Recent Publications by Anil K. Lalwani, MD
Publications
| 1. | Coelho, Daniel H; Yeh, Joseph; Kim, Jung T; Lalwani, Anil K. "Cochlear implantation is associated with minimal anesthetic risk in the elderly". Laryngoscope. 2009; 119: 355 (#J0164917) |
| 2. | Lalwani, Anil K; Budenz, Cameron L; Weisstuch, Adam S; Babb, James; Roland, J Thomas Jr; Waltzman, Susan B. "Predictability of cochlear implant outcome in families". Laryngoscope. 2009; 119: 131 (#J0160343) |
| 3. | Mallur, Pavan S; Harirchian, Sanaz; Lalwani, Anil K. "Preoperative and postoperative intracranial complications of acute mastoiditis". Annals of otology rhinology & laryngology. 2009; 118: 118 (#J0165194) |
| 4. | Mhatre, Anand N; Janssens, Sandra; Nardi, Michael A; Li, Yan; Lalwani, Anil K. "Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss". European journal of medical genetics. 2009; 52: 185 (#J0174770) |
| 5. | Reitzen, Shari D; Babb, James S; Lalwani, Anil K. "Significance and reliability of the House-Brackmann grading system for regional facial nerve function". Otolaryngology, head & neck surgery. 2009; 140: 154 (#J0161348) |
| 6. | Zeitler, Daniel M; Lalwani, Anil K; Roland, J Thomas Jr; Habib, Mirette G; Gudis, David; Waltzman, Susan B. "The effects of cochlear implant electrode deactivation on speech perception and in predicting device failure". Otology & neurotology. 2009; 30: 7 (#J0158585) |
| 7. | Zeitler, Daniel M; Lalwani, Anil K. "Retraction. Are postoperative hearing results better with titanium ossicular reconstruction prostheses?". Laryngoscope. 2009; 119: 1 (#J0176199) |
| 8. | Coelho, Daniel H; Lalwani, Anil K. "Medical management of Meniere's disease". Laryngoscope. 2008; 118: 1099 (#J0140631) |
| 9. | Lalwani, Anil K; Atkin, Graham; Li, Yan; Lee, Jennifer Y; Hillman, Dean E; Mhatre, Anand N. "Localization in stereocilia, plasma membrane, and mitochondria suggests diverse roles for NMHC-IIa within cochlear hair cells". Brain research. 2008; 1197: 13 (#J0135233) |
| 10. | Li Y; Lalwani AK; Mhatre AN. "Alternative Splice Variants of MYH9". DNA & cell biology. 2008; 27: 117 (#J0131300) |
| 11. | Li Y; Friedmann DR; Mhatre AN; Lalwani AK. "MYH9-siRNA and MYH9 mutant alleles: Expression in cultured cell lines and their effects upon cell structure and function". Cell motility & the cytoskeleton. 2008; 65: 393 (#J0135237) |
| 12. | Mallur, Pavan S; Wisoff, Jeffrey H; Lalwani, Anil K. "Steroid responsive fluctuating sensorineural hearing loss due to juvenile pilocytic astrocytoma involving the cerebellopontine angle". International journal of pediatric otorhinolaryngology. 2008; 72: 529 (#J0135234) |
| 13. | Shapiro, WH; Huang, T; Shaw, T; Roland, JT; Lalwani, AK. "Remote intraoperative monitoring during cochlear implant surgery is feasible and efficient". Otology & neurotology. 2008; 29: 495 (#J0150303) |
| 14. | Zeitler, Daniel M; Kessler, Megan A; Terushkin, Vitaly; Roland, Thomas J Jr; Svirsky, Mario A; Lalwani, Anil K; Waltzman, Susan B. "Speech perception benefits of sequential bilateral cochlear implantation in children and adults: a retrospective analysis". Otology & neurotology. 2008; 29: 314 (#J0139243) |
| 15. | Lalwani, Anil K. "Endolymphatic sac tumors in von Hippel-Lindau disease [comment]". Archives of otolaryngology, head & neck surgery. 2007; 133: 857 (#J0131303) |
| 16. | Lanson, Biana G; Green, Janet E; Roland, J Thomas Jr; Lalwani, Anil K; Waltzman, Susan B. "Cochlear implantation in Children with CHARGE syndrome: therapeutic decisions and outcomes". Laryngoscope. 2007; 117: 1260 (#J0128182) |
| 17. | Mallur, Pavan S; Lalwani, Anil K. "Fluctuating corticosteroid-responsive auditory neuropathy/dyssynchrony is suggestive of central nervous system pathology". Otology & neurotology. 2007; 28: 1002 (#J0131301) |
| 18. | Mhatre, Anand N; Li, Yan; Bhatia, Nitin; Wang, Kevin H; Atkin, Graham; Lalwani, Anil K. "Generation and characterization of mice with Myh9 deficiency". Neuromolecular medicine. 2007; 9: 205 (#J0131302) |
| 19. | Morris, Luc G; Mallur, Pavan S; Roland, J Thomas Jr; Waltzman, Susan B; Lalwani, Anil K. "Implication of central asymmetry in speech processing on selecting the ear for cochlear implantation". Otology & neurotology. 2007; 28: 25 (#J0124576) |
| 20. | Grandis, Jennifer R; Battey, James F; Califf, Robert M; Chole, Richard A; Gantz, Bruce J; Gates, George A; Gorelic, Lester; Hannley, Maureen T; Hardwick, Kevin S; Harris, Jeffrey P; Kapoor, Wishwa N; Lai, Stephen Y; Lalwani, Anil K; Minor, Lloyd B; Nadol, Joseph P; Post, J Christopher; Roland, Peter S; Schechter, Alan M; Schuller, David E; Sklare, Daniel A; Wackym, P Ashley; Weber, Randal S; Weymuller, Ernest A Jr; Wolf, Gregory T; Woodson, Gayle E. "Research education and training in otolaryngology: meeting summary and research opportunities". Otolaryngology, head & neck surgery. 2006; 135: 361 (#J0131304) |
| 21. | Mhatre, Anand N; Li, Yan; Atkin, Graham; Maghnouj, Abdel; Lalwani, Anil K. "Expression of Myh9 in the mammalian cochlea: localization within the stereocilia". Journal of neuroscience research. 2006; 84: 809 (#J0121131) |
| 22. | Purcell, Derk D; Fischbein, Nancy J; Patel, Andrew; Johnson, Jacob; Lalwani, Anil K. "Two temporal bone computed tomography measurements increase recognition of malformations and predict sensorineural hearing loss". Laryngoscope. 2006; 116: 1439 (#J0131305) |
| 23. | Wareing, Michael J; Lalwani, Anil; Jackler, Robert K. "Development of the ear" IN: Head & neck surgery -- otolaryngology Philadelphia PA : Lippincott Williams & Wilkins, 2006. 2006; (#C0003142) |
| 24. | Young, R J; Shatzkes, D R; Babb, J S; Lalwani, A K. "The cochlear-carotid interval: anatomic variation and potential clinical implications". AJNR. American journal of neuroradiology. 2006; 27: 1486 (#J0123383) |
| 25. | Gurtler, Nicolas; Schmuziger, Nicolas; Kim, Yuil; Mhatre, Anand N; Jungi, Manuel; Lalwani, Anil K. "Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides". Laryngoscope. 2005; 115: 640 (#J0131308) |
| 26. | Gurtler, Nicolas; Kim, Yuil; Mhatre, Anand; Schlegel, Christoph; Mathis, Adolf; Daniels, Robert; Shelton, Clough; Lalwani, Anil K. "Two families with nonsyndromic low-frequency hearing loss harbor novel mutations in Wolfram syndrome gene 1". Journal of Molecular Medicine (Berlin). 2005; 83: 553 (#J0131307) |
| 27. | Karmody, Collin S; Blevins, Nikolas H; Lalwani, Anil K. "Sensorineural hearing loss, early greying, and essential tremor: a new hereditary syndrome?". Otolaryngology, head & neck surgery. 2005; 133: 94 (#J0131306) |
| 28. | Chatelin, Veronique; Kim, Eugene J; Driscoll, Colin; Larky, Jannine; Polite, Colleen; Price, Laura; Lalwani, Anil K. "Cochlear implant outcomes in the elderly". Otology & neurotology. 2004; 25: 298 (#J0131310) |
| 29. | Gurtler, Nicolas; Kim, Yuil; Mhatre, Anand; Schlegel, Christoph; Mathis, Alfons; Lalwani, Anil K. "DFNA54, a third locus for low-frequency hearing loss". Journal of Molecular Medicine (Berlin). 2004; 82: 775 (#J0131309) |
| 30. | Gurtler, Nicolas; Kim, Yuil; Mhatre, Anand; Muller, Rene; Probst, Rudolf; Lalwani, Anil K. "GJB2 mutations in the Swiss hearing impaired". Ear & hearing. 2003; 24: 440 (#J0131312) |
| 31. | Purcell D; Johnson J; Fischbein N; Lalwani AK. "Establishment of normative cochlear and vestibular measurements to aid in the diagnosis of inner ear malformations". Otolaryngology, head & neck surgery. 2003; 128: 78 (#J0046785) |
| 32. | Purcell, Derk D; Fischbein, Nancy; Lalwani, Anil K. "Identification of previously "undetectable" abnormalities of the bony labyrinth with computed tomography measurement". Laryngoscope. 2003; 113: 1908 (#J0131311) |
| 33. | Shin EJ; Guertler N; Kim E; Lalwani AK. "Screening of middle ear effusion for the common sinus pathogen Bipolaris". European archives of oto-rhino-laryngology. 2003; 260: 78 (#J0046784) |
| 34. | Wilson, Leslie; Lin, Eddie; Lalwani, Anil. "Cost-effectiveness of intraoperative facial nerve monitoring in middle ear or mastoid surgery". Laryngoscope. 2003; 113: 1736 (#J0131313) |
| 35. | Yen TL; Driscoll CL; Lalwani AK. "Significance of house-brackmann facial nerve grading global score in the setting of differential facial nerve function". Otology & neurotology. 2003; 24: 118 (#J0046786) |
| 36. | Goldstein JA; Lalwani AK. "Further evidence for a third deafness gene within the DFNA2 locus". American journal of medical genetics. 2002; 108: 304 (#J0046800) |
| 37. | Gurtler N; Lalwani AK. "Etiology of syndromic and nonsyndromic sensorineural hearing loss". Otolaryngologic clinics of North America. 2002; 35: 891 (#J0046787) |
| 38. | Hegarty JL; Patel S; Fischbein N; Jackler RK; Lalwani AK. "The value of enhanced magnetic resonance imaging in the evaluation of endocochlear disease". Laryngoscope. 2002; 112: 8 (#J0046801) |
| 39. | Kim EJ; Catten MD; Lalwani AK. "Detection of fungal DNA in effusion associated with acute and serous otitis media". Laryngoscope. 2002; 112: 2037 (#J0046789) |
| 40. | Laane CJ; Murr AH; Mhatre AN; Jones KD; Lalwani AK. "Role of Epstein-Barr virus and cytomegalovirus in the etiology of benign parotid tumors". Head & neck. 2002; 24: 443 (#J0046799) |
| 41. | Lalwani AK; Goldstein JA; Mhatre AN. "Auditory phenotype of DFNA17". Advances in oto-rhino-laryngology. 2002; 61: 107 (#J0046792) |
| 42. | Lalwani AK; Jero J; Mhatre AN. "Current issues in cochlear gene transfer". Audiology & neuro-otology. 2002; 7: 146 (#J0046798) |
| 43. | Lalwani AK; Jero J; Mhatre AN. "Developments in cochlear gene therapy". Advances in oto-rhino-laryngology. 2002; 61: 28 (#J0046794) |
| 44. | Lalwani AK. "Evaluation of childhood sensorineural hearing loss in the post-genome world". Archives of otolaryngology, head & neck surgery. 2002; 128: 88 (#J0046803) |
| 45. | Lalwani AK; Han JJ; Castelein CM; Carvalho GJ; Mhatre AN. "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". Laryngoscope. 2002; 112: 1325 (#J0046797) |
| 46. | Leon PE; Lalwani AK. "Auditory phenotype of DFNA1". Advances in oto-rhino-laryngology. 2002; 61: 34 (#J0046793) |
| 47. | Mafong DD; Pletcher SD; Hoyt C; Lalwani AK. "Ocular findings in children with congenital sensorineural hearing loss". Archives of otolaryngology, head & neck surgery. 2002; 128: 1303 (#J0046790) |
| 48. | Mafong DD; Shin EJ; Lalwani AK. "Use of laboratory evaluation and radiologic imaging in the diagnostic evaluation of children with sensorineural hearing loss". Laryngoscope. 2002; 112: 1 (#J0046802) |
| 49. | Mhatre AN; Jero J; Chiappini I; Bolasco G; Barbara M; Lalwani AK. "Aquaporin-2 expression in the mammalian cochlea and investigation of its role in Meniere's disease". Hearing research. 2002; 170: 59 (#J0046796) |
| 50. | Mhatre AN; Stern RE; Li J; Lalwani AK. "Aquaporin 4 expression in the mammalian inner ear and its role in hearing". Biochemical & biophysical research communications. 2002; 297: 987 (#J0046795) |
| 51. | Pfister MH; Lalwani AK. "Clinical phenotype of DFN2, DFN4 and DFN6". Advances in oto-rhino-laryngology. 2002; 61: 168 (#J0046791) |
| 52. | Stern RE; Lalwani AK. "Audiologic evidence for further genetic heterogeneity at DFNA2". Acta oto-laryngologica. 2002; 122: 730 (#J0046788) |
| 53. | Bork, JM; Peters, LM; Riazuddin, S; Bernstein, SL; Ahmed, ZM; Ness, SL; Polomeno, R; Ramesh, A; Schloss, M; Srisailpathy, CRS; Wayne, S; Bellman, S; Desmukh, D; Ahmed, Z; Khan, SN; Kaloustian, VMD; Li, XC; Lalwani, A; Riazuddin, S; Bitner-Glindzicz, M; Nance, WE; Liu, XZ; Wistow, G; Smith, RJH; Griffith, AJ; Wilcox, ER; Friedman, TB; Morell, RJ. "Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23". American journal of human genetics. 2001; 68: 26 (#J0181082) |
| 54. | Catten MD; Murr AH; Goldstein JA; Mhatre AN; Lalwani AK. "Detection of fungi in the nasal mucosa using polymerase chain reaction". Laryngoscope. 2001; 111: 399 (#J0046809) |
| 55. | Jero J; Mhatre AN; Tseng CJ; Stern RE; Coling DE; Goldstein JA; Hong K; Zheng WW; Hoque AT; Lalwani AK. "Cochlear gene delivery through an intact round window membrane in mouse". Human gene therapy. 2001; 12: 539 (#J0046808) |
| 56. | Jero J; Tseng CJ; Mhatre AN; Lalwani AK. "A surgical approach appropriate for targeted cochlear gene therapy in the mouse". Hearing research. 2001; 151: 106 (#J0046812) |
| 57. | Jero J; Coling DE; Lalwani AK. "The use of Preyer's reflex in evaluation of hearing in mice". Acta oto-laryngologica. 2001; 121: 585 (#J0046804) |
| 58. | Lin D; Goldstein JA; Mhatre AN; Lustig LR; Pfister M; Lalwani AK. "Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2)". Human mutation. 2001; 18: 42 (#J0046806) |
| 59. | Noss RS; Lalwani AK; Yingling CD. "Facial nerve monitoring in middle ear and mastoid surgery". Laryngoscope. 2001; 111: 831 (#J0046807) |
| 60. | Yu KC; Hegarty JL; Gantz BJ; Lalwani AK. "Conservative management of infections in cochlear implant recipients". Otolaryngology, head & neck surgery. 2001; 125: 66 (#J0046805) |
| 61. | Bikhazi, PH; Messina, L; Mhatre, AN; Goldstein, JA; Lalwani, AK. "Molecular pathogenesis in sporadic head and neck paraganglioma". Laryngoscope. 2000; 110: 1346 (#J0181069) |
| 62. | Johnson J; Lalwani AK. "Sensorineural and conductive hearing loss associated with lateral semicircular canal malformation". Laryngoscope. 2000; 110: 1673 (#J0046815) |
| 63. | Kho ST; Pettis RM; Mhatre AN; Lalwani AK. "Cochlear microinjection and its effects upon auditory function in the guinea pig". European archives of oto-rhino-laryngology. 2000; 257: 469 (#J0046811) |
| 64. | Kho, ST; Pettis, RM; Mhatre, AN; Lalwani, AK. "Safety of adeno-associated virus as cochlear gene transfer vector: Analysis of distant spread beyond injected cochleae". Molecular therapy. 2000; 2: 368 (#J0181068) |
| 65. | Lalwani AK; Mhatre AN. "Cochlear gene therapy". Advances in oto-rhino-laryngology. 2000; 56: 275 (#J0046820) |
| 66. | Lalwani AK; Goldstein JA; Kelley MJ; Luxford W; Castelein CM; Mhatre AN. "Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9". American journal of human genetics. 2000; 67: 1121 (#J0046816) |
| 67. | Pfister M; Lalwani AK. "DFN4: non-syndromic autosomal dominant X-linked sensorineural hearing impairment". Advances in oto-rhino-laryngology. 2000; 56: 196 (#J0046821) |
| 68. | Riazuddin, S; Castelein, CM; Friedman, TB; Lalwani, AK; Griffith, AJ; Naz, S; Smith, TN; Liburd, NA; Mastroianni, MA; Riazuddin, S; Wilcox, ER. "A dominant modifier, DFNM1 protects seven individuals from DFNB26 hearing impairment [Abstract]". American journal of human genetics. 2000; 67: 56 (#J0181083) |
| 69. | Riazuddin S; Castelein CM; Ahmed ZM; Lalwani AK; Mastroianni MA; Naz S; Smith TN; Liburd NA; Friedman TB; Griffith AJ; Riazuddin S; Wilcox ER. "Dominant modifier DFNM1 suppresses recessive deafness DFNB26". Nature genetics. 2000; 26: 431 (#J0046813) |
| 70. | Shin EJ; Lalwani AK; Dowd CF. "Role of angiography in the evaluation of patients with pulsatile tinnitus". Laryngoscope. 2000; 110: 1916 (#J0046814) |
| 71. | Tseng CJ; Lalwani AK. "Cracking the auditory genetic code: part II. Syndromic hereditary hearing impairment". American journal of otology. 2000; 21: 437 (#J0046823) |
| 72. | Wilcox ER; Everett LA; Li XC; Lalwani AK; Green ED. "The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4". Advances in oto-rhino-laryngology. 2000; 56: 145 (#J0046822) |
| 73. | Yasunaga S; Grati M; Chardenoux S; Smith TN; Friedman TB; Lalwani AK; Wilcox ER; Petit C. "OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9". American journal of human genetics. 2000; 67: 591 (#J0046819) |
| 74. | Yu KC; Lalwani AK. "Inner ear malformations and hearing loss in linear nevus sebaceous syndrome". International journal of pediatric otorhinolaryngology. 2000; 56: 211 (#J0046810) |
| 75. | Ahn MS; Hayashi GM; Hilsinger RL Jr; Lalwani AK. "Familial mixed tumors of the parotid gland". Head & neck. 1999; 21: 772 (#J0046825) |
| 76. | Bikhazi PH; Roeder E; Attaie A; Lalwani AK. "Familial paragangliomas: the emerging impact of molecular genetics on evaluation and management". American journal of otology. 1999; 20: 639 (#J0046827) |
| 77. | Carvalho GJ; Song CS; Vargervik K; Lalwani AK. "Auditory and facial nerve dysfunction in patients with hemifacial microsomia". Archives of otolaryngology, head & neck surgery. 1999; 125: 209 (#J0046832) |
| 78. | Carvalho GJ; Lalwani AK. "The effect of cochleostomy and intracochlear infusion on auditory brain stem response threshold in the guinea pig". American journal of otology. 1999; 20: 87 (#J0046834) |
| 79. | Chen D; Lalwani AK; House JW; Choo D. "Aspergillus mastoiditis in acquired immunodeficiency syndrome". American journal of otology. 1999; 20: 561 (#J0046828) |
| 80. | Han JJ; Mhatre AN; Wareing M; Pettis R; Gao WQ; Zufferey RN; Trono D; Lalwani AK. "Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector". Human gene therapy. 1999; 10: 1867 (#J0046829) |
| 81. | Lalwani AK; Castelein CM. "Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment". American journal of otology. 1999; 20: 115 (#J0046833) |
| 82. | Lalwani AK; Luxford WM; Mhatre AN; Attaie A; Wilcox ER; Castelein CM. "A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [Letter]". American journal of human genetics. 1999; 64: 318 (#J0046836) |
| 83. | Lalwani AK. "Progress in congenital hearing loss [Editorial]". American journal of otology. 1999; 20: 2 (#J0046835) |
| 84. | Mhatre AN; Steinbach S; Hribar K; Hoque AT; Lalwani AK. "Identification of aquaporin 5 (AQP5) within the cochlea: cDNA cloning and in situ localization". Biochemical & biophysical research communications. 1999; 264: 157 (#J0046826) |
| 85. | Pfister MH; Apaydin F; Turan O; Bereketoglu M; Bilgen V; Braendle U; Kose S; Zenner HP; Lalwani AK. "Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4". Laryngoscope. 1999; 109: 730 (#J0046830) |
| 86. | Riazuddin, S; Castelein, CM; Friedman, TB; Lalwani, AK; Liburd, N; Naz, S; Smith, TN; Riazuddin, S; Wilcox, ER. "A novel nonsyndromic recessive form of deafness maps to 4q28 and demonstrates incomplete penetrance [Abstract]". American journal of human genetics. 1999; 65: 530 (#J0181086) |
| 87. | Shah SB; Lalwani AK; Dowd CF. "Transverse/sigmoid sinus dural arteriovenous fistulas presenting as pulsatile tinnitus". Laryngoscope. 1999; 109: 54 (#J0046837) |
| 88. | Wareing M; Mhatre AN; Pettis R; Han JJ; Haut T; Pfister MH; Hong K; Zheng WW; Lalwani AK. "Cationic liposome mediated transgene expression in the guinea pig cochlea". Hearing research. 1999; 128: 61 (#J0046831) |
| 89. | Wareing MJ; Lalwani AK. "Cochlear gene therapy: current perspectives". International journal of pediatric otorhinolaryngology. 1999; 49 Suppl 1: S27 (#J0046824) |
| 90. | Bikhazi PH; Lalwani AK; Kim EJ; Bikhazi N; Attaie A; Slattery WH; Jackler RK; Brackmann DE. "Germline screening of the NF-2 gene in families with unilateral vestibular schwannoma". Otolaryngology, head & neck surgery. 1998; 119: 1 (#J0046843) |
| 91. | DeStefano AL; Cupples LA; Arnos KS; Asher JH Jr; Baldwin CT; Blanton S; Carey ML; da Silva EO; Friedman TB; Greenberg J; Lalwani AK; Milunsky A; Nance WE; Pandya A; Ramesar RS; Read AP; Tassabejhi M; Wilcox ER; Farrer LA. "Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations". Human genetics. 1998; 102: 499 (#J0046844) |
| 92. | Goodarzi MO; Broberg TG; Lalwani AK. "Lymphoma of the tympanic membrane in acquired immunodeficiency syndrome". Auris, nasus, larynx. 1998; 25: 89 (#J0046851) |
| 93. | Griffith AJ; Telian SA; Downs C; Gorski JL; Gebarski SS; Lalwani AK; Sheldon S. "Familial Mondini dysplasia". Laryngoscope. 1998; 108: 1368 (#J0046841) |
| 94. | Jain PK; Lalwani AK; Li XC; Singleton TL; Smith TN; Chen A; Deshmukh D; Verma IC; Smith RJ; Wilcox ER. "A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene". Genomics. 1998; 50: 290 (#J0046845) |
| 95. | Lalwani AK; Abaza MM; Makariou EV; Armstrong M. "Audiologic presentation of vestibular schwannomas in neurofibromatosis type 2". American journal of otology. 1998; 19: 352 (#J0046850) |
| 96. | Lalwani AK; Larky JB; Wareing MJ; Kwast K; Schindler RA. "The Clarion Multi-Strategy Cochlear Implant--surgical technique, complications, and results: a single institutional experience". American journal of otology. 1998; 19: 66 (#J0046853) |
| 97. | Lalwani AK; Walsh BJ; Carvalho GJ; Muzyczka N; Mhatre AN. "Expression of adeno-associated virus integrated transgene within the mammalian vestibular organs". American journal of otology. 1998; 19: 390 (#J0046849) |
| 98. | Lalwani AK; Jackler RK; Sweetow RW; Lynch ED; Raventos H; Morrow J; King MC; Leon PE. "Further characterization of the DFNA1 audiovestibular phenotype". Archives of otolaryngology, head & neck surgery. 1998; 124: 699 (#J0046846) |
| 99. | Lalwani, AK; Walsh, BJ; Reilly, PG; Carvalho, GJ; Zolotukhin, S; Muzyczka, N; Mhatre, AN. "Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus". Gene therapy. 1998; 5: 277 (#J0181071) |
| 100. | Lalwani AK; Attaie A; Randolph FT; Deshmukh D; Wang C; Mhatre A; Wilcox E. "Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family". American journal of medical genetics. 1998; 80: 406 (#J0046838) |
| 101. | Lattyak BV; Rosenthal P; Mudge C; Roberts JP; Renze JF; Osorio RW; Emond JC; Lalwani AK. "Posttransplant lymphoproliferative disorder presenting in the head and neck". Laryngoscope. 1998; 108: 1195 (#J0046842) |
| 102. | Liang Y; Wang A; Probst FJ; Arhya IN; Barber TD; Chen KS; Deshmukh D; Dolan DF; Hinnant JT; Carter LE; Jain PK; Lalwani AK; Li XC; Lupski JR; Moeljopawiro S; Morell R; Negrini C; Wilcox ER; Winata S; Camper SA; Friedman TB. "Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2". American journal of human genetics. 1998; 62: 904 (#J0046848) |
| 103. | Li XC; Everett LA; Lalwani AK; Desmukh D; Friedman TB; Green ED; Wilcox ER. "A mutation in PDS causes non-syndromic recessive deafness [Letter]". Nature genetics. 1998; 18: 215 (#J0046852) |
| 104. | Mhatre, AN; Charachon, G; Alper, SL; Lalwani, AK. "The guinea pig cochlear AE2 anion exchanger: cDNA cloning and in situ localization within the cochlea". Biochimica & biophysica acta. Biomembranes. 1998; 1414: 1 (#J0181070) |
| 105. | Mhatre AN; Charachon G; Alper SL; Lalwani AK. "The guinea pig cochlear AE2 anion exchanger: cDNA cloning and in situ localization within the cochlea". Biochimica & biophysica acta. 1998; 1414: 1 (#J0046839) |
| 106. | Pfister MH; Apaydin F; Turan O; Bereketoglu M; Bylgen V; Braendle U; Zenner HP; Lalwani AK. "A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD". Genomics. 1998; 53: 377 (#J0046840) |
| 107. | Shah SB; Lalwani AK; Koerper MA. "Perioperative management of von Willebrand's disease in otolaryngologic surgery". Laryngoscope. 1998; 108: 32 (#J0046855) |
| 108. | Wang C; Kim E; Attaie A; Smith TN; Wilcox ER; Lalwani AK. "A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2". Molecular & cellular probes. 1998; 12: 55 (#J0046847) |
| 109. | Attaie A; Kim E; Wilcox ER; Lalwani AK. "A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type I (WS1)". Molecular & cellular probes. 1997; 11: 233 (#J0046858) |
| 110. | Bikhazi NB; Slattery WH 3rd; Lalwani AK; Jackler RK; Bikhazi PH; Brackmann DE. "Familial occurrence of unilateral vestibular schwannoma". Laryngoscope. 1997; 107: 1176 (#J0046857) |
| 111. | Jain, PK; Lalwani, AK; Li, XC; McDuffie, T; Deshmukh, D; Verma, IC; Wilcox, ER. "A gene for recessive nonsyndromic sensorineural hearing impairment (DFNB18) maps to the chromosomal region containing the Usher Syndrome type 1C gene [Abstract]". American journal of human genetics. 1997; 61: 1632 (#J0181088) |
| 112. | Lalwani AK; Linthicum FH; Wilcox ER; Moore JK; Walters FC; San Agustin TB; Mislinski J; Miller MR; Sinninger Y; Attaie A; Luxford WM. "A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration". Audiology & neuro-otology. 1997; 2: 139 (#J0046856) |
| 113. | Lalwani AK; Han JJ; Walsh BJ; Zolotukhin S; Muzyczka N; Mhatre AN. "Green fluorescent protein as a reporter for gene transfer studies in the cochlea". Hearing research. 1997; 114: 139 (#J0046854) |
| 114. | Lustig, LR; Lalwani, A. "The history of Meniere's disease". Otolaryngologic clinics of North America. 1997; 30: 917 (#J0181087) |
| 115. | Morell R; Carey ML; Lalwani AK; Friedman TB; Asher JH Jr. "Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1". Human heredity. 1997; 47: 38 (#J0046860) |
| 116. | Peterson-Falzone SJ; Golabi M; Lalwani AK. "Otolaryngologic manifestations of Kabuki syndrome". International journal of pediatric otorhinolaryngology. 1997; 38: 227 (#J0046859) |
| 117. | Abaza MM; Makariou E; Armstrong M; Lalwani AK. "Growth rate characteristics of acoustic neuromas associated with neurofibromatosis type 2". Laryngoscope. 1996; 106: 694 (#J0046864) |
| 118. | Lalwani AK; Walsh BJ; Reilly PG; Muzyczka N; Mhatre AN. "Development of in vivo gene therapy for hearing disorders: introduction of adeno-associated virus into the cochlea of the guinea pig". Gene therapy. 1996; 3: 588 (#J0046861) |
| 119. | Lalwani AK; Mhatre AN; San Agustin TB; Wilcox ER. "Genotype-phenotype correlations in type 1 Waardenburg syndrome". Laryngoscope. 1996; 106: 895 (#J0046862) |
| 120. | Lalwani AK; Carey TE; Goldstein IJ; Peters BP. "Lectin binding characteristics of squamous cell carcinomas of the head and neck". Acta oto-laryngologica. 1996; 116: 125 (#J0046865) |
| 121. | Mhatre AN; Lalwani AK. "Molecular genetics of deafness". Otolaryngologic clinics of North America. 1996; 29: 421 (#J0046863) |
| 122. | BIKHAZI, NB; SLATTERY, W; LALWANI, AK; JACKLER, RK; BRACKMANN, DE. "FAMILIAL UNILATERAL ACOUSTIC NEUROMA - A NEW HEREDITARY-DISEASE OR AN INCOMPLETE FORM OF NEUROFIBROMATOSIS TYPE-2 [Abstract]". American journal of human genetics. 1995; 57: 452 (#J0181090) |
| 123. | Jain PK; Fukushima K; Deshmukh D; Ramesh A; Thomas E; Lalwani AK; Kumar S; Plopis B; Skarka H; Srisailapathy CR; et al.. "A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus". Human molecular genetics. 1995; 4: 2391 (#J0046866) |
| 124. | JAIN, PK; DESHMUKH, D; THOMAS, E; KUMAR, S; LALWANI, AK; PLOPLIS, B; SKARKA, H; VERMAN, IC; WILCOX, ER. "MAPPING A GENE FOR RECESSIVE NONSYNDROMIC HEARING IMPAIRMENT TO CHROMOSOME 9P21-Q21 [Abstract]". American journal of human genetics. 1995; 57: 1112 (#J0181091) |
| 125. | Lalwani AK; Butt FY; Jackler RK; Pitts LH; Yingling CD. "Delayed onset facial nerve dysfunction following acoustic neuroma surgery". American journal of otology. 1995; 16: 758 (#J0046867) |
| 126. | LALWANI, AK; WALSH, B; REILLY, G; MHATRE, AN; ZOLOTUKHIN, S; MUZYCZKA, N. "DEVELOPMENT OF IN-VIVO GENE-THERAPY FOR HEARING DISORDERS - INTRODUCTION OF ADENOASSOCIATED VIRUS INTO THE COCHLEA OF THE GUINEA-PIG [Abstract]". American journal of human genetics. 1995; 57: 1417 (#J0181073) |
| 127. | Lalwani AK; Brister JR; Fex J; Grundfast KM; Ploplis B; San Agustin TB; Wilcox ER. "Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families". American journal of human genetics. 1995; 56: 75 (#J0046868) |
| 128. | Farrer LA; Arnos KS; Asher JH Jr; Baldwin CT; Diehl SR; Friedman TB; Greenberg J; Grundfast KM; Hoth C; Lalwani AK; et al.. "Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes". American journal of human genetics. 1994; 55: 728 (#J0046870) |
| 129. | Lalwani AK; Butt FY; Jackler RK; Pitts LH; Yingling CD. "Facial nerve outcome after acoustic neuroma surgery: a study from the era of cranial nerve monitoring". Otolaryngology, head & neck surgery. 1994; 111: 561 (#J0046869) |
| 130. | Lalwani AK; Brister JR; Fex J; Grundfast KM; Pikus AT; Ploplis B; San Agustin T; Skarka H; Wilcox ER. "A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2". American journal of human genetics. 1994; 55: 685 (#J0046871) |
| 131. | Chang CY; Lalwani AK; Lanser MJ. "Actinomycosis of the external auditory canal". Otolaryngology, head & neck surgery. 1993; 108: 73 (#J0046879) |
| 132. | FARRER, LA; ASHER, JH; BALDWIN, CT; FRIEDMAN, TB; GREENBERG, J; GRUNDFAST, KM; LALWANI, AK; MILUNSKY, A; MORELL, R; NEWTON, V; RAMESAR, R; RAO, VS; AGUSTIN, TBS; WILCOX, ER; WINSHIP, I; READ, AP. "LOCUS HETEROGENEITY FOR WAARDENBURG SYNDROME IS NOT PREDICTIVE OF CLINICAL SUBTYPES [Abstract]". American journal of human genetics. 1993; 53: 1156 (#J0181093) |
| 133. | Kingdom TT; Lalwani AK; Pitts LH. "Isolated metastatic melanoma of the cerebellopontine angle: case report". Neurosurgery. 1993; 33: 142 (#J0046874) |
| 134. | Lalwani AK; Jackler RK; Harsh GR 4th; Butt FY. "Bilateral temporal bone encephaloceles after cranial irradiation. Case report". Journal of neurosurgery. 1993; 79: 596 (#J0046872) |
| 135. | Lalwani AK; Dowd CF; Halbach VV. "Grading venous restrictive disease in patients with dural arteriovenous fistulas of the transverse/sigmoid sinus". Journal of neurosurgery. 1993; 79: 11 (#J0046876) |
| 136. | Lalwani AK; Lalwani RB; Bartlett PC. "Heterotopic gastric mucosal cyst of the tongue". Otolaryngology, head & neck surgery. 1993; 108: 204 (#J0046878) |
| 137. | Lalwani AK; Jackler RK; Gutin PH. "Lethal fibrosarcoma complicating radiation therapy for benign glomus jugulare tumor". American journal of otology. 1993; 14: 398 (#J0046877) |
| 138. | LALWANI, AK; BRISTER, R; FEX, J; GRUNDFAST, KM; PLOPLIS, B; AGUSTIN, TS; SKARKA, H; WILCOX, ER. "A NEW NONSYNDROMIC X-LINKED SENSORINEURAL HEARING-LOSS LINKED TO XP11.3-21.1 [Abstract]". American journal of human genetics. 1993; 53: 1027 (#J0181092) |
| 139. | Lalwani AK; Jackler RK. "Preoperative differentiation between meningioma of the cerebellopontine angle and acoustic neuroma using MRI". Otolaryngology, head & neck surgery. 1993; 109: 88 (#J0046875) |
| 140. | Lalwani AK; Grundfast KM. "A role for the otolaryngologist in identification and discovery of genetic disorders and chromosomal abnormalities". Archives of otolaryngology, head & neck surgery. 1993; 119: 1074 (#J0046873) |
| 141. | Grundfast KM; Lalwani AK. "Practical approach to diagnosis and management of hereditary hearing impairment (HHI)". Ear, nose & throat journal. 1992; 71: 479 (#J0046882) |
| 142. | Lalwani AK; Jackler RK. "Endaural encephalocele". Otolaryngology, head & neck surgery. 1992; 106: 309 (#J0046884) |
| 143. | LALWANI, AK; CHANG, CYJ; LALWANI, RB. "INDIUM-111-LABELED WHITE BLOOD-CELL SCAN IN DIAGNOSIS OF OCCULT SINUS INFECTION". American journal of rhinology. 1992; 6: 215 (#J0181094) |
| 144. | Lalwani AK; Tami TA; Gelber RH. "Lepromatous leprosy: nasal manifestations and treatment with minocycline". Annals of otology rhinology & laryngology. 1992; 101: 261 (#J0046885) |
| 145. | Lalwani AK. "Meningiomas, epidermoids, and other nonacoustic tumors of the cerebellopontine angle". Otolaryngologic clinics of North America. 1992; 25: 707 (#J0046883) |
| 146. | Lalwani AK; Engel TL. "Teratoma of the tongue: a case report and review of the literature". International journal of pediatric otorhinolaryngology. 1992; 24: 261 (#J0046881) |
| 147. | Lalwani AK; Kaplan MJ; Gutin PH. "The transsphenoethmoid approach to the sphenoid sinus and clivus". Neurosurgery. 1992; 31: 1008 (#J0046880) |
| 148. | Lee KC; Tami TA; Lalwani AK; Schecter G. "Contemporary management of cervical tuberculosis". Laryngoscope. 1992; 102: 60 (#J0046886) |
| 149. | Lalwani AK; Kaplan MJ. "Mediastinal and thoracic complications of necrotizing fasciitis of the head and neck". Head & neck. 1991; 13: 531 (#J0046888) |
| 150. | Lalwani AK; Snyderman NL. "Pharyngeal ulceration in AIDS patients secondary to cytomegalovirus infection". Annals of otology rhinology & laryngology. 1991; 100: 484 (#J0046890) |
| 151. | Lalwani AK; Engelstad BL; Boles R. "Significance of abnormal indium In 111-labeled leukocyte accumulation in the head and neck region". Archives of otolaryngology, head & neck surgery. 1991; 117: 1138 (#J0046889) |
| 152. | Lalwani AK; Jackler RK. "Spontaneous hemotympanum associated with chronic middle ear effusion". American journal of otology. 1991; 12: 455 (#J0046887) |
| 153. | Lalwani AK; Kaplan MJ. "Paranasal sinus leiomyosarcoma after cyclophosphamide and irradiation". Otolaryngology, head & neck surgery. 1990; 103: 1039 (#J0046891) |
| 154. | LALWANI, AK; PETERS, BP; CAREY, TE; GOLDSTEIN, IJ. "CELL-SURFACE PHENOTYPING OF HUMAN SQUAMOUS-CELL CARCINOMAS USING FLUORESCEIN-CONJUGATED LECTINS [Abstract]". Clinical research. 1983; 31: A814 (#J0181095) |
All data from NYU School of Medicine Ehrman Medical Library Faculty Bibliography
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