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24篇 您的检索式:作者名="Villamar"
    题名 作者 年代 出处 被引量
1A mutational analysis of the SLC26A4 gene in Spanish hearing- impaired families provides new insights into the genetic causes of Pendred syn- drome and DFNIM hearing loss显示文摘Pera A Villamar M Vinuela A 2008Eur J Hum Genet2008,16,:1
2A deletion involving the Connexin 30 gene in nonsyndromic hearing impairment显示文摘del Castillo I Villamar M Moreno--Pelayo MA 2002N Engl J Med2002,346,:1
3Maternally inherity nonsyndromic hearing impairment in a Spanish family with the T7 510C mutation in the mitoehondrial tRNASer (UCN) gene显示文摘Castillo FJ Villamar M Moreno-Pelayo MA 2002J Med Genet2002,39,:1
4SIMULTANEOUS DETERMINATION OF ADENOSINE AND RELATED PURINES IN TISSUES AND HEMOLYMPH OF MUSSEL BY HPLC显示文摘Sonia Prado Antonio Villamarín Izaskun Ibarguren 2013Journal of Liquid Chromatography & Related Technologies2013,,4:1
5A deletion involving the connexin 30 gene in nonsyndromic hearing impairment 显示文摘del Castillo I Villamar M Moreno - Pelayo MA 2002N Engl J Med2002,346,4:1
6Focal modulation of the primary motor cortex in fibromyalgia using 4x 1-ring high-definition transcranial direct current stimulation (HD-tDCS): immediate and delayed analgesic effects of cathod- al and anodal stimulation 显示文摘Villamar MF Wivatvongvana P Patumanond J 2013J Pain2013,14,4:1
7Delivery of dietary components of larval shrimp (Penaeus vannamei) by means of complex micro capsules 显示文摘Villamar D Langdon C J 1993Mar Biol1993,115,:1
8A novel locus for non--syndromic sensorineural deafness (DFN6) maps to chromosome Xp22显示文摘del Castillo I Villamar M Sarduy M 1996Hum Mol Genet1996,5,:1
9A deletion involving the connexin 30 gene in nonsyndromic hearing impairment 显示文摘DEL CASTILLO I VILLAMAR M MORENO- PELAYO M A 2002N Engl J Med2002,346,:1
10A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy显示文摘Rodri?guez-Ballesteros M Reynoso R Olarte M Villamar M Morera C Santarelli R Arslan E 0,,06:1
11A deletion involving the connexin 30 gene in nonsyndromic hearing impairment显示文摘del Castillo I Villamar M Moreno-Pelayo MA 2002N Engl J Med2002,346,4:1
12Delivery of dietary components of larval shrimp (Penaeus vannamei) by means of complex micro caopsules显示文摘VILLAMAR D LANGDON C J 1993Marine Biology1993,115,:1
13Focal modulation of the primary motor cortex in fibromyalgia using 4×1-ring high-definition transcranial direct current stimulation(HD-tDCS):Immediate and delayed analgesic effects of cathodal and anodal stimulation显示文摘Villamar M Wivatvongvana P Patumanond J 2013The Journal of Pain2013,45,26:1
14Nondisjunction in a 49,XXXXY male using recombinant-DNA techniques显示文摘 Benitez J Fernandez E 198936:152-1551989,36,:1
15A eysteine substitution in the zona pellucida domain of alpha-- tectorin results in autosomal dominant, postlingual, progres- sive, mid frequency hearing loss in a Spanish family显示文摘Moreno--pelayo MA Del Castillo I Villamar M 2001J Med Genet2001,38,:1
16Maternally inherited non-syndromic hearing impair- ment in a Spanish family with the 7510T > C mutation in the mitoehondrial tRNA ( Ser ( UCN ) ) gene 显示文摘DEL CASTILLO F J VILLAMAR M MORENO-PELAYO M A 2002J Med Goner2002,39,12:1
17Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing impaired subjects:a multicenter study显示文摘del Castillo I Moreno-Pelayo MA del Castillo FJ Brown-stein Z Marlin S Adina Q Cockburn DJ Pandya A Siemering KR Chamberlin GP Ballana E WuytsW Maciel-Guerra AT Alva-rez A Villamar M Shohat M Abeliovich D Dahl HHM Estivill X Gasparini P Hutchin T Nance WE 0,,:1
18A deletion involving the connexin 30 gene in nonsyndromic hearing impairment显示文摘DEL CASTILLO I VILLAMAR M MMRENOPELAYO M A 2002N Engl J Med2002,346,:1
19Noninvasive brain stimulation to modulate neuroplasticity in traumatic brain injury 显示文摘Villamar MF Portilla AS Fregni F 2012Neuromodulation2012,15,4:1
20A dele-tion involving the connexin 30 gene in nonsyndromic hearing impairment显示文摘Castillo I Villamar M Moreno-Pelayo MA 2002N Engl J Med2002,23,2:1
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