Publications

  1. Tintle S, Alikhan A, Horner ME, Hand JL, Davis DM. Cutaneous porphyrias part II: treatment strategies. Int J Dermatol. 2014 Jan; 53(1):3-24. Epub 2013 Oct 18
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  2. Ness MJ, Lowe GC, Davis DM, Hand JL. Narrowband ultraviolet B light in Langerhans cell histiocytosis: a case report. Pediatr Dermatol. 2014 Jan-Feb; 31(1):e10-2. Epub 2013 Nov 14
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  3. Horner ME, Alikhan A, Tintle S, Tortorelli S, Davis DM, Hand JL. Cutaneous porphyrias part I: epidemiology, pathogenesis, presentation, diagnosis, and histopathology. Int J Dermatol. 2013 Dec; 52(12):1464-80.
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  4. Storan ER, McEvoy MT, Wetter DA, el-Azhary RA, Hand JL, Davis DM, Bridges AG, Camilleri MJ, Davis MD. Pediatric hospital dermatology: experience with inpatient and consult services at the Mayo Clinic. Pediatr Dermatol. 2013 Jul-Aug; 30(4):433-7. Epub 2013 Feb 14.
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  5. Kottschade LA, Grotz TE, Dronca RS, Salomao DR, Pulido JS, Wasif N, Jakub JW, Bagaria SP, Kumar R, Kaur JS, Morita SY, Moran SL, Nguyen JT, Nguyen EC, Hand JL, Erickson LA, Brewer JD, Baum CL, Miller RC, Swanson DL, Lowe V, Markovic SN. Rare Presentations of Primary Melanoma and Special Populations: A Systematic Review. Am J Clin Oncol. 2013 Apr 03. [Epub ahead of print]
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  6. Brick K, Hand JL, Frankel AS, Siegel DH, Thomas KB, El-Azhary R, Krol A. Epidermolysis bullosa pruriginosa: further clarification of the phenotype. Pediatr Dermatol. 2012 Nov-Dec; 29(6):732-7.
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  7. Hand JL. Retinoic acid: a familiar teratogen. Pediatr Dermatol. 2012 Nov-Dec; 29(6):774-6.
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  8. Dabade TS, Davis DM, Wetter DA, Hand JL, McEvoy MT, Pittelkow MR, el-Azhary RA, Davis MD. Wet dressing therapy in conjunction with topical corticosteroids is effective for rapid control of severe pediatric atopic dermatitis: experience with 218 patients over 30 years at Mayo Clinic. J Am Acad Dermatol. 2012 Jul; 67(1):100-6. Epub 2011 Oct 05.
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  9. Brick K, Hand JL, Frankel AS, Siegel DH, Thomas KB, El-Azhary R, Krol A. Epidermolysis Bullosa Pruriginosa: Further Clarification of the Phenotype. Pediatr Dermatol. 2012 May 29. [Epub ahead of print]
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  10. Podjasek JO, Hand JL. Marie-Unna hereditary hypotrichosis: case report and review of the literature. Pediatr Dermatol. 2011 Mar-Apr; 28(2):202-4.
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  11. Ayo DS, Aughenbaugh GL, Yi ES, Hand JL, Ryu JH. Cystic lung disease in Birt-Hogg-Dube syndrome. Chest. 2007 Aug; 132(2):679-84. Epub 2007 May 15.
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  12. Markovic SN, Erickson LA, Rao RD, Weenig RH, Pockaj BA, Bardia A, Vachon CM, Schild SE, McWilliams RR, Hand JL, Laman SD, Kottschade LA, Maples WJ, Pittelkow MR, Pulido JS, Cameron JD, Creagan ET, Melanoma Study Group of Mayo Clinic Cancer Center. Malignant melanoma in the 21st century, part 2: staging, prognosis, and treatment. Mayo Clin Proc. 2007 Apr; 82(4):490-513.
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  13. Markovic SN, Erickson LA, Rao RD, Weenig RH, Pockaj BA, Bardia A, Vachon CM, Schild SE, McWilliams RR, Hand JL, Laman SD, Kottschade LA, Maples WJ, Pittelkow MR, Pulido JS, Cameron JD, Creagan ET, Melanoma Study Group of the Mayo Clinic Cancer Center. Malignant melanoma in the 21st century, part 1: epidemiology, risk factors, screening, prevention, and diagnosis. Mayo Clin Proc. 2007 Mar; 82(3):364-80.
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  14. Mensink KA, Hand JL. Autosomal recessive inheritance: an updated review. Pediatr Dermatol. 2006 Jul-Aug; 23(4):404-9.
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  15. Kuhl J, Davis MD, Kalaaji AN, Kamath PS, Hand JL, Peine CJ. Skin signs as the presenting manifestation of severe nutritional deficiency: report of 2 cases. Arch Dermatol. 2004 May; 140(5):521-4.
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  16. Hand JL, Rogers RS. Oral manifestations of genodermatoses. Dermatol Clin. 2003 Jan; 21(1):183-94.
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  17. Hand JL, Frieden IJ. Vascular birthmarks of infancy: Resolving nosologic confusion. Am J Med Genet. 2002 Apr 1; 108(4):257-64.
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  18. Lindor NM, Hand J, Burch PA, Gibson LE. Birt-Hogg-Dube syndrome: an autosomal dominant disorder with predisposition to cancers of the kidney, fibrofolliculomas, and focal cutaneous mucinosis. Int J Dermatol. 2001 Oct; 40(10):653-6.
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  19. Yiannias JA, el-Azhary RA, Hand JH, Pakzad SY, Rogers RS III. Relevant contact sensitivities in patients with the diagnosis of oral lichen planus. J Am Acad Dermatol. 2000 Feb; 42(2 Pt 1):177-82.
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  20. Hand JL, Michels VV, Marinello MJ, Ketterling RP, Jalal SM. Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation. Prenat Diagn. 2000 Feb; 20(2):144-8; discussion 149-51.
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  21. Khan JH, Ahmed I. A case of relapsing polychondritis involving the tragal and the conchal bowl areas with sparing of the helix and the antihelix. J Am Acad Dermatol. 1999 Aug; 41(2 Pt 2):299-302.
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