-G M Terwindt Researcher Activity Profile

Research Author Detailed Information 

G M Terwindt Publication Rate By Year

G M Terwindt has published 1 paper(s) in 1995, 2 paper(s) in 1996, 1 paper(s) in 1999, 1 paper(s) in 2001, 1 paper(s) in 2002, 1 paper(s) in 2005, 1 paper(s) in 2006, 4 paper(s) in 2007, 4 paper(s) in 2008, for a total of 16 research publications in total.

G M Gm Terwindt Author Information

LAST NAME: terwindt

FIRST NAME: G M

INITIALS: gm

AFFILIATION:

Papers

G M Terwindt's Publication Record

1. Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. Year Published: 2007
Departments of Human Genetics, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlands.
2. Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. Year Published: 2007
Departments of Human Genetics, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlands.
3. A review of the genetic relation between migraine and epilepsy. Year Published: 2008
Department of Neurology, Leiden University Medical Centre, Leiden, the Netherlands. jhaan@rijnland.nl
4. A review of the genetic relation between migraine and epilepsy. Year Published: 2008
Department of Neurology, Leiden University Medical Centre, Leiden, the Netherlands. jhaan@rijnland.nl
5. A review of the genetic relation between migraine and epilepsy. Year Published: 2008
Department of Neurology, Leiden University Medical Centre, Leiden, the Netherlands. jhaan@rijnland.nl
6. Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene. Year Published: 2001
Department of Neurology, Leiden University Medical Centre, The Netherlands.
7. No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache. Year Published: 2002
Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands. jhaan@rijnland.nl
8. Association study in migraine. Year Published: 1995
9. Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG. Year Published: 1996
Department of Neurology, Leiden University Hospital, The Netherlands.
10. Is familial hemiplegic migraine a hereditary form of basilar migraine? Year Published: 1996
Department of Neurology, University Hospital Leiden, Netherlands.
11. Search for mitochondrial DNA mutations in migraine subgroups. Year Published: 1999
Department of Neurology, Leiden University Medical Centre, The Netherlands.
12. The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine. Year Published: 2005
Department of Human Genetics, Leiden University Medical Centre, Leiden, and Department of Neurology, Rijnland Hospital, Leiderdorp, The Netherlands.
13. The prevalence of premonitory symptoms in migraine: a questionnaire study in 461 patients. Year Published: 2006
Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands. g.g.schoonman@lumc.nl
14. A review of the genetic relation between migraine and epilepsy. Year Published: 2008
Department of Neurology, Leiden University Medical Centre, Leiden, the Netherlands. jhaan@rijnland.nl
15. Migraine: a complex genetic disorder. Year Published: 2007
16. C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Year Published: 2007
Department of Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.