Cormand B - Search Results

1

Molecular genetics of cocaine use disorders in humans.

Fernàndez-Castillo N, Cabana-Domínguez J, Corominas R, Cormand B. Fernàndez-Castillo N, et al. Among authors: cormand b. Mol Psychiatry. 2022 Jan;27(1):624-639. doi: 10.1038/s41380-021-01256-1. Epub 2021 Aug 27. Mol Psychiatry. 2022. PMID: 34453125 Free PMC article. Review.

2

Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study.

Macaya A, Brunso L, Fernández-Castillo N, Arranz JA, Ginjaar HB, Cuenca-León E, Corominas R, Roig M, Cormand B. Macaya A, et al. Among authors: cormand b. Neuropediatrics. 2005 Dec;36(6):389-94. doi: 10.1055/s-2005-872877. Neuropediatrics. 2005. PMID: 16429380

3

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.

Ribasés M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, Artigas J, Rodriguez-Ben S, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Among authors: cormand b. Mol Psychiatry. 2009 Jan;14(1):71-85. doi: 10.1038/sj.mp.4002100. Epub 2007 Oct 16. Mol Psychiatry. 2009. PMID: 17938636

4

Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.

Cuenca-León E, Corominas R, Fernàndez-Castillo N, Volpini V, Del Toro M, Roig M, Macaya A, Cormand B. Cuenca-León E, et al. Among authors: cormand b. Cephalalgia. 2008 Oct;28(10):1039-47. doi: 10.1111/j.1468-2982.2008.01645.x. Epub 2008 Jul 17. Cephalalgia. 2008. PMID: 18644040

5

Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred.

Cuenca-León E, Corominas R, Montfort M, Artigas J, Roig M, Bayés M, Cormand B, Macaya A. Cuenca-León E, et al. Among authors: cormand b. Neurogenetics. 2009 Jul;10(3):191-8. doi: 10.1007/s10048-008-0169-6. Epub 2009 Jan 20. Neurogenetics. 2009. PMID: 19153782

6

Lack of association of hormone receptor polymorphisms with migraine.

Corominas R, Ribasés M, Cuenca-León E, Cormand B, Macaya A. Corominas R, et al. Among authors: cormand b. Eur J Neurol. 2009 Mar;16(3):413-5. doi: 10.1111/j.1468-1331.2008.02499.x. Eur J Neurol. 2009. PMID: 19175383

7

The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition.

Serra SA, Fernàndez-Castillo N, Macaya A, Cormand B, Valverde MA, Fernández-Fernández JM. Serra SA, et al. Among authors: cormand b. Pflugers Arch. 2009 Jul;458(3):489-502. doi: 10.1007/s00424-009-0637-3. Epub 2009 Feb 3. Pflugers Arch. 2009. PMID: 19189122

8

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene.

Cuenca-León E, Banchs I, Serra SA, Latorre P, Fernàndez-Castillo N, Corominas R, Valverde MA, Volpini V, Fernández-Fernández JM, Macaya A, Cormand B. Cuenca-León E, et al. Among authors: cormand b. J Neurol Sci. 2009 May 15;280(1-2):10-4. doi: 10.1016/j.jns.2009.01.005. Epub 2009 Feb 20. J Neurol Sci. 2009. PMID: 19232643

9

Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population.

Corominas R, Ribasés M, Cuenca-León E, Narberhaus B, Serra SA, del Toro M, Roig M, Fernández-Fernández JM, Macaya A, Cormand B. Corominas R, et al. Among authors: cormand b. Neurosci Lett. 2009 May 15;455(2):105-9. doi: 10.1016/j.neulet.2009.03.011. Epub 2009 Mar 6. Neurosci Lett. 2009. PMID: 19368856

10

Association study of the serotoninergic system in migraine in the Spanish population.

Corominas R, Sobrido MJ, Ribasés M, Cuenca-León E, Blanco-Arias P, Narberhaus B, Roig M, Leira R, López-González J, Macaya A, Cormand B. Corominas R, et al. Among authors: cormand b. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):177-84. doi: 10.1002/ajmg.b.30972. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19455600

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