Zobrazeno 1 - 10
of 195
pro vyhledávání: '"W. Hammerstein"'
Autor:
W, Hammerstein
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 224(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef33930fed64b90fe869b735c348174f
https://pubmed.ncbi.nlm.nih.gov/17455390
https://pubmed.ncbi.nlm.nih.gov/17455390
Autor:
W. Hammerstein, S. Kohnen
Publikováno v:
7. Kongreß der Deutschsprachigen Gesellschaft für Intraokularlinsen Implantation ISBN: 9783642501845
Es wird uber eine Methode zur Nachstarresektion bei dichten Kapselfibrosen und Pseudophakie berichtet. Das chirurgische Vorgehen wurde erforderlich, wenn dichte Kapselfibrosen mit dem Neodymium-YAG-Laser nicht eroffnet werden konnten. Uber einen Pars
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::420d0e3f144a12ab4c88f0b395e3d6c8
https://doi.org/10.1007/978-3-642-50183-8_66
https://doi.org/10.1007/978-3-642-50183-8_66
Autor:
W, Küster, W, Hammerstein
Publikováno v:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 43(12)
Schöpf syndrome is an unusual genodermatosis categorized within the heterogeneous group of ectodermal dysplasias. Since the first description of this syndrome in 1971, ten further cases have been published. The diagnostic features include eyelid cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47a62141d01dc7c54617c1b79ac6feac
https://pubmed.ncbi.nlm.nih.gov/1473970
https://pubmed.ncbi.nlm.nih.gov/1473970
Autor:
W, Hammerstein
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 199(3)
In premature infants there is a temporal and causal relation between the change in the erythropoiesis after birth and the manifestation of retinopathy. The physiological substitution of the fetal erythrocytes can be controlled by an analysis of the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c74d2f16b8805b6ac202fec4d847caf6
https://pubmed.ncbi.nlm.nih.gov/1721664
https://pubmed.ncbi.nlm.nih.gov/1721664
Publikováno v:
Fortschritte der Ophthalmologie : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 88(5)
We discuss a paraneoplastic retinopathy in a 6-year-old boy who had an embryonal rhabdomyosarcoma of the thorax. Opacities of the vitreous body, optical atrophy, contracted arteries and changes in the structure of the retina--especially the retinal p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::582d61593b4cc160a0f494f0165a9630
https://pubmed.ncbi.nlm.nih.gov/1757033
https://pubmed.ncbi.nlm.nih.gov/1757033
Autor:
W, Hammerstein
Publikováno v:
Fortschritte der Ophthalmologie : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 87(5)
In this paper we discuss a female patient with retinitis pigmentosa. Pronounced pigmentation in the periphery, together with yellow waxlike optical atrophy and contracted arteries, characterized the ophthalmological findings. The ERG was extinguished
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72d6a32a5cd16097171b8d889273326a
https://pubmed.ncbi.nlm.nih.gov/2272569
https://pubmed.ncbi.nlm.nih.gov/2272569
Publikováno v:
Albrecht von Graefes Archiv f�r Klinische und Experimentelle Ophthalmologie. 195:161-173
The authors report about observations they made in two sisters. One sister showed a fibroid degeneration of the cornea, the other a band-shaped keratopathy respectively, together with an ichthyosis and an alopecia as a result of capillary fractures d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1cc43a6ea24d9b34a330e5619d0e97f
https://doi.org/10.1007/bf00410468
https://doi.org/10.1007/bf00410468
Publikováno v:
Dermatology. 153:163-171
Corneal lesions in ichthyosis, here combined with alopecia, are rarely described in the literature. The present observation relates to two sisters, whose grandparents were siblings. The mode of inheritance is autosomal recessive, as is usual in ichth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b97048bd4458984dc328b99df51123d
https://doi.org/10.1159/000251111
https://doi.org/10.1159/000251111
Autor:
T. F. Wienker, Andreas Gal, K. Rüther, D. Ahlert, F. Brunsmann, D. Hogenkamp, I. H. Pawlowitzki, W. Hammerstein
Publikováno v:
Human Genetics. 73:123-126
Choroideremia is a progressive tapetochoroidal dystrophy with X-linked transmission leading frequently to blindness in affected males. The choroideremia-locus (TCD) has recently been assigned to the long arm of the X chromosome by linkage to polymorp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e840e18b79e0e479078e0829fa0df7e1
https://doi.org/10.1007/bf00291600
https://doi.org/10.1007/bf00291600
Publikováno v:
European Neurology. 21:249-255
Tapetoretinal degeneration in 3 members of a family is documented with fundus photographs and fluorescein angiograms. Computer tomograms showed intracranial symmetrical calcifications of the central nervous system in 2 patients. Laboratory examinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cddc3a2d4500f63b2f64bf8fbebc1c64
https://doi.org/10.1159/000115488
https://doi.org/10.1159/000115488