References of "Misson, Jean-Paul"
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See detailLa Biologie clinique en pédiatrie: hypotonie et retard moteur
Misson, Jean-Paul ULg; Leroy, Patricia; Dubru, Jean-Marie ULg et al

in Acta Paediatrica Belgica (1996), 28(2), 95

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See detailHeterogeneity of sponastrime dysplasia: Delineation of a variant form with severe mental retardation
Verloes, Alain ULg; Misson, Jean-Paul ULg; Dubru, J. M. et al

in Clinical Dysmorphology (1995), 4(3), 208-215

We report a child with short stature, osteopenia with metaphyseal striations and severe mental retardation. This child shows radiological and clinical features of SPONASTRIME dysplasia. Only three ... [more ▼]

We report a child with short stature, osteopenia with metaphyseal striations and severe mental retardation. This child shows radiological and clinical features of SPONASTRIME dysplasia. Only three sibships with this disorder have been reported. In two families, affected patients were of normal intelligence. In the third one, as well as our case, the dysplasia was complicated by severe mental retardation of unknown origin. The severity of the retardation in our case and a previous report, and some difference in the gestalt and radiological aspects, suggest that SPONASTRIME dysplasia is a heterogeneous disorder. We provisionally propose to split SPONASTRIME dysplasia in two phenotypically distinct subgroups, and to delineate here a 'new' variant with microcephaly and severe mental impairment. [less ▲]

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See detailCaractéristiques neuroradiologiques du déficit en Pyruvate Carboxylase
Misson, Jean-Paul ULg; Lombet, J.; Rigo, Jacques ULg et al

in Société Européenne de Neurologie Pédiatrique (1995)

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See detailMéningiome volumineux chez l'enfant: discussion à propos d'un cas chez une fillette de 5 ans
Misson, Jean-Paul ULg; Dacier, Ph; Leroy, P. et al

in Société Belge de Neurologie Pédiatrique (1995)

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See detailCentral neuroblastoma in a 14 year-old girl
Hoyoux, Cl; Dresse, Marie-Françoise ULg; Misson, Jean-Paul ULg et al

in 4th International Symposium on Neuroblastoma Screening (1995)

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See detailGliomatose méningée cérébro-spinale diffuse chez un enfant traité par hormone de croissance dans le cadre d!un syndrome de Turner
Dacier, Ph; Leroy, P.; Ernould, Ch et al

in Société Belge de Neurologie Pédiatrique (1995)

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See detailLambdoid synostosis - pachycephaly: diagnosis and treatment
Misson, Jean-Paul ULg; Born, Jacques; Collignon, L. et al

in Developmental Medicine and Child Neurology. Supplement (1995), 37(3), 87

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See detailLeber-associateddystonia with putamen necrosis
Van Coster, R.; Misson, Jean-Paul ULg; Meire, F. et al

in Annals of Neurology (1994)

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See detailSponastrime dysplasia with mental retardation: A distinct entity
Verloes, A.; Misson, Jean-Paul ULg; Dubru, Jean-Marie ULg et al

in 3ème Dysmorphology Meeting (1994)

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See detailEffet préventif du Sabril dans un cas présymtomatique de maladie de Bourneville
Leroy, P.; Bakri, A.; Dubru, Jean-Marie ULg et al

in Société Belge de Neurologie Pédiatrique (1994)

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See detailHeterogeneity versus variability in Neuhauser megalocornea-mental retardation (MMR) syndromes: Report of new cases and delineation of 4 probable types
Verloes, Alain ULg; Journel, H.; Elmer, C. et al

in American Journal of Medical Genetics (1993), 46(2), 132-137

Megalocornea (corneal diameter > or = 13 mm) is associated with mental and neurological impairment, and minor anomalies in Neuhauser syndrome (megalocornea-mental retardation syndrome). Here we report 4 ... [more ▼]

Megalocornea (corneal diameter > or = 13 mm) is associated with mental and neurological impairment, and minor anomalies in Neuhauser syndrome (megalocornea-mental retardation syndrome). Here we report 4 new cases of megalocornea and mental retardation. Those unrelated patients have a consistent pattern of anomalies with possible recessive inheritance which clearly differs from that of the original patients of Neuhauser et al. [1975]. We discuss the heterogeneity of the syndromes with megalocornea and mental retardation. Based on these cases and on a review of the literature, we suggest a provisional clinically oriented classification in 5 subtypes: (1) a recessive form type Neuhauser (with iris hypoplasia and minor anomalies), (2) a recessive form type Frank-Temtamy (with camptodactyly, scoliosis and growth retardation), (3) a recessive type 3, including our 4 personal cases (with normal irides, severe hypotonia, relative or absolute macrocephaly and minor anomalies), (4) a possible Frydman type (with normal irides, megalencephaly and obesity), and (5) provisionally unclassifiable cases. [less ▲]

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See detailNeuroblastome primitif du système nerveux central
Jamblin, Paul; Collignon, J.; Flandroy, P. et al

in Revue Neurologique (1993), 149

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See detailSclérodermie en coup de sabre et hémiatrophie faciale de Perry-Romberg: A propos d'un cas
Leroy, P.; Dubru, Jean-Marie ULg; Pierrard, A. et al

in 30ème Congrès de l'Association des Pédiatres de Langue Française (1993)

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See detailSchizencephaly of the frontal opercula mimicing sylvian arachnoidal cyst
Misson, Jean-Paul ULg; Collignon, Jacques ULg

in 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology (1993)

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See detailSyndrome oculo-cérébro-cutané de Delleman
Leroy, P.; Verloes, Alain ULg; Born, J. et al

in 30ème Congrès de l'Association des Pédiatres de Langue Française (1993)

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See detailEpilepsie frontale et trouble du comportement: diagnostic, exploration et traitement
Misson, Jean-Paul ULg; Reynaers, A.; Ernould, C. et al

in 30ème Congrès de l'Association des Pédiatres de Langue Française (1993)

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See detailKyste arachnoïdien suprasellaire post méningitique
Grossman, D.; Misson, Jean-Paul ULg; Quacoe, M. et al

in Revue Neurologique (1993)

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See detailTransient multiple arterial spasms: stenosis in the corse of a cerebral trauma
Misson, Jean-Paul ULg; Leroy, P.; Born, J. et al

in 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology (1993)

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See detailPostnatal ulegyria due to prolonged postoperative status epilepticus
Misson, Jean-Paul ULg; Robbe-Dechamps, M.; Pauly, F. et al

in 3rd biennal Meeting of European Society of Magnetic Resonance in Pediatric Neurology (1993)

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