References of "Misson, Jean-Paul"
     in
Bookmark and Share    
Full Text
Peer Reviewed
See detailManagement of diffuse glioma in children: a retrospective study of 27 cases and review of literature
Piette, Caroline ULg; Deprez, Manuel; Born, Jacques et al

in Acta Neurologica Belgica (2008), 108

Gliomas are the most common CNS tumours in children and present either as circumscribed tumours or diffusely infiltrative neoplasms. Diffuse gliomas develop both in the cerebral hemispheres and the ... [more ▼]

Gliomas are the most common CNS tumours in children and present either as circumscribed tumours or diffusely infiltrative neoplasms. Diffuse gliomas develop both in the cerebral hemispheres and the brainstem and have a poor prognosis. Guidelines for the therapy of these tumours are still debated. In this study, we reviewed the clinical features of 27 consecutive patients with diffuse gliomas admitted to the Department of Paediatrics of CHR Citadelle, University of Liège, between 1985 and 2005. We review their clinical presentation, diagnosis, treatment and outcome with reference to the published literature. [less ▲]

Detailed reference viewed: 28 (1 ULg)
Full Text
Peer Reviewed
See detailManagement of diffuse glioma in children: a retrospective study of 27 cases and review of literature.
Piette, Caroline ULg; Deprez, Manuel ULg; Born, Jacques et al

in Acta Neurologica Belgica (2008), 108(2), 35-43

Gliomas are the most common CNS tumours in children and present either as circumscribed tumours or diffusely infiltrative neoplasms. Diffuse gliomas develop both in the cerebral hemispheres and the ... [more ▼]

Gliomas are the most common CNS tumours in children and present either as circumscribed tumours or diffusely infiltrative neoplasms. Diffuse gliomas develop both in the cerebral hemispheres and the brainstem and have a poor prognosis. Guidelines for the therapy of these tumours are still debated. In this study, we reviewed the clinical features of 27 consecutive patients with diffuse gliomas admitted to the Department of Paediatrics of CHR Citadelle, University of Liege, between 1985 and 2005. We review their clinical presentation, diagnosis, treatment and outcome with reference to the published literature. [less ▲]

Detailed reference viewed: 85 (12 ULg)
See detailUrgences Pédiatriques
Carvelli, Thierry ULg; Viellevoye, Renaud ULg; Misson, Jean-Paul ULg

Book published by Université de Liège (2008)

Detailed reference viewed: 99 (8 ULg)
Full Text
Peer Reviewed
See detailPrise en charge du médulloblastome de l'enfant
Fransolet, A. C.; Born, J. D.; Misson, Jean-Paul ULg et al

in Revue Médicale de Liège (2007), 62(4), 200-4

We present the experience of the Citadelle Hospital (Liege, B) in the diagnosis, treatment and follow-up of medulloblastoma in children. A retrospective study of 10 cases of medulloblastoma was performed ... [more ▼]

We present the experience of the Citadelle Hospital (Liege, B) in the diagnosis, treatment and follow-up of medulloblastoma in children. A retrospective study of 10 cases of medulloblastoma was performed. Five years after diagnosis, the event-free survival was 77%. [less ▲]

Detailed reference viewed: 166 (2 ULg)
Full Text
Peer Reviewed
See detailActualites therapeutiques en neuropediatrie
Leroy, Patricia; Dubru, Jean-Marie ULg; Misson, Jean-Paul ULg

in Revue Médicale de Liège (2007), 62(5-6, May-Jun), 449-450

The most recent antiepileptic drugs used in children are lamotrigine, topiramate, oxcarbamaz6pine and levetiracetam. Their efficacy is proven, depending on the type of crisis, but in Belgium they are ... [more ▼]

The most recent antiepileptic drugs used in children are lamotrigine, topiramate, oxcarbamaz6pine and levetiracetam. Their efficacy is proven, depending on the type of crisis, but in Belgium they are reimbursed only in certain conditions. The treatment of children with attention deficit hyperactivity disorder (ADHD), which was only constituted of methylphenidate, can now benefit from atomoxetine whose mechanism of action is different. [less ▲]

Detailed reference viewed: 294 (6 ULg)
Full Text
Peer Reviewed
See detailIntoxication au CO: Mouvements athétosiques
Mohring, M.-P.; Dadoumont, Caroline ULg; Daron, A. et al

in Journal de Pédiatrie belge (2007)

Detailed reference viewed: 37 (3 ULg)
Full Text
Peer Reviewed
See detailEpilepsie chez des enfants infirmes moteurs-cérébraux
Peduzzi, M.; Defontaine, E.; Misson, Jean-Paul ULg

in Revue Médicale de Liège (2006), 61(4), 237-239

The incidence of epilepsy in 110 patients with cerebral palsy (the majority with spastic tetraplegia) was 46,4%. Almost half of the patients with spastic tetraplegia (45%) and hemiplegia (52%) had ... [more ▼]

The incidence of epilepsy in 110 patients with cerebral palsy (the majority with spastic tetraplegia) was 46,4%. Almost half of the patients with spastic tetraplegia (45%) and hemiplegia (52%) had epilepsy. The incidence was lower in patients with spastic diplegia (32%). Half of epilepsy in spastic hemiplegia were partial seizures and the other half consisted of generalized seizures, while generalized tonic-clonic episodes predominated in all other forms of C.P. A high incidence of West syndrome was observed in patients with spastic tetraplegia. Etiological factors of C.P. were perinatal in 75%. 16,65% had neonatal antecedents of convulsions; most of them had spastic tetraplegia (75%) and a significant mental retardation. A low intelligence quotient (I.Q.) was seen in most of the children with epilepsy, and patients with tetraplegia had significantly lower intelligence quotient than other groups. [less ▲]

Detailed reference viewed: 190 (13 ULg)
Full Text
Peer Reviewed
See detailLe syndrome de Prader Willi: intérêt d'une prise en charge pluridisciplinaire
Salmon, C.; Gaillez, Stephanie ULg; Pieltain, Catherine ULg et al

in Revue Médicale de Liège (2006), 61(7-8, Jul-Aug), 593-599

Prader Willi syndrome can be viewed as a physiopathological model of obesity. Such patients deserve specific management, preferably in a multidisciplinary setting. The paper reports on 6 patients followed ... [more ▼]

Prader Willi syndrome can be viewed as a physiopathological model of obesity. Such patients deserve specific management, preferably in a multidisciplinary setting. The paper reports on 6 patients followed in the paediatric endocrine service at the University of Liege. [less ▲]

Detailed reference viewed: 164 (12 ULg)
Full Text
Peer Reviewed
See detailMigraine specificities during childhood to adulthood: diagnosis and treatment
de Tourtchaninoff, M.; Misson, Jean-Paul ULg

in Acta Neurologica Belgica (2006)

Detailed reference viewed: 24 (0 ULg)
Full Text
Peer Reviewed
See detailEmpyème extradural et ostéite de la voûte crânienne associés à des infections ORL et un déficit immunitaire
Liegeois, S.; Lerusse, C.; Leroy, P. et al

in Revista de Neurologia (2006)

Detailed reference viewed: 56 (0 ULg)
Full Text
Peer Reviewed
See detailA propos d'un cas d'hémiparésie aigue chez l'enfant
Daron, Aurore; Leroy, Patricia; Misson, Jean-Paul ULg

in Percentile (2005), 10

Detailed reference viewed: 114 (12 ULg)
Full Text
Peer Reviewed
See detailEncéphalocéle frontoethimoidale: Encéphalite herpétique comme premier signe d'une méningite récurrente
Leroy, P.; Daron, A.; Weerts, E. et al

in Revista de Neurologia (2005)

Detailed reference viewed: 22 (0 ULg)
Full Text
Peer Reviewed
See detailEpilepsy in children with cerebral palsy
Peduzzi, M.; Defontaine, E.; Leroy, P. et al

in European Journal of Paediatric Neurology : Official Journal of the European Paediatric Neurology Society (2005)

Detailed reference viewed: 30 (0 ULg)
Full Text
Peer Reviewed
See detailBony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias
Verloes, Alain ULg; Raoul, M.; Genevieve, D. et al

in Clinical Dysmorphology (2004), 13(4), 205-211

Congenital bony fusion of the maxilla and mandible is a rare condition. Two classifications were previously proposed dealing exclusively with craniofacial malformations. Most of the reported cases to date ... [more ▼]

Congenital bony fusion of the maxilla and mandible is a rare condition. Two classifications were previously proposed dealing exclusively with craniofacial malformations. Most of the reported cases to date represent either aglossia-aclactylia or hemifacial microsomia syndromes. We report a young girl with bony syngnathia associated with multiple defects (severe microcephaly, coloboma, vertebral segmentation defects), growth and mental delay. This patient is very similar to the patient described by Dobrow in 1983 and confirms the existence of this extremely rare disorder. (C) 2004 Lippincott Williams Wilkins. [less ▲]

Detailed reference viewed: 123 (5 ULg)
Full Text
Peer Reviewed
See detailDéveloppement normal et anormal du cortex cérébral: un up-date
Misson, Jean-Paul ULg; Dubru, Jean-Marie ULg; Leroy, Patricia

in Percentile (2004), 9(1), 3-6

Detailed reference viewed: 25 (2 ULg)
Full Text
Peer Reviewed
See detailHypertrichosis, fallot tetralogy, growth and developmental delay
Verloes, Alain ULg; Massin, Martial; Fransolet, Anne-Catherine et al

in Clinical Dysmorphology (2004), 13

Detailed reference viewed: 12 (1 ULg)
Full Text
Peer Reviewed
See detailSpontaneous arachnoid cyst rupture in a previously asymptomatic child: a case report
Poirrier, Anne-Lise ULg; Ngosso-Tetanye, I.; Mouchamps, M. et al

in European Journal of Paediatric Neurology : Official Journal of the European Paediatric Neurology Society (2004), 8(5), 247-251

Arachnoid cysts are benign congenital cavities arising in the subarachnoid space. Non-traumatic subdural effusion of cerebrospinal fluid is a rare complication requiring surgical treatment. Case Report: A ... [more ▼]

Arachnoid cysts are benign congenital cavities arising in the subarachnoid space. Non-traumatic subdural effusion of cerebrospinal fluid is a rare complication requiring surgical treatment. Case Report: A 15-year-old boy was admitted to the hospital because of symptoms related to acute intracranial hypertension (headache and vomiting). The cerebral CT-scan revealed a subdural hygroma adjoining a voluminous Sylvian arachnoid cyst. Two arachnoid cysts were incidentally discovered 11 years before this dramatic complication. Moreover, the patient had suffered a cerebral concussion 2 years earlier, but interestingly did not develop cystic hemorrhage or rupture, contrary to numerous cases previously described in the literature. The location of the cysts and their regular follow-up did not allow foreseeing a cystic rupture. Hygroma evacuation was first performed after which a subdural peritoneal. shunting, using a programmable opening pressure valve, was implanted. Spontaneous rupture into the subdural space represents an unusual complication of arachnoid cysts. Clinical aspects, radiographic findings, pathogenesis and surgical management are described. It is important to point out that subdural hygroma or haematoma should never be excluded in the absence of trauma history, even in the case of small non-progressive cysts regularly supervised. (C) 2004 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved. [less ▲]

Detailed reference viewed: 24 (0 ULg)
Full Text
Peer Reviewed
See detailFebrile convulsions: an update
Lagae, L.; Ceulemans, B.; Misson, Jean-Paul ULg

in Acta Neurologica Belgica (2004)

Detailed reference viewed: 19 (1 ULg)
Full Text
Peer Reviewed
See detailLa tachycardie ventriculaire catecholergique du jeune enfant: un diagnostic souvent meconnu
Massin, M.; Leroy, P.; Misson, Jean-Paul ULg et al

in Archives de Pédiatrie (2003), 10(6), 524-526

Catecholaminergic polymorphic ventricular tachycardia is important to be diagnosed as an underlying disease in children with syncope and normal heart, because of its poor prognosis. CASE REPORT: A 3-year ... [more ▼]

Catecholaminergic polymorphic ventricular tachycardia is important to be diagnosed as an underlying disease in children with syncope and normal heart, because of its poor prognosis. CASE REPORT: A 3-year-old boy was referred for stress and emotion induced syncope. Primary ventricular arrhythmia, consisting of salvos of bidirectional ventricular tachycardia, was reproducibly induced by physical exertion. The syncopal events and severe arrhythmia disappeared with beta-blocking therapy. CONCLUSION: Despite its rare occurrence, catecholaminergic polymorphic ventricular tachycardia is an important cause of stress and emotion induced syncope and sudden death in children. [less ▲]

Detailed reference viewed: 46 (1 ULg)
Full Text
Peer Reviewed
See detailDuane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?
Verloes, Alain; Misson, Jean-Paul ULg; Gillet, Philippe ULg et al

in Annales de Génétique (2003), 46(4), 449-52

We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling-Turk-Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but ... [more ▼]

We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling-Turk-Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but normal intelligence, severe, early onset scoliosis, and short stature. Muscular biopsy revealed numerous regenerating fibers, but no specific abnormalities among the non-regenerating fibers. This combination of anomalies has not been previously reported, and could represent a new autosomal recessive syndrome. The only differential diagnosis is Crisfield-Dretakis-Sharpe syndrome, a combination of lateral gaze palsy, ptosis, and scoliosis without hypotonia, recessively inherited. [less ▲]

Detailed reference viewed: 23 (0 ULg)