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- 2002
-
Mark
Spinal sensorimotor transformation: Relation between cutaneous somatotopy and a reflex network
Levinsson, Anders LU ; Holmberg, Hans LU ; Broman, Jonas LU ; Zhang, Mengliang LU and Schouenborg, Jens LU
(2002)
In The Journal of Neuroscience
22(18).
p.8170-8182
- Contribution to journal › Article
-
Mark
Migration patterns and phenotypic differentiation of long-term expanded human neural progenitor cells after transplantation into the adult rat brain.
Englund Johansson, Ulrica LU ; Björklund, Anders LU
and Wictorin, Klas
LU
(2002)
In Developmental Brain Research
134(1-2).
p.123-141
- Contribution to journal › Article
-
Mark
Cataract surgery and quality of life in patients with age related macular degeneration.
- Contribution to journal › Article
-
Mark
Clinical features of achromatopsia in Swedish patients with defined genotypes.
- Contribution to journal › Article
-
Mark
Optic nerve hypoplasia: Risk factors and epidemiology.
- Contribution to journal › Article
-
Mark
Long-term survival and glial differentiation of the brain-derived precursor cell line RN33B after subretinal transplantation to adult normal rats
Blixt Wojciechowski, Anita LU ; Englund Johansson, Ulrica LU ; Lundberg, Cecilia LU
and Warfvinge, Karin
LU
(2002)
In Stem Cells
20(2).
p.163-173
- Contribution to journal › Article
-
Mark
Retinal dysfunction and anterior segment deposits in a patient treated with rifabutin
Ponjavic, Vesna LU ; Gränse, Lotta LU
; Bengtsson-Stigmar, Elisabeth
LU
and Andréasson, Sten
LU
(2002)
In Acta Ophthalmologica Scandinavica
80(5).
p.553-556
- Contribution to journal › Article
-
Mark
Tracing local hyaluronan after ocular anterior segment trauma
(2002)
- Thesis › Doctoral thesis (compilation)
-
Mark
In vivo properties of neural stem cells after transplantation into the rat brain-Studies of phenotypic differentiation and functional integration using cell-specific labelling and electrophysiological techniques
(2002)
- Thesis › Doctoral thesis (compilation)
-
Mark
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene
- Contribution to journal › Article