Human Genome Epidemiology Literature Finder
Rare Diseases
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Records 1 - 24 (of 24 Records) |
| Query Trace: Familial Hemiplegic Migraine[original query] |
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| Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology 2001 Apr 56 (8): 1028-32. Terwindt G M, Ophoff R A, van Eijk R, Vergouwe M N, Haan J, Frants R R, Sandkuijl L A, Ferrari M D, |
| Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine. Archives of neurology 2002 Jun 59 (6): 1016-8. Terwindt Gisela, Kors Esther, Haan Joost, Vermeulen Frans, Van den Maagdenberg Arn, Frants Rune, Ferrari Mich |
| CACNA1A gene polymorphisms in cluster headache. Cephalalgia : an international journal of headache 2001 Dec 21 (10): 953-8. Sjöstrand C, Giedratis V, Ekbom K, Waldenlind E, Hillert |
| Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. American journal of medical genetics 2001 Dec 105 (8): 707-12. Lea R A, Curtain R P, Hutchins C, Brimage P J, Griffiths L |
| [An update on the familial headache syndromes]. Rinsho shinkeigaku = Clinical neurology 2005 1 44 (11): 944-7. Takeshima Takao, Kusumi Masayoshi, Fukuhara Yoko, Kowa Hisanori, Adachi Yoshiki, Nakashima Ken |
| Haplotype-based systematic association studies of ATP1A2 in migraine with aura. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006 Apr 141B (3): 257-60. Netzer Christian, Todt Unda, Heinze Axel, Freudenberg Jan, Zumbroich Vera, Becker Tim, Goebel Ingrid, Ohlraun Stephanie, Goebel Hartmut, Kubisch Christi |
| Association analysis of chromosome 1 migraine candidate genes. BMC medical genetics 2007 8 (1): 57. Fernandez Francesca, Curtain Robert P, Colson Natalie J, Ovcaric Micky, MacMillan John, Griffiths Lyn |
| A high-density association screen of 155 ion transport genes for involvement with common migraine. Human molecular genetics 2008 Nov 17 (21): 3318-31. Nyholt Dale R, LaForge K Steven, Kallela Mikko, Alakurtti Kirsi, Anttila Verneri, Färkkilä Markus, Hämaläinen Eija, Kaprio Jaakko, Kaunisto Mari A, Heath Andrew C, Montgomery Grant W, Göbel Hartmut, Todt Unda, Ferrari Michel D, Launer Lenore J, Frants Rune R, Terwindt Gisela M, de Vries Boukje, Verschuren W M Monique, Brand Jan, Freilinger Tobias, Pfaffenrath Volker, Straube Andreas, Ballinger Dennis G, Zhan Yiping, Daly Mark J, Cox David R, Dichgans Martin, van den Maagdenberg Arn M J M, Kubisch Christian, Martin Nicholas G, Wessman Maija, Peltonen Leena, Palotie Aar |
| Investigation of the NOTCH3 and TNFSF7 genes on C19p13 as candidates for migraine. The open neurology journal 2008 2 1-7. Smith Robert A, Curtain Robert, Ovcaric Mick, Tajouri Lotti, Macmillan John, Griffiths L |
| A genotype-phenotype analysis of the 8q22.1 variant in migraine with aura. European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Apr 19 (4): 603-9. Esserlind A-L, Kirchmann M, Hauge A W, Le H, Olesen |
| Identification of novel genes involved in migraine. Headache 2012 Oct 52 Suppl 2 107-10. Lafrenière Ronald G, Rouleau Guy |
| Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2013 Mar 18 (Suppl 1): S6-S10. Meamar Rokhsareh, Ostadsharif Maryam, Saadatnia Mohammad, Ghorbani Abbas, Nouri Nayereh, Dehghani Leila, Salehi Manso |
| Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study. SpringerPlus 2013 Dec 2 (1): 46. Harriott Andrea M, Dueker Nicole, Cheng Yu-Ching, Ryan Kathleen A, O'Connell Jeffrey R, Stine O Colin, McArdle Patrick F, Wozniak Marcella A, Stern Barney J, Mitchell Braxton D, Kittner Steven J, Cole John |
| Involvement of astrocyte and oligodendrocyte gene sets in migraine. Cephalalgia : an international journal of headache 2015 Dec . Eising Else, de Leeuw Christiaan, Min Josine L, Anttila Verneri, Verheijen Mark Hg, Terwindt Gisela M, Dichgans Martin, Freilinger Tobias, Kubisch Christian, , Ferrari Michel D, Smit August B, de Vries Boukje, Palotie Aarno, van den Maagdenberg Arn Mjm, Posthuma Daniel |
| Molecular factors in migraine. Oncotarget 2016 May . Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan |
| Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes. Human genomics 2016 10 (1): 3. Domitrz Izabela, Kosiorek Michalina, ?ekanowski Cezary, Kami?ska An |
| Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes. Headache 2017 Jun . Ambrosini Anna, D'Onofrio Mara, Buzzi Maria Gabriella, Arisi Ivan, Grieco Gaetano S, Pierelli Francesco, Santorelli Filippo M, Schoenen Je |
| Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine. Journal of medical genetics 2020 1 57 (9): 610-616. Rasmussen Andreas Hoiberg, Olofsson Isa, Chalmer Mona Ameri, Olesen Jes, Hansen Thomas Folkma |
| Epilepsy in patients with familial hemiplegic migraine. Seizure 2021 4 88 87-94. Has?rc? Bay?r Buse Rahime, Tutkavul Kemal, Eser Metin, Baykan Bet |
| Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study. Neurology 2021 10 98 (1): e51-e61. Riant Florence, Roos Caroline, Roubertie Agathe, Barbance Cécile, Hadjadj Jessica, Auvin Stéphane, Baille Guillaume, Beltramone Marion, Boulanger Cécile, Cahn Alice, Cata Florina, Cheuret Emmanuel, Cuvellier Jean-Christophe, Defo Antoine, Demarquay Genevieve, Donnet Anne, Gaillard Nicolas, Massardier Evelyne, Guy Nathalie, Lamoureux Sylvie, Le Moigno Laurence, Lucas Christian, Ratiu Diana, Redon Sylvain, Rey Caroline, Thauvin Christel, Viallet François, Tournier-Lasserve Elisabeth, Ducros An |
| Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study. Headache 2023 6 . Giuseppe Donato Mangano, Maria Rita Capizzi, Elide Mantuano, Liana Veneziano, Giuseppe Santangelo, Giuseppe Quatrosi, Rosaria Nardello, Vincenzo Raie |
| Efficacy of galcanezumab in proline-rich transmembrane protein 2 (PRRT2)-associated familial hemiplegic migraine: A case series. Headache 2024 9 . Costanza Sottani, Giulia Di Lazzaro, Paolo Calabresi, Maria Grazia Pomponi, Francesco Danilo Tiziano, Anna Rita Bentivoglio, Serenella Servidei, Catello Vollo |
| De novo SCN1A missense variant in a patient with Parkinson's disease. Frontiers in genetics 2024 11 15 1496683. Majed Alluqmani, Abdulfatah M Alayoubi, Jamil A Hashmi, Sulman Bas |
| Exploring the association between familial hemiplegic migraine genes (CACNA1A, ATP1A2 and SCN1A) with migraine and epilepsy: A UK Biobank exome-wide association study. Cephalalgia : an international journal of headache 2025 1 45 (1): 3331024241306103. Christian Staehr, Mette Nyegaard, Flemming W Bach, Palle Duun Rohde, Vladimir V Matchk |
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