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. Präsentiert bei: 172. Tagung der Schweizerischen Neurologischen Gesellschaft (Interlaken), 172. Tagung der Schweizerischen Neurologischen Gesellschaft (Interlaken)
21.12.2004Hereditary transthyretin amyloidosis:a case report of a newly described TTR variant Ile 107Met
21.12.2004172. 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.
01.01.2004Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
01.01.2004Schweiz 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. Präsentiert bei: Joint Meeting of the Swiss Society for Neurology (SNG) and the Swiss Society for Sleep Research, Sleep Medicine and Chronobiology (SGSSC), Zürich
20.10.2003Hereditary transthyretin amyloidosis: a case report of a newly described TTR variant Ile 107 Met
20.10.2003Joint 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