Search Results

Phenotype and genotype in females with POU3F4 mutations

Authors: Marlin, S; Moizard, MP; David, A; Chaissang, N; Raynaud, M; Jonard, L; Feldmann, D; Loundon, N; Denoyelle, F; Toutain, A

Source: Clinical Genetics, Volume 76, Number 6, December 2009 , pp. 558-563(6)

Publisher: Blackwell Publishing

MYH9 related disease: A novel missense Ala95Asp mutation of the MYH9 gene

Authors: de Rocco, Daniela; Heller, Paula G.; Girotto, Giorgia; Pastore, Annalisa; Glembotsky, Ana C.; Marta, Rosana F.; Bozzi, Valeria; Pecci, Alessandro; Molinas, Felisa C.; Savoia, Anna

Source: Platelets, Volume 20, Number 8, June 2009 , pp. 598-602(5)

Publisher: Informa Healthcare

Dental team management for a patient with Klippel-Feil syndrome: Case report

Authors: de Deus Moura de Lima, Marina; Ortega, Karem Lopez; Araújo, Luis Carlos Arias; Soares, Marcelo Melo; de Magalhães, Marina Helena Cury Gallottini

Source: Special Care in Dentistry, Volume 29, Number 6, November/December 2009 , pp. 244-248(5)

Publisher: Blackwell Publishing

The Importance of Sound for Cognitive Sequencing Abilities: The Auditory Scaffolding Hypothesis

Authors: Conway, Christopher M.; Pisoni, David B.; Kronenberger, William G.

Source: Current Directions in Psychological Science, Volume 18, Number 5, October 2009 , pp. 275-279(5)

Publisher: Blackwell Publishing

Spontaneous intracranial hypotension

Author: GORDON, NEIL

Source: Developmental Medicine & Child Neurology, Volume 51, Number 12, December 2009 , pp. 932-935(4)

Publisher: Blackwell Publishing

Peginterferon-α-2a/ribavirin: Sudden hearing loss and anaemia: case report

Source: Reactions, Volume 1, Number 1278, 2009-11-14 , pp. 24-24(1)

Publisher: Adis International

A CitationRank algorithm inheriting Google technology designed to highlight genes responsible for serious adverse drug reaction

Authors: Yang, Lun; Xu, Langlai; He, Lin

Source: Bioinformatics, Volume 25, Number 17, 1 September 2009 , pp. 2244-2250(7)

Publisher: Oxford University Press

Cisplatin/ifosfamide: Renal impairment, pancytopenia, hearing loss and encephalopathy: case report

Source: Reactions, Volume 1, Number 1274, 2009-10-17 , pp. 17-17(1)

Publisher: Adis International

Wolfram syndrome: a clinicopathologic correlation

Authors: Hilson, Justin; Merchant, Saumil; Adams, Joe; Joseph, Jeffrey

Source: Acta Neuropathologica, Volume 118, Number 3, September 2009 , pp. 415-428(14)

Publisher: Springer

Oblique multiplanar reformation in multislice temporal bone CT

Authors: Blanco Ulla, Miguel; Vázquez, Fernando; Pumar, José; del Río, María; Romero, Giselle

Source: Surgical and Radiologic Anatomy, Volume 31, Number 6, July 2009 , pp. 475-479(5)

Publisher: Springer

Chromosome imbalances in syndromic hearing loss

Authors: Catelani, ALPM; Krepischi, ACV; Kim, CA; Kok, F; Otto, PA; Auricchio, MTBM; Mazzeu, JF; Uehara, DT; Costa, SS; Knijnenburg, J; Tabith, A; Vianna-Morgante, AM; Mingroni-Netto, RC; Rosenberg, C

Source: Clinical Genetics, Volume 76, Number 5, November 2009 , pp. 458-464(7)

Publisher: Blackwell Publishing

Otosclerosis 1: the aetiopathogenesis of otosclerosis

Authors: Uppal, S.; Bajaj, Y.; Rustom, I.; Coatesworth, A. P.

Source: International Journal of Clinical Practice, Volume 63, Number 10, October 2009 , pp. 1526-1530(5)

Publisher: Blackwell Publishing

Ciprofloxacin/quinine: Permanent deafness in a patient with typhoid fever: case report

Source: Reactions, Volume 1, Number 1270, 2009-09-19 , pp. 12-12(1)

Publisher: Adis International

Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26

Authors: Todt, Ingo; Mazereeuw-Hautier, Juliette; Binder, Barbara; Willems, Patrick J.

Source: Clinical Genetics, Volume 76, Number 4, October 2009 , pp. 404-408(5)

Publisher: Blackwell Publishing

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15

Authors: Waryah, AM; Rehman, A; Ahmed, ZM; Bashir, Z-H; Khan, SY; Zafar, AU; Riazuddin, S; Friedman, TB

Source: Clinical Genetics, Volume 76, Number 3, September 2009 , pp. 270-275(6)

Publisher: Blackwell Publishing

Role of speechreading in audiovisual interactions during the recovery of speech comprehension in deaf adults with cochlear implants

Authors: STRELNIKOV, K.; ROUGER, J.; BARONE, P.; DEGUINE, O.

Source: Scandinavian Journal of Psychology, Volume 50, Number 5, October 2009 , pp. 437-444(8)

Publisher: Blackwell Publishing

Development of social-cognitive and communication skills in children born deaf

Author: PETERSON, CANDIDA C.

Source: Scandinavian Journal of Psychology, Volume 50, Number 5, October 2009 , pp. 475-483(9)

Publisher: Blackwell Publishing

Working memory, deafness and sign language

Authors: RUDNER, MARY; ANDIN, JOSEFINE; RÖNNBERG, JERKER

Source: Scandinavian Journal of Psychology, Volume 50, Number 5, October 2009 , pp. 495-505(11)

Publisher: Blackwell Publishing

Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss

Authors: Mackenzie, F. E.; Parker, A.; Parkinson, N. J.; Oliver, P. L.; Brooker, D.; Underhill, P.; Lukashkina, V. A.; Lukashkin, A. N.; Holmes, C.; Brown, S. D. M.

Source: Genes, Brain & Behavior, Volume 8, Number 7, October 2009 , pp. 699-713(15)

Publisher: Blackwell Publishing

Sildenafil/tadalafil: Sudden sensorineural hearing loss: 2 case reports

Source: Reactions, Volume 1, Number 1272, 2009-10-03 , pp. 28-29(2)

Publisher: Adis International