E-LIB Suche - Ergebnisse für: WISSINGER, B

1

A case of X-linked retinoschisis with atypical fundus appea..:

Nasser, F. ; Kohl, S. ; Kuehlewein, L....
Documenta Ophthalmologica. 139 (2019) 1 - p. 75-81 , 2019

Link: https://doi.org/10.1007/..

2

Mutation detection of Pakistani families with autosomal rec..:

Ravesh, Z. ; Wissinger, B. ; Ansar, M.
Acta Ophthalmologica. 95 (2017) S259 - p. , 2017

Link: https://doi.org/10.1111/..

3

Antisense oligonucleotide therapy for splicing defects in O..:

Wissinger, B. ; Synofzik, M. ; Schöls, L..
Acta Ophthalmologica. 95 (2017) S259 - p. , 2017

Link: https://doi.org/10.1111/..

4

Loss of function of Ywhah in mice induces deafness and coch..:

Buret, L ; Rebillard, G ; Brun, E...
Cell Death Discovery. 2 (2016) 1 - p. , 2016

Link: https://doi.org/10.1038/..

5

Dominant Optic Atrophy plus phenotype caused by a deep intr..:

Wissinger, B. ; Bonifert, T. ; Gonzalez‐Menendez, I....
Acta Ophthalmologica. 93 (2015) S255 - p. , 2015

Link: https://doi.org/10.1111/..

6

Pure and syndromic optic atrophy explained by deep intronic..:

Bonifert, T. ; Karle, K. N. ; Tonagel, F....
Brain. 137 (2014) 8 - p. 2164-2177 , 2014

Link: https://doi.org/10.1093/..

7

Altered nitrogen and precipitation along urban gradients af..:

Wissinger, B.D. ; Eigenbrode, S.D. ; Marshall, J.D...
Journal of Arid Environments. 104 (2014) - p. 96-105 , 2014

Link: https://doi.org/10.1016/..

8

Hope: Hereditary retinal disorders

from patients towards therapies ; Schlussbericht des Gesamt...

Wissinger, B. , [ca. 2012]

Link: http://edok01.tib.uni-ha..

9

Establishing baseline rod electroretinogram values in achro..:

Wang, Isaac ; Khan, Naheed W. ; Branham, Kari...
Documenta Ophthalmologica. 125 (2012) 3 - p. 229-233 , 2012

Link: https://doi.org/10.1007/..

10

Lebersche Optikusneuropathie:

Leo-Kottler, B. ; Wissinger, B.
Der Ophthalmologe. 108 (2011) 12 - p. 1179-1194 , 2011

Link: https://doi.org/10.1007/..

11

Blue cone nonochromacy gene mutation in Asia: phenotype var..:

BITOUN, P ; RIGAUDIERE, F ; PAPKE, M..
Acta Ophthalmologica. 88 (2010) s246 - p. 0-0 , 2010

Link: https://doi.org/10.1111/..

12

Induction of STAT3-related genes in fast degenerating cone ..:

Schaeferhoff, K. ; Michalakis, S. ; Tanimoto, N....
Cellular and Molecular Life Sciences. 67 (2010) 18 - p. 3173-3186 , 2010

Link: https://doi.org/10.1007/..

13

Zapfendystrophien – von der Bedeutsamkeit einer Minderheit ..:

Wissinger, B.
Der Ophthalmologe. 106 (2009) 2 - p. 97-98 , 2009

Link: https://doi.org/10.1007/..

14

A novel mutation in the FOXC1 gene in a family with Axenfel..:

Weisschuh, N ; Wolf, C ; Wissinger, B.
Clinical Genetics. 74 (2008) 5 - p. 476-480 , 2008

Link: https://doi.org/10.1111/..

15

OPA1 mutations induce mitochondrial DNA instability and opt..:

Amati-Bonneau, P. ; Valentino, M. L. ; Reynier, P....
Brain. 131 (2008) 2 - p. 338-351 , 2008

Link: https://doi.org/10.1093/..