Cormand B - Search Results

1

Candidate-gene association study searching for genetic factors involved in migraine chronification.

Louter MA, Fernandez-Morales J, de Vries B, Winsvold B, Anttila V, Fernandez-Cadenas I, Vila-Pueyo M, Sintas C, van Duijn CM, Cormand B, Álvarez-Sabin J, Montaner J, Ferrari MD, van den Maagdenberg A, Palotie A, Zwart JA, Macaya A, Terwindt GM, Pozo-Rosich P. Louter MA, et al. Among authors: cormand b. Cephalalgia. 2015 May;35(6):500-7. doi: 10.1177/0333102414547141. Epub 2014 Aug 28. Cephalalgia. 2015. PMID: 25169732

2

Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.

Cuenca-Leon E, Cormand B, Thomson T, Macaya A. Cuenca-Leon E, et al. Among authors: cormand b. Neuropediatrics. 2002 Dec;33(6):288-93. doi: 10.1055/s-2002-37079. Neuropediatrics. 2002. PMID: 12571782

3

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

4

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

5

Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder.

Ribasés M, Hervás A, Ramos-Quiroga JA, Bosch R, Bielsa A, Gastaminza X, Fernández-Anguiano M, Nogueira M, Gómez-Barros N, Valero S, Gratacòs M, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Among authors: cormand b. Biol Psychiatry. 2008 May 15;63(10):935-45. doi: 10.1016/j.biopsych.2007.11.004. Epub 2008 Jan 7. Biol Psychiatry. 2008. PMID: 18179783

6

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

7

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

8

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

9

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

10

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

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