Williams ML - Search Results

1

Giant congenital melanocytic nevi: the significance of neurocutaneous melanosis in neurologically asymptomatic children.

Foster RD, Williams ML, Barkovich AJ, Hoffman WY, Mathes SJ, Frieden IJ. Foster RD, et al. Among authors: williams ml. Plast Reconstr Surg. 2001 Apr 1;107(4):933-41. doi: 10.1097/00006534-200104010-00005. Plast Reconstr Surg. 2001. PMID: 11252085

2

MR of neurocutaneous melanosis.

Barkovich AJ, Frieden IJ, Williams ML. Barkovich AJ, et al. Among authors: williams ml. AJNR Am J Neuroradiol. 1994 May;15(5):859-67. AJNR Am J Neuroradiol. 1994. PMID: 8059652 Free PMC article.

3

Giant congenital melanocytic nevi: brain magnetic resonance findings in neurologically asymptomatic children.

Frieden IJ, Williams ML, Barkovich AJ. Frieden IJ, et al. Among authors: williams ml. J Am Acad Dermatol. 1994 Sep;31(3 Pt 1):423-9. doi: 10.1016/s0190-9622(94)70204-7. J Am Acad Dermatol. 1994. PMID: 8077466

4

Neonatal erosions and ulcerations in giant congenital melanocytic nevi.

Giam YC, Williams ML, Leboit PE, Orlow SJ, Eichenfield LF, Frieden IJ. Giam YC, et al. Among authors: williams ml. Pediatr Dermatol. 1999 Sep-Oct;16(5):354-8. doi: 10.1046/j.1525-1470.1999.00092.x. Pediatr Dermatol. 1999. PMID: 10571832

5

Genetic changes in neoplasms arising in congenital melanocytic nevi: differences between nodular proliferations and melanomas.

Bastian BC, Xiong J, Frieden IJ, Williams ML, Chou P, Busam K, Pinkel D, LeBoit PE. Bastian BC, et al. Among authors: williams ml. Am J Pathol. 2002 Oct;161(4):1163-9. doi: 10.1016/S0002-9440(10)64393-3. Am J Pathol. 2002. PMID: 12368190 Free PMC article.

6

The stiff skin syndrome: case series, differential diagnosis of the stiff skin phenotype, and review of the literature.

Liu T, McCalmont TH, Frieden IJ, Williams ML, Connolly MK, Gilliam AE. Liu T, et al. Among authors: williams ml. Arch Dermatol. 2008 Oct;144(10):1351-9. doi: 10.1001/archderm.144.10.1351. Arch Dermatol. 2008. PMID: 18936399 Review.

7

Sweet's syndrome leading to acquired cutis laxa (Marshall's syndrome) in an infant with alpha 1-antitrypsin deficiency.

Hwang ST, Williams ML, McCalmont TH, Frieden IJ. Hwang ST, et al. Among authors: williams ml. Arch Dermatol. 1995 Oct;131(10):1175-7. Arch Dermatol. 1995. PMID: 7574835

8

Familial site-specific congenital melanocytic nevus: report of two families.

Frieden IJ, Williams ML. Frieden IJ, et al. Among authors: williams ml. Arch Dermatol. 1994 Aug;130(8):1075-6. Arch Dermatol. 1994. PMID: 8053712 No abstract available.

9

Cutaneous manifestations of maternal engraftment in patients with severe combined immunodeficiency: a clinicopathologic study.

Denianke KS, Frieden IJ, Cowan MJ, Williams ML, McCalmont TH. Denianke KS, et al. Among authors: williams ml. Bone Marrow Transplant. 2001 Aug;28(3):227-33. doi: 10.1038/sj.bmt.1703128. Bone Marrow Transplant. 2001. PMID: 11535989

10

Trichothiodystrophy: clinical spectrum, central nervous system imaging, and biochemical characterization of two siblings.

Chen E, Cleaver JE, Weber CA, Packman S, Barkovich AJ, Koch TK, Williams ML, Golabi M, Price VH. Chen E, et al. Among authors: williams ml. J Invest Dermatol. 1994 Nov;103(5 Suppl):154S-158S. doi: 10.1111/1523-1747.ep12399493. J Invest Dermatol. 1994. PMID: 7963680 Free article.

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