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Late Lesion Growth following Endovascular Therapy: Is 24 h Too Early to Assess Acute Infarct Size Including the Effects of Secondary Injury? Enthalten in Cerebrovascular diseases Bd. 54, 2025, Nr. 1: 129-137. 9 S.
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Outcomes of allogeneic haematopoietic cell transplantation for myelofibrosis in children and adolescents: the retrospective study of the EBMT Paediatric Diseases WP Enthalten in Bone marrow transplantation 16.4.2024: 1-13
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Real-world use of defibrotide for veno-occlusive disease/sinusoidal obstruction syndrome: the DEFIFrance Registry Study Enthalten in Bone marrow transplantation 23.12.2022: 1-10
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TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT Enthalten in European Molecular Biology Organization: EMBO molecular medicine Bd. 8, 2016, Nr. 12: 1390-1408. 19 S.
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Menschen & Andere. Einleitung in den Schwerpunkt Angerer, Marie-Luise. - Marburg : Philipps-Universität Marburg, 2011
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A discharge summary adapted to the frail elderly to ensure transfer of relevant information from the hospital to community settings: a model Enthalten in BMC geriatrics Bd. 10, 23.9.2010, Nr. 1, date:12.2010: 1-10
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Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect Enthalten in Orphanet journal of rare diseases Bd. 13, 1.10.2018, Nr. 1, date:12.2018: 1-12
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8 |
Allogeneic stem cell transplantation for peripheral T cell lymphomas: a retrospective study in 285 patients from the Société Francophone de Greffe de Moelle et de Thérapie Cellulaire (SFGM-TC) Enthalten in Journal of hematology & oncology Bd. 13, 19.5.2020, Nr. 1, date:12.2020: 1-12
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Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death Enthalten in Acta Neuropathologica Communications Bd. 5, 14.7.2017, Nr. 1, date:12.2017: 1-15
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Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study Enthalten in Orphanet journal of rare diseases Bd. 18, 21.7.2023, Nr. 1, date:12.2023: 1-12
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