Works by Utermann, G.

Results: 25

Mutation spectrum of type I glycogen storage disease in Hungary.

Published in:

Journal of Inherited Metabolic Disease, 2005, v. 28, n. 6, p. 939, doi. 10.1007/s10545-005-0186-7

By:

Miltenberger-Miltenyi, G.;
Szonyi, L.;
Balogh, L.;
Utermann, G.;
Janecke, A.

Publication type:

Article

Herpes Simplex Virus Binds to Human Serum Lipoprotein.

Published in:

Intervirology, 1988, v. 29, n. 2, p. 68, doi. 10.1159/000150031

By:

Huemer, H.P.;
Menzel, H.J.;
Potratz, D.;
Brake, B.;
Falke, D.;
Utermann, G.;
Dierich, M.P.

Publication type:

Article

Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

Published in:

Clinical Genetics, 2014, v. 86, n. 4, p. 361, doi. 10.1111/cge.12288

By:

Spreiz, A.;
Haberlandt, E.;
Baumann, M.;
Baumgartner Sigl, S.;
Fauth, C.;
Gautsch, K.;
Karall, D.;
Janetschek, C.;
Rostasy, K.;
Scholl‐Bürgi, S.;
Zotter, S.;
Utermann, G.;
Zschocke, J.;
Kotzot, D.

Publication type:

Article

Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 1, p. 45, doi. 10.1038/sj.ejhg.5200579

By:

Witsch-Baumgartner, M;
Ciara, E;
Löffler, J;
Menzel, H J;
Seedorf, U;
Burn, J;
Gillessen-Kaesbach, G;
Hoffmann, G F;
Fitzky, B U;
Mundy, H;
Clayton, P;
Kelley, R I;
Krajewska-Walasek, M;
Utermann, G

Publication type:

Article

Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system.

Published in:

British Journal of Cancer, 1999, v. 81, n. 2, p. 242, doi. 10.1038/sj.bjc.6690684

By:

Culig, Z;
Hoffmann, J;
Erdel, M;
Eder, I E;
Hobisch, A;
Hittmair, A;
Bartsch, G;
Utermann, G;
Schneider, M R;
Parczyk, K;
Klocker, H

Publication type:

Article

Corrigendum: Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause severe childhood-onset retinal dystrophy.

Published in:

2004

By:

Janecke, A. R.;
Thompson, D. A.;
Utermann, G.;
Becker, C.;
Hübner, C. A.;
Schmid, E.;
McHenry, C. L.;
Nair, A. R.;
Rüschendorf, F.;
Heckenlively, J.;
Wissinger, B.;
Nürnberg, P.;
Gal, A.

Publication type:

Correction Notice

Polymorphism of apolipoprotein E and occurrence of dysbetalipoproteinaemia in man.

Published in:

Nature, 1977, v. 269, n. 5629, p. 604, doi. 10.1038/269604a0

By:

UTERMANN, G.;
HEES, M.;
STEINMETZ, A.

Publication type:

Article

Plasma apolipoprotein A-IV metabolism in patients with chronic renal disease.

Published in:

European Journal of Clinical Investigation, 1992, v. 22, n. 3, p. 166, doi. 10.1111/j.1365-2362.1992.tb01822.x

By:

DIEPLINGER, H.;
LOBENTANZ, E.-M.;
KÖNIG, P.;
GRAF, H.;
SANDHOLZER, C.;
MATTHYS, E.;
ROSSENEU, M.;
UTERMANN, G.

Publication type:

Article

The human gene encoding SCYB9B, a putative novel CXC chemokine, maps to human chromosome 4q21 like the closely related genes for MIG (SCYB9) and INP10 (SCYB10).

Published in:

Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 271, doi. 10.1159/000015043

By:

Erdel, M.;
Laich, A.;
Utermann, G.;
Werner, E. R.;
Werner-Felmayer, G.

Publication type:

Article

Zur Differenzierurg des Lp(a)-Lipoptoteins mit Hilfe der Agarosegel-Elektrophorese.

Published in:

Clinical Chemistry & Laboratory Medicine, 1973, v. 11, n. 7, p. 291

By:

VOGELBERG, K. H.;
UTERMANN, G.;
GRIES, F. A.

Publication type:

Article

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis Grossmann et al.

Published in:

Clinical Genetics, 2010, v. 78, n. 6, p. 548, doi. 10.1111/j.1399-0004.2010.01419.x

By:

Grossmann, V.;
Höckner, M.;
Karmous-Benailly, H.;
Liang, D.;
Puttinger, R.;
Quadrelli, R.;
Röthlisberger, B.;
Huber, A.;
Wu, L.;
Spreiz, A.;
Fauth, C.;
Erdel, M.;
Zschocke, J.;
Utermann, G.;
Kotzot, D.

Publication type:

Article

DHCR7mutations and genotype–phenotype correlation in 37 Polish patients with Smith–Lemli–Opitz syndrome.

Published in:

Clinical Genetics, 2004, v. 66, n. 6, p. 517, doi. 10.1111/j.1399-0004.2004.00350.x

By:

Ciara, E.;
Nowaczyk, M. J. M.;
Witsch-Baumgartner, M.;
Malunowicz, E.;
Popowska, E.;
Jezela-Stanek, A.;
Piotrowicz, M.;
Waye, J. S.;
Utermann, G.;
Krajewska-Walasek, M.

Publication type:

Article

Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations.

Published in:

Cytogenetic & Genome Research, 2012, v. 136, n. 4, p. 242, doi. 10.1159/000337923

By:

Höckner, M.;
Spreiz, A.;
Frühmesser, A.;
Tzschach, A.;
Dufke, A.;
Rittinger, O.;
Kalscheuer, V.;
Singer, S.;
Erdel, M.;
Fauth, C.;
Grossmann, V.;
Utermann, G.;
Zschocke, J.;
Kotzot, D.

Publication type:

Article

Whole Genome Amplification from Microdissected Chromosomes.

Published in:

Cytogenetic & Genome Research, 2009, v. 125, n. 2, p. 98, doi. 10.1159/000227832

By:

Höckner, M.;
Erdel, M.;
Spreiz, A.;
Utermann, G.;
Kotzot, D.

Publication type:

Article

Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy.

Published in:

Human Mutation, 2005, v. 25, n. 4, p. 412, doi. 10.1002/humu.9328

By:

Witsch-Baumgartner, M.;
Clayton, P.;
Clusellas, N.;
Haas, D.;
Kelley, R.I.;
Krajewska-Walasek, M.;
Lechner, S.;
Rossi, M.;
Zschocke, J.;
Utermann, G.

Publication type:

Article

Apolipoprotein A-IV polymorphism in the Hungarian population: Gene frequencies, effect on lipid levels, and sequence of two new variants.

Published in:

Human Mutation, 1995, v. 5, n. 1, p. 58, doi. 10.1002/humu.1380050108

By:

Menzel, H. J.;
Dieplinger, H.;
Sandholzer, C.;
Karádi, I.;
Utermann, G.;
Császár, A.

Publication type:

Article

Lipoproteinstoffwechsel und koronare Herzkrankheit.

Published in:

Medizinische Genetik, 2011, v. 23, n. 1, p. 7, doi. 10.1007/s11825-010-0259-3

By:

Utermann, G.

Publication type:

Article

Lipoprotein(a): resurrected by genetics.

Published in:

Journal of Internal Medicine, 2013, v. 273, n. 1, p. 6, doi. 10.1111/j.1365-2796.2012.02592.x

By:

Kronenberg, F.;
Utermann, G.

Publication type:

Article

Genetic Architecture of the Atherogenic Lipoprotein(a).

Published in:

Annals of the New York Academy of Sciences, 1994, v. 748, n. 1, p. 301, doi. 10.1111/j.1749-6632.1994.tb17328.x

By:

UTERMANN, G.;
HAIBACH, C.;
TROMMSDORFF, M.;
KÖCHL, S.;
LINGENHEL, A.;
ABE, A.;
KRAFT, H. G.

Publication type:

Article

Lecithin-cholesterol-acyltransferase deficiency: autosomal recessive transmission in a large kindred.

Published in:

Clinical Genetics, 1981, v. 19, n. 6, p. 448, doi. 10.1111/j.1399-0004.1981.tb02063.x

By:

Utermann, G.;
Menzel, H. J.;
Dieker, P.;
Langer, K. H.;
Fiorelli, G.

Publication type:

Article

Polymorphism of apolipoprotein E.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 63, doi. 10.1111/j.1399-0004.1979.tb02028.x

By:

Utermann, G.;
Pruin, N.;
Steinmetz, A.

Publication type:

Article

Polymorphism of apolipoprotein E.

Published in:

Clinical Genetics, 1979, v. 15, n. 1, p. 37, doi. 10.1111/j.1399-0004.1979.tb02027.x

By:

Utermann, G.;
Vogelberg, K. H.;
Steinmetz, A.;
Schoenborn, W.;
Pruin, N.;
Jaeschke, M.;
Hees, M.;
Canzler, H.

Publication type:

Article

Polymorphism of apolipoprotein E.

Published in:

Clinical Genetics, 1978, v. 14, n. 6, p. 351, doi. 10.1111/j.1399-0004.1978.tb02101.x

By:

Utermann, G.;
Albrecht, G.;
Steinmetz, A.

Publication type:

Article

Studies on the metabolic defect in Broad-ß disease (hyperlipoproteinaemia type III).

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 139, doi. 10.1111/j.1399-0004.1977.tb00917.x

By:

Utermann, G.;
Canzler, H.;
Hees, M.;
Jaeschke, M.;
Mühlfellner, G.;
Schoenborn, W.;
Vogelberg, K. H.

Publication type:

Article

Plasma lipoprotein abnormalities in a case of primary high-density-lipoprotein (HDL) deficiency.

Published in:

Clinical Genetics, 1975, v. 8, n. 4, p. 258, doi. 10.1111/j.1399-0004.1975.tb01501.x

By:

Utermann, G.;
Menzel, H. J.;
Schoenborn, W.

Publication type:

Article