Tendero A - Search Results

Year	Number of Results
1975	1
1976	1
1977	2
1978	1
1980	2
1995	1
1996	1
1998	2
1999	1
2000	1
2001	4
2002	1
2003	1
2004	1
2005	1
2006	1
2017	1
2019	1
2021	1
2024	0

1

[A study of Gobbi's syndrome in Spanish population].

Martínez-Bermejo A, Polanco I, Royo A, López-Martín V, Arcas J, Tendero A, Fernández-Jaén A, Pascual-Castroviejo I. Martínez-Bermejo A, et al. Among authors: tendero a. Rev Neurol. 1999 Jul 16-31;29(2):105-10. Rev Neurol. 1999. PMID: 10528319 Review. Spanish.

2

Mietens-Weber syndrome: two new patients and a review.

Martínez-Glez V, Lapunzina P, Delicado A, Tendero A, Mori MÁ, de Torres ML, Fernández L, Palomares M, Pajares IL. Martínez-Glez V, et al. Among authors: tendero a. Clin Dysmorphol. 2006 Jul;15(3):175-177. doi: 10.1097/01.mcd.0000204985.54366.a7. Clin Dysmorphol. 2006. PMID: 16760739 Review.

3

Hypomelanosis of ITO. A study of 76 infantile cases.

Pascual-Castroviejo I, Roche C, Martinez-Bermejo A, Arcas J, Lopez-Martin V, Tendero A, Esquiroz JL, Pascual-Pascual SI. Pascual-Castroviejo I, et al. Among authors: tendero a. Brain Dev. 1998 Jan;20(1):36-43. doi: 10.1016/s0387-7604(97)00097-1. Brain Dev. 1998. PMID: 9533559

4

The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.

Vidal S, Brandi N, Pacheco P, Gerotina E, Blasco L, Trotta JR, Derdak S, Del Mar O'Callaghan M, Garcia-Cazorla À, Pineda M, Armstrong J; Rett Working Group. Vidal S, et al. Sci Rep. 2017 Sep 25;7(1):12288. doi: 10.1038/s41598-017-11620-3. Sci Rep. 2017. PMID: 28947817 Free PMC article.

5

[Is benign childhood paroxysmal eye deviation a non-epileptic disorder?].

Merino-Andreu M, Arcas J, Izal- Linares E, Tendero A, Roche-Herrero MC, Martínez-Bermejo A. Merino-Andreu M, et al. Among authors: tendero a. Rev Neurol. 2004 Jul 16-31;39(2):129-32. Rev Neurol. 2004. PMID: 15264162 Free article. Spanish.

6

Developmental defects of the cerebellum. A radiologic and anatomic investigation.

Pascual-Castroviejo I, Santolaya JM, Tendero A. Pascual-Castroviejo I, et al. Among authors: tendero a. Acta Radiol Suppl. 1976;347:553-60. doi: 10.1177/0284185175016s34769. Acta Radiol Suppl. 1976. PMID: 207146

7

X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients.

Xiol C, Vidal S, Pascual-Alonso A, Blasco L, Brandi N, Pacheco P, Gerotina E, O'Callaghan M, Pineda M, Armstrong J; Rett Working Group. Xiol C, et al. Sci Rep. 2019 Aug 19;9(1):11983. doi: 10.1038/s41598-019-48385-w. Sci Rep. 2019. PMID: 31427717 Free PMC article.

8

Preference structure for lamb meat consumers. A Spanish case study.

Bernabéu R, Tendero A. Bernabéu R, et al. Among authors: tendero a. Meat Sci. 2005 Nov;71(3):464-70. doi: 10.1016/j.meatsci.2005.04.027. Epub 2005 Jun 16. Meat Sci. 2005. PMID: 22060921

9

Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.

Vidal S, Brandi N, Pacheco P, Gerotina E, Blasco L, Trotta JR, Derdak S, Del Mar O'Callaghan M, Garcia-Cazorla À, Pineda M, Armstrong J; Rett Working Group. Vidal S, et al. Sci Rep. 2021 Sep 7;11(1):18146. doi: 10.1038/s41598-021-97262-y. Sci Rep. 2021. PMID: 34493777 Free PMC article. No abstract available.

10

[Lafora disease. A new case of confirmation of diagnosis on molecular genetic studies].

Martínez-Bermejo A, López-Martín V, Serratosa JM, Gutiérrez-Molina M, Gómez-Garre P, Arcas J, Tendero A, Roche C, Pérez-Mies B. Martínez-Bermejo A, et al. Among authors: tendero a. Rev Neurol. 2002 Jan 16-31;34(2):117-20. Rev Neurol. 2002. PMID: 11988905 Free article. Spanish.

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