A. Jung

Promotor polymorphisms of plasminogen activator inhibitor-1 and other thrombophilic genotypes in cerebral venous thrombosis: a case-control study in adults

K. Berger, M. Stoll, F. Schlachetzki, 2012, Journal of Neurology.

Genetic causes of goiter and deafness: Pendred syndrome in a girl and cooccurrence of Pendred syndrome and resistance to thyroid hormone in her sister.

C. Kubisch, G. Borck, E. Schönau, 2009, The Journal of clinical endocrinology and metabolism.

Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura

K. Berger, S. Evers, G. Kuhlenbäumer, 2010, Journal of Neural Transmission.

Nummular headache: Six new cases and lancinating pain attacks as possible manifestation

S. Evers, R. Ruscheweyh, A. Buchheister, 2010, Cephalalgia : an international journal of headache.

Intracerebral mass lesion diagnosed as cryptococcoma in a patient with sarcoidosis, a rare opportunistic manifestation induced by immunosuppression with corticosteroids

T. Kuhlmann, I. Husstedt, C. Korsukewitz, 2012, Journal of Neurology.

An Association of Migraine with Hereditary Haemorrhagic Telangiectasia Independently of Pulmonary Right-to-Left Shunts

S. Evers, J. Prudlo, M. Marziniak, 2009, Cephalalgia : an international journal of headache.