Chen AH - Search Results

1

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

Greinwald JH Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ. Greinwald JH Jr, et al. Among authors: chen ah. Am J Med Genet. 1998 Jun 30;78(2):107-13. Am J Med Genet. 1998. PMID: 9674898

2

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ. Chen AH, et al. Hum Mol Genet. 1995 Jun;4(6):1073-6. doi: 10.1093/hmg/4.6.1073. Hum Mol Genet. 1995. PMID: 7655461

3

Incidence of vocal fold paralysis in infants undergoing ligation of patent ductus arteriosus.

Zbar RI, Chen AH, Behrendt DM, Bell EF, Smith RJ. Zbar RI, et al. Among authors: chen ah. Ann Thorac Surg. 1996 Mar;61(3):814-6. doi: 10.1016/0003-4975(95)01152-8. Ann Thorac Surg. 1996. PMID: 8619698

4

Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.

Chen AH, Mueller RF, Prasad SD, Greinwald JH Jr, Manaligod J, Muilenburg AC, Verhoeven K, Van Camp G, Smith RJ. Chen AH, et al. Arch Otolaryngol Head Neck Surg. 1998 Jan;124(1):20-4. doi: 10.1001/archotol.124.1.20. Arch Otolaryngol Head Neck Surg. 1998. PMID: 9440775 Review.

5

Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13.

McGuirt WT, Lesperance MM, Wilcox ER, Chen AH, Van Camp G, Smith RJ. McGuirt WT, et al. Among authors: chen ah. Adv Otorhinolaryngol. 2000;56:84-96. doi: 10.1159/000059085. Adv Otorhinolaryngol. 2000. PMID: 10868218 Review. No abstract available.

6

DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance?

Chen AH, Fukushima K, McGuirt WT, Smith RJ. Chen AH, et al. Adv Otorhinolaryngol. 2000;56:171-5. doi: 10.1159/000059089. Adv Otorhinolaryngol. 2000. PMID: 10868231 No abstract available.

7

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Bearer EL, Chen AF, Chen AH, Li Z, Mark HF, Smith RJ, Jackson CL. Bearer EL, et al. Among authors: chen af, chen ah. Ann Hum Genet. 2000 May;64(Pt 3):189-96. doi: 10.1046/j.1469-1809.2000.6430189.x. Ann Hum Genet. 2000. PMID: 11409409 Free PMC article.

8

MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.

Chen AH, Stephan DA, Hasson T, Fukushima K, Nelissen CM, Chen AF, Jun AI, Ramesh A, Van Camp G, Smith RJ. Chen AH, et al. Among authors: chen af. Arch Otolaryngol Head Neck Surg. 2001 Aug;127(8):921-5. doi: 10.1001/archotol.127.8.921. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11493199

9

Evolving mucocutaneous eruptions following chemotherapy.

Chen A, Patrick AP, Sharif-Sidi Z, Liu V, Fairley JA. Chen A, et al. JAAD Case Rep. 2022 Aug 10;28:67-70. doi: 10.1016/j.jdcr.2022.08.004. eCollection 2022 Oct. JAAD Case Rep. 2022. PMID: 36105754 Free PMC article. No abstract available.

10

Adalimumab therapy used successfully for recalcitrant Hailey-Hailey disease.

Chen A, DaCunha M, Harms J. Chen A, et al. JAAD Case Rep. 2022 Sep 22;29:173-176. doi: 10.1016/j.jdcr.2022.09.014. eCollection 2022 Nov. JAAD Case Rep. 2022. PMID: 36304476 Free PMC article. No abstract available.

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