Schnur RE - Search Results

1

Tuberous sclerosis. The persistent challenge of clinical diagnosis.

Schnur RE. Schnur RE. Arch Dermatol. 1995 Dec;131(12):1460-2. doi: 10.1001/archderm.131.12.1460. Arch Dermatol. 1995. PMID: 7492142 No abstract available.

2

Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.

Payne AS, Yan AC, Ilyas E, Li W, Seykora JT, Young TL, Pawel BR, Honig PJ, Camacho J, Imaizumi S, Heymann WR, Schnur RE. Payne AS, et al. Among authors: schnur re. Arch Dermatol. 2005 Dec;141(12):1567-73. doi: 10.1001/archderm.141.12.1567. Arch Dermatol. 2005. PMID: 16365259

3

Clustered angiofibromas on the ear of a patient with neurofibromatosis type 2.

Jaffe AT, Heymann WR, Schnur RE. Jaffe AT, et al. Among authors: schnur re. Arch Dermatol. 1998 Jun;134(6):760-1. doi: 10.1001/archderm.134.6.760. Arch Dermatol. 1998. PMID: 9645657 No abstract available.

4

Magnetization transfer in the investigation of patients with tuberous sclerosis.

Girard N, Zimmerman RA, Schnur RE, Haselgrove J, Christensen K. Girard N, et al. Among authors: schnur re. Neuroradiology. 1997 Jul;39(7):523-8. doi: 10.1007/s002340050459. Neuroradiology. 1997. PMID: 9258933

5

Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome.

Schnur RE, Greenbaum BH, Heymann WR, Christensen K, Buck AS, Reid CS. Schnur RE, et al. Am J Med Genet. 1997 Oct 3;72(1):24-9. Am J Med Genet. 1997. PMID: 9295069 Review.

6

Melanoma and basal cell carcinoma in the hereditary leiomyomatosis and renal cell cancer syndrome. An expansion of the oncologic spectrum.

Sommer LL, Schnur RE, Heymann WR. Sommer LL, et al. Among authors: schnur re. J Dermatol Case Rep. 2016 Nov 30;10(3):53-55. doi: 10.3315/jdcr.2016.1234. eCollection 2016 Nov 30. J Dermatol Case Rep. 2016. PMID: 28400895 Free PMC article.

7

Reticulate hyperpigmentation.

Schnur RE, Heymann WR. Schnur RE, et al. Semin Cutan Med Surg. 1997 Mar;16(1):72-80. doi: 10.1016/s1085-5629(97)80038-7. Semin Cutan Med Surg. 1997. PMID: 9125768 Review.

8

Variability in the Michelin tire syndrome. A child with multiple anomalies, smooth muscle hamartoma, and familial paracentric inversion of chromosome 7q.

Schnur RE, Herzberg AJ, Spinner N, Kant JA, Magnusson M, McDonald-McGinn D, Rehberg K, Honig PJ, Zackai EH. Schnur RE, et al. J Am Acad Dermatol. 1993 Feb;28(2 Pt 2):364-70. J Am Acad Dermatol. 1993. PMID: 8436660 Review.

9

Genodermatoses 2003-2004.

Schnur RE. Schnur RE. Curr Opin Pediatr. 2004 Dec;16(6):678-88. doi: 10.1097/01.mop.0000145727.95637.d6. Curr Opin Pediatr. 2004. PMID: 15548932 Review.

10

Reevaluation of a kindred with congenital absence of dermal ridges, syndactyly, and facial milia.

Cirillo-Hyland VA, Zackai EH, Honig PJ, Grace KR, Schnur RE. Cirillo-Hyland VA, et al. Among authors: schnur re. J Am Acad Dermatol. 1995 Feb;32(2 Pt 2):315-8. doi: 10.1016/0190-9622(95)90394-1. J Am Acad Dermatol. 1995. PMID: 7829732

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