C. Seitz

Publication List Details

Period

1990 - 2009

Number

20

Co-Authors

The registry of the German Network for Systemic Scleroderma: frequency of disease subsets and patterns of organ involvement (2008)

Hunzelmann, N., Genth, E., Krieg, T., Lehmacher, W., Melchers, I., Meurer, M., ...

Objective. Systemic sclerosis (SSc) is a rare, heterogeneous disease, which affects different organs and therefore requires interdisciplinary diagnostic and therapeutic management. To improve the...

Association and linkage of allelic variants of the dopamine transporter gene in ADHD (2007)

Friedel, S., Saar, K., Sauer, S., Dempfle, A., Walitza, S., Renner, T., ...

Previously, we had reported a genome-wide scan for attention-deficit/hyperactivity disorder (ADHD) in 102 families with affected sibs of German ancestry; the highest multipoint LOD score of 4.75 was...

Association and linkage of allelic variants of the dopamine transporter gene in ADHD (2007)

Friedel, S., Saar, K., Sauer, S., Dempfle, A., Walitza, S., Renner, T., ...

Previously, we had reported a genome-wide scan for attention-deficit/hyperactivity disorder (ADHD) in 102 families with affected sibs of German ancestry; the highest multipoint LOD score of 4.75 was...

In situ Er-doping of SiC bulk single crystals (2004)

Müller, R., Desperrier, P., Seitz, C., Weisser, M., Magerl, A., Maier, M., ...

In this work the first PVT grown in-situ erbium doped SiC bulk crystal, to our knowledge, is presented. The crystal was characterised by secondary ion mass spectrometry (SIMS) and photoluminescence...

Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III (2001)

Schaper, J, Meinecke, P, Momeni, P, Gross, S, Von Holtum D, ...

Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...

Lp(a) glycoprotein phenotypes. Inheritance and relation to Lp(a)-lipoprotein concentrations in plasma.

Utermann, G, Menzel, H J, Kraft, H G, Duba, H C, Kemmler, H G, Seitz, C

The Lp(a) lipoprotein represents a quantitative genetic trait. It contains two different polypeptide chains, the Lp(a) glycoprotein and apo B-100. We have demonstrated the Lp(a) glycoprotein directly...

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

Schaper, J., Meinecke, P., Momeni, P., Groß, S., Von Holtum, D., ...

Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...

Lp(a) glycoprotein phenotypes. Inheritance and relation to Lp(a)-lipoprotein concentrations in plasma.

Utermann, G, Menzel, H J, Kraft, H G, Duba, H C, Kemmler, H G, Seitz, C

The Lp(a) lipoprotein represents a quantitative genetic trait. It contains two different polypeptide chains, the Lp(a) glycoprotein and apo B-100. We have demonstrated the Lp(a) glycoprotein directly...

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

Schaper, J., Meinecke, P., Momeni, P., Groß, S., Von Holtum, D., ...

Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities. Three subtypes have been described: TRPS I, caused by mutations in the TRPS1 gene on chromosome 8;...

The registry of the German Network for Systemic Scleroderma: frequency of disease subsets and patterns of organ involvement

Hunzelmann, N., Genth, E., Krieg, T., Lehmacher, W., Melchers, I., Meurer, M., ...

Objective. Systemic sclerosis (SSc) is a rare, heterogeneous disease, which affects different organs and therefore requires interdisciplinary diagnostic and therapeutic management. To improve the...