Literature DB >> 18765143

Genetics of headache in children: where are we headed?

Andrew D Hershey1.   

Abstract

A history of headaches in a family is very frequently noted when evaluating a child for recurrent, episodic headaches. Oftentimes, these headaches have migraine features, although the family may deny a history of migraine. This positive family history implies an inherited or genetic basis as a component to the underlying pathophysiology of primary headaches. A variety of methodology has begun to elucidate this contribution, including historical observation, population-based studies of families and twins, gene polymorphism association studies, and specific gene identification for isolated migraine subtypes. This line of investigation should progress in the future to a better understanding of migraine and clarification of the diagnostic subtypes for a genotype-phenotype association.

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Year:  2008        PMID: 18765143     DOI: 10.1007/s11916-008-0062-x

Source DB:  PubMed          Journal:  Curr Pain Headache Rep        ISSN: 1534-3081


  45 in total

1.  Possible risk factors and precipitants for migraine with aura in discordant twin-pairs: a population-based study.

Authors:  V Ulrich; J Olesen; M Gervil; M B Russell
Journal:  Cephalalgia       Date:  2000-11       Impact factor: 6.292

2.  Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Authors:  G M Terwindt; R A Ophoff; J Haan; M N Vergouwe; R van Eijk; R R Frants; M D Ferrari
Journal:  Neurology       Date:  1998-04       Impact factor: 9.910

3.  The relative role of genetic and environmental factors in migraine without aura.

Authors:  M Gervil; V Ulrich; J Kaprio; J Olesen; M B Russell
Journal:  Neurology       Date:  1999-09-22       Impact factor: 9.910

Review 4.  Serotonin receptors and the acute attack of migraine.

Authors:  P J Goadsby
Journal:  Clin Neurosci       Date:  1998

5.  Association of the insertion/deletion polymorphism of the angiotensin I-converting enzyme gene in patients of migraine with aura.

Authors:  Hisanori Kowa; Emi Fusayasu; Tamami Ijiri; Kumiko Ishizaki; Kenichi Yasui; Kazuhiro Nakaso; Masayoshi Kusumi; Takao Takeshima; Kenji Nakashima
Journal:  Neurosci Lett       Date:  2005-02-10       Impact factor: 3.046

6.  A gene for familial hemiplegic migraine maps to chromosome 19.

Authors:  A Joutel; M G Bousser; V Biousse; P Labauge; H Chabriat; A Nibbio; J Maciazek; B Meyer; M A Bach; J Weissenbach
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

7.  Inheritance of cluster headache and its possible link to migraine.

Authors:  L Kudrow; D B Kudrow
Journal:  Headache       Date:  1994 Jul-Aug       Impact factor: 5.887

Review 8.  Migraine: a complex genetic disorder.

Authors:  Maija Wessman; Gisela M Terwindt; Mari A Kaunisto; Aarno Palotie; Roel A Ophoff
Journal:  Lancet Neurol       Date:  2007-06       Impact factor: 44.182

9.  Genomic abnormalities in patients with migraine and chronic migraine: preliminary blood gene expression suggests platelet abnormalities.

Authors:  Andrew D Hershey; Yang Tang; Scott W Powers; Marielle A Kabbouche; Donald L Gilbert; Tracy A Glauser; Frank R Sharp
Journal:  Headache       Date:  2004 Nov-Dec       Impact factor: 5.887

10.  Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

Authors:  Maurizio De Fusco; Roberto Marconi; Laura Silvestri; Luigia Atorino; Luca Rampoldi; Letterio Morgante; Andrea Ballabio; Paolo Aridon; Giorgio Casari
Journal:  Nat Genet       Date:  2003-01-21       Impact factor: 38.330

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