Mycophenolate mofetil for severe childhood atopic dermatitis: experience in 14 patients von Heller, M., Shin, H.T., Orlow, S.J., Schaffer, J.V.

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Androgenetic alopecia in the paediatric population: a retrospective review of 57 patients von Gonzalez, M. E., Cantatore-Francis, J., Orlow, S. J.

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Inhibition of the CRAF/prohibitin interaction reverses CRAF-dependent resistance to vemurafenib von Doudican, N A, Orlow, S J

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Increased risk of symptomatic hemangiomas of the airway in association with cutaneous hemangiomas in a “beard” distribution von Orlow, Seth J., Isakoff, Michael S., Blei, Francine

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Ulcerated haemangioma of infancy: a retrospective review of 47 patients von Shin, H.T., Orlow, S.J., Chang, M.W.

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Melanosomes Are Specialized Members of the Lysosomal Lineage of Organelles von Orlow, Seth J.

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Undifferentiated pleomorphic sarcoma in a child with type 1 neurofibromatosis von Patel, R.R., Meehan, S., Orlow, S.J.

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Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome von Przylepa, Kelly A, Paznekas, William, Zhang, Minghuang, Golabi, Mahin, Bias, Wilma, Bamshad, Michael J, Carey, John C, Hall, Bryan D, Stevenson, Roger, Orlow, Seth J, Cohen Jr, M. Michael, Jabs, Ethylin Wang

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A study of large congenital melanocytic nevi and associated malignant melanomas: Review of cases in the New York University registry and the world literature von DeDavid, Maria, Orlow, Seth J., Provost, Nathalie, Marghoob, Ashfaq A., Rao, Babar K., Huang, Carol L., Wasti, Qasim, Kopf, Alfred W., Bart, Robert S.

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Fibroblast growth factor receptor 3 ( FGFR3 ) transmembrane mutation in Crouzon syndrome with acanthosis nigricans von Meyers, Gregory A, Orlow, Seth J, Munro, Ian R, Przylepa, Kelly A, Jabs, Ethylin Wang

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Unilateral cutaneous heterotopic meningeal nodules with neural, smooth muscle and connective tissue hamartomas: a field defect of cephalic neural crest-derived tissues von Hunzeker, C.M., Borys, D., Greco, M.A., Orlow, S.J., Schaffer, J.V.

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High-Molecular-Weight Forms of Tyrosinase and the Tyrosinase-Related Proteins: Evidence for a Melanogenic Complex von Orlow, Seth J, Zhou, Bao-Kang, Drucker, Michael, Pifko-Hirst, Sharon, Chakraborty, Ashok K, Pawelek, John M

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Lines of Blaschko von Bolognia, Jean L., Orlow, Seth J., Glick, Sharon A.

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Neurocutaneous melanosis: Clinical features of large congenital melanocytic nevi in patients with manifest central nervous system melanosis von DeDavid, Maria, Orlow, Seth J, Provost, Nathalie, Marghoob, Ashfaq A, Rao, Babar K, Wasti, Qasim, Huang, Carol L, Kopf, Alfred W, Bart, Robert S

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The pink-eyed dilution locus controls the biogenesis of melanosomes and levels of melanosomal proteins in the eye von ORLOW, S. J, BRILLIANT, M. H

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A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma ( NEMO) von Zonana, Jonathan, Elder, Melissa E., Schneider, Lynda C., Orlow, Seth J., Moss, Celia, Golabi, Mahin, Shapira, Stuart K., Farndon, Peter A., Wara, Diane W., Emmal, Stephanie A., Ferguson, Betsy M.

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Cimetidine therapy for multiple viral warts in children von Orlow, Seth J., Paller, Amy

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Identification of a Melanosomal Membrane Protein Encoded by the Pink-Eyed Dilution (Type II Oculocutaneous Albinism) Gene von Rosemblat, Susana, Durham-Pierre, Donna, Gardner, John M., Nakatsu, Yoshimichi, Brilliant, Murray H., Orlow, Seth J.

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The Pmel 17/silver locus protein. Characterization and investigation of its melanogenic function von Kobayashi, T, Urabe, K, Orlow, S J, Higashi, K, Imokawa, G, Kwon, B.S., Potterf, B, Hearing, V.J.

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Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability von Park, Woo-Jin, Meyers, Gregory A., Li, Xiang, Theda, Christiane, Day, Donald, Oriow, Seth J., Jones, Marilyn C., Jabs, Ethylin Wang

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