Pivnick EK - Search Results

1

Treatment of diffuse basal cell carcinomas and basaloid follicular hamartomas in nevoid basal cell carcinoma syndrome by wide-area 5-aminolevulinic acid photodynamic therapy.

Oseroff AR, Shieh S, Frawley NP, Cheney R, Blumenson LE, Pivnick EK, Bellnier DA. Oseroff AR, et al. Among authors: pivnick ek. Arch Dermatol. 2005 Jan;141(1):60-7. doi: 10.1001/archderm.141.1.60. Arch Dermatol. 2005. PMID: 15655143

2

Complications of the nevoid basal cell carcinoma syndrome: a case report.

Walter AW, Pivnick EK, Bale AE, Kun LE. Walter AW, et al. Among authors: pivnick ek. J Pediatr Hematol Oncol. 1997 May-Jun;19(3):258-62. doi: 10.1097/00043426-199705000-00016. J Pediatr Hematol Oncol. 1997. PMID: 9201152

3

Gorlin syndrome associated with midline nasal dermoid cyst.

Pivnick EK, Walter AW, Lawrence MD, Smith ME. Pivnick EK, et al. J Med Genet. 1996 Aug;33(8):704-6. doi: 10.1136/jmg.33.8.704. J Med Genet. 1996. PMID: 8863166 Free PMC article.

4

Phenocopy of warfarin syndrome in an infant born to a mother with sickle cell anemia and severe transfusional iron overload.

Xie Y, Pivnick EK, Cohen HL, Adams-Graves PE, Pourcyrous M, Aygun B, Hankins JS. Xie Y, et al. Among authors: pivnick ek. J Pediatr Hematol Oncol. 2013 Aug;35(6):e265-8. doi: 10.1097/MPH.0b013e3182678f68. J Pediatr Hematol Oncol. 2013. PMID: 23018567

5

Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.

Pivnick EK, Furman WL, Velagaleti GV, Jenkins JJ, Chase NA, Ribeiro RC. Pivnick EK, et al. J Med Genet. 1998 Apr;35(4):328-32. doi: 10.1136/jmg.35.4.328. J Med Genet. 1998. PMID: 9598730 Free PMC article.

6

Hair whorl as an indicator of a mediastinal plexiform neurofibroma.

Pivnick EK, Lobe TE, Fitch SJ, Riccardi VM. Pivnick EK, et al. Pediatr Dermatol. 1997 May-Jun;14(3):196-8. doi: 10.1111/j.1525-1470.1997.tb00236.x. Pediatr Dermatol. 1997. PMID: 9192411

7

Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review.

Pivnick EK, Angle B, Kaufman RA, Hall BD, Pitukcheewanont P, Hersh JH, Fowlkes JL, Sanders LP, O'Brien JM, Carroll GS, Gunther WM, Morrow HG, Burghen GA, Ward JC. Pivnick EK, et al. Am J Med Genet. 2000 Jan 17;90(2):131-40. Am J Med Genet. 2000. PMID: 10607952 Review.

8

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Pivnick EK, Velagaleti GV, Wilroy RS, Smith ME, Rose SR, Tipton RE, Tharapel AT. Pivnick EK, et al. J Med Genet. 1996 Sep;33(9):772-8. doi: 10.1136/jmg.33.9.772. J Med Genet. 1996. PMID: 8880580 Free PMC article. Review.

9

Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome?

Pivnick EK, Wilroy RS, Martens PR, Teather TC, Hashimoto K. Pivnick EK, et al. Am J Med Genet. 1996 Apr 24;62(4):386-90. doi: 10.1002/(SICI)1096-8628(19960424)62:4<386::AID-AJMG11>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8723069

10

A jumping Robertsonian translocation: a molecular and cytogenetic study.

Gross SJ, Tharapel AT, Phillips OP, Shulman LP, Pivnick EK, Park VM. Gross SJ, et al. Among authors: pivnick ek. Hum Genet. 1996 Sep;98(3):291-6. doi: 10.1007/s004390050209. Hum Genet. 1996. PMID: 8707296

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