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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 2
1991 1
1993 2
1994 2
1995 3
1996 6
1997 1
1998 2
1999 4
2002 2
2003 1
2004 1
2005 2
2006 1
2007 1
2008 3
2009 1
2010 4
2011 3
2012 2
2013 2
2014 2
2015 1
2016 2
2017 1
2019 5
2020 3
2024 1
2025 0

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55 results

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Page 1
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.
Gutiérrez Gutiérrez G, Díaz-Manera J, Almendrote M, Azriel S, Eulalio Bárcena J, Cabezudo García P, Camacho Salas A, Casanova Rodríguez C, Cobo AM, Díaz Guardiola P, Fernández-Torrón R, Gallano Petit MP, García Pavía P, Gómez Gallego M, Gutiérrez Martínez AJ, Jericó I, Kapetanovic García S, López de Munaín Arregui A, Martorell L, Morís de la Tassa G, Moreno Zabaleta R, Muñoz-Blanco JL, Olivar Roldán J, Pascual Pascual SI, Peinado Peinado R, Pérez H, Poza Aldea JJ, Rabasa M, Ramos A, Rosado Bartolomé A, Rubio Pérez MÁ, Urtizberea JA, Zapata-Wainberg G, Gutiérrez-Rivas E. Gutiérrez Gutiérrez G, et al. Among authors: cobo am. Neurologia (Engl Ed). 2020 Apr;35(3):185-206. doi: 10.1016/j.nrl.2019.01.001. Epub 2019 Apr 16. Neurologia (Engl Ed). 2020. PMID: 31003788 Free article. English, Spanish.
Calpainopathy-a survey of mutations and polymorphisms.
Richard I, Roudaut C, Saenz A, Pogue R, Grimbergen JE, Anderson LV, Beley C, Cobo AM, de Diego C, Eymard B, Gallano P, Ginjaar HB, Lasa A, Pollitt C, Topaloglu H, Urtizberea JA, de Visser M, van der Kooi A, Bushby K, Bakker E, Lopez de Munain A, Fardeau M, Beckmann JS. Richard I, et al. Among authors: cobo am. Am J Hum Genet. 1999 Jun;64(6):1524-40. doi: 10.1086/302426. Am J Hum Genet. 1999. PMID: 10330340 Free PMC article.
Une cause inhabituelle d’hyperCKémie.
Modrego PJ, Gazulla J, Cobo AM, Andoni Urtizberea J. Modrego PJ, et al. Among authors: cobo am. Med Sci (Paris). 2016 Nov;32 Hors série n°2:12-13. doi: 10.1051/medsci/201632s204. Epub 2016 Nov 21. Med Sci (Paris). 2016. PMID: 27869070 Free article. French. No abstract available.
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
Sáenz A, Leturcq F, Cobo AM, Poza JJ, Ferrer X, Otaegui D, Camaño P, Urtasun M, Vílchez J, Gutiérrez-Rivas E, Emparanza J, Merlini L, Paisán C, Goicoechea M, Blázquez L, Eymard B, Lochmuller H, Walter M, Bonnemann C, Figarella-Branger D, Kaplan JC, Urtizberea JA, Martí-Massó JF, López de Munain A. Sáenz A, et al. Among authors: cobo am. Brain. 2005 Apr;128(Pt 4):732-42. doi: 10.1093/brain/awh408. Epub 2005 Feb 2. Brain. 2005. PMID: 15689361
Carotid Ultrasound-Based Plaque Score for the Allocation of Aspirin for the Primary Prevention of Cardiovascular Disease Events: The Multi-Ethnic Study of Atherosclerosis and the Atherosclerosis Risk in Communities Study.
Dzaye O, Razavi AC, Dardari ZA, Nasir K, Matsushita K, Mok Y, Santilli F, Cobo AML, Johri AM, Albrecht G, Blaha MJ. Dzaye O, et al. Among authors: cobo aml. J Am Heart Assoc. 2024 Jun 18;13(12):e034718. doi: 10.1161/JAHA.123.034718. Epub 2024 Jun 11. J Am Heart Assoc. 2024. PMID: 38860391 Free PMC article.
[Alterations in functional proteins. Calpaine-3 deficiency].
López de Munain A, Urtasun A, Poza JJ, Ruiz J, Sáenz A, Cobo AM, Lasa A, Gallano P, Baiget M, Martí-Massó JF. López de Munain A, et al. Among authors: cobo am. Rev Neurol. 1999 Jan 16-31;28(2):158-64. Rev Neurol. 1999. PMID: 10101785 Review. Spanish.
[Basic concepts in molecular genetics].
Cobo AM, Poza JJ, Sáenz A, López de Munain A. Cobo AM, et al. Rev Neurol. 1996 Mar;24(127):315-9. Rev Neurol. 1996. PMID: 8742399 Review. Spanish. No abstract available.
Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations.
Savarese M, Palmio J, Poza JJ, Weinberg J, Olive M, Cobo AM, Vihola A, Jonson PH, Sarparanta J, García-Bragado F, Urtizberea JA, Hackman P, Udd B. Savarese M, et al. Among authors: cobo am. Ann Neurol. 2019 Jun;85(6):899-906. doi: 10.1002/ana.25470. Epub 2019 Apr 3. Ann Neurol. 2019. PMID: 30900782
[Diseases due to instability of DNA].
López de Muniain A, Cobo AM, Poza JJ, Sáenz A. López de Muniain A, et al. Among authors: cobo am. Neurologia. 1995 Dec;10 Suppl 1:12-9. Neurologia. 1995. PMID: 8838555 Review. Spanish.
55 results