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Search Results - Seydewitz, Hans
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The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients
by
Roth, Eva K
,
Hirtz, Stephanie
,
Duerr, Julia
,
Wenning, Daniel
,
Eichler, Irmgard
,
Seydewitz, Hans H
,
Amaral, Margarida D
,
Mall, Marcus A
Published in
PloS one
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Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes
by
Mall, Marcus
,
Wissner, Andreas
,
Seydewitz, Hans H
,
Hübner, Martin
,
Kuehr, Joachim
,
Brandis, Matthias
,
Greger, Rainer
,
Kunzelmann, Karl
Published in
British journal of pharmacology
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Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations
by
Seydewitz, Hans H.
,
Matern, Dietrich
Published in
Human mutation
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The K.sup.+ Channel Opener 1-EBIO Potentiates Residual Function of Mutant CFTR in Rectal Biopsies from Cystic Fibrosis Patients
by
Roth, Eva K
,
Hirtz, Stephanie
,
Duerr, Julia
,
Wenning, Daniel
,
Eichler, Irmgard
,
Seydewitz, Hans H
,
Amaral, Margarida D
,
Mall, Marcus A
Published in
PloS one
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Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
by
DÖRK, T
,
DWORNICZAK, B
,
PANDER, H.-J
,
SPERLING, H
,
RATJEN, F
,
PASSARGE, E
,
SCHMIDTKE, J
,
STUHRMANN, M
,
AULEHLA-SCHOLZ, C
,
WIECZOREK, D
,
BÖHM, I
,
MAYEROVA, A
,
SEYDEWITZ, H. H
,
NIESCHLAG, E
,
MESCHEDE, D
,
HORST, J
Published in
Human genetics
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Glycogen storage disease type I: diagnosis and phenotype/genotype correlation
by
Matern, Dietrich
,
Seydewitz, Hans Hermann
,
Bali, Deeksha
,
Lang, Christine
,
Chen, Yuan-Tsong
Published in
European journal of pediatrics
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A novel missense mutation, S1159F, in exon 19 of the CFTR gene
by
Seydewitz, Hans Hermann
,
Mall, Marcus
,
Kuehr, Joachim
Published in
Human mutation
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A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene
by
Seydewitz, Hans Hermann
,
Gonska, Tanja
,
Mall, Marcus
,
Kueh, Joachim
Published in
Human mutation
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Glycogen storage disease type I: diagnosis and phenotype/genotype correlation
by
Matern, Dietrich
,
Seydewitz, Hans
,
Bali, Deeksha
,
Lang, Christine
,
Chen, Yuan-Tsong
Published in
European journal of pediatrics
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Primary treatment of propionic acidemia complicated by acute thiamine deficiency
by
Matern, Dietrich
,
Seydewitz, Hans H.
,
Lehnert, Willy
,
Niederhoff, Helmut
,
Leititis, Jekabs U.
,
Brandis, Matthias
Published in
The Journal of pediatrics
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Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case-control study
by
Menne, Jan
,
Nitschke, Martin
,
Stingele, Robert
,
Abu-Tair, Mariam
,
Beneke, Jan
,
Bramstedt, Jörn
,
Bremer, Jan P
,
Brunkhorst, Reinhard
,
Busch, Veit
,
Dengler, Reinhard
,
Deuschl, Günther
,
Fellermann, Klaus
,
Fickenscher, Helmut
,
Gerigk, Christoph
,
Goettsche, Alexander
,
Greeve, Jobst
,
Hafer, Carsten
,
Hagenmüller, Friedrich
,
Haller, Hermann
,
Herget-Rosenthal, Stefan
,
Hertenstein, Bernd
,
Hofmann, Christina
,
Lang, Melanie
,
Kielstein, Jan T
,
Klostermeier, Ulrich C
,
Knobloch, Johannes
,
Kuehbacher, Markus
,
Kunzendorf, Ulrich
,
Lehnert, Hendrik
,
Manns, Michael P
,
Menne, Tobias F
,
Meyer, Tobias N
,
Michael, Claus
,
Münte, Thomas
,
Neumann-Grutzeck, Christine
,
Nuernberger, Jens
,
Pavenstaedt, Hermann
,
Ramazan, Leyla
,
Renders, Lutz
,
Repenthin, Jonas
,
Ries, Wolfgang
,
Rohr, Axel
,
Rump, Lars Christian
,
Samuelsson, Ola
,
Sayk, Friedhelm
,
Schmidt, Bernhard M W
,
Schnatter, Sabine
,
Schöcklmann, Harald
,
Schreiber, Stefan
,
von Seydewitz, Cay U
,
Steinhoff, Jürgen
,
Stracke, Sylvia
,
Suerbaum, Sebastian
,
van de Loo, Andreas
,
Vischedyk, Martin
,
Weissenborn, Karin
,
Wellhöner, Peter
,
Wiesner, Monika
,
Zeissig, Sebastian
,
Büning, Jürgen
,
Schiffer, Mario
,
Kuehbacher, Tanja
Published in
BMJ (Online)
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