbrisseau A, de Veber G
Neurology
. 2000 Feb;
54(2):371-8.
PMID: 10668698
Objective: To characterize the risk factors for stroke in children and their relationship to outcomes. Methods: We reviewed charts of children with ischemic and hemorrhagic stroke seen at Hopital Sainte-Justine,...
5.
Proulx F, Weber M, Collu R, Lelievre M, Larbrisseau A, Delisle M
Eur J Pediatr
. 1993 Jun;
152(6):526-9.
PMID: 7687546
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...
6.
Roux A, Mercier C, Larbrisseau A, Dube L, Dupuis C, del Carpio R
J Neurosurg
. 1992 Mar;
76(3):528-33.
PMID: 1738035
Epidermoid cysts are tumors familiar to neurosurgeons, but intramedullary epidermoid cysts are rare. The authors report the case of a 6-year-old girl presenting with progressive paraparesis. A midthoracic intramedullary mass...
7.
Mitchell G, Larochelle J, Lambert M, Michaud J, Grenier A, Ogier H, et al.
N Engl J Med
. 1990 Feb;
322(7):432-7.
PMID: 2153931
Hereditary tyrosinemia results from an inborn error in the final step of tyrosine metabolism. The disease is known to cause acute and chronic liver failure, renal Fanconi's syndrome, and hepatocellular...
8.
Huot C, Gauthier M, Lebel M, Larbrisseau A
Can J Neurol Sci
. 1987 Aug;
14(3):290-3.
PMID: 3117346
Two children born with birth defects after intrauterine exposure to valproic acid are reported. The mothers took the drug throughout pregnancy as sole treatment for primary generalized epilepsy. The first...
9.
Yazbeck S, Larbrisseau A, ORegan S
J Urol
. 1985 Oct;
134(4):720-1.
PMID: 2993677
We report 2 cases of cadaveric renal transplantation in which the grafts were placed in the right iliac fossa. Postoperatively, both patients complained of ipsilateral thigh weakness. Electromyography and nerve...
10.
Vanasse M, Masson P, Geoffroy G, Larbrisseau A, David P
Can J Neurol Sci
. 1984 Aug;
11(3):377-9.
PMID: 6467089
Intermittent oral or rectal administration of diazepam for the prophylactic treatment of febrile convulsions has given results comparable to the continuous use of phenobarbital while limiting side effects and risks...