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Edi Lúcia Sartorato Selected Research

Nonsyndromic sensorineural hearing loss

12/2011Searching for digenic inheritance in deaf Brazilian individuals using the multiplex ligation-dependent probe amplification technique.
11/2009C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
10/2009Screening for the GJB2 c.-3170 G>A (IVS 1+1 G>A) mutation in Brazilian deaf individuals using multiplex ligation-dependent probe amplification.

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Edi Lúcia Sartorato Research Topics

Disease

5Hearing Loss (Hearing Impairment)
03/2013 - 05/2006
3Sensorineural Hearing Loss
01/2016 - 05/2006
3Nonsyndromic sensorineural hearing loss
12/2011 - 10/2009
3Deafness (Deaf Mutism)
04/2009 - 11/2007
2Optic Nerve Diseases (Optic Neuropathy)
01/2016 - 01/2011
2Ototoxicity
05/2010 - 11/2009
1Auditory neuropathy
07/2016
1Nonsyndromic Deafness
01/2016
1Meniere Disease (Menieres Disease)
01/2016
1Pendred syndrome
03/2013
1Autosomal Recessive 4 Deafness
03/2013
1Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy)
09/2010
1Inborn Genetic Diseases (Disease, Hereditary)
02/2009
1Skin Diseases (Skin Disease)
02/2009
1Keratitis
02/2009
1leuconychia and sensorineural deafness Knuckle pads
07/2005

Drug/Important Bio-Agent (IBA)

6Mitochondrial DNA (mtDNA)IBA
01/2016 - 04/2009
4AminoglycosidesIBA
01/2016 - 04/2009
3Connexin 26IBA
12/2011 - 07/2005
2Anti-Bacterial Agents (Antibiotics)IBA
05/2010 - 11/2009
1A-Form DNA (A-DNA)IBA
07/2016
1IGF-I-IGFBP-3 complexFDA Link
01/2016
1Lys Transfer RNAIBA
01/2016
1Aquaporins (Water Channels)IBA
01/2016
1Potassium Channels (Potassium Channel)IBA
01/2016
1GoldIBA
01/2016
1AnionsIBA
03/2013
1human GJB3 proteinIBA
12/2011
1NADH DehydrogenaseIBA
01/2011
1Cytochromes b (Cytochrome b)IBA
01/2011
1Pharmaceutical PreparationsIBA
05/2010
1Glutathione Transferase (Glutathione S-Transferase)IBA
05/2010
112S ribosomal RNAIBA
11/2009
1Connexin 43 (Connexin43)IBA
02/2009
1ConnexinsIBA
02/2009

Therapy/Procedure

1Lasers (Laser)
01/2016
1Ligation
10/2009
1Cochlear Implantation
05/2006