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[Endovascular treatment of epistaxis of the internal carotid artery. Vessel occlusion and vessel preservation].

M. Forsting, J. Lautermann, I. Wanke, 2009, HNO.

NDUFS8-related Complex I Deficiency Extends Phenotype from "PEO Plus" to Leigh Syndrome.

M. Santibanez-Koref, P. Chinnery, H. Lochmüller, 2013, JIMD reports.

Treacher Collins syndrome: clinical implications for the paediatrician—a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature

D. Wieczorek, D. Lohmann, A. Stein, 2012, European Journal of Pediatrics.

A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation

D. Wieczorek, P. Nürnberg, J. Altmüller, 2016, American Journal of Medical Genetics. Part A.

Telmisartan on Top of Antihypertensive Treatment Does Not Prevent Progression of Cerebral White Matter Lesions in the Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) MRI Substudy

A. Demchuk, R. Sacco, H. Diener, 2012, Stroke.

Risk of Recurrent Stroke in Patients With Silent Brain Infarction in the Prevention Regimen for Effectively Avoiding Second Strokes (PRoFESS) Imaging Substudy

A. Demchuk, R. Sacco, H. Diener, 2012, Stroke.

Neuro-Quiz

D. Timmann, M. Obermann, C. Möller-Hartmann, 2013, Aktuelle Neurologie.

A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation

D. Wieczorek, P. Nürnberg, J. Altmüller, 2016, American Journal of Medical Genetics. Part A.