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Daniel D Miller

19982019
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Fingerprint The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.

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Skin Medicine & Life Sciences
Skin Diseases Medicine & Life Sciences
Melanoma Medicine & Life Sciences
Stevens-Johnson Syndrome Medicine & Life Sciences
Virus Diseases Medicine & Life Sciences
Biopsy Medicine & Life Sciences
Papillomaviridae Medicine & Life Sciences
Squamous Cell Carcinoma Medicine & Life Sciences

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Projects 2016 2019

Allogeneic skin grafting in the treatment of chronic

Shih, T. L. & Miller, D. D.

WOMEN'S DERMATOLOGIC SOCIETY

7/15/16 → 7/14/19

Project: Research project

Skin Transplantation
Graft vs Host Disease
Skin
Therapeutics

Research Output 1998 2019

9 Citations (Scopus)

Development and Validation of a Risk Prediction Model for In-Hospital Mortality among Patients with Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis - ABCD-10

Noe, M. H., Rosenbach, M., Hubbard, R. A., Mostaghimi, A., Cardones, A. R., Chen, J. K., Cotliar, J., Davis, M. D. P., Dominguez, A., Fox, L. P., Hughey, L. C., Kaffenberger, B. H., Kroshinsky, D., Kwong, B. Y., Miller, D. D., Musiek, A., Ortega-Loayza, A. G., Sharon, V. R., Shinkai, K., Summers, E. M. & 6 others, Wanat, K. A., Wetter, D. A., Worswick, S., Margolis, D. J., Gelfand, J. M. & Micheletti, R. G., Apr 2019, In : JAMA Dermatology. 155, 4, p. 448-454 7 p.

Research output: Contribution to journal › Article

Stevens-Johnson Syndrome
Bicarbonates
Hospital Mortality
Dialysis
Neoplasms

Diagnosis of epidermodysplasia verruciformis: Two cases highlighting the role of direct HPV L1 gene sequencing

Bushara, O., Miller, D. D., Giubellino, A., Schomaker, M., Thyagarajan, B. & Nelson, A. C., Jun 2019, In : Journal of cutaneous pathology. 46, 6, p. 436-441 6 p.

Research output: Contribution to journal › Article

Epidermodysplasia Verruciformis
Genes
Warts
Papillomavirus Infections
Rare Diseases

Diffuse, mottled hyperpigmentation and mutations in LMNA gene in a 5-year-old boy, his mother, and his grandmother: Atypical progeroid syndrome

Schultz, B., Miller, D. D. & Maguiness, S., Nov 1 2019, In : Pediatric Dermatology. 36, 6, p. 913-917 5 p.

Research output: Contribution to journal › Article

Hyperpigmentation
Mothers
Mutation
Lamin Type A
Genes

Fibrous hamartoma of infancy associated with bony remodeling and muscle atrophy

Kozlowski, A., Murati, M., Ogilvie, C., Hess, D., Miller, D. & Hook, K., Sep 1 2019, In : Pediatric Dermatology. 36, 5, p. 677-680 4 p.

Research output: Contribution to journal › Article

Hamartoma
Muscular Atrophy
Fats
Therapeutics

Image Gallery: A case of gadolinium-associated plaques requiring confirmation with mass spectrometry

Olayiwola, O., Ronkainen, S., Miller, D. D., High, W. & Farah, R. S., Mar 2019, In : British Journal of Dermatology. 180, 3, p. e66

Research output: Contribution to journal › Letter

Gadolinium
Mass Spectrometry