Classificação Internacional das Cefaléias - HGF – Neurologia

Newman DS, Levine SR, Curtis VL, Welch KMA: Migraine like visual phenomena associated with
cerebral venous thrombosis. Headache 1989;29:82–5.
Tehindrazanarivelo AD, Evrard S, Schaison M, Mas JL, Dormont D, Bousser MG: Prospective
study of cereral sinus venous thrombosis in patients presenting with benign intracranial
hypertension. Cerebrovasc Dis 1992;2:22–7.
6.7.1 Arteriopatia cerebral autossômica dominante com infartos subcorticais e
leucoencefalopatia (CADASIL)
Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escailla JP, Iba-Zizen MT,
Bracard S, Tehindrazanarivelo A, Gastaut JL, Bousser MG. Autosomal dominant migraine with
MRI white matter abnormalities mapping to the CADASIL locus. Neurology 1995;45:1086–91.
Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B,
Ducrocq X, Levasseur M, Homeyer P, Mas JL, Lyon-Caen O, Tournier-Lasserve E, Bousser MG.
Clinical spectrum of CADASIL: a study of 7 families. Lancet 1995;346:934–9.
Joutel A, Corpechot C, Ducros A, Katayoun V, Chabriat H, Mouton P, Alamowitch S, Domenga V,
Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis EA, Ruchoux MM,
Weissenbach J, Bacxh JF, Bousser MG, Tournier-Lasserve E. ‘Notch 3’ mutations in CADASIL, a
hereditary adult-onset condition causing stroke and dementia. Nature 1996;383:707–10.
Verin M, Rolland Y, Landgraf F Chabriat H, Bompais B, Michel A, Vahedi K, Martinet JP,
Tournier-Lasserve E, Lemaitre MH, Edan G. New phenotype of the cerebral autosomal
dominant arteriopathy mapped to chromosome 19 migraine as the prominent clinical feature. J
Neurol Neurosurg Psychiat 1995;59:579–85.
6.7.2 Encefalopatia mitocondrial, acidose lática e episódios semelhantes a acidente vascular
encefálico (MELAS)
Klopstock A, May P, Siebel E, Papagiannuli E, Diener NC, Heichmann H. Mitochondrial DNA in
migraine with aura. Neurology 1996;46:1735–8.
Koo B, Becker L, Chuang S, Merante F, Robinson BH, Mac Gregor D, Tein I, Ho VB, McGreal DA,
Wherrett JR, Logan WJ. Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes
(MELAS): clinical, radiological, pathological and genetic observations. Ann Neurol
1993;34:25–32.
Ojaimi J, Katsabanis S, Bower S, Quigley A, Byrne E. Mitochondrial DNA in stroke and migraine
with aura. Cerebrovasc Dis 1998;8:102–6.
Pavlakis SG, Phillips PC, Di Mauro S, De Vivo DC, Rowland P. Mitochondrial myopathy,
encephalopathy, lactic acidosis and stroke-like episodes: a distinct clinical syndrome. Ann
Neurol 1984;16:481–8.
6.7.3 Cefaléia atribuída a angioplastia benigna do sistema nervoso central
Call GK, Fleming MC, Sealfon S, Levine H, Kistler JP, Fisher CM. Reversible cerebral segmental
vasoconstriction. Stroke 1988;19:1159–70.
Dodick DW, Brown RD, Britton JW, Huston J. Non aneurysmal thunderclap headache with
diffuse, multifocal segmental and reversible vasospasm. Cephalalgia 1999;19:118–213.
Lee KY, Sohn YH, Kim SH, Sunwoo IN. Basilar artery vasospasm in postpartum cerebral
angiopathy. Neurology 2000;54:2003–5.
McColl GJ, Fraser K. Pheochromocytoma and pseudovasculitis. J Rheumatol 1995;22:1441–2.
Razavi M, Bendixen B, Maley JE, Schoaib M, Zargarian M, Razavi B, Adams HP. CNS
pseudovasculitis in a patient with pheochromocytoma. Neurology 1999;52:1088–90. Serdaru
M, Chiras J, Cujas M, Lhermitte F. Isolated benign cerebral vasculitis or migrainous
vasospasm? J Neurol Neurosurg Psychiat 1984;47:73–6.
6.7.4 Cefaléia atribuída à apoplexia pituitária
Carral F. Pituitary apoplexy. Arch Neurol 2001;58:1143–4.
Chakeres DW, Curtin A, Ford G. Magnetic resonance imaging of pituitary and parasellar
abnormalities. Radiol Clin North Am 1989;27:265–81.