W. Kress

Publication List Details

Period

1981 - 2006

Number

24

Co-Authors

Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionary conserved non-transcribed region (2006)

Tagariello, A., Heller, R., Greven, A., Kalscheuer, Vera M., Molter, T., Rauch, A., ...

Craniosynostosis is a congenital developmental disorder involving premature fusion of cranial sutures, which results in an abnormal shape of the skull. Significant progress in understanding the...

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 (2005)

Loeys, B, Chen, J, Neptune, E, Judge, D, Podowski, M, Holm, T, ...

We report heterozygous mutations in the genes encoding either type I or type II transforming growth factor beta receptor in ten families with a newly described human phenotype that includes...

Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...

Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...

Intolerance to neuroleptics and susceptibility for malignant hyperthermia in a patient with proximal myotonic myopathy (PROMM) and schizophrenia (2002)

Schneider, C, Gil, FP, Schneider, M, Anetseder, M, Kress, W, Müller, CR

We report a patient with proximal myotonic myopathy who was treated with neuroleptics because of exacerbating schizophrenia. Under therapy with fluanxol, the patient developed muscle stiffness and...

LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)

Kugel, G., Carabatos, C., Kress, W.

The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...

PHONONS IN MIXED VALENCE COMPOUNDS (1981)

Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.

Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...

LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)

Kugel, G., Carabatos, C., Kress, W.

The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...

PHONONS IN MIXED VALENCE COMPOUNDS (1981)

Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.

Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...

LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)

Kugel, G., Carabatos, C., Kress, W.

The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...

PHONONS IN MIXED VALENCE COMPOUNDS (1981)

Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.

Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...

Linkage studies in a large fragile X family.

Patterson, M, Bell, M, Kress, W, Davies, K E, Froster-Iskenius, U

We have analyzed the segregation of five loci in the region Xq27/28 in a large family affected by the fragile X syndrome. The marker DXS115 (767) is shown to be polymorphic with the enzyme PstI, as...

Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene

Felbor, U., Mutsch, Y., Grehn, F., Muller, C., Kress, W.

AIMS—To assess the involvement of the recently identified human homogentisate 1,2-dioxygenase gene (HGO) in alkaptonuria (AKU) in two unrelated patients with ochronosis of the conjunctiva, sclera,...

Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome.

Merienne, K, Jacquot, S, Trivier, E, Pannetier, S, Rossi, A, Scott, C, ...

Coffin-Lowry syndrome (CLS) is a syndromal form of X linked mental retardation, in which some associated facial, hand, and skeletal abnormalities are diagnostic features. Accurate diagnosis, critical...

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec, I, Kress, W, Meng, G, Müller, B, Müller, C R, Grimm, T

Ninety-five percent of cases of severe muscular dystrophy with early childhood onset result from mutations in the dystrophin region of the human X chromosome (DMD, McKusick 310200), whereas 5% are...