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The Journal of Comparative Neurology
|
December 1, 1994
GABAA receptor alpha 1 subunit, an early marker for area specification in developing rat cerebral cortex
J Paysan, J Bolz, H Mohler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 24, 1997
Area-specific regulation of gamma-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortex
J Paysan, A Kossel, J Bolz, et al.
Ophthalmology
|
April 14, 2015
Ophthalmic Features of Children Not Yet Diagnosed with Alstrom Syndrome
Arif O Khan, Inam N Bifari, Hanno J Bolz
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
December 6, 2014
[Genetics of congenital aniridia]
C Neuhaus, C Betz, C Bergmann, et al.
Clinical Genetics
|
January 21, 2016
Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian Peninsula
A O Khan, M Tamimi, S Lenzner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 5, 1998
Membrane-associated molecules guide limbic and nonlimbic thalamocortical projections
F Mann, V Zhukareva, A Pimenta, et al.
The British Journal of Ophthalmology
|
October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian Peninsula
Arif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Neuroscience
|
September 13, 2005
Neurogenesis in the adult dentate gyrus after cortical infarcts: effects of infarct location, N-methyl-D-aspartate receptor blockade and anti-inflammatory treatment
M M Kluska, O W Witte, J Bolz, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")
Arif O Khan, Sandra Nagl, Carsten Bergmann, et al.
Ophthalmic Genetics
|
December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutations
Arif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 148) with videos related to
Sort By:
Page
of 15
The Journal of Comparative Neurology
|
December 1, 1994
GABAA receptor alpha 1 subunit, an early marker for area specification in developing rat cerebral cortex
J Paysan, J Bolz, H Mohler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 24, 1997
Area-specific regulation of gamma-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortex
J Paysan, A Kossel, J Bolz, et al.
Ophthalmology
|
April 14, 2015
Ophthalmic Features of Children Not Yet Diagnosed with Alstrom Syndrome
Arif O Khan, Inam N Bifari, Hanno J Bolz
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
December 6, 2014
[Genetics of congenital aniridia]
C Neuhaus, C Betz, C Bergmann, et al.
Clinical Genetics
|
January 21, 2016
Hermansky-Pudlak syndrome genes are frequently mutated in patients with albinism from the Arabian Peninsula
A O Khan, M Tamimi, S Lenzner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 5, 1998
Membrane-associated molecules guide limbic and nonlimbic thalamocortical projections
F Mann, V Zhukareva, A Pimenta, et al.
The British Journal of Ophthalmology
|
October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian Peninsula
Arif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Neuroscience
|
September 13, 2005
Neurogenesis in the adult dentate gyrus after cortical infarcts: effects of infarct location, N-methyl-D-aspartate receptor blockade and anti-inflammatory treatment
M M Kluska, O W Witte, J Bolz, et al.
Journal of Pediatric Ophthalmology and Strabismus
|
July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")
Arif O Khan, Sandra Nagl, Carsten Bergmann, et al.
Ophthalmic Genetics
|
December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutations
Arif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Page
of 15