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Results: 1-25 | 26-43
Results: 1-25/43
GENETIC-MAPPING REFINES DFNB3 TO 17P11.2, SUGGESTS MULTIPLE ALLELES OF DFNB3, AND SUPPORTS HOMOLOGY TO THE MOUSE MODEL SHAKER-2
Authors: LIANG Y WANG AH PROBST FJ ARHYA IN BARBER TD CHEN KS DESHMUKH D DOLAN DF HINNANT JT CARTER LE JAIN PK LALWANI AK LI XYC LUPSKI JR MOELJOPAWIRO S MORELL R NEGRINI C WILCOX ER WINATA S CAMPER SA FRIEDMAN TB
Citation: Y. Liang et al., 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, 62(4), 1998, pp. 904-915
A MUTATION IN PDS CAUSES NON-SYNDROMIC RECESSIVE DEAFNESS
Authors: LI XC EVERETT LA LALWANI AK DESMUKH D FRIEDMAN TB GREEN ED WILCOX ER
Citation: Xc. Li et al., A MUTATION IN PDS CAUSES NON-SYNDROMIC RECESSIVE DEAFNESS, Nature genetics, 18(3), 1998, pp. 215-217
LONG-TERM IN-VIVO COCHLEAR TRANSGENE EXPRESSION MEDIATED BY RECOMBINANT ADENOASSOCIATED VIRUS
Authors: LALWANI AK WALSH BJ REILLY PG CARVALHO GJ ZOLOTUKHIN S MUZYCZKA N MHATRE AN
Citation: Ak. Lalwani et al., LONG-TERM IN-VIVO COCHLEAR TRANSGENE EXPRESSION MEDIATED BY RECOMBINANT ADENOASSOCIATED VIRUS, Gene therapy, 5(2), 1998, pp. 277-281
A PAX3 POLYMORPHISM (T315K) IN A FAMILY EXHIBITING WAARDENBURG-SYNDROME TYPE-2 (WS2)
Authors: WANG C KIM E ATTAIE A SMITH TN WILCOX ER LALWANI AK
Citation: C. Wang et al., A PAX3 POLYMORPHISM (T315K) IN A FAMILY EXHIBITING WAARDENBURG-SYNDROME TYPE-2 (WS2), Molecular and cellular probes, 12(1), 1998, pp. 55-57
A 2ND FAMILY WITH NONSYNDROMIC SENSORINEURAL HEAVING LOSS LINKED TO XP21.2 - REFINEMENT OF THE DFN4 LOCUS WITHIN DMD
Authors: PFISTER MHF APAYDIN F TURAN O BEREKETOGLU M BYLGEN V BRAENDLE U ZENNER HP LALWANI AK
Citation: Mhf. Pfister et al., A 2ND FAMILY WITH NONSYNDROMIC SENSORINEURAL HEAVING LOSS LINKED TO XP21.2 - REFINEMENT OF THE DFN4 LOCUS WITHIN DMD, Genomics (San Diego, Calif.), 53(3), 1998, pp. 377-382
A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS (DFNB18) MAPS TO THE CHROMOSOMAL REGION 11P14-P15.1 CONTAINING THE USHER-SYNDROME TYPE 1C GENE
Authors: JAIN PK LALWANI AK LI XC SINGLETON TL SMITH TN CHEN A DESHMUKH D VERMA IC SMITH RJH WILCOX ER
Citation: Pk. Jain et al., A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS (DFNB18) MAPS TO THE CHROMOSOMAL REGION 11P14-P15.1 CONTAINING THE USHER-SYNDROME TYPE 1C GENE, Genomics, 50(2), 1998, pp. 290-292
FURTHER CHARACTERIZATION OF THE DFNA1 AUDIOVESTIBULAR PHENOTYPE
Authors: LALWANI AK JACKLER RK SWEETOW RW LYNCH ED RAVENTOS H MORROW J KING MC LEON PE
Citation: Ak. Lalwani et al., FURTHER CHARACTERIZATION OF THE DFNA1 AUDIOVESTIBULAR PHENOTYPE, Archives of otolaryngology, head & neck surgery, 124(6), 1998, pp. 699-702
CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS
Authors: DESTEFANO AL CUPPLES LA ARNOS KS ASHER JH BALDWIN CT BLANTON S CAREY ML DASILVA EO FRIEDMAN TB GREENBERG J LALWANI AK MILUNSKY A NANCE WE PANDYA A RAMESAR RS READ AP TASSABEJHI M WILCOX ER FARRER LA
Citation: Al. Destefano et al., CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS, Human genetics, 102(5), 1998, pp. 499-506
GERMLINE SCREENING OF THE NF-2 GENE IN FAMILIES WITH UNILATERAL VESTIBULAR SCHWANNOMA
Authors: BIKHAZI PH LALWANI AK KIM EJ BIKHAZI M ATTAIE L SLATTERY WH JACKLER RK BRACKMANN DE
Citation: Ph. Bikhazi et al., GERMLINE SCREENING OF THE NF-2 GENE IN FAMILIES WITH UNILATERAL VESTIBULAR SCHWANNOMA, Otolaryngology and head and neck surgery, 119(1), 1998, pp. 1-6
THE CLARION MULTI-STRATEGY COCHLEAR IMPLANT - SURGICAL TECHNIQUE, COMPLICATIONS, AND RESULTS - A SINGLE INSTITUTIONAL EXPERIENCE
Authors: LALWANI AK LARKY JB WAREING MJ KWAST K SCHINDLER RA
Citation: Ak. Lalwani et al., THE CLARION MULTI-STRATEGY COCHLEAR IMPLANT - SURGICAL TECHNIQUE, COMPLICATIONS, AND RESULTS - A SINGLE INSTITUTIONAL EXPERIENCE, The American journal of otology, 19(1), 1998, pp. 66-70
FAMILIAL MONDINI-DYSPLASIA
Authors: GRIFFITH AJ TELIAN SA DOWNS C GORSKI JL GEBARSKI SS LALWANI AK SHELDON S
Citation: Aj. Griffith et al., FAMILIAL MONDINI-DYSPLASIA, The Laryngoscope, 108(9), 1998, pp. 1368-1373
POSTTRANSPLANT LYMPHOPROLIFERATIVE DISORDER PRESENTING IN THE HEAD AND NECK
Authors: LATTYAK BV ROSENTHAL P MUDGE C ROBERTS JP RENZE JF OSORIO RW EMOND JC LALWANI AK
Citation: Bv. Lattyak et al., POSTTRANSPLANT LYMPHOPROLIFERATIVE DISORDER PRESENTING IN THE HEAD AND NECK, The Laryngoscope, 108(8), 1998, pp. 1195-1198
PERIOPERATIVE MANAGEMENT OF VON-WILLEBRANDS-DISEASE IN OTOLARYNGOLOGIC SURGERY
Authors: SHAH SB LALWANI AK KOERPER MA
Citation: Sb. Shah et al., PERIOPERATIVE MANAGEMENT OF VON-WILLEBRANDS-DISEASE IN OTOLARYNGOLOGIC SURGERY, The Laryngoscope, 108(1), 1998, pp. 32-36
THE GUINEA-PIG COCHLEAR AE2 ANION-EXCHANGER - CDNA CLONING AND IN-SITU LOCALIZATION WITHIN THE COCHLEA
Authors: MHATRE AN CHARACHON G ALPER SL LALWANI AK
Citation: An. Mhatre et al., THE GUINEA-PIG COCHLEAR AE2 ANION-EXCHANGER - CDNA CLONING AND IN-SITU LOCALIZATION WITHIN THE COCHLEA, Biochimica et biophysica acta. Biomembranes, 1414(1-2), 1998, pp. 1-15
A 5-GENERATION FAMILY WITH LATE-ONSET PROGRESSIVE HEREDITARY HEARING IMPAIRMENT DUE TO COCHLEOSACCULAR DEGENERATION
Authors: LALWANI AK LINTHICUM FH WILCOX ER MOORE JK WALTERS FC SANAGUSTIN TB MISLINSKI J MILLER MR SINNINGER Y ATTAIE A LUXFORD WM
Citation: Ak. Lalwani et al., A 5-GENERATION FAMILY WITH LATE-ONSET PROGRESSIVE HEREDITARY HEARING IMPAIRMENT DUE TO COCHLEOSACCULAR DEGENERATION, Audiology & neuro-otology, 2(3), 1997, pp. 139-154
A SPLICE-SITE MUTATION AFFECTING THE PAIRED BOX OF PAX3 IN A 3 GENERATION FAMILY WITH WAARDENBURG SYNDROME TYPE-I (WS1)
Authors: ATTAIE A KIM E WILCOX ER LALWANI AK
Citation: A. Attaie et al., A SPLICE-SITE MUTATION AFFECTING THE PAIRED BOX OF PAX3 IN A 3 GENERATION FAMILY WITH WAARDENBURG SYNDROME TYPE-I (WS1), Molecular and cellular probes, 11(3), 1997, pp. 233-236
GREEN FLUORESCENT PROTEIN AS A REPORTER FOR GENE-TRANSFER STUDIES IN THE COCHLEA
Authors: LALWANI AK HAN JJ WALSH BJ ZOLOTUKHIN S MUZYCZKA N MHATRE AN
Citation: Ak. Lalwani et al., GREEN FLUORESCENT PROTEIN AS A REPORTER FOR GENE-TRANSFER STUDIES IN THE COCHLEA, Hearing research, 114(1-2), 1997, pp. 139-147
OTOLARYNGOLOGIC MANIFESTATIONS OF KABUKI SYNDROME
Authors: PETERSONFALZONE SJ GOLABI M LALWANI AK
Citation: Sj. Petersonfalzone et al., OTOLARYNGOLOGIC MANIFESTATIONS OF KABUKI SYNDROME, International journal of pediatric otorhinolaryngology, 38(3), 1997, pp. 227-236
FAMILIAL OCCURRENCE OF UNILATERAL VESTIBULAR SCHWANNOMA
Authors: BIKHAZI NB SLATTERY WH LALWANI AK JACKLER RK BIKHAZI PH BRACKMANN DE
Citation: Nb. Bikhazi et al., FAMILIAL OCCURRENCE OF UNILATERAL VESTIBULAR SCHWANNOMA, The Laryngoscope, 107(9), 1997, pp. 1176-1180
A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL HEARING IMPAIRMENT (DFNB18) MAPS TO THE CHROMOSOMAL REGION CONTAINING THE USHER-SYNDROME TYPE 1C GENE
Authors: JAIN PK LALWANI AK LI XC MCDUFFIE T DESHMUKH D VERMA IC WILCOX ER
Citation: Pk. Jain et al., A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL HEARING IMPAIRMENT (DFNB18) MAPS TO THE CHROMOSOMAL REGION CONTAINING THE USHER-SYNDROME TYPE 1C GENE, American journal of human genetics, 61(4), 1997, pp. 1632-1632
3 MUTATIONS IN THE PAIRED HOMEODOMAIN OF PAX3 THAT CAUSE WAARDENBURG SYNDROME TYPE-1
Authors: MORELL R CAREY ML LALWANI AK FRIEDMAN TB ASHER JH
Citation: R. Morell et al., 3 MUTATIONS IN THE PAIRED HOMEODOMAIN OF PAX3 THAT CAUSE WAARDENBURG SYNDROME TYPE-1, Human heredity, 47(1), 1997, pp. 38-41
DEVELOPMENT OF IN-VIVO GENE-THERAPY FOR HEARING DISORDERS - INTRODUCTION OF ADENOASSOCIATED VIRUS INTO THE COCHLEA OF THE GUINEA-PIG
Authors: LALWANI AK WALSH BJ REILLY PG MUZYCZKA N MHATRE AN
Citation: Ak. Lalwani et al., DEVELOPMENT OF IN-VIVO GENE-THERAPY FOR HEARING DISORDERS - INTRODUCTION OF ADENOASSOCIATED VIRUS INTO THE COCHLEA OF THE GUINEA-PIG, Gene therapy, 3(7), 1996, pp. 588-592
FACIAL-NERVE DYSFUNCTION - REPLY
Authors: LALWANI AK
Citation: Ak. Lalwani, FACIAL-NERVE DYSFUNCTION - REPLY, The American journal of otology, 17(3), 1996, pp. 497-497
MOLECULAR-GENETICS OF DEAFNESS
Authors: MHATRE AN LALWANI AK
Citation: An. Mhatre et Ak. Lalwani, MOLECULAR-GENETICS OF DEAFNESS, Otolaryngologic clinics of North America, 29(3), 1996, pp. 421
GENOTYPE-PHENOTYPE CORRELATIONS IN TYPE-1 WAARDENBURG SYNDROME
Authors: LALWANI AK MHATRE AN SANAGUSTIN TB WILCOX ER
Citation: Ak. Lalwani et al., GENOTYPE-PHENOTYPE CORRELATIONS IN TYPE-1 WAARDENBURG SYNDROME, The Laryngoscope, 106(7), 1996, pp. 895-902
Risultati: 1-25 | 26-43