The primary headaches, migraine with (MA) and without aura (MO) and cluster headache,
all carry a substantial genetic liability. Familial hemiplegic migraine (FHM), an autosomal …

In the last two decades, migraine research has greatly advanced our current knowledge of
the genetic contributions and the pathophysiology of this common and debilitating disorder …

The issue of interictal excitability of cortical neurons in migraine patients is controversial:
some studies have reported hypo-, others hyperexcitability. The aim of the present study was …

Biomarkers are physical signs or laboratory measurements that occur in association with a
pathological process and have putative diagnostic and/or prognostic utility. In migraine …

Migraine with aura (MA) and migraine without aura (MO) are primary headaches prevalent
in the general population that carry a substantial familial liability. Based on the model of …

Many novel ATP1A2 mutations were identified in patients with familial and sporadic
hemiplegic migraine. In sporadic patients, ATP1A2 screening has the highest chance of …

Migraines carry a substantial genetic liability, and in families affected with the typical
migraines (migraine with, MA, and without aura, MO) linkage to some chromosomal loci has …

Zwillings-und Familienstudien belegen die Bedeutung genetischer Faktoren für die Migräne,
insbesondere die Migräne mit Aura (MA). Für die familiäre hemiplegische Migräne (FHM) …

Liability to spontaneous and experimental pain is genetically determined and there is
considerable variability in the antinociceptive effects of drugs commonly used in treating …

Background Migraine is a polygenic multifactorial disease, possessing environmental and
genetic causative factors with multiple involved genes. Mutations in various ion channel …