Sturge Weber syndrome in a multinational pediatric cohort: a systematic analysis of different types.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
