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Vigabatrin as initial therapy for infantile spasms: a European retrospective survey. Sabril IS Investigator and Peer Review Groups

Autor: Aicardi, J, Hauser, E, Steinbock, H, Szyper, M, Holsteen, V, Ostergaard, J, Pedersen, SA, Taudorf, K, BarthezCarpentier, MA, BadinandHubert, N, Berquin, P, Boulloche, J, Bourgeois, M, Carriere, JP, Chabrol, B, Chiron, C, Claris, O, Echenne, B, GauthierMorel, D, Livet, MO, Lopez, N, Mancini, J, Netter, JC, Quillerou, D, Richelme, CH, Rousselle, C, DeStMartin, A, DeSwarte, M, Auerswald, G, Brandl, U, Kurlemann, G, Siemes, H, Spohr, HL, Aarts, WFM, Begeer, JH, Heersma, DJ, Laan, LAEM, Peters, ACB, Cavazzutti, GB, Curatolo, P, Fois, A, Franzoni, E, Gobbi, G, Incorpora, G, Vigevano, F, Campistol-Plana J, Campos, J, Casas, C, Herranz, JL, Nieto, M, Prats, JM, Amark, P, Blennow, G, Theorell, K, Tonnby, B, Haenggeli, CA, Weissert, M, Appleton, UKR, Robinson, R, deSousa, C, Thomas, N, Andermann, F, Appleton, R, Arzimanoglou, Boyd, S, Brandt, W, Buti, D, Dulac, O, Farrell, K, Moshe, S, Motte, J, Plouin, P, Shields, WD, Mumford, JP, Dumas, C, Wood, S

Publikováno v: Epilepsia
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
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The efficacy and tolerability of vigabatrin (VGB) as an add-on therapy in the treatment of infantile spasm (IS) prompted physicians to explore its use as the first drug in this seizure type.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0125bcb5e04650d00e5dac68d9d2fd5e
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=8811

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THE SYNDROME OF AUTOSOMAL RECESSIVE PONTOCEREBELLAR HYPOPLASIA, MICROCEPHALY, AND EXTRAPYRAMIDAL DYSKINESIA (PONTOCEREBELLAR HYPOPLASIA TYPE-2) - COMPILED DATA FROM 10 PEDIGREES

Autor: BARTH, PG, BLENNOW, G, LENARD, HG, BEGEER, JH, VANDERKLEY, JM, HANEFELD, F, PETERS, ACB, Valk, J.

Publikováno v: Neurology, 45(2), 311-317. LIPPINCOTT WILLIAMS & WILKINS

The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, severely impaired mental and motor development, and extrapyramidal dyskinesia is a distinct system degeneration, previously designated pontocerebellar hypoplasia type 2 (PC

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::f85a4264817351221be64bbae0043d66
https://research.rug.nl/en/publications/fcced7fe-7f75-4e50-887c-0240a5ed2505

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Congenital malformations and structural developmental anomalies in groups at high risk for psychosis

Autor: Blennow G, Thomas F. McNeil, L. Lundberg

Publikováno v: The American journal of psychiatry. 149(1)

OBJECTIVE: Early somatic developmental anomalies may be one expression of a genetic influence toward psychosis. The purpose of this study was to investigate whether higher rates of early developmental anomalies are associated with heightened genetic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb625e571ffcb32043cf3e53a51e7562
https://pubmed.ncbi.nlm.nih.gov/1728186

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Importance of creatinine analyses of urine when screening for abused drugs

Autor: Lafolie P, Beck O, Blennow G, Boréus L, Borg S, Ce, Elwin, Karlsson L, Odelius G, Paul Hjemdahl

Publikováno v: Europe PubMed Central

We report here a simple method involving urine creatine measurements for testing authenticity and reducing false-negative results in urine testing for drugs of abuse. Urinary creatinine in consecutive patient samples (n = 176) ranged between 0.1 and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::86044d48651cbdba86cf449cb3dc927e
https://pubmed.ncbi.nlm.nih.gov/8472375

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