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Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.

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Title: Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.
Authors: Disse S; University Children's Hospital Regensburg (KUNO) - Hospital St. Hedwig of the Order of St. John, University of Regensburg, Linik St. Hedwig, Steinmetzstraße 1-3, 93049, Regensburg, Germany. sigdisse@gmx.de., Ramantani G; Department of Neuropaediatrics, University Children's Hospital Zürich, Zürich, Switzerland., Küpper H; University Children's Hospital Tübingen, Tübingen, Germany., Bock A; University Hospital Essen, Essen, Germany., Korenke GC; Department of Neuropaediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany., Weidner B; Paediatric Practice, Cottbus, Germany., Preisel M; University Hospital Salzburg, Salzburg, Austria., Trollmann R; Paediatric Neurology, University Children's Hospital, Erlangen, Germany., Wiemer-Kruel A; Paediatric Epilepsy Center Kehl-Kork, Kork, Germany., Wellmann S; University Children's Hospital Regensburg (KUNO) - Hospital St. Hedwig of the Order of St. John, University of Regensburg, Linik St. Hedwig, Steinmetzstraße 1-3, 93049, Regensburg, Germany., Brockmann K; University Medical Center Göttingen and German Center for Child and Adolescent Health (DZKJ), Göttingen, Germany., Schroeder S; University Medical Center Göttingen and German Center for Child and Adolescent Health (DZKJ), Göttingen, Germany., Meyer S; Franz-Lust Klinik Für Kinder Und Jugendliche, Karlsruhe, Germany.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2025 Jul 02; Vol. 20 (1), pp. 336. Date of Electronic Publication: 2025 Jul 02.
Publication Type: Journal Article; Observational Study
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.
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  Data: <searchLink fieldCode="AU" term="%22Disse+S%22">Disse S</searchLink>; University Children's Hospital Regensburg (KUNO) - Hospital St. Hedwig of the Order of St. John, University of Regensburg, Linik St. Hedwig, Steinmetzstraße 1-3, 93049, Regensburg, Germany. sigdisse@gmx.de.<br /><searchLink fieldCode="AU" term="%22Ramantani+G%22">Ramantani G</searchLink>; Department of Neuropaediatrics, University Children's Hospital Zürich, Zürich, Switzerland.<br /><searchLink fieldCode="AU" term="%22Küpper+H%22">Küpper H</searchLink>; University Children's Hospital Tübingen, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Bock+A%22">Bock A</searchLink>; University Hospital Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Korenke+GC%22">Korenke GC</searchLink>; Department of Neuropaediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany.<br /><searchLink fieldCode="AU" term="%22Weidner+B%22">Weidner B</searchLink>; Paediatric Practice, Cottbus, Germany.<br /><searchLink fieldCode="AU" term="%22Preisel+M%22">Preisel M</searchLink>; University Hospital Salzburg, Salzburg, Austria.<br /><searchLink fieldCode="AU" term="%22Trollmann+R%22">Trollmann R</searchLink>; Paediatric Neurology, University Children's Hospital, Erlangen, Germany.<br /><searchLink fieldCode="AU" term="%22Wiemer-Kruel+A%22">Wiemer-Kruel A</searchLink>; Paediatric Epilepsy Center Kehl-Kork, Kork, Germany.<br /><searchLink fieldCode="AU" term="%22Wellmann+S%22">Wellmann S</searchLink>; University Children's Hospital Regensburg (KUNO) - Hospital St. Hedwig of the Order of St. John, University of Regensburg, Linik St. Hedwig, Steinmetzstraße 1-3, 93049, Regensburg, Germany.<br /><searchLink fieldCode="AU" term="%22Brockmann+K%22">Brockmann K</searchLink>; University Medical Center Göttingen and German Center for Child and Adolescent Health (DZKJ), Göttingen, Germany.<br /><searchLink fieldCode="AU" term="%22Schroeder+S%22">Schroeder S</searchLink>; University Medical Center Göttingen and German Center for Child and Adolescent Health (DZKJ), Göttingen, Germany.<br /><searchLink fieldCode="AU" term="%22Meyer+S%22">Meyer S</searchLink>; Franz-Lust Klinik Für Kinder Und Jugendliche, Karlsruhe, Germany.
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  Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2025 Jul 02; Vol. 20 (1), pp. 336. <i>Date of Electronic Publication: </i>2025 Jul 02.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE
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