The information explosion.

Por Zlotogorski, A, Lenga, S
Publicado em 1990

The use of textbooks in evaluating the impact of medical journals.

Por Zlotogorski, A, Israeli, A
Publicado em 1988

Oxodipine-induced gingival hyperplasia in beagle dogs.

Por Nyska, A., Waner, T., Zlotogorski, A., Pirak, M., Scolnik, M., Nyska, M., Galiano, A.
Publicado em 1990

Epidermolysis bullosa simplex: a keratin 5 mutation is a fully dominant allele in epidermal cytoskeleton function.

Por Stephens, K, Zlotogorski, A, Smith, L, Ehrlich, P, Wijsman, E, Livingston, R J, Sybert, V P
Publicado em 1995

Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic origins.

Por Rogers, G R, Rizzo, W B, Zlotogorski, A, Hashem, N, Lee, M, Compton, J G, Bale, S J
Publicado em 1995

Cutaneous lymphoma in Israel, 1985-1993: a population-based incidence study.

Por Iscovich, J., Paltiel, O., Azizi, E., Kuten, A., Gat, A., Lifzchitz-Mercer, B., Zlotogorski, A., Polliack, A.
Publicado em 1998

Histological and Immunohistochemical Features of the Skin Lesions in CANDLE Syndrome

Por Torrelo, A, Colmenero, I, Requena, L, Paller, A, Ramot, Y, Lee, C-CR, Vera, A, Zlotogorski, A, Goldbach-Mansky, R, Kutzner, H
Publicado no Pediatr Rheumatol Online J (2015)

Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24

Por Martinez-Mir, A, Zlotogorski, A, Londono, D, Gordon, D, Grunn, A, Uribe, E, Horev, L, Ruiz, I, Davalos, N, Alayan, O, Liu, J, Gilliam, T, Salas-Alanis, J, Christiano, A
Publicado em 2003

What causes alopecia areata?

Por McElwee, K. J., Gilhar, A., Tobin, D. J., Ramot, Y., Sundberg, J. P., Nakamura, M., Bertolini, M., Inui, S., Tokura, Y., Jr, L. E. King, Duque-Estrada, B., Tosti, A, Keren, A., Itami, S., Shoenfeld, Y., Zlotogorski, A., Paus, R.
Publicado em 2013

Preliminary response to Janus kinase inhibition with baricitinib in chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperatures (CANDLE)

Por Montealegre, G, Reinhardt, A, Brogan, P, Berkun, Y, Zlotogorski, A, Brown, D, Chira, P, Gao, L, Dare, J, Schalm, S, Merino, R, Chapelle, D, Kim, H, Judd, S, O'Brien, M, De Jesus, A Almeida, Kim, Y, Kost, B, Huang, Y, Paul, S, Brofferio, A, Lee, C-C, Hadigan, C, Heller, T, Minniti, C, Rother, K, Goldbach-Mansky, R
Publicado no Pediatr Rheumatol Online J (2015)

OR13-002 Recessive mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause systemic and cutaneous polyarteritis nodosa (PAN)

Por Levy-Lahad, E, Elkan-Navon, P, Segel, R, Pierce, SB, Walsh, T, Barash, J, Padeh, S, Zlotogorski, A, Berkun, YY, Press, JJ, Mukamel, M, Hashkes, PJ, Harel, LL, Tekin, M, Yalcinkaya, F, Kasapcopur, O, Emirogullari, EF, Lee, MK, Klevit, RE, Renbaum, PF, Weinberg-Shukron, A, Zeligson, S, Marek-Yagel, D, Shohat, M, Singer, A, Pras, E, Rubinow, AA, Anikster, Y, King, M-C
Publicado em 2013