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Anil K. Lalwani

Department of Otolaryngology

Head and Neck Surgery

University of California

San Francisco

USA

[email]@*.ucsf.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Otolaryngology, Head and Neck Surgery, University of California, San Francisco, USA. 1996 - 2002
  • Laboratory of Molecular Otology, Epstein Laboratories, Division of Otology, Neurotology, USA. 2002
  • Laboratory of Molecular Otology, Epstein Laboratories, Department of Otolaryngology-Head and Neck Surgery, University of California, USA. 2000

References

  1. Current issues in cochlear gene transfer. Lalwani, A.K., Jero, J., Mhatre, A.N. Audiol. Neurootol. (2002) [Pubmed]
  2. In vitro and in vivo assessment of the ability of adeno-associated virus-brain-derived neurotrophic factor to enhance spiral ganglion cell survival following ototoxic insult. Lalwani, A.K., Han, J.J., Castelein, C.M., Carvalho, G.J., Mhatre, A.N. Laryngoscope (2002) [Pubmed]
  3. Developments in cochlear gene therapy. Lalwani, A.K., Jero, J., Mhatre, A.N. Adv. Otorhinolaryngol. (2002) [Pubmed]
  4. Auditory phenotype of DFNA17. Lalwani, A.K., Goldstein, J.A., Mhatre, A.N. Adv. Otorhinolaryngol. (2002) [Pubmed]
  5. Cochlear gene therapy. Lalwani, A.K., Mhatre, A.N. Adv. Otorhinolaryngol. (2000) [Pubmed]
  6. Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. Lalwani, A.K., Goldstein, J.A., Kelley, M.J., Luxford, W., Castelein, C.M., Mhatre, A.N. Am. J. Hum. Genet. (2000) [Pubmed]
  7. Sensorineural and conductive hearing loss associated with lateral semicircular canal malformation. Johnson, J., Lalwani, A.K. Laryngoscope (2000) [Pubmed]
  8. Further characterization of the DFNA1 audiovestibular phenotype. Lalwani, A.K., Jackler, R.K., Sweetow, R.W., Lynch, E.D., Raventós, H., Morrow, J., King, M.C., León, P.E. Arch. Otolaryngol. Head Neck Surg. (1998) [Pubmed]
  9. Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family. Lalwani, A.K., Attaie, A., Randolph, F.T., Deshmukh, D., Wang, C., Mhatre, A., Wilcox, E. Am. J. Med. Genet. (1998) [Pubmed]
  10. A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration. Lalwani, A.K., Linthicum, F.H., Wilcox, E.R., Moore, J.K., Walters, F.C., San Agustin, T.B., Mislinski, J., Miller, M.R., Sinninger, Y., Attaie, A., Luxford, W.M. Audiol. Neurootol. (1997) [Pubmed]
  11. Green fluorescent protein as a reporter for gene transfer studies in the cochlea. Lalwani, A.K., Han, J.J., Walsh, B.J., Zolotukhin, S., Muzyczka, N., Mhatre, A.N. Hear. Res. (1997) [Pubmed]
  12. Lectin binding characteristics of squamous cell carcinomas of the head and neck. Lalwani, A.K., Carey, T.E., Goldstein, I.J., Peters, B.P. Acta Otolaryngol. (1996) [Pubmed]
 
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