Schittkowski, Michael P.

[["dc.bibliographiccitation.firstpage","1175"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Der Ophthalmologe"],["dc.bibliographiccitation.lastpage","1177"],["dc.bibliographiccitation.volume","108"],["dc.contributor.author","Atili, A."],["dc.contributor.author","Holke, Karin"],["dc.contributor.author","Karimdadian, Desiree"],["dc.contributor.author","Schittkowski, Michael P."],["dc.date.accessioned","2018-11-07T08:49:26Z"],["dc.date.available","2018-11-07T08:49:26Z"],["dc.date.issued","2011"],["dc.description.abstract","A 22-year-old patient presented with persistent epiphora over a period of about 7 months. The clinical examination revealed a canalicular swelling in both lacrimal ducts, which postoperatively transpired to be an exophytic tumor. The histopathology result of the excised tumor showed an epithelial lesion, a partially inverted papilloma without malignancy. For tumors arising from lachrimal ducts the first-line therapy is complete tumor resection."],["dc.identifier.doi","10.1007/s00347-011-2437-3"],["dc.identifier.isi","000297709800014"],["dc.identifier.pmid","22016192"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/21456"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0941-293X"],["dc.title","Recurrent canaliculitis in a 22-year-old patient"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1051"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Der Ophthalmologe"],["dc.bibliographiccitation.lastpage","1057"],["dc.bibliographiccitation.volume","110"],["dc.contributor.author","Atili, A."],["dc.contributor.author","Richter, C."],["dc.contributor.author","Bahn, Erik"],["dc.contributor.author","Rustenbeck, Hans Heino"],["dc.contributor.author","Schittkowski, Michael P."],["dc.date.accessioned","2018-11-07T09:18:02Z"],["dc.date.available","2018-11-07T09:18:02Z"],["dc.date.issued","2013"],["dc.description.abstract","This paper summarizes the possible ocular manifestations of Churg-Straus syndrome (CCS) from the literature and presents an unusual case report from routine clinical practice with conjunctival granuloma, orbital pseudotumor and choroidal folds. The CSS is an ANCA-associated granulomatous vasculitis which can be manifested in various organs and represents a life-threatening situation for the patient. Ocular manifestations are rare and can spread to all segments of the eye and orbit. The most frequent forms of ocular involvement described in the literature are retinal occlusion and orbital pseudotumor with various degrees of expression."],["dc.identifier.doi","10.1007/s00347-013-2815-0"],["dc.identifier.isi","000327084900008"],["dc.identifier.pmid","23765370"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28317"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","1433-0423"],["dc.relation.issn","0941-293X"],["dc.title","Ocular manifestations of Churg-Strauss syndrome. Review article and case report"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","160"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Der Ophthalmologe"],["dc.bibliographiccitation.lastpage","163"],["dc.bibliographiccitation.volume","110"],["dc.contributor.author","Atili, A."],["dc.contributor.author","Luebke, Jennifer"],["dc.contributor.author","Shoukier, Moneef"],["dc.contributor.author","Schittkowski, Michael P."],["dc.date.accessioned","2018-11-07T09:28:37Z"],["dc.date.available","2018-11-07T09:28:37Z"],["dc.date.issued","2013"],["dc.description.abstract","A 1-year-old female child suffering from nystagmus and abnormal head posture (AHP) was presented by the parents in our clinic. The family history revealed the presence of von Willebrand's disease in both parents. General examination showed a female child with light blond colored skin accompanied by black-haired parents. Physical and ophthalmic examination revealed nystagmus, AHP and oculocutaneous albinism. The molecular genetic analysis showed a mutation in the HPS-1 gene which confirmed the suspected diagnosis of Hermansky-Pudlak syndrome (HPS). Of clinical significance, patients with HPS commonly have hemorrhagic diathesis, granulomatous colitis or restrictive lung fibrosis. A detailed full medical history, ophthalmic examination as well as genetic analyses are essential in establishing the diagnosis of HPS. Treatment includes correcting refraction anomalies with spectacles or contact lenses, prescription of tinted glasses or surgical correction of the AHP. An internal medical consultation is also necessary for the management of other associated symptoms, such as hemorrhagic diathesis."],["dc.identifier.doi","10.1007/s00347-012-2621-0"],["dc.identifier.isi","000314716500008"],["dc.identifier.pmid","22806537"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30820"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0941-293X"],["dc.title","Hermansky-Pudlak syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]