Items where Author is "Huber, Andreas R."

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Number of items: 6.


Killer, Hanspeter Esriel and Jaggi, Gregor Peter and Miller, Neil R. and Huber, Andreas R. and Landolt, Hans and Mironov, Angel and Meyer, Peter and Remonda, Luca. (2011) Cerebrospinal fluid dynamics between the basal cisterns and the subarachnoid space of the optic nerve in patients with papilloedema. British journal of ophthalmology, Vol. 95, no. 6. pp. 822-827.

Filges, Isabel and Shimojima, Keiko and Okamoto, Nobuhiko and Röthlisberger, Benno and Weber, Peter and Huber, Andreas R. and Nishizawa, Tsutomu and Datta, Alexandre N. and Miny, Peter and Yamamoto, Toshiyuki. (2011) Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome. Journal of medical genetics, Vol. 48, H. 2. pp. 117-122.


Hergersberg, Martin and Brunner-Agten, Saskia and Kühne, Thomas and Paulussen, Michael and Huber, Andreas R.. (2010) A new stable alpha chain variant : Hb Basel [alpha14(A12)Trp--<Leu (alpha1)]. Hemoglobin, Vol. 34, H. 3. pp. 327-331.

Filges, Isabel and Röthlisberger, Benno and Boesch, Nemya and Weber, Peter and Wenzel, Friedel and Huber, Andreas R. and Heinimann, Karl and Miny, Peter. (2010) Interstitial deletion 1q42 in a patient with agenesis of corpus callosum : Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome. American journal of medical genetics. Part A, Vol. 152, H. 4. pp. 987-993.

Schuetz, Philipp and Christ-Crain, Mirjam and Huber, Andreas R. and Müller, Beat. (2010) Long-term stability of procalcitonin in frozen samples and comparison of Kryptor and VIDAS automated immunoassays. Clinical biochemistry, 43 (3). pp. 341-344.


Filges, Isabel and Röthlisberger, Benno and Noppen, Christoph and Boesch, Nemya and Wenzel, Friedel and Necker, Judith and Binkert, Franz and Huber, Andreas R. and Heinimann, Karl and Miny, Peter. (2009) Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33 : clinical and array-CGH study of a benign phenotype in a three-generation family. American journal of medical genetics, Vol. 149. pp. 237-241.

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