Heinrich Heimann

Prof. Heinrich Heimann


Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2007 in Ophthalmology
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Journal Article
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HHHeinrich Heimann
Heinrich Heimann
KBKarl Ulrich Bartz-Schmidt
Karl Ulrich Bartz-Schmidt
NBNorbert Bornfeld
Norbert Bornfeld
CWClaudia Weiss
Claudia Weiss
RHRalf-Dieter Hilgers
Ralf-Dieter Hilgers
SGScleral Buckling versus Primary Vitrectomy in Rhegmatogenous Retinal Detachment Study Group
Scleral Buckling versus Primary Vitrectomy in Rhegmatogenous Retinal Detachment Study Group

29 October 2004 in Graefe's Archive for Clinical and Experimental Ophthalmology
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Journal Article
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Sarah E. CouplandSarah E. Coupland
Sarah E. Coupland
HHHeinrich Heimann
Heinrich Heimann
NBNikolaos E. Bechrakis
Nikolaos E. Bechrakis

26 July 2005 in Graefe's Archive for Clinical and Experimental Ophthalmology
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Journal Article
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HHHeinrich Heimann
Heinrich Heimann
XZXiulan Zou
Xiulan Zou
CJClaudia Jandeck
Claudia Jandeck
UKUlrich Kellner
Ulrich Kellner
NBNikolaos E. Bechrakis
Nikolaos E. Bechrakis
MFMichael H. Foerster
Michael H. Foerster

1 October 2000 in British Journal of Ophthalmology
Verified
Journal Article
Open access
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HHHeinrich Heimann
Heinrich Heimann
NBNorbert Bornfeld
Norbert Bornfeld
OVOliver Vij
Oliver Vij
Sarah E. CouplandSarah E. Coupland
Sarah E. Coupland
NBNikolaos E Bechrakis
Nikolaos E Bechrakis
MFMichael H Foerster
Michael H Foerster
BACKGROUND Vasoproliferative tumours of the retina (VPTR) are benign tumours of unknown origin, occurring mostly in otherwise healthy patients. VPTR may be associated with other chorioretinal diseases, such as uveitis. The tumours, which histologically represent reactive gliovascular proliferations, are characterised by a pink to yellow appearance on funduscopy and are accompanied by exudative and haemorrhagic changes of the retina. METHODS 22 cases of VPTR in 21 patients were examined with a follow up period between 1 month and 6 years. Ophthalmological changes associated with VPTR were intraretinal and subretinal exudations (n=18), exudative detachments of the surrounding sensory retina (n=13), intraretinal and subretinal haemorrhages (n=10), exudative changes within the macula (n=10), hyperpigmentation of the retinal pigment epithelium at the border of the exudative retinal changes (n=9), and vitreous haemorrhages (n=4). Tumour biopsy was performed in two cases. Treatment consisted of plaque radiotherapy (n=14), plaque radiotherapy and cryotherapy (two), cryotherapy only (two), observation (three), and enucleation in one case of a blind and painful eye. RESULTS Regression of the tumour and the associated exudative changes could be observed in all treated cases. Visual acuity at last follow up improved two lines or more in two cases, remained within two lines of the initial visual acuity in 15 cases, and worsened in the remaining five. Histopathological examination of the biopsy specimens and the tumour of the enucleated eye showed massive capillary proliferation with perivascular spindle-shaped glial cells of retinal origin. CONCLUSION The correct diagnosis of VPTR is of importance as these lesions may lead to visual loss. Further, VPTR must be differentiated from angiomas associated with von Hippel-Lindau disease as well as from ocular and systemic malignancies. Regression of tumour thickness and associated retinal changes can be achieved with brachytherapy or cryotherapy.

1 January 2012 in American Journal of Ophthalmology
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Journal Article
Closed access
EZElsbeth J.T. van Zeeburg
Elsbeth J.T. van Zeeburg
KMKristel J.M. Maaijwee
Kristel J.M. Maaijwee
TMTom O.A.R. Missotten
Tom O.A.R. Missotten
HHHeinrich Heimann
Heinrich Heimann
JMJan C. van Meurs
Jan C. van Meurs

14 March 2008 in Eye
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Journal Article
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HHHeinrich Heimann
Heinrich Heimann
TST Stappler
T Stappler
DWD Wong
D Wong
Heavier than water intraocular tamponades have several theoretical advantages over conventional tamponades, especially in the treatment of complicated retinal detachments and proliferative viteroretinopathy of the lower fundus periphery. However, initial clinical series of various heavy tamponades have reported significant complication rates. Therefore, heavy tamponades have not found widespread acceptance. Three recently developed heavy silicone oil tamponades, Oxane HD, Densiron 68, and HWS 46-3000, are much better tolerated and presently seem to enter routine clinical practice. Literature review of 21 publications on the clinical application of 9 different heavy tamponades (fluorosilicone, C10F18, F6H8, OL62HV, Oxane HD, O62, F6H8-silicone oil mixture, Densiron 68, and HWS 46-3000). The first generation (fluorinated silicone and perfluorocarbon liquids) and second generation (partially fluorinated alkanes) of heavy tamponades were associated with relatively high complication rates, for example, tamponade emulsification, intraocular inflammation, and rise in intraocular pressure. The complication spectrum of the new generation of heavy silicone oils (Oxane HD, Densiron 68, and HWS 46-3000) seems to be comparable to conventional silicone oil tamponades while providing better support for the inferior retina and the posterior pole. The recently developed heavy silicone oil tamponades are safe and effective tools for the use of complicated retinal detachments of the inferior fundus.