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List of works by Douglas E Crompton

A neurologist's guide to genome-wide association studies.

scientific article published on February 2009

Acquired Chiari 1 malformation and syringomyelia following lumboperitoneal shunting for pseudotumour cerebri.

scientific article published in February 2005

Adverse clinical outcomes after dabigatran reversal with idarucizumab to facilitate acute stroke thrombolysis

scientific article published on 06 February 2017

Analysis of a cDNA from the neurologically active locus shaking-B (Passover) of Drosophila melanogaster

scientific article published on December 15, 1992

Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation

scientific article published on 2 December 2006

Deconstruction of Interhospital Transfer Workflow in Large Vessel Occlusion: Real-World Data in the Thrombectomy Era.

scientific article

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

article

Epileptic spasms are a feature of DEPDC5 mTORopathy.

scientific article published on 23 July 2015

Essential and neural transcripts from the Drosophila shaking-B locus are differentially expressed in the embryonic mesoderm and pupal nervous system.

scientific article published on July 1995

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.

scientific article published on 24 December 2015

Extensive cerebral venous sinus thrombosis after romiplostim treatment for immune thrombocytopenia (ITP) despite severe thrombocytopenia

scientific article published on 01 June 2015

Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families

scientific article published on 16 March 2020

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus

scientific article

Familial mesial temporal lobe epilepsy and the borderland of déjà vu.

scientific article

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance

scientific article published on 23 September 2010

Genetic Basis of Sudden Unexpected Death in Epilepsy.

scientific article

Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases.

scientific article published in August 2014

Glut1 deficiency syndrome: Absence epilepsy and La Soupe du Jour

scientific article published on 3 September 2015

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2.

scientific article published on July 2016

Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

scientific article published on 29 October 2019

Large basilar tip aneurysm causing anterior internuclear ophthalmoplegia.

scientific article published on 10 February 2015

Mortality in Dravet syndrome

scientific article published on 26 October 2016

Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.

scientific article published on 14 April 2014

Neuroferritinopathy: a window on the role of iron in neurodegeneration.

scientific article published on November 2002

Optic perineuritis as a rare initial presentation of sarcoidosis

scientific article published on 01 September 2007

The borderland of epilepsy: a clinical and molecular view, 100 years on.

scientific article published in February 2010

The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures

scientific article published in April 2009

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