Wu YH - Search Results

1

Netherton syndrome: mutation analysis of two Taiwanese families.

Lin SP, Huang SY, Tu ME, Wu YH, Lin CY, Lin HY, Lee-Chen GJ. Lin SP, et al. Among authors: wu yh. Arch Dermatol Res. 2007 Jun;299(3):145-50. doi: 10.1007/s00403-007-0751-z. Epub 2007 Apr 6. Arch Dermatol Res. 2007. PMID: 17415575

2

Isotopic response of fungal granuloma following facial herpes zoster infections - report of three cases.

Huang CW, Tu ME, Wu YH, Lin YC. Huang CW, et al. Among authors: wu yh. Int J Dermatol. 2007 Nov;46(11):1141-5. doi: 10.1111/j.1365-4632.2007.03265.x. Int J Dermatol. 2007. PMID: 17988332

3

Necrolytic acral erythema without hepatitis C infection.

Wu YH, Tu ME, Lee CS, Lin YC. Wu YH, et al. J Cutan Pathol. 2009 Mar;36(3):355-8. doi: 10.1111/j.1600-0560.2008.01037.x. J Cutan Pathol. 2009. PMID: 19220632

4

Allergic contact dermatitis from incense.

Yang CC, Tu ME, Wu YH. Yang CC, et al. Among authors: wu yh. Contact Dermatitis. 2009 Sep;61(3):185-6. doi: 10.1111/j.1600-0536.2009.01595.x. Contact Dermatitis. 2009. PMID: 19780782 No abstract available.

5

Lafora disease and congenital generalized lipodystrophy: a case report.

Tseng CF, Ho CS, Chiu NC, Lin SP, Tzen CY, Wu YH. Tseng CF, et al. Among authors: wu yh. Kaohsiung J Med Sci. 2009 Dec;25(12):663-8. doi: 10.1016/S1607-551X(09)70572-8. Kaohsiung J Med Sci. 2009. PMID: 19951852 Free article.

6

NEMO gene mutations in Chinese patients with incontinentia pigmenti.

Hsiao PF, Lin SP, Chiang SS, Wu YH, Chen HC, Lin YC. Hsiao PF, et al. Among authors: wu yh. J Formos Med Assoc. 2010 Mar;109(3):192-200. doi: 10.1016/S0929-6646(10)60042-3. J Formos Med Assoc. 2010. PMID: 20434027 Free article.

7

Sebaceous nevus syndrome, central nervous system malformations, aplasia cutis congenita, limbal dermoid, and pigmented nevus syndrome.

Hsieh CW, Wu YH, Lin SP, Peng CC, Ho CS. Hsieh CW, et al. Among authors: wu yh. Pediatr Dermatol. 2012 May-Jun;29(3):365-7. doi: 10.1111/j.1525-1470.2011.01639.x. Epub 2011 Nov 28. Pediatr Dermatol. 2012. PMID: 22122611

8

Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

Yang CF, Lin SP, Chiang CP, Wu YH, H'ng WS, Chang CP, Chen YT, Wu JY. Yang CF, et al. Among authors: wu yh, wu jy. Am J Hum Genet. 2018 Feb 1;102(2):219-232. doi: 10.1016/j.ajhg.2017.12.012. Epub 2018 Jan 11. Am J Hum Genet. 2018. PMID: 29336782 Free PMC article.

9

Folliculosebaceous cystic hamartoma or trichofolliculoma? A spectrum of hamartomatous changes inducted by perifollicular stroma in the follicular epithelium.

Wu YH. Wu YH. J Cutan Pathol. 2008 Sep;35(9):843-8. doi: 10.1111/j.1600-0560.2007.00914.x. Epub 2008 May 20. J Cutan Pathol. 2008. PMID: 18494824

10

Generalized Dowling-Degos disease.

Wu YH, Lin YC. Wu YH, et al. J Am Acad Dermatol. 2007 Aug;57(2):327-34. doi: 10.1016/j.jaad.2006.12.023. J Am Acad Dermatol. 2007. PMID: 17637446

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