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Results of search for 'au:"Elçioglu, M"'
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Authors
Akalin, F
Akpolat, Ç
Aslankurt, M
Aydin, A
Aytuğ, A F
Bolukbasi, S
Cakir, A
Cenani, A
Child, A H
Comeglio, P
Elcioglu, M
Elcioglu, M N
Elçioglu, M
Elçioglu, N H
Elçioğlu, M
Elçioğlu, N
Elçioğlu, N H
Erden, B
Ergun, T
Fuhrmann, W
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Alkaptonuria
Angiogenesis Inhibitors
Biopsy
Diabetic Retinopathy
Female
Genetic Counseling
Humans
Infant
Infant, Newborn
Intravitreal Injections
Macular Edema
Male
Middle Aged
administration & dosage
complications
genetics
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Languages
English
Polish
Your search returned 7 results.
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1.
The frequency of genetic eye diseases in a genetic counseling center.
[electronic resource]
by
Elçioğlu, N
Elçioğlu, M
Fuhrmann, W
Producer:
19961017
In:
Genetic counseling (Geneva, Switzerland)
vol. 6
Availability:
No items available.
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2.
[The role of vitrectomy in the treatment of retinal detachment with macular holes].
[electronic resource]
by
Nawrocki, J
Elcioglu, M
Ghoraba, H
Gabel, V P
Producer:
19920902
In:
Klinika oczna
vol. 94
Availability:
No items available.
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3.
Tuberous sclerosis: clinical evaluation in a family and implications for genetic counseling.
[electronic resource]
by
Elçioğlu, N
Karatekin, G
Elçioğlu, M
Nuhoğlu, M
Cenani, A
Producer:
19980922
In:
Genetic counseling (Geneva, Switzerland)
vol. 9
Availability:
No items available.
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4.
Vessel diameter study: intravitreal vs posterior subtenon triamcinolone acetonide injection for diabetic macular edema.
[electronic resource]
by
Kurt, M M
Çekiç, O
Akpolat, Ç
Aslankurt, M
Elçioğlu, M
Producer:
20171221
In:
Eye (London, England)
vol. 31
Online resources:
Available from publisher's website
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5.
Neonatal Marfan syndrome caused by an exon 25 mutation of the fibrillin-1 gene.
[electronic resource]
by
Elçioglu, N H
Akalin, F
Elçioglu, M
Comeglio, P
Child, A H
Producer:
20041014
In:
Genetic counseling (Geneva, Switzerland)
vol. 15
Availability:
No items available.
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6.
Comparison of the effect of ranibizumab and dexamethasone implant in diabetic macular edema with concurrent epiretinal membrane.
[electronic resource]
by
Cakir, A
Erden, B
Bolukbasi, S
Aydin, A
Yurttaser Ocak, S
Maden, G
Elcioglu, M N
Producer:
20200128
In:
Journal francais d'ophtalmologie
vol. 42
Online resources:
Available from publisher's website
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7.
Alkaptonuria caused by compound heterozygote mutations.
[electronic resource]
by
Elçioğlu, N H
Aytuğ, A F
Müller, C R
Gürbüz, O
Ergun, T
Kotiloğlu, E
Elçioğlu, M
Producer:
20031104
In:
Genetic counseling (Geneva, Switzerland)
vol. 14
Availability:
No items available.
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