Med. pract. Stefanie Müller
Neurologie · Dept. III
Hereditary transthyretin amyloidosis:a case report of a newly described TTR variant Ile 107Met
Müller S, Tettenborn B, Schött D, Altland K (2004). Hereditary transthyretin amyloidosis:a case report of a newly described TTR variant Ile 107Met. Presented at: 172. Tagung der Schweizerischen Neurologischen Gesellschaft (Interlaken), 172. Tagung der Schweizerischen Neurologischen Gesellschaft (Interlaken)
Dec 21, 2004Hereditary transthyretin amyloidosis:a case report of a newly described TTR variant Ile 107Met
Dec 21, 2004172. Tagung der Schweizerischen Neurologischen Gesellschaft (Interlaken)
Müller Stefanie, Tettenborn Barbara, Schött Dagmar, Altland K.
Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
Müller S, Schött D, Altland K, Tettenborn B. Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met. Schweiz Arch Neurol Psych 2004; 155:91-92.
Jan 1, 2004Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
Jan 1, 2004Schweiz Arch Neurol Psych 2004; 155:91-92
Müller Stefanie, Schött Dagmar, Altland K, Tettenborn Barbara
Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
Müller S, Schött D, Altland K, Tettenborn B (2003). Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met. Presented at: Joint Meeting of the Swiss Society for Neurology (SNG) and the Swiss Society for Sleep Research, Sleep Medicine and Chronobiology (SGSSC), Zürich
Oct 20, 2003Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
Oct 20, 2003Joint Meeting of the Swiss Society for Neurology (SNG) and the Swiss Society for Sleep Research, Sleep Medicine and Chronobiology (SGSSC)
Müller Stefanie, Schött Dagmar, Altland K, Tettenborn Barbara