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Results of search for 'au:"Weidle, E"', page 4 of 4
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Authors
Auw-Haedrich, C
Baur, M P
Clausen, I
Duncker, G
Emmig, C T
Froster, U
Grünauer-Kloevekorn, C
Heinritz, W
Lisch, W
Naumann, G O
Pleyer, U
Rohrbach, J M
Steuhl, K P
Thiel, H J
Tost, F
Waetjen, R
Weidle, E
Weidle, E G
Wolter-Roessler, M
Zierhut, M
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Adolescent
Adult
Aged
Aged, 80 and over
Cataract Extraction
Child
Child, Preschool
Cornea
Corneal Dystrophies, Hereditary
Corneal Transplantation
Diagnosis, Differential
Female
Follow-Up Studies
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Male
Middle Aged
Pedigree
diagnosis
genetics
pathology
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German
Your search returned 66 results.
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61.
[Bullous dermatosis with conjunctival and corneal involvement: differential diagnostic scope and explanation of the "overlap syndrome" concept].
[electronic resource]
by
Zierhut, M
Thiel, H J
Weidle, E G
Steuhl, K P
Sönnichsen, K
Müller, C
Hübner, H
Producer:
19880920
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 192
Online resources:
Available from publisher's website
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62.
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].
[electronic resource]
by
Grünauer-Kloevekorn, C
Bräutigam, S
Wolter-Roessler, M
Tost, F
Weidle, E
Froster, U
Duncker, G I W
Producer:
20060228
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 222
Online resources:
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63.
[Clinical types of immunologic transplant reactions following perforating keratoplasty].
[electronic resource]
by
Pleyer, U
Weidle, E G
Lisch, W
Steuhl, K P
Möhrle, C
Richter, U
Zierhut, M
Selbmann, H K
Producer:
19900521
In:
Fortschritte der Ophthalmologie : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 87
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64.
A new, band-shaped and whorled microcystic dystrophy of the corneal epithelium.
[electronic resource]
by
Lisch, W
Steuhl, K P
Lisch, C
Weidle, E G
Emmig, C T
Cohen, K L
Perry, H D
Producer:
19920731
In:
American journal of ophthalmology
vol. 114
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65.
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy].
[electronic resource]
by
Grünauer-Kloevekorn, C
Braeutigam, S
Weidle, E
Wolter-Roessler, M
Tost, F
Auw-Haedrich, C
Völcker, H E
Heinritz, W
Froster, U
Duncker, G
Producer:
20061213
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 223
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66.
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings.
[electronic resource]
by
Gruenauer-Kloevekorn, C
Clausen, I
Weidle, E
Wolter-Roessler, M
Tost, F
Völcker, H E
Schulze, D P
Heinritz, W
Reinhard, T
Froster, U
Duncker, G
Schorderet, D
Auw-Haedrich, C
Producer:
20090715
In:
The British journal of ophthalmology
vol. 93
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