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

Year Number of Results
1990 3
1991 4
1992 4
1994 2
1995 2
1996 1
1998 1
1999 2
2000 1
2001 1
2004 2
2005 1
2006 1
2007 1
2009 1
2011 1
2012 3
2013 1
2014 1
2016 1
2019 1
2020 1
2022 1
2023 1
2024 0

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34 results

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Page 1
Clinical description, molecular delineation and genotype-phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients.
Martinez-Cayuelas E, Blanco-Kelly F, Lopez-Grondona F, Swafiri ST, Lopez-Rodriguez R, Losada-Del Pozo R, Mahillo-Fernandez I, Moreno B, Rodrigo-Moreno M, Casas-Alba D, Lopez-Gonzalez A, García-Miñaúr S, Ángeles Mori M, Pacio-Minguez M, Rikeros-Orozco E, Santos-Simarro F, Cruz-Rojo J, Quesada-Espinosa JF, Sanchez-Calvin MT, Sanchez-Del Pozo J, Bernado Fonz R, Isidoro-Garcia M, Ruiz-Ayucar I, Alvarez-Mora MI, Blanco-Lago R, De Azua B, Eiris J, Garcia-Peñas JJ, Gil-Fournier B, Gomez-Lado C, Irazabal N, Lopez-Gonzalez V, Madrigal I, Malaga I, Martinez-Menendez B, Ramiro-Leon S, Garcia-Hoyos M, Prieto-Matos P, Lopez-Pison J, Aguilera-Albesa S, Alvarez S, Fernández-Jaén A, Llano-Rivas I, Gener-Querol B, Ayuso C, Arteche-Lopez A, Palomares-Bralo M, Cueto-González A, Valenzuela I, Martinez-Monseny A, Lorda-Sanchez I, Almoguera B. Martinez-Cayuelas E, et al. Among authors: martinez menendez b. J Med Genet. 2023 Jul;60(7):644-654. doi: 10.1136/jmg-2022-108632. Epub 2022 Nov 29. J Med Genet. 2023. PMID: 36446582
[Febrile seizures: is EEG useful?].
Martínez Menéndez B, Simón de las Heras R, de la Peña Mayor P, Pérez Sempere A, Alvarez Tejerina J, Mateos Beato F. Martínez Menéndez B, et al. An Esp Pediatr. 1999 Feb;50(2):126-8. An Esp Pediatr. 1999. PMID: 10199020 Spanish.
[Mononeuropathy in chronic lymphatic leukaemia].
Escolar E, García-Vela J, Aladro Y, Martínez-Menéndez B, Martín A. Escolar E, et al. Among authors: martinez menendez b. Rev Neurol. 2007 Aug 16-31;45(4):233-5. Rev Neurol. 2007. PMID: 17668406 Free article. Spanish.
Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: De novo mutation of the KIF1A gene, a new hope in prognosis.
Urtiaga Valle S, Fournier Gil B, Ramiro León MS, Martínez Menéndez B. Urtiaga Valle S, et al. Among authors: martinez menendez b. Neurologia (Engl Ed). 2020 Sep;35(7):535-538. doi: 10.1016/j.nrl.2018.07.001. Epub 2019 Mar 10. Neurologia (Engl Ed). 2020. PMID: 30862385 Free article. English, Spanish. No abstract available.
Has clinical activity in paediatric neurology changed in the past 11 years?
Martínez Menéndez B, Escolar Escamilla E, Pinel González A, Cerezo García M, Martínez Sarries FJ, Morlán Gracia L. Martínez Menéndez B, et al. Neurologia. 2016 Nov-Dec;31(9):606-612. doi: 10.1016/j.nrl.2014.09.011. Epub 2014 Dec 17. Neurologia. 2016. PMID: 25529177 Free article. English, Spanish.
[Migraine in childhood: a trivial condition?].
Martínez-Menéndez B, Pinel-González A. Martínez-Menéndez B, et al. Rev Neurol. 2006 Jun 1-15;42(11):643-6. Rev Neurol. 2006. PMID: 16736398 Free article. Spanish.
34 results