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 *

513 related articles for article (PubMed ID: 24898624)

  • 1. 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]  

  • 2. 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]  

  • 3. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P
    Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CACNA1A nonsense mutation is associated with basilar-type migraine and episodic ataxia type 2.
    Robbins MS; Lipton RB; Laureta EC; Grosberg BM
    Headache; 2009 Jul; 49(7):1042-6. PubMed ID: 19486177
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
    García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E
    J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT
    J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Progressive Ataxia with Hemiplegic Migraines: a Phenotype of CACNA1A Missense Mutations, Not CAG Repeat Expansions.
    Duque KR; Marsili L; Sturchio A; Mahajan A; Merola A; Espay AJ; Kauffman MA
    Cerebellum; 2021 Feb; 20(1):134-139. PubMed ID: 32888184
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. 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]  

  • 14. Early-onset cerebellar atrophy associated with mutation in the CACNA1A gene.
    Naik S; Pohl K; Malik M; Siddiqui A; Josifova D
    Pediatr Neurol; 2011 Nov; 45(5):328-30. PubMed ID: 22000314
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
    Bürk K; Kaiser FJ; Tennstedt S; Schöls L; Kreuz FR; Wieland T; Strom TM; Büttner T; Hollstein R; Braunholz D; Plaschke J; Gillessen-Kaesbach G; Zühlke C
    Eur J Med Genet; 2014 Apr; 57(5):207-11. PubMed ID: 24486772
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
    Ducros A; Denier C; Joutel A; Vahedi K; Michel A; Darcel F; Madigand M; Guerouaou D; Tison F; Julien J; Hirsch E; Chedru F; Bisgård C; Lucotte G; Després P; Billard C; Barthez MA; Ponsot G; Bousser MG; Tournier-Lasserve E
    Am J Hum Genet; 1999 Jan; 64(1):89-98. PubMed ID: 9915947
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular genetic findings in migraine].
    Østergaard E; Thomsen LL; Russell MB
    Ugeskr Laeger; 2001 Nov; 163(45):6260-5. PubMed ID: 11723684
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The complexities of CACNA1A in clinical neurogenetics.
    Hommersom MP; van Prooije TH; Pennings M; Schouten MI; van Bokhoven H; Kamsteeg EJ; van de Warrenburg BPC
    J Neurol; 2022 Jun; 269(6):3094-3108. PubMed ID: 34806130
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
    Coutinho P; Cruz VT; Tuna A; Silva SE; Guimarães J
    Arch Neurol; 2006 Apr; 63(4):553-5. PubMed ID: 16606768
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 26.