|
1
|
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
|
Eur J Neurol
|
2004
|
1.09
|
|
2
|
Replication and meta-analysis of TMEM132D gene variants in panic disorder.
|
Transl Psychiatry
|
2012
|
1.02
|
|
3
|
Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.
|
J Neurol Neurosurg Psychiatry
|
1998
|
0.93
|
|
4
|
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
|
Hum Mol Genet
|
1997
|
0.90
|
|
5
|
The norepinephrine transporter gene is a candidate gene for panic disorder.
|
J Neural Transm (Vienna)
|
2011
|
0.90
|
|
6
|
Probenecid inhibition of the outward transport of fluorescein across the human blood-retina barrier.
|
Acta Ophthalmol (Copenh)
|
1994
|
0.85
|
|
7
|
Interferon alpha-2a treatment of patients with subfoveal neovascular macular degeneration. A pilot investigation.
|
Acta Ophthalmol (Copenh)
|
1993
|
0.83
|
|
8
|
No association between the -399 C > T polymorphism of the neuropeptide Y gene and schizophrenia, unipolar depression or panic disorder in a Danish population.
|
Acta Psychiatr Scand
|
2006
|
0.79
|
|
9
|
Symptomatic type 1 protein C deficiency caused by a de novo Ser270Leu mutation in the catalytic domain.
|
Br J Haematol
|
2001
|
0.78
|
|
10
|
Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
|
J Neurol Neurosurg Psychiatry
|
1998
|
0.75
|
|
11
|
[The future of social pediatrics].
|
Ugeskr Laeger
|
1980
|
0.75
|