These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 11061267)

  • 1. CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.
    Vahedi K; Denier C; Ducros A; Bousson V; Levy C; Chabriat H; Haguenau M; Tournier-Lasserve E; Bousser MG
    Neurology; 2000 Oct; 55(7):1040-2. PubMed ID: 11061267
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
    Ducros A; Denier C; Joutel A; Cecillon M; Lescoat C; Vahedi K; Darcel F; Vicaut E; Bousser MG; Tournier-Lasserve E
    N Engl J Med; 2001 Jul; 345(1):17-24. PubMed ID: 11439943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial hemiplegic migraine resulting in recurrent coma].
    Lee H; Aramideh M; Ginjaar HB
    Ned Tijdschr Geneeskd; 2008 Feb; 152(7):393-6. PubMed ID: 18380388
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.
    Terwindt G; Kors E; Haan J; Vermeulen F; Van den Maagdenberg A; Frants R; Ferrari M
    Arch Neurol; 2002 Jun; 59(6):1016-8. PubMed ID: 12056940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
    Kors EE; Terwindt GM; Vermeulen FL; Fitzsimons RB; Jardine PE; Heywood P; Love S; van den Maagdenberg AM; Haan J; Frants RR; Ferrari MD
    Ann Neurol; 2001 Jun; 49(6):753-60. PubMed ID: 11409427
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial hemiplegic migraine with prolonged coma and cerebellar atrophy: CACNA1A T666M mutation in a Korean family.
    Choi KH; Kim JS; Lee SY; Ryu SW; Kim SS; Lee SH; Kim S; Park HK
    J Korean Med Sci; 2012 Sep; 27(9):1124-7. PubMed ID: 22969264
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine.
    Sánchez-Albisua I; Schöning M; Jurkat-Rott K; Lerche H
    Pediatr Neurol; 2013 Oct; 49(4):286-8. PubMed ID: 23831250
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation.
    Freilinger T; Bohe M; Wegener B; Müller-Myhsok B; Dichgans M; Knoblauch H
    Cephalalgia; 2008 Apr; 28(4):403-7. PubMed ID: 18279427
    [No Abstract]   [Full Text] [Related]  

  • 9. The prevalence of familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in Portugal.
    Barros J; Ruano L; Domingos J; Tuna A; Damásio J; Alonso I; Silveira I; Sequeiros J; Coutinho P
    Headache; 2014 May; 54(5):911-5. PubMed ID: 24898624
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cerebellar ataxia, hemiplegic migraine, and related phenotypes due to a CACNA1A missense mutation: 12-year follow-up of a large Portuguese family.
    Barros J; Damásio J; Tuna A; Alves I; Silveira I; Pereira-Monteiro J; Sequeiros J; Alonso I; Sousa A; Coutinho P
    JAMA Neurol; 2013 Feb; 70(2):235-40. PubMed ID: 23407676
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stepwise developmental regression associated with novel CACNA1A mutation.
    Guerin AA; Feigenbaum A; Donner EJ; Yoon G
    Pediatr Neurol; 2008 Nov; 39(5):363-4. PubMed ID: 18940563
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brain atrophy following hemiplegic migraine attacks.
    Pelzer N; Hoogeveen ES; Ferrari MD; Poll-The BT; Kruit MC; Terwindt GM
    Cephalalgia; 2018 May; 38(6):1199-1202. PubMed ID: 28750589
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.
    Romozzi M; Primiano G; Rollo E; Travaglini L; Calabresi P; Servidei S; Vollono C
    J Headache Pain; 2021 Jul; 22(1):85. PubMed ID: 34320921
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family.
    Yabe I; Kitagawa M; Suzuki Y; Fujiwara K; Wada T; Tsubuku T; Takeichi N; Sakushima K; Soma H; Tsuji S; Niino M; Saitoh S; Sasaki H
    J Neurol; 2008 Oct; 255(10):1541-4. PubMed ID: 18670797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant.
    Nardello R; Plicato G; Mangano GD; Gennaro E; Mangano S; Brighina F; Raieli V; Fontana A
    BMC Neurol; 2020 Apr; 20(1):155. PubMed ID: 32336275
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.
    Zangaladze A; Asadi-Pooya AA; Ashkenazi A; Sperling MR
    Epilepsy Behav; 2010 Feb; 17(2):293-5. PubMed ID: 20071244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.
    Wada T; Kobayashi N; Takahashi Y; Aoki T; Watanabe T; Saitoh S
    Pediatr Neurol; 2002 Jan; 26(1):47-50. PubMed ID: 11814735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
    Stam AH; Luijckx GJ; Poll-Thé BT; Ginjaar IB; Frants RR; Haan J; Ferrari MD; Terwindt GM; van den Maagdenberg AM
    J Neurol Neurosurg Psychiatry; 2009 Oct; 80(10):1125-9. PubMed ID: 19520699
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.
    Battistini S; Stenirri S; Piatti M; Gelfi C; Righetti PG; Rocchi R; Giannini F; Battistini N; Guazzi GC; Ferrari M; Carrera P
    Neurology; 1999 Jul; 53(1):38-43. PubMed ID: 10408534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation.
    Chan YC; Burgunder JM; Wilder-Smith E; Chew SE; Lam-Mok-Sing KM; Sharma V; Ong BK
    J Clin Neurosci; 2008 Aug; 15(8):891-4. PubMed ID: 18313928
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.